NOVEL COMPOUND FOR INHIBITING NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE AND COMPOSITION CONTAINING SAME

TECHNICAL FIELD

The present invention relates to novel compounds for inhibiting nicotinamide phosphoribosyltransferase (NamPT) and a composition comprising the same and various uses thereof.

BACKGROUND ART

NAD+(nicotinamide adenine dinucleotide) is a coenzyme that plays an important role in many physiologically essential processes (Ziegkel, M. Eur. J. Biochem. 267, 1550-1564, 2000). NAD is essential for several signaling pathways including mono-ADP-ribosylation in both the immune system and G-protein-coupled receptor signaling among other poly ADP-ribosylation in DNA repair, and is also essential for the activity of Sirtuin deacetylase (Garten, A. et al., Trends in Endocrinology and Metabolism, 20, 130-138, 2008).

Nicotinamide phosphoribosyltransferase (NamPT) is an enzyme catalyzing the phosphorylation of nicotinamide and is a rate-limiting enzyme in one of two pathways that restore NAD.

The evidence is increasing that NamPT inhibitors have efficacy as anticancer agents. Cancer cells have a higher basal turnover of NAD and also require higher energy with comparing to normal cells. Furthermore, increased NamPT expression was reported in colorectal cancer (Van Beijnum, J. R. et al., Int. J. Cancer 101, 118-127, 2002), and it has been reported that NamPT is involved in angiogenesis (Kim, S. R. et al., Biochem. Biophys. Res. Commun. 357, 150-156, 2007). Small molecule inhibitors of NamPT cause depletion of intracellular NAD+ levels and ultimately induce tumor cell death (Hansen, C M et al., Anticancer Res. 20, 42111-4220, 2000), as well as inhibit tumor growth in a xenograft model.

Also, NamPT inhibitors have potential as therapeutic agents in inflammatory and metabolic disorders (Galli, M. et al., Cancer Res. 70, 8-11, 2010). For example, NamPT is a predominant enzyme in T and B lymphocytes. In selective inhibition of NamPT, lymphocytes can inhibit the occurrence of autoimmune disease by decreasing NAD+, but cell types with other NAD+ synthesis pathways cannot. The small molecule NamPT inhibitor (FK866) inhibited the proliferation of activated T cells and induced apoptosis and was effective in arthritis animal models (collagen-induced arthritis) (Busso, N. et al., Plos One 3, e2267, 2008). NamPT activity increases NF-kB transcriptional activity in human vascular endothelial cells and induces MMP-2 and MMP-9 activity, suggesting a role for NamPT inhibitors in the prevention of inflammation-mediated complications of obesity and type 2 diabetes (Adya, R. et al., Diabetes Care, 31, 758-760, 2008).

As one of the NamPT inhibitors, (E)-N-[4-(1-benzoylpiperidin-4-yl)butyl]-3-(pyridin-3-yl)-acrylamide (also known as AP0866, FK866, WK175 or WK22.175, hereinafter referred to as ‘FK866’ [international non-trade name]) is known in particular as an anti-cancer agent. FK866 can be used for the treatment of diseases associated with deregulated apoptosis such as cancer. In the prior art, FK866 has been confirmed to hinder the biosynthesis of nicotinamide adenyl dinucleotides (also known as NAD and also referred to hereinafter) without any DNA damage effect and induce apoptotic cell death.

In addition, FK866 induces apoptosis in HepG2 cells without a major effect on cellular energy metabolism (Hasmann M, Schemainda I. FK866, a Highly Specific Noncompetitive Inhibitor of Nicotinamide Phosphoribosyltransferase, Represents a Novel Mechanism for Induction of Tumor Cell Apoptosis. Cancer Res 2003; 63:7436-7442. [PubMed: 14612543]). Instead of causing immediate cytotoxicity, inhibiting NamPT and depleting NAD in cells suggests that FK866 may be an effectively active agent for cancer cells depending on nicotinamide to synthesize NAD. The crystal structure of the NamPT-FK866 complex indicates that the compound binds to the nicotinamide-binding site of NamPT to inhibit its activity. FK866 was tested in a murine neoplastic cell carcinoma model and has been proved to exhibit antitumor, antimetastasis and antiangiogenic activity (Drevs J, et al., Antiangiogenic potency of FK866/K22.175, a new inhibitor of intracellular NAD biosynthesis, in murine renal cell carcinoma. Anticancer Res 2003; 23:4853-4858. [PubMed:14981935]).

A drug inhibiting NamPT may have a number of uses other than inflammatory diseases or cancer as described above. Deficiency of NamPT expression may strongly affect the development of both T and B lymphocytes. In addition, NamPT can affect endothelial cells in association with high glucose level, oxidative stress and aging, and further, NamPT is known to be able to use excess of glucose productively so that human endothelial cells on the process of the proliferation can be endured from aging and high oxidative stress of glucose and the replicative longevity and angiogenic activity are possible.

DISCLOSURE
Technical Problem

It is an object of the present invention to provide a novel compound capable of inhibiting nicotinamide phospholibosyltransferase (NamPT).

Another object of the present invention is to provide a composition capable of preventing, improving or treating NamPT-related diseases, comprising novel compounds capable of inhibiting NamPT.

It is still another object of the present invention to provide a method of preventing, improving or treating NamPT-related diseases by using a novel compound capable of inhibiting NamPT.

However, the technical problem to be solved by the present invention is not limited to the above-mentioned problems, and other problems not mentioned can be clearly understood by those skilled in the art from the following description.

Technical Solution

The inventors of the present invention have found a novel compound capable of inhibiting the activity of nicotinamide phosphoribosyltransferase (hereinafter, referred to as ‘NamPT’) and completed the present invention.

An embodiment of the present invention provides a compound selected from a compound represented by the following Chemical Formula 1, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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wherein X₁and X₂are each independently N or C(R₃);

L₁is a direct bond or C₂-C₄alkenylene group;

R₁and R₂are each independently hydrogen, —(CH₂)m-R₄or —N═C(R₅)(R₆), the R₁and R₂are bonded to each other to form heterocycloalkyl ring having nuclear atoms of 5 to 7, heteroaryl ring having nuclear atoms of 5 to 14, or non-aromatic fused heteropolycyclic ring having nuclear atoms of 5 to 14;

R₃is hydrogen or C₁˜C₆alkyl group;

R₄is -L₂-R₇;

L₂is a direct bond, C₆˜C₁₀arylene group or heteroarylene group having nuclear atoms of 5 to 14;

R₅and R₆can be bonded to each other to form non-aromatic fused heteropolycyclic ring having nuclear atoms of 5 to 14;

R₇is selected from the group consisting of C₁-C₆alkyl group, heterocycloalkyl group having nuclear atoms of 5 to 7, C₆-C₁₄aryl, heteroaryl group having nuclear atoms of 5 to 14, C₅-C₁₄non-aromatic fused polycyclic group, non-aromatic fused hetero polycyclic group having nuclear atoms of 5 to 14, —C(═O)—R₈, —S(═O)(═O)—R₉, —(CH₂)n-N(R₁₀)(R₁₁) and —(CH₂)n-O-(L₃)-(R₁₂);

R₈is selected from the group consisting of C₁-C₆alkyl group, C₁-C₆alkoxy group, C₃-C₇cycloalkoxy group, heterocycloalkyl group having nuclear atoms of 5 to 7, heteroaryl group having nuclear atoms of 5 to 14 and non-aromatic fused hetero polycyclic group having nuclear atoms of 5 to 14;

R₉is heterocycloalkyl having nuclear atoms of 5 to 7;

R₁₀and R₁₁are each independently, hydrogen, C₁˜C₆alkyl group or —C(═O)—R₁₃;

L₃is a direct bond or C₁˜C₄alkylene group;

R₁₂is C₆˜C₁₄aryl group or heteroaryl having nuclear atoms of 5 to 14;

R₁₃is -(L₄)-(R₁₄),

L₄is a direct bond or heteroarylene group having nuclear atoms 5 to 14;

R₁₄is C₆˜C₁₄aryl group or heteroaryl having nuclear atoms 5 to 14;

m and n are each independently integer of 0 to 4;

heterocycloalkyl ring, heteroaryl ring and non-aromatic fused heteropoly ring formed by bonding the R₁and R₂together are each independently unsubstituted or substituted with at least one substituent selected from the group consisting of -(L₅)-(L₆)-(R₁₅) and —NH—C(═O)—R₁₆, and when they are substituted with a plurality of substituents, they are the same as or different from each other;

L₅is a direct bond or C₁˜C₄alkylene group;

L₆is a direct bond or heteroarylene group having nuclear atoms of 5 to 14;

R₁₅is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

R₁₆is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

non-aromatic fused hetero polycyclic ring formed by bonding the R₅and R₆together, is substituted with at least one C₁˜C₆alkyl group or unsubstituted and when it is substituted with a plurality of substituents, they are the same as or different from each other;

the alkyl group, heterocycloalkyl group, aryl group, heteroaryl group, non-aromatic fused polycyclic ring group and non-aromatic fused hetero polycyclic ring group of R₇are each independently unsubstituted or substituted with at least one substituent selected from the group consisting of halogen, nitro group, C₁˜C₆alkyl, C₁˜C₆alkoxy group, C₆˜C₁₄aryl group and heteroaryl group having nuclear atoms of 5 to 14 and when it is substituted with a plurality of substituents, they are the same as or different from each other;

the aryl group and heteroaryl group of R₁₄are each independently unsubstituted or substituted with at least one substituent selected from the group consisting of halogen, C₁˜C₆alkyl and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they are the same as or different from each other;

aryl group and heteroaryl group of the R₁₅and R₁₆are each independently unsubstituted or substituted with at least one substituent selected from the group consisting of C₁˜C₆alkyl and C₁˜C₆haloalkyl and when it is substituted with a plurality of substituents, they are the same as or different from each other.

Another embodiment of the present invention provides a pharmaceutical composition and a pharmaceutical formulation comprising therapeutically effective amount of the compound.

The term ‘halogen’ as used herein, unless otherwise indicated, means fluorine, chlorine, bromine or iodine.

As used herein, the term of ‘C₁˜C₆alkyl’ means a linear or branched hydrocarbon residue having carbon atoms of 1 to 6, unless otherwise specified. Examples thereof include methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, t-butyl, n-pentyl and n-hexyl, etc., but it is not limited thereto.

As used herein, the term of ‘C₁-C₆alkoxy’ means a linear or branched hydrocarbon residue having carbon atoms of 1 to 6, unless otherwise specified, Examples thereof include methoxy, ethoxy, propoxy, isobutoxy, n-butoxy, sec-butoxy, t-butoxy, pentoxy and hexoxy, etc. but it is not limited thereto.

As used herein, the term of ‘C₃˜C₇cycloalkoxy’ means a cyclic hydrocarbon residue having carbon atoms of 3 to 6 linked to oxygen, unless otherwise specified. Examples thereof include cyclopropoxy, cyclobutoxy, cyclopentoxy, cyclohexoxy and cycloheptoxy, etc., but it is not limited.

As used herein, the term of ‘C₃˜C₇cycloalkyl’ means a cyclic hydrocarbon residue having carbon atoms of 3 to 7, unless otherwise specified. Examples thereof include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl, etc., but it is not limited thereto.

As used herein, the term of ‘heterocycloalkyl having nuclear atoms of 5 to 7’ means a 5 to 7 membered cyclic residue containing from one to three optionally selected from N, O, S, SO and SO₂, unless otherwise specified. Examples thereof include tetrahydrofuran-3-yl, tetrahydro-2H-pyran-4-yl, tetrahydro-2H-pyran-3-yl, oxepan-4-yl, oxepan-3-yl, piperadin-1-yl, piperadin-3-yl, piperadin-4-yl, piperazin-1-yl, morpholin-4-yl, thiomorpholin-4-yl, 1,1-dioxido-thiomorpholin-4-yl, pyrrolidin-1-yl, pyrrolidin-3-yl, azepan-1-yl, azepan-3-yl and azepan-4-yl, etc. but it is not limited thereto.

As used herein, the term of ‘C₆˜C₁₄aryl’ means a mono- or poly-cyclic carbocyclic ring system having carbon atoms of 6 to 14 carbon atoms with at least one fused or non-fused aromatic ring, unless otherwise specified and examples of aryl include phenyl, naphthyl, tetrahydronaphthyl, indenyl and anthracenyl, etc., but it is not limited thereto.

As used herein, the term of heteroaryl having nuclear atoms of 5 to 14′ means 5 to 14-membered aromatic group such as monocyclic or bicyclic or more cyclic aromatic group containing at least one, e.g. one to four heteroatoms selected from O, N and S, unless otherwise specified. Examples of monocyclic heteroaryl include thiazolyl, oxazolyl, thiophenyl, furanyl, pyrrolyl, imidazolyl, benzo[d]oxazolyl, isoxazolyl, oxazolopyridinyl, pyrazolyl, triazolyl, thiazolyl, benzo[d]thiazolyl, thiadiazolyl, tetrazolyl, oxadiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, quinolinyl, naphthoxazolyl and groups similar thereto, but it is not limited thereto. Examples of bicyclic heteroaryl include indolyl, benzothiophenyl, benzofuranyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzthiadiazolyl, benztriazolyl, quinolinyl, isoquinolinyl, furinyl, furopyridinyl, carbazolyl, dibenzofuranyl, dibenzothiophenyl and groups similar thereof, but it is not limited thereto.

As used herein, the term of ‘C₅-C₁₄non-aromatic fused polycyclic ring’ means rings in which at least two rings are condensed with each other and contain only carbon atoms having 6 to 14 as ring forming atoms and have non-aromacity in the entire molecule. Examples thereof include fluorenyl, etc., but it is not limited thereto.

As used herein, the term of ‘non-aromatic fused hetero polycyclic rings having nuclear atoms of 5 to 14’ means rings in which at least two rings are condensed with each other and contain at least one, e.g. one to four heteroatom selected from N, O and S, in addition to carbon as ring forming atoms and have non-aromacity in the entire molecule of member of 5 to 14. Examples of the non-aromatic fused heteropolycyclic ring include indolinyl, isoindolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, 2,3-dihydro-1H-benzo [d]imidazolyl, 2,3-dihydrobenzazo[d]oxazolyl, 2,3-dihydrobenzo[d]thiazolyl, 3,3a-dihydropyrazolo[1,5-a]pyrimidinyl, 2,3,3a,7a-tetrahydrobenzo[d]thiazolyl and 2,3,3a,7a-tetrahydro-1H-isoindolyl, etc., but it is not limited thereto.

As used herein, the term of ‘C₂-C₄alkenylene group’ is a divalent residue derived from a hydrogen carbide chain containing at least one carbon-carbon double bond, and the alkenylene group is, for example, alkylene group having carbon atoms of 2 to 4. The alkylene group may be substituted with at least one polymerizable functional group or other substituents, and the hydrocarbon chain may contain a hetero atom such as nitrogen (N) or oxygen (O) in the chain. Examples thereof include ethylenyl, propylenyl and butylenyl, etc., but it is not limited.

As used herein, the term of “fused ring” means a condensed aliphatic ring, a condensed aromatic ring, a condensed heteroaliphatic ring, a condensed heteroaromatic ring, or a combination thereof.

Advantageous Effects

The compound represented by Chemical Formula 1 according to the present invention is excellent effect inhibiting nicotinamide phosphoribosyltransferase (NamPT), and can prevent, improve or treat various diseases associated with NamPT, and further, It can be used particularly useful as a remedy for preventing, improving or treating cancer.

DESCRIPTION OF DRAWINGS

FIG. 1 shows NMR spectrum of N-(4-(6-methylbenzo[d]oxazol-2-yl) benzyl)nicotinamide (A4276) prepared in Synthesis Example 1 according to an example of the present invention.

FIG. 2 shows NMR spectrum of N-(4-(6-chlorobenzo[d]oxazol-2-yl) benzyl)nicotinamide (A4266) prepared in Synthesis Example 2 according to an example of the present invention.

FIG. 3 shows NMR spectrum of N-(4-(6-methylbenzo[d]oxazol-2-yl) benzyl)nicotinamide (A4265) prepared in Synthesis Example 3 according to an example of the present invention.

FIG. 4 shows NMR spectrum of N-(4-(oxazolo[4,5-c]pyridin-2-yl)benzyl)nicotinamide (B1471) prepared in Synthesis Example 4 according to an example of the present invention.

FIG. 5 shows NMR spectrum of N-ethyl-N-(4-(nicotinamidomethyl) benzyl) ethanaminium (Drug 3) prepared in Synthesis Example 33 according to an example of the present invention.

FIG. 6 shows the results measuring the change of absorbance according to the treatment time when the compound (A4276) prepared in Synthesis Example 1 was treated at various concentrations according to an example of the present invention for NamPT in Evaluation Example 1.

FIG. 7 shows the results measuring the change of absorbance according to the treatment time when the compound (A4266) prepared in Synthesis Example 2 was treated at various concentrations according to an example of the present invention for NamPT in Evaluation Example 1.

FIG. 8 shows the results measuring the change of absorbance according to the treatment time when the compound (A4265) prepared in Synthesis Example 3 was treated at various concentrations according to an example of the present invention for NamPT in Evaluation Example 1.

FIG. 9 shows the results measuring the change of absorbance according to the treatment time when the compound (B1471) prepared in Synthesis Example 4 was treated at various concentrations according to an example of the present invention for NamPT in Evaluation Example 1.

FIG. 10 shows the results measuring the change of absorbance according to the treatment time when the compound (FK866) prepared in Comparative Example 1 was treated at various concentrations according to an example of the present invention for NamPT in Evaluation Example 1.

FIG. 11 is a graph showing the change in Vmax/min according to the treatment concentration of the A4276 compound according to the results of FIG. 6 in Evaluation Example 1.

FIG. 12 is a graph showing the change in Vmax/min according to the treatment concentration of the A4266 compound according to the results of FIG. 7 in Evaluation Example 1.

FIG. 13 is a graph showing the change in Vmax/min according to the treatment concentration of the A4265 compound according to the results of FIG. 8 in Evaluation Example 1.

FIG. 14 is a graph showing the change in Vmax/min according to the treatment concentration of the A1471 compound according to the results of FIG. 9 in Evaluation Example 1.

FIG. 15 is a graph showing the change in Vmax/min according to the treatment concentration of the FK866 compound according to the results of FIG. 10 in Evaluation Example 1.

FIG. 16 shows the result of measuring the change in the viability of the cancer cell line according to concentration after treating the compound (A4276) prepared in Synthesis Example 1 at various concentrations according to an example of the present invention for various cancer cell lines in Evaluation Example 2.

FIG. 17 shows the result of measuring the change in the viability of the cancer cell line according to concentration after treating the compound (A4266) prepared in Synthesis Example 2 at various concentrations according to an example of the present invention for various cancer cell lines in Evaluation Example 2.

FIG. 18 shows the result of measuring the change in the viability of the cancer cell line according to concentration after treating the compound (A4265) prepared in Synthesis Example 3 at various concentrations according to an example of the present invention for various cancer cell lines in Evaluation Example 2.

FIG. 19 shows the result of measuring the change in the viability of the cancer cell line according to concentration after treating the compound (B1471) prepared in Synthesis Example 4 at various concentrations according to an example of the present invention for various cancer cell lines in Evaluation Example 2.

FIG. 20 is a graph showing changes in the content of intracellular NAD, ATP and total protein after treatment with 2.5 μM of the compound (B1471) prepared in Synthesis Example 4 according to an example of the present invention for the cancer cell line H322 in Evaluation Example 4.

FIG. 21 shows the result analyzing expression level of NAPRT and NamPT by Western blot analysis using the cell lysate obtained after culturing primary cardiomyocyte, retinal pigment epithelium cell (RPE) and liver cell which are the normal cell line in Evaluation Example 5. FIG. 22 shows the result measuring the change of the cell viability according to the concentration of the compounds (A4276, A4265) prepared in Synthesis Example 1 and 3, respectively and the compound (FK866) of Comparative Example 1 according to an example of the present invention for primary cardiomyocyte in Evaluation Example 5.

FIG. 23 shows the result measuring the change of the cell viability according to the concentration of the compounds (A4276, A4265) prepared in Synthesis Example 1 and 3, respectively and the compound (FK866) of Comparative Example 1 according to an example of the present invention for retinal pigment epithelium cell (RPE) in Evaluation Example 5.

FIG. 24 shows the result measuring the change of the cell viability according to the concentration of the compounds (A4276, A4265) prepared in Synthesis Example 1 and 3, respectively and the compound (FK866) of Comparative Example 1 according to an example of the present invention for liver cell (THLE-2) in Evaluation Example 5.

FIG. 25 shows the result measuring the change of the cell viability according to the concentration of the compounds (B1471, B1468, B1477) prepared in Synthesis Example 4, 8 and 13, respectively and the compound (FK866, GNE617) of Comparative Example 1 and 2 according to an example of the present invention for liver cell (THLE-2) in Evaluation Example 6.

FIG. 26 shows the result measuring the change of the cell viability according to the concentration of the compounds (B1471, B1468, B1477) prepared in Synthesis Example 4, 8 and 13, respectively and the compound (FK866, GNE617) of Comparative Example 1 and 2 according to an example of the present invention for liver cell (THLE-3) in Evaluation Example 6.

BEST MODE

Hereinafter, the present invention will be described in detail.

An aspect of the present invention provides a compound selected from a compound represented by following Chemical Formula 1, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 1,

wherein X₁and X₂are each independently N or C(R₃);

L₁is a direct bond or C₂-C₄alkenylene group;

R₃is hydrogen or C₁-C₆alkyl;

R₄is -L₂-R₇;

L₂is a direct bond, C₆˜C₁₀arylene group or heteroarylene group having nuclear atoms of 5 to 14;

R₅and R₆can be bonded to each other to form non-aromatic fused heteropolycyclic ring having nuclear atoms of 5 to 14;

R₉is heterocycloalkyl having nuclear atoms of 5 to 7;

R₁₀and R₁₁are each independently, hydrogen, C₁˜C₆alkyl or —C(═O)—R₁₃,

L₃is a direct bond or C₁˜C₄alkylene group;

R₁₂is C₆˜C₁₄aryl group or heteroaryl having nuclear atoms of 5 to 14;

R₁₃is -(L₄)-(R₁₄),

L₄is a direct bond or heteroarylene group having nuclear atoms 5 to 14;

R₁₄is C₆˜C₁₄aryl group or heteroaryl having nuclear atoms 5 to 14;

m and n are each independently integer of 0 to 4;

L₅is a direct bond or C₁˜C₄alkylene group;

L₆is a direct bond or heteroarylene group having nuclear atoms of 5 to 14;

R₁₅is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

R₁₆is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

non-aromatic fused hetero polycyclic ring formed by bonding the R₅and R₆together, is substituted with at least one C₁˜C₆alkyl or unsubstituted and when it is substituted with a plurality of substituents, they are the same as or different from each other;

Hereinafter, the present invention will be described in detail.

The present invention relates to a novel compound having a specific inhibitory activity against nicotinamide phosphoribosyltransferase (hereinafter referred to as ‘NamPT’), a pharmaceutically acceptable salt thereof, an optical isomer, a hydrate and a solvate thereof, and a pharmaceutical composition for preventing or treating various diseases related to NamPT, comprising the same.

Specially, an aspect of the present invention provides a compound selected from a compound represented by following Chemical Formula 1, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 1,

X₁and X₂are each independently N or C(R₃);

L₁is a direct bond or C₂-C₄alkenylene group;

R₃is hydrogen or C₁-C₆alkyl;

R₄is -L₂-R₇;

L₂is a direct bond, C₆˜C₁₀arylene group or heteroarylene group having nuclear atoms of 5 to 14;

R₅and R₆can be bonded to each other to form non-aromatic fused heteropolycyclic ring having nuclear atoms of 5 to 14;

R₉is heterocycloalkyl having nuclear atoms of 5 to 7;

R₁₀and R₁₁are each independently, hydrogen, C₁˜C₆alkyl or —C(═O)—R₁₃;

L₃is a direct bond or C₁˜C₄alkylene group;

R₁₂is C₆˜C₁₄aryl group or heteroaryl having nuclear atoms of 5 to 14;

R₁₃is -(L₄)-(R₁₄);

L₄is a direct bond or heteroarylene group having nuclear atoms 5 to 14;

R₁₄is C₆˜C₁₄aryl group or heteroaryl having nuclear atoms 5 to 14;

m and n are each independently an integer of 0 to 4;

L₅is a direct bond or C₁˜C₄alkylene group;

L₆is a direct bond or heteroarylene group having nuclear atoms of 5 to 14;

R₁₅is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

R₁₆is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

An aspect of the present invention provides a compound selected from a compound represented by following Chemical Formula 2, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 2,

p is an integer of 0 to 3;

L₆is a direct bond, oxo group(*—C(═O)—*), or sulfonyl group(*—S(═O)(═O)—*);

R₁₇is heterocycloalkyl group having nuclear atoms of 5 to 7, heteroaryl group having nuclear atoms of 5 to 14, —O—(CH₂)q-R₁₈or —(CH₂)r-N(R₁₉)(R₂₀);

R₁₈is hydrogen, C₁˜C₆alkyl group, C₃˜C₇cycloalkyl or heteroaryl group having nuclear atoms of 5 to 14;

R₁₉and R₂₀are each independently hydrogen or C₁˜C₆alkyl group;

q and r are each independently an integer of 0 to 2;

the heterocycloalkyl group and heteroaryl group of R₁₇and the alkyl group cycloalkyl group and heteroaryl group of R₁₈are each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, nitro group, C₁˜C₆alkyl, C₁˜C₆alkoxy group, C₆˜C₁₄aryl group and heteroaryl group having nuclear atoms of 5 to 14;

X₁, X₂and L₁are each as defined in claim 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the X₁may be N and X₂may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 2, both X₁and X₂may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the L₁may be a direct bond or C₂-C₃alkenylene group and more preferably a direct bond.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the p may be an integer of 0 to 2 and more preferably an integer of 0 or 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the q may be an integer of 0 or 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, heterocycloalkyl and heteroaryl group of the R₁₇may be each independently unsubstituted or substituted with at least one substituent selected from the group consisting of halogen, nitro group, C₁˜C₆alkyl group, C₁˜C₆alkoxy group and C₆˜C₁₄aryl group.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be substituent represented by the following Chemical Formula 3:

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in the Chemical Formula 3,

* is a bonding site;

Y₁is O or S;

Y₂is N or C(R₂₁);

Z₁to Z₄are each independently N or C(R₂₂);

R₂₁is hydrogen or C₁˜C₆alkyl group;

in case that R₂₂is plural, they are the same or different from each other, and selected from the group consisting of hydrogen, halogen, nitro group, C₁˜C₆alkyl, C₁˜C₆alkoxy group, C₆˜C₁₄aryl group and heteroaryl group having nuclear atoms of 5 to 14 or in case that R₂₂is plural, R₂₂adjacent to each other can form fused ring by bonding with each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 3, the Y₁may be 0 and Y₂may be N or C(R₂₁) and more preferably the Y₁may be O and the Y₂may be N.

According to one preferred embodiment of the present invention, in the Chemical Formula 3, the Y₁may be S and the Y₂may be N.

According to one preferred embodiment of the present invention, in the Chemical Formula 3, the Z₁to Z₄may be all C(R₂₂), and a plurality of R₂₂may be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 3, at least one of the Z₁to Z₄is N and the others are C(R₂₂), and a plurality of R₂₂may be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 3, any one of the Z₁to Z₄is N and the others are C(R₂₂), and a plurality of R₂₂may be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 3, at least one of the Z₁to Z₄is C(R₂₂) and a plurality of R₂₂may be the same as or different from each other.

According to one preferred embodiment of the present invention, the Chemical Formula 3 may be represented by any one of the following Chemical Formulas a1 to a8, but it is not limited thereto:

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in Chemical Formula a1 to a8,

* is a bonding site;

o is an integer of 0 to 2;

R₂₃can be selected from the group consisting of halogen, nitro group, C₁˜C₆alkyl, C₁˜C₆alkoxy group, C₆˜C₁₄aryl group and heteroaryl group having nuclear atoms of 5 to 14, in case that the R₂₃is plural, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula a1 to a8, the o may be an integer of 0 or 1.

According to a preferred embodiment of the present invention, in Chemical Formula 2, R₁₇may be a substituent represented by the following Chemical Formula 4:

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the Chemical Formula 4,

* is a bonding site;

Y₃is O or S,

R₂₄may be hydrogen, C₁˜C₆alkyl group or C₆˜C₁₄aryl group.

According to one preferred embodiment of the present invention, in the Chemical Formula 4, the Y₃may be S.

According to one preferred embodiment of the present invention, in the Chemical Formula 4, the R₂₄may be hydrogen or C₁˜C₆alkyl group.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be —(CH₂)r-N(R₁₉)(R₂₀), wherein the r may be an integer of 0 to 2, R₁₉and R₂₀may be each independently hydrogen or C₁˜C₆alkyl group.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be —(CH₂)r-N(R₁₉)(R₂₀), wherein the r may be 0 or 1, R₁₉and R₂₀may be each independently C₁˜C₆alkyl group.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be heterocycloalkyl group having nuclear atoms of 5 to 7, and more preferably piperidinyl, piperazinyl, morpholinyl or thiomorpholinyl.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be heteroaryl group having nuclear atoms of 5 to 6, and heteroaryl group of the R₁₇may be unsubstituted or substituted with at least one C₁˜C₆alkyl group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be pyrrolyl, imidazolyl or triazolyl, and the pyrrolyl, imidazolyl or triazolyl of the R₁₇may be each independently unsubstituted substituted with at least one C₁-C₆alkyl group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be —O—(CH₂)q-R₁₈.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be —O—(CH₂)q-R₁₈, q may be an integer of 0 to 2, and R₁₈may be heteroaryl group having nuclear atoms of 5 to 14.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the R₁₇may be —O—(CH₂)q-R₁₈, q may be an integer of 1 or 2, and R₁₈may be pyridinyl, pyrimidinyl or triazinyl.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the L₆may be oxo group, the R₁₇may be —O—(CH₂)q-R₁₈or heteroaryl group having nuclear atoms of 5 to 14, and more preferably the L₆may be oxo group, the R₁₇may be C₁˜C₆alkoxy group, C₃˜C₆cycloalkoxy group or heteroaryl group having nuclear atoms 5 to 10.

According to one preferred embodiment of the present invention, in the Chemical Formula 2, the L₆may be sulfonyl group, the R₁₇may be heterocycloalkyl having nuclear atoms 5 to 7, and more preferably the L₆may be sulfonyl group and the R₁₇may be piperidinyl, piperazinyl, morpholinyl or thiomorpholinyl.

According to a preferred embodiment of the present invention, the compound may be selected from a compound represented by the following Chemical Formula 5, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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the Chemical Formula 5,

X₁, X₂, R₃, p, L₆and R₁₇are each as defined in the Chemical Formula 2.

According to one preferred embodiment of the present invention, in the Chemical Formula 5, X₁and X₂are each independently N or C(R₃),

R₃is hydrogen or C₁˜C₆alkyl group;

p, L₆and R₁₇are each as defined in the Chemical Formula 2.

According to an embodiment of the present invention, in the Chemical Formula 1, the R₁and R₂are bonded with each other to form heterocycloalkyl ring having nuclear atoms of 5 to 7 or non-aromatic fused heteropolycyclic ring having nuclear atoms of 5 to 14, and heterocycloalkyl ring and non-aromatic fused hetero polycyclic ring formed by bonding with the R₁and R₂are each independently unsubstituted or substituted by -(L₅)-(L₆)-(R₁₅) or —NH—C(═O)—R₁₆, and the L₅, L₆, R₁₅and R₁₆are each as defined in the Chemical Formula 1.

According to one preferred embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 6, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 6,

X₁, X₂, L₅, L₆and R₁₅are each as defined in the Chemical Formula 1.

According to a preferred embodiment of the present invention, in the Chemical Formula 6, one of the X₁and X₂may be N and the other may be C(R₃), and more preferably X₁may be N, and X₂may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 6, the L₅may be C₁˜C₄alkylene group, more preferably C₁˜C₃alkylene group.

According to one preferred embodiment of the present invention, in the Chemical Formula 6, the L₆may be heteroarylene group having nuclear atoms of 5 to 14, more preferably heteroarylene group having nuclear atoms 5 to 10.

According to one preferred embodiment of the present invention, in the Chemical Formula, the L₆may be thiazolyl, oxazolyl or thiophenyl, and more preferably thiazolyl, but it is not limited thereto.

According to one preferred embodiment of the present invention, in the Chemical Formula 6, the R₁₅may be heteroaryl group having nuclear atoms of 5 to 14, and more preferably heteroaryl group having nuclear atoms of 5 to 10.

According to one preferred embodiment of the present invention, in the Chemical Formula 6, the R₁₅may be thiophenyl, furanyl or pyrrolyl, and more preferably furanyl, but it is not limited thereto.

According to one preferred embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 7, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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the Chemical Formula 7,

X₁, X₂, L₅, L₆and R₁₅are each as defined in the Chemical Formula 1.

According to one preferred embodiment of the present invention, in Chemical Formula 7, one of the X₁and X₂may be N and the other may be C(R₃), more preferably X1 may be N and X₂may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 7, at least one of the L₅and L₆may be a direct bond, and preferably L₅and L₆may all be a direct bond.

According to one preferred embodiment of the present invention, in the Chemical Formula 7, the R₁₅may be heteroaryl group having nuclear atoms of 5 to 14, heteroaryl group of the R₁₅may be unsubstituted or substituted by at least one substituents selected from the group consisting of C₁˜C₆alkyl group and C₁˜C₆haloalkyl, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 7, the R₁₅may be indolizinyl, pyrazolopyrimidinyl, pyrrolopyrimidinyl or pyrazolopyridinyl, and more preferably may be pyrazolopyrimidinyl, but it is not limited thereto.

According to one preferred embodiment of the present invention, the compound may be selected from a compound represented by the following Chemical Formula 8, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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the Chemical Formula 8,

X₁, X₂and R₁₆are each as defined in the Chemical Formula 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 8, one of the X₁and X₂may be N and the other may be C(R₃), more preferably X₁may be N and X₂may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 8, the R₁₆may be C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14, more preferably phenyl group, a pyridinyl group, a pyrimidinyl group or a triazinyl group, but it is limited thereto.

According to one preferred embodiment of the present invention, the Chemical Formula 8, the R₁₆may be heteroaryl group having nuclear atoms of 5 to 14, more preferably pyridinyl group, a pyrimidinyl group or a triazinyl group, but it is not limited thereto.

According to an embodiment of the present invention, in Chemical Formula 1, the R₁may be hydrogen, the R₂may be —(CH₂)m-R₄.

According to one preferred embodiment of the present invention, in the Chemical Formula 1, the R₁may be hydrogen, and the R₂may be —(CH₂)m-R₄;

the m is an integer of 0 to 4, more preferably an integer of 0 to 3;

the R₄is -L₂-R₇;

L₂is a direct bond;

R₇may be C₅˜C₁₄non-aromatic fused polycyclic group or non-aromatic fused hetero polycyclic group having nuclear atoms of 5 to 14.

According to one preferred embodiment of the present invention, in the Chemical Formula 1, the R₂may be indolinyl, isoindolinyl, tetrahydroquinolinyl or tetrahydroisoquinolinyl, and more preferably indolinyl, but it is not limited thereto.

According to one preferred embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 9, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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the Chemical Formula 9,

s and t are each independently an integer of 0 to 4;

X₁and X₂are each as defined in the Chemical Formula 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 9, one of the X₁and X₂may be N, and the other may be C(R₃), and more preferably X₁may be N and X₂may be C(R₃).

According to an embodiment of the present invention, in the Chemical Formula 1, the R₁may be hydrogen and the R₂may be —N═C(R₅)(R₆).

According to one preferred embodiment of the present invention, in the Chemical Formula 1, R₁may be hydrogen and R₂may be —N═C(R₅)(R₆);

the R₅and R₆are bonded with each other to form non-aromatic fused hetero polycyclic ring having nuclear atoms of 5 to 10; and

non-aromatic fused hetero polycyclic ring formed by bonding with R₅and R₆to each other is unsubstituted or substituted by at least one C₁˜C₆alkyl group, and when it is with a plurality of substituents which are the same as or different to each other.

According to one preferred embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 10, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 10,

Y₄is N(R₂₇), O or S;

R₂₅and R₂₇are each independently hydrogen, C₁˜C₆alkyl group or C₆˜C₁₄aryl group;

u is an integer of 0 to 2;

R₂₆is C₁˜C₆alkyl group or C₆˜C₁₄aryl group, when the R₂₆is plural, they can be the same as or different from to each other;

X₁and X₂are each as defined in claim 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 10, the Y₄may be O or S and more preferably S.

According to one preferred embodiment of the present invention, in the Chemical Formula 10, the R₂₅may be hydrogen or C₁˜C₆alkyl group.

According to an embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 11, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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the Chemical Formula 11,

v is an integer of 0 to 4;

L₇is a direct bond or heteroarylene group having nuclear atoms of 5 to 14;

R₂₈is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

aryl group and heteroaryl group of the R₂₈are each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl and C₁˜C₆alkoxy group, when they are substituted by a plurality of substituents which are the same as or different to each other;

X₁, X₂and L₁are each as defined in claim 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 11, one of the X₁and X₂may be N and the other may be C(R₃), and more preferably X₁may be N and X₂may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 11, the L₁may be a direct bond.

According to one preferred embodiment of the present invention, in the Chemical Formula 11, the v may be an integer of 0 to 3, more preferably an integer of 1 or 2.

According to one preferred embodiment of the present invention, in the Chemical Formula 11, the L₇may be a direct bond or selected from the group consisting of furanyl group, isoxazolyl group, oxazolyl group and an oxadiazolyl group, and more preferably oxadiazolyl group.

According to the preferred embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 12, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 12,

v, L₇and R₂₈are each as defined in the Chemical Formula 11.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the v may be an integer of 0 to 3, more preferably an integer of 1 or 2.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the R₂₈may be selected from the group consisting of phenyl group, pyridinyl group, pyrimidinyl group, triazinyl group, naphthalenyl group, pyrrolyl group, furanyl group, thiophenyl group, quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group, phthalazinyl group, indenyl group, benzimidazolyl group, benzoxazolyl group, benzothiazolyl group, indolyl group, benzofuranyl group and benzothiophenyl group,

phenyl group, pyridinyl group, pyrimidinyl group, triazinyl group, naphthalenyl group, pyrrolyl group, furanyl group, thiophenyl group, quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group, phthalazinyl group, indenyl group, benzimidazolyl group, benzoxazolyl group, benzothiazolyl group, indolyl group, benzofuranyl group and benzothiophenyl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the L₇is a direct bond, the R₂₈is heteroaryl group having nuclear atoms of 5 to 14, heteroaryl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the L₇is a direct bond, the R₂₈may be selected from the group consisting of naphthalenyl group, quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group, phthalazinyl group, indenyl group, benzimidazolyl group, benzoxazolyl group, benzothiazolyl group, indolyl group, benzofuranyl group and benzothiophenyl group, and the naphthalenyl group, quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group, phthalazinyl group, indenyl group, benzimidazolyl group, benzoxazolyl group, benzothiazolyl group, indolyl group, benzofuranyl group and benzothiophenyl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the L₇is a direct bond, the R₂₈may be selected from the group consisting of quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group, phthalazinyl group, benzimidazolyl group, benzoxazolyl group and benzothiazolyl group, and the quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group, phthalazinyl group, benzimidazolyl group, benzoxazolyl group and benzothiazolyl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the L₇is heteroarylene group having nuclear atoms of 5 to 14, the R₂₈is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14, the aryl group and heteroaryl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the L₇is selected from the group consisting of furanyl group, isoxazolyl group, oxazolyl group and oxadiazolyl group, the R₂₈is C₆˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14, the aryl group and heteroaryl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 12, the L₇is selected from the group consisting of furanyl group, isoxazolyl group, oxazolyl group and oxadiazolyl group, the R₂₈is selected from the group consisting of phenyl group, naphthalenyl group, pyrrolyl group, furanyl group, thiophenyl group, quinolinyl group and isoquinolinyl group, and the phenyl group, naphthalenyl group, pyrrolyl group, furanyl group, thiophenyl group, quinolinyl group and isoquinolinyl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 13, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 13,

v and R₂₈may be each as defined in the Chemical Formula 11.

According to one preferred embodiment of the present invention, in the Chemical Formula 13, the v may be an integer of 0 to 3, more preferably an integer of 1 or 2.

According to one preferred embodiment of the present invention, in the Chemical Formula 13, the R₂₈is C₆-˜C₁₀aryl group or heteroaryl group having nuclear atoms of 5 to 10,

the R₂₈aryl group and heteroaryl group may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, in the Chemical Formula 13, the R₂₈may be selected from the group consisting of phenyl group, naphthalenyl group, pyrrolyl group, furanyl group, thiophenyl group, quinolinyl group and isoquinolinyl group,

the phenyl group, naphthalenyl group, pyrrolyl group, furanyl group, thiophenyl group, quinolinyl group and isoquinolinyl group of the R₂₈may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of halogen, C₁˜C₆alkyl group and C₁˜C₆alkoxy group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to an embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 14, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 14,

R₂₉is C₁-˜C₆alkyl group;

X₁and X₂are each as defined in the Chemical Formula 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 14, one of the X₁and X₂may be N, and the other may be C(R₃), and more preferably X₂may be N and X₁may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 14, the X₁and X₂are all C(R₃), and at this time, the R₃may be hydrogen or C₁˜C₆alkyl group.

According to an embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 15, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 15,

L₈is heteroarylene group having nuclear atoms of 5 to 14;

R₃₀is C₆-˜C₁₄aryl group or heteroaryl group having nuclear atoms of 5 to 14;

the aryl group and heteroaryl group of the R₃₀are each independently unsubstituted or substituted by at least one substituents selected from the group consisting of C₁˜C₆alkyl group, when it is substituted with a plurality of substituents and they are the same as or different from each other;

X₁, X₂and L₁are each as defined in claim 1.

According to one preferred embodiment of the present invention, in the Chemical Formula 15, one of X₁and X₂may be N, the other may be C(R₃), and more preferably X₁may be N and X₂may be C(R₃).

According to one preferred embodiment of the present invention, in the Chemical Formula 15, L₁may be a direct bond.

According to one preferred embodiment of the present invention, the Chemical Formula 15 may be a linker represented by the following Chemical Formula 16:

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in the Chemical Formula 16,

* is a bonding site;

Y₅is O or S;

Z₅is N or C(R₃₁);

R₃₁is hydrogen or C₁˜C₆alkyl group.

According to one preferred embodiment of the present invention, in the Chemical Formula 15, the R₃₀may be selected from the group consisting of phenyl group, pyridinyl group, pyrimidinyl group, triazinyl group, naphthalenyl group, quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group and phthalazinyl group,

the phenyl group, pyridinyl group, pyrimidinyl group, triazinyl group, naphthalenyl group, quinolinyl group, isoquinolinyl group, cinnolinyl group, quinazolinyl group and phthalazinyl group of the R₃₀may be each independently unsubstituted or substituted by at least one substituents selected from the group consisting of C₁˜C₆alkyl group, and when it is substituted with a plurality of substituents, they can be the same as or different from each other.

According to one preferred embodiment of the present invention, the compound may be selected from a compound represented by following Chemical Formula 17, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof:

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in the Chemical Formula 17,

Y₅is O or S;

Z₅is N or C(R₃₂);

w is an integer of 0 to 3;

R₃₁is C₁˜C₆alkyl group, when the R₃₁is a plural, they are same as or different to each other;

R₃₂is hydrogen or C₁˜C₆alkyl group.

An embodiment of the present invention may be methyl 4-(2-(imidazo[1,2-a]pyridine-6-carboxamido)ethyl)benzoate represented by the following Chemical Formula 18:

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Preferred examples of the compound according to the present invention include, but are not limited to:

1) N-(4-(benzo[d]oxazol-2-yl)benzyl)nicotinamide;
2) N-(4-(6-methylbenzo[d]oxazol-2-yl)benzyl)nicotinamide;
3) N-(4-(6-methylbenzo[d]oxazol-2-yl)benzyl)benzamide;
4) N-(4-(5-methylbenzo[d]oxazol-2-yl)benzyl)nicotinamide;
5) N-(4-(5-ethylbenzo[d]oxazol-2-yl)benzyl)nicotinamide;
6) N-(4-(6-ethylbenzo[d]oxazol-2-yl)benzyl)nicotinamide;
7) N-(4-(5-isopropylbenzo[d]oxazol-2-yl)benzyl)nicotinamide;
8) N-(4-(6-(tert-butyl)benzo[d]oxazol-2-yl)benzyl)nicotinamide;
9) N-(4-(5-methoxybenzo[d]oxazol-2-yl)benzyl)nicotinamide;
10) N-(4-(6-chlorobenzo[d]oxazol-2-yl)benzyl)nicotinamide;
11) N-(4-(6-nitrobenzo[d]oxazol-2-yl)benzyl)nicotinamide;
12) N-(4-(5-phenylbenzo[d]oxazol-2-yl)benzyl)nicotinamide;
13) N-(4-(naphtho[2,3-d]oxazol-2-yl)benzyl)nicotinamide;
14) N-(4-(oxazolo[5,4-b]pyridin-2-yl)benzyl)nicotinamide;
15) N-(4-(oxazolo[4,5-c]pyridin-2-yl)benzyl)nicotinamide;
16) N-(4-(oxazolo[4,5-b]pyridin-2-yl)benzyl)nicotinamide;
17) N-(4-(benzo[d]thiazol-2-yl)benzyl)nicotinamide;
18) N-(4-(5-isopropylbenzo[d]oxazol-2-yl)phenyl)nicotinamide;
19) methyl 4-(nicotinamido)benzoate;
20) isopropyl 4-(nicotinamido)benzoate;
20) cyclohexyl 4-(nicotinamido)benzoate;
21) N-(4-(benzofuran-2-carbonyl)phenyl)nicotinamide;
22) N-(4-(piperidin-1-ylsulfonyl)benzyl)nicotinamide;
23) N-(4-(morpholinosulfonyl)benzyl)nicotinamide;
24) N-(4-([1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)phenyl)nicotinamide;
25) N-(4-(3-methyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)phenyl)nicotinamide;
26) N-(4-(3-ethyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)phenyl)nicotinamide;
27) N-(4-([1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)benzyl)nicotinamide;
28) N-(4-(3-methyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)benzyl)nicotinamide;
29) N-(4-(3-ethyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-yl)benzyl)nicotinamide;
30) N-(4-((diethylamino)methyl)benzyl)nicotinamide;
31) N-(4-(piperidin-1-yl)benzyl)nicotinamide;
32) N-(4-(2-methyl-1H-imidazol-1-yl)benzyl)nicotinamide;
33) N-(4-(pyridin-2-ylmethoxy)benzyl)nicotinamide;
34) N-ethyl-N-(4-(nicotinamidomethyl)benzyl)ethanaminium;
35) (E)-N-(3-(indolin-1-yl)propyl)-3-(pyridin-3-yl)acrylamide;
36) (2E, N′Z)—N′-(3-methylbenzo[d]thiazol-2(3H)-ylidene)-3-(pyridin-3-yl)acrylohydrazide;
37) (E)-1-(44(2-(furan-2-yl)thiazol-4-yl)methyl)piperazin-1-yl)-3-(pyridin-3-yl)prop-2-en-1-one;
38) (E)-N-(2-(3-(pyridin-3-yl)acryloyl)-1,2,3,4-tetrahydroisoquinolin-7-yl)isonicotinamide;
39) (S, E)-1-(3-(5-isopropyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-2-yl)pyrrolidin-1-yl)-3-(pyridin-3-yl)prop-2-en-1-one;
40) N-(2-(nicotinamido)ethyl)-3-(p-tolyl)-1,2,4-oxadiazole-5-carboxamide;
41) 3-(4-chlorophenyl)-N-(2-(nicotinamido)ethyl)-1,2,4-oxadiazole-5-carboxamide;
42) N-(2-(nicotinamido)ethyl)-3-(thiophen-2-yl)-1,2,4-oxadiazole-5-carboxamide;
43) 3-(4-methoxyphenyl)-N-(2-(nicotinamido)ethyl)-1,2,4-oxadiazole-5-carboxamide;
44) N-(2-(nicotinamido)ethyl)quinoline-7-carboxamide;
45) N-(2-(nicotinamido)ethyl)isoquinoline-3-carboxamide;
46) N-(2-(nicotinamido)ethyl)quinoline-3-carboxamide;
47) N-methylisonicotinamide;
48) N,4-dimethylbenzamide;
49) N-(2-(3,4-dimethylphenyl)benzo[d]oxazol-5-yl)nicotinamide;
50) methyl 4-(2-(imidazo[1,2-a]pyridine-6-carboxamido)ethyl)benzoate;
51) N-(2-(nicotinamido)ethyl)quinoline-2-carboxamide; and
52) N-(2-(nicotinamido)ethyl)benzo[d]thiazole-2-carboxamide.

In the present invention, the compounds represented by Chemical Formula 1 and Chemical Formula 18 can be prepared by the following Reaction Scheme 1, but are not limited thereto:

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In the Reaction Scheme 1, X₁, X₂, L₁, R₁and R₂are each as defined in the Chemical Formula 1.

As a specific example, a compound represented by Chemical Formula 1 are synthesized by dissolving an acid represented by the Chemical Formula 19 and an amine compound represented by the Chemical Formula 20 in a solvent such as DMF (dimethylformamide) in the presence of EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride), HOBt (1-hydroxybenzotriazole monohydrate) and DIPEA (N,N-diisopropylethylamine) and refluxing for 12 to 36 hours.

Also, in the present invention, the compounds represented by Chemical Formula 2 can be prepared by the following Reaction Scheme 2, but are not limited thereto:

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In the Reaction Scheme 2, X₁, X₂, L₁, L₆, p and R₁₇are each as defined in the Chemical Formula 2.

As a specific example, a compound represented by Chemical Formula 2 are synthesized by dissolving an acid represented by the Chemical Formula 21 and an amine compound represented by the Chemical Formula 22 in a solvent such as DMF (dimethylformamide) in the presence of EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride), HOBt (1-hydroxybenzotriazole monohydrate) and DIPEA (N,N-diisopropylethylamine) and refluxing for 12 to 36 hours.

In the present invention, the compound represented by Chemical Formula 1 or Chemical Formula 18 can prevent, improve or treat the NamPT-related diseases by effectively inhibiting the activity of nicotinamide phospholibosyl transferase (NamPT).

In the present invention, the NamPT-related diseases are at least one selected from the group consisting of cancer, viral infection, human immunodeficiency virus, hepatitis virus, herpes virus, herpes simplex, inflammatory disorder, irritable bowel syndrome, inflammatory bowel disease, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, osteoarthritis, osteoporosis, dermatitis, atopic dermatitis, psoriasis, systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, graft-versus-host disease, Alzheimer's disease, cerebrovascular accident, atherosclerosis, diabetes, glomerulonephritis, and metabolic syndrome, and preferably, it may be a cancer.

In the present invention, the cancer is at least on selected from the group consisting of liver cancer, biliary cancer, gallbladder cancer, esophageal cancer, gastric cancer, ovarian cancer, breast cancer, uterine cancer, colon cancer, rectal cancer, cervical cancer, prostate cancer, skin cancer, pancreatic cancer, leukemia, lymphoma, Hodgkin's disease, lung cancer, bronchial cancer, multiple myeloma, lymphoma, squamous cell cancer, kidney cancer, urethral cancer, bladder cancer, head and neck cancer, brain cancer and central nervous system cancer, preferably it may be lung cancer or gastric cancer.

The present invention also provides a pharmaceutically acceptable salt of a compound represented by the Chemical Formula 1 or Chemical Formula 18. Pharmaceutically acceptable salts should be low in toxicity to humans and should not adversely affect the biological activity and physicochemical properties of the parent compound. Pharmaceutically acceptable salts include, pharmaceutically acceptable free acids and acid addition salts of basic compounds of Chemical Formula 1, but are not limited thereto.

Preferred salts of the compounds according to the invention include salts with inorganic or organic acids. The inorganic acid may be hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, perchloric acid, bromic acid, etc. Also, the organic acid may be acetic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, fumaric acid, maleic acid, malonic acid, phthalic acid, succinic acid, lactic acid, citric acid, citric acid, gluconic acid, tartaric acid, salicylic acid, malic acid, oxalic acid, benzoic acid, embonic acid, aspartic acid, glutamic acid, etc. Organic bases that can be used in the production of organic base addition salts include tris(hydroxymethyl)methylamine, dicyclohexylamine, and the like. Amino acids that can be used in the production of amino acid addition salts are natural amino acids such as alanine and glycine, etc. It will be apparent to those skilled in the art that other acid or base other than the exemplified inorganic acids, organic acids, organic bases and amino acids may be used.

The salt may be prepared by conventional methods. For example, the salt may be prepared by dissolving the compound of the Chemical Formula 1 or the Chemical Formula 18 in a solvent which can be mixed with water, such as methanol, ethanol, acetone, or 1,4-dioxane, and then adding free acid or free base followed by crystallizing.

Meanwhile, the compounds according to the present invention may have an asymmetric carbon center, and thus may be R or S isomers or racemic compounds, and all these optical isomers and mixtures may be included in the scope of the present invention.

In addition, the hydrate or solvate forms of the compounds of Chemical Formula 1 may be included within the scope of the present invention.

The present invention provides a pharmaceutical composition comprising a compound selected from the compounds represented by Chemical Formula 1 or Chemical Formula 18, a pharmaceutically acceptable salt thereof, an optical isomer, a hydrate and a solvate, as an active ingredient.

In the pharmaceutical composition according to the present invention, the compound represented by Chemical Formula 1 or Chemical Formula 18 can prevent, improve or treat the NamPT-related diseases by effectively inhibiting the activity of nicotinamide phospholibosyl transferase (NamPT).

The pharmaceutical composition of the present invention can provide a synergistic effect to NamPT inhibition by further comprising a compound represented by the following Chemical Formula 23:

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in the Chemical Formula 23,

Y₆is hydrogen or halogen;

Y₇is hydrogen or hydroxyl group (—OH).

According to one preferred embodiment of the present invention, in the Chemical Formula 23, Y₆may be hydrogen and Y₇may be hydroxyl group.

According to one preferred embodiment of the present invention, in the Chemical Formula 23, Y₆may be halogen and Y₇may be hydrogen.

According to one preferred embodiment of the present invention, the pharmaceutical composition of the present invention may comprise a compound represented by Chemical Formula 1 and the Chemical Formula 23.

According to one preferred embodiment of the present invention, the pharmaceutical composition according to the present invention comprises a compound represented by the Chemical Formula 14 and further comprises a compound represented by the Chemical Formula 23. In the Chemical Formula 14, the X₂may be N, the X₁may be C(H), the R₂₉may be C₁-C₃alkyl group and in the Chemical Formula 23, the Y₆may be hydrogen and the Y₇may be hydroxyl group.

According to one preferred embodiment of the present invention, the pharmaceutical composition according to the present invention comprises a compound represented by the Chemical Formula 14 and further comprises a compound represented by the Chemical Formula 23. In the Chemical Formula 14, the X₂may be C(R₃), the X₁may be C(H), the R₃and the R₂₉may be each independently C₁-C₃alkyl group and in the Chemical Formula 23, the Y₆may be hydrogen and the Y₇may be hydroxyl group.

According to one preferred embodiment of the present invention, the pharmaceutical composition according to the present invention comprises at least one compound selected from N-methylisonicotinamide, N,4-dimethylbenzamide, 4-chloro-2-(iminoethyl)phenol and 4-(iminoethyl)benzene-1,3-diol.

According to one preferred embodiment of the present invention, the pharmaceutical composition according to the present invention comprises at least one from N-methyl isonicotinamide and N,4-dimethylbenzamide, and further comprises at least one from 4-chloro-2-(iminoethyl)phenol and 4-(iminoethyl)benzene-1,3-diol.

According to one preferred embodiment of the present invention, the pharmaceutical composition according to the present invention comprises N-methyl isonicotinamide, and further comprises at least one from 4-chloro-2-(iminoethyl) phenol and 4-(iminoethyl)benzene-1,3-diol.

According to one preferred embodiment of the present invention, the pharmaceutical composition according to the present invention comprises N,4-dimethylbenzamide, and further may comprise at least one from 4-chloro-2-(iminoethyl)phenol and 4-(iminoethyl)benzene-1,3-diol, and more preferably 4-(iminoethyl)benzene-1,3-diol.

According to one preferred embodiment of the present invention, the pharmaceutical composition of the present invention may contain the compound represented by the Chemical Formula 14 and the compound represented by the Chemical Formula 23 in a weight ratio of 1:100 to 100:1, more preferably in a weight ratio of 40:60 to 60:40. In the present invention, when the two compounds are included beyond the weight ratio, the NamPT inhibitory effect may be significantly lowered.

In the present invention, “treatment” and “improvement” can include, without limitation, any action to improve or conducive to a NamPT related disease using a pharmaceutical composition.

In the present invention, “prevention” can include, without limitation, any action to block the symptoms or to suppress or delay the symptoms of NamPT related disease using a pharmaceutical composition.

The pharmaceutical composition of the present invention can be administered in combination with other anticancer drugs, thereby further enhancing the effect of radiation therapy on cancer stem cells.

Herein, the anticancer agents include at least one selected from the group consisting of nitrogen mustard, imatinib, oxaliplatin, rituximab, erlotinib, neratinib, lapatinib, gefitinib, vandetanib, nilotinib, semaxanib, bosutinib, axitinib, cediranib, lestaurtinib, trastuzumab, gefitinib, bortezomib, sunitinib, carboplatin, sorafenib, bevacizumab, cisplatin, cetuximab, Viscum album, asparaginase, tretinoin, hydroxycarbamide, dasatinib, estramustine, gemtuzumab ozogamicin, ibritumomab tiuxetan, heptaplatin, methyl aminolevulinic acid, amsacrine, alemtuzumab, procarbazine, alprostadil, holmium nitrate chitosan, gemcitabine, doxifluridine, pemetrexed, tegafur, capecitabine, gimeracil, oteracil, azacitidine, methotrexate, uracil, cytarabine, fluorouracil, fludarabine, enocitabine, flutamide, decitabine, mercaptopurine, thioguanine, cladribine, carmofur, raltitrexed, docetaxel, paclitaxel, irinotecan, belotecan, topotecan, vinorelbine, etoposide, vincristine, vinblastine, teniposide, doxorubicin, idarubicin, epirubicin, mitoxantrone, mitomycin, bleomycin, daunorubicin, dactinomycin, pirarubicin, aclarubicin, peplomycin, temozolomide, busulfan, ifosfamide, cyclophosphamide, melphalan, altretamine, dacarbazine, thiotepa, nimustine, chlorambucil, mitolactol, leucovorin, tretinoin, exemestane, aminogluthetimide, anagrelide, olaparib, navelbine, fadrozole, tamoxifen, toremifene, testolactone, anastrozole, letrozole, vorozole, bicalutamide, lomustine, vorinostat, entinostat and carmustine, but it is not limited thereto.

According to the present invention, the pharmaceutical composition may be in the form of capsules, tablets, granules, injections, ointments, powders or beverages, and the pharmaceutical composition may be targeted to humans.

The pharmaceutical composition of the present invention is not limited to, but may be used as a formulation in the form of an oral preparation such as powders, granules, capsules, tablets, aqueous suspensions, etc., an external preparation, a suppository and a sterilized injection solution. The pharmaceutical composition of the present invention may include a pharmaceutically acceptable carrier. The pharmaceutically acceptable carrier may be a binder, a lubricant, a disintegrant, an excipient, a solubilizing agent, a dispersing agent, a stabilizer, a suspending agent, a pigment, a perfume or the like for oral administration and a buffer, a preservative, an analgesic agent, a solubilizer, an isotonic agent, a stabilizer and the like may be mixed and used for injections, and a base, an excipient, a lubricant, a preservative and the like may be used for topical administration. Formulations of the pharmaceutical compositions of the present invention may be prepared in a variety of ways by mixing with a pharmaceutically acceptable carrier as described above. For example, it can be prepared in the form of tablets, troches, capsules, elixirs, suspensions, syrups, wafers and the like in the case of oral administration. Injections may be prepared in the form of unit dosage ampoules or multiple doses. It may be formulated as other solutions, suspensions, tablets, capsules, sustained-release preparations and the like.

Meanwhile, Examples of carriers, excipients and diluents suitable for formulation include lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, malditol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methylcellulose, microcrystalline cellulose, polyvinylpyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate or mineral oil, etc. Further, it may further include fillers, anti-coagulants, lubricants, wetting agents, perfumes, emulsifiers, preservatives and the like.

The route of administration of the pharmaceutical compositions according to the present invention may be, but is not limited to, oral, intravenous, intramuscular, intraarterial, intramedullary, intradural, intracardiac, transdermal, subcutaneous, intraperitoneal, intranasal, intestinal, topical, sublingual or rectal. Oral or parenteral administration is preferred.

In the present invention, “parenteral” includes subcutaneous, intradermal, intravenous, intramuscular, intraarticular, intrasynovial, intrasternal, intradural, intralesional and intracranial injection or infusion techniques. The pharmaceutical compositions of the present invention may also be administered in the form of suppositories for rectal administration.

The pharmaceutical composition of the present invention may be changed according to various factors including the activity of the used specific compound, age, body weight, general health, sex, diet, time of administration, route of administration, rate of excretion, drug formulation and severity of specific diseases to be prevented or treated, and the dosage of the pharmaceutical composition varies depending on the condition of the patient, the body weight, the degree of disease, the type of drug, the route of administration, and the period of time, but may be suitably selected by those skilled in the art and is preferably from 0.0001 to 50 mg/kg or 0.001 to 50 mg/kg per a day. The administration may be carried out once a day or divided into several times. The dosage amount is not intended to limit the scope of the invention in any way. The pharmaceutical composition according to the present invention can be formulated into pills, sugar-coated tablets, capsules, solutions, gels, syrups, slurries, suspensions.

The pharmaceutical composition of the present invention can be used alone or in combination with methods using surgery, radiotherapy, hormone therapy, chemotherapy and biological response modifiers.

The present invention provides a food composition comprising a compound selected from a compound represented by the Chemical Formula 1 or the Chemical Formula 18, a pharmaceutically acceptable salt thereof, an optical isomer, a hydrate and a solvate thereof, as an active ingredient.

According to food composition of the present invention, the compound represented by Chemical Formula 1 or Chemical Formula 18 can prevent or improve the NamPT-related diseases by effectively inhibiting the activity of nicotinamide phospholibosyl transferase (NamPT).

The food composition of the present invention can provide a synergistic effect to NamPT inhibition by further comprising a compound represented by the Chemical Formula 23.

However, description regarding the compound represented by Chemical Formula 23 is the same as that of the pharmaceutical composition, and details thereof will be omitted below.

The food composition of the present invention may be manufactured in the form of various foods such as beverage, gum, tea, vitamin complex, powder, granule, tablet, capsule, snack, rice cakes, bread and the like. Since the food composition of the present invention is composed of a plant extract having little toxicity and side effects, it can be safely used for long-term use for prophylactic purposes.

When the compound of the present invention is contained in the food composition, the amount thereof may be added 0.1 to 50% of the total weight.

Here, when the food composition is prepared in a beverage form, there are no particular limitations other than containing the food composition in the indicated ratios, and may contain various flavors or natural carbohydrates as an additional ingredient such as general beverages. Namely, as natural carbohydrates, monosaccharide such as glucose, etc., disaccharides such as fructose, etc. and polysaccharides such as sucrose, etc., and typical sugar such as dextrin and cyclodextrin, etc. and sugar alcohols such as xylitol, sorbitol and erythritol, etc. can be included. Examples of the flavoring agents include natural flavoring agents (thaumatin and stevia extract (e.g. rebaudioside A and glycyrrhizin, etc.) and synthetic flavorings (e.g. saccharin and aspartame, etc.) and the like.

In addition, the food composition of the present invention can contain various nutrients, vitamins, minerals (electrolytes), a flavoring agent such as synthetic flavoring agents and natural flavoring agents, coloring agents, pectic acid and its salts, alginic acid and its salts, organic acid, protective colloid thickener, a pH adjusting agent, a stabilizer, a preservative, a glycerin, an alcohol, a carbonating agent used in a carbonated drink, and the like.

These ingredients can be used independently or in combination. The proportion of such additives is not so critical, but is generally selected in the range of 0.1 to about 50 parts by weight per 100 parts by weight of the composition of the present invention.

The present invention provides a cosmetic composition comprising a compound selected from a compound represented by Chemical Formula 1 or Chemical Formula 18, a pharmaceutically acceptable salt thereof, an optical isomer, a hydrate and a solvate, as an active ingredient.

In the cosmetic composition according to the present invention, the compound represented by Chemical Formula 1 or Chemical Formula 18 can prevent or improve the NamPT-related diseases by effectively inhibiting the activity of nicotinamide phospholibosyl transferase (NamPT).

In the present invention, the NamPT related diseases may be dermatitis, atopic dermatitis or psoriasis.

The cosmetic composition of the present invention can provide a synergistic effect to NamPT inhibition by further comprising a compound represented by the Chemical Formula 23.

However, description regarding the compound represented by Chemical Formula 23 is the same as that of the pharmaceutical composition, and details thereof will be omitted below.

The cosmetic composition according to the present invention can be prepared in the form of toner, nutrition lotion, nutrition essence, massage cream, cosmetic bath additives, body lotion, body milk, bath oil, baby oil, baby powder, shower gel, shower cream, sunscreen lotion, sunscreen cream, suntan cream, skin lotion, skin cream, UV protection cosmetic, cleansing milk, hair loss treatment agent (cosmetic), face and body lotion, face and body cream, skin whitening cream, hand lotion, hair lotion, cosmetic cream, jasmine oil, bath soap, water soap, beauty soap, shampoo, hand cleaner, medicinal soap (non-medical), cream soap, facial wash, body cleansing agent, scalp detergent, hair conditioner, cosmetic soap, tooth whitening gel, toothpaste, and the like. For this, the composition of the present invention may further comprise a solvent commonly used in the production of a cosmetic composition, or a suitable carrier, excipient or diluent.

The type of the solvent that can be further added to the cosmetic composition of the present invention is not particularly limited and for example, water, saline, DMSO or a combination thereof can be used. Examples of the carrier, excipient or diluent include purified water, oil, wax, fatty acids, fatty alcohols, fatty acid esters, surfactants, humectants, thickeners, antioxidants, viscosity stabilizers, chelating agents, buffers, and lower alcohols, etc., but they are not limited thereto. In addition, it may contain a whitening agent, a moisturizer, a vitamin, an ultraviolet screening agent, a perfume, a dye, an antibiotic, an antibacterial agent and an antifungal agent, if necessary.

As the oil, hydrogenated vegetable oil, castor oil, cottonseed oil, olive oil, palm oil, jojoba oil and avocado oil may be used and examples of the wax include beewax, spermaceti wax, carnauba, candelilla, montan, ceresin, liquid paraffin, lanolin.

As the fatty acid, stearic acid, linoleic acid, linolenic acid and oleic acid may be used. As the fatty acid alcohol, cetyl alcohol, octyldodecanol, oleyl alcohol, panthenol, lanolin alcohol, stearyl alcohol and hexadecanol may be used. As the fatty acid ester, isopropyl myristate, isopropyl palmitate and butyl stearate may be used. As the surfactant, cationic surfactants, anionic surfactants and nonionic surfactants known in the art can be used, and as far as possible, surfactants derived from natural materials are preferable.

In addition, a moisture absorbent, a thickener, an antioxidant and the like widely known in the field of cosmetics can be included, and the kind and amount thereof are well known in the art.

The present invention also relates to a method of preventing or treating NamPT-related diseases comprising a step of administering a compound selected from a compound of the Chemical Formula 1 or Chemical Formula 18 of the present invention, a pharmaceutically acceptable salt, an optical isomer, a hydrate and a solvate thereof, to a subject in need of administration (e.g. humans) in a pharmaceutically effective amount.

The “administration” in the present invention means providing a certain compound of the present invention to a subject in any suitable manner.

The “subject” in which the administration is required in the present invention may include both mammals and non-mammals. Here, examples of the mammals include humans, non-human primates such as chimpanzees, and other apes and monkey species; livestock animals such as cattle, horses, sheep, goats, pigs; breeding animals such as rabbits, dogs and cats; laboratory animals such as rodents, e.g. rats, mice and guinea pigs, and the like, but it is not limited thereto. Also, examples of non-mammals in the present invention include birds and fishes, and the like, but it is not limited thereto.

The formulation of the compound to be administered as described above is not particularly limited and may be administered in the form of a solid form, a liquid formulation or an aerosol formulation for aspiration and a solid form preparation intended to be converted to a liquid form preparation for oral or parenteral administration immediately prior to use, for example, oral formulation such as powders, granules, capsules, tablets, aqueous suspensions, etc., and formulation in the form of external preparations, suppositories and sterile injectable solutions, but it is not limited thereto.

In addition, in the administration of the present invention, a pharmaceutically acceptable carrier may be further administered together with the compound of the present invention. Here, the pharmaceutically acceptable carrier may be a binder, a lubricant, a disintegrant, an excipient, a solubilizing agent, a dispersing agent, a stabilizer, a suspending agent, a pigment, a perfume or the like for oral administration and a buffer, a preservative, an analgesic agent, a solubilizer, an isotonic agent, a stabilizer and the like may be mixed and used for injections, and a base, an excipient, a lubricant, a preservative and the like may be used for topical administration. Formulations of the compound of the present invention may be prepared in a variety of ways by mixing with a pharmaceutically acceptable carrier as described above. For example, it can be prepared in the form of tablets, troches, capsules, elixirs, suspensions, syrups, wafers and the like in the case of oral administration. Injections may be prepared in the form of unit dosage ampoules or multiple doses. It may be formulated as other solutions, suspensions, tablets, capsules, sustained-release preparations and the like.

In the present invention, “pharmaceutically effective amount” refers to a sufficient amount of an agent to provide a desired biological result. The results may be indicative of a disease, a reduction and/or mitigation in symptoms or causes, or any other desired change in the biological system. For example, “effective amount” for therapeutic use is the amount of a compound disclosed the present invention that is required to provide clinically significant reduction in disease. Appropriate “effective” amounts in any individual case may be determined by one of ordinary skill in the art using routine experiment. Thus, the expression of “effective amount” generally refers to the amount that the active substance has a therapeutic effect. In the present invention, the active substance is an inhibitor of the formation of nicotinamide phosphoribosyl transferase (NAMPT).

The compound of the present invention may be changed according to various factors including the activity of the used specific compound, age, body weight, general health, sex, diet, time of administration, route of administration, rate of excretion, drug formulation and severity of specific diseases to be prevented or treated, and the dosage of the compound varies depending on the condition of the patient, the body weight, the degree of disease, the type of drug, the route of administration, and the period of time, but may be suitably selected by those skilled in the art and is preferably from 0.0001 to 50 mg/kg or 0.001 to 50 mg/kg per a day. The administration may be carried out once a day or divided into several times. The dosage amount is not intended to limit the scope of the invention in any way. The pharmaceutical composition according to the present invention can be formulated into pills, sugar-coated tablets, capsules, solutions, gels, syrups, slurries, suspensions.

The compound of the present invention can be used alone or in combination with methods using surgery, radiotherapy, hormone therapy, chemotherapy and biological response modifiers.

Hereinafter, the present invention will be described in more detail based on the following Synthesis Example and Example, but the present invention is not limited thereto.

EXAMPLE
[Preparation Example 1] Preparation of Intermediate 1((4-(6-methylbenzo[d]oxazol-2-yl)phenyl)methanamine)

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4-(Aminomethyl)benzoic acid (1.99 mmol) and 6-amino-m-cresol (1.99 mmol) were dissolved in polyphosphoric acid (PPA, excess) and refluxed at 200° C. for 12 hours. The reactant was dissolved in an excess of distilled water and precipitated salt was filtered, vacuum dried and used in the next step without further purification.

[Preparation Example 2] Preparation of Intermediate 2((4-(6-chlorobenzo[d]oxazol-2-yl)phenyl)methanamine)

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4-(Aminomethyl)benzoic acid (1.32 mmol) and 2-amino-5-chlorophenol (1.32 mmol) were dissolved in polyphosphoric acid (PPA, excess) and refluxed at 200° C. for 12 hours. The reactant was dissolved in an excess of distilled water and precipitated salt was filtered, vacuum dried and used in the next step without further purification.

[Preparation Example 3] Preparation of Intermediate 3(4-(naphtho[2,3-d]oxazol-2-yl)phenyl)methanamine)

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4-(Aminomethyl)benzoic acid (1.32 mmol) and 3-amino-2-naphthol (1.32 mmol) were dissolved in polyphosphoric acid (PPA, excess) and refluxed at 200° C. for 12 hours. The reactant was dissolved in an excess of distilled water and precipitated salt was filtered, vacuum dried and used in the next step without further purification.

[Synthesis Example 1] Preparation of N-(4-(6-methylbenzo[d]oxazol-2-yl)benzyl)nicotinamide

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Nicotinic acid (1.06 mmol), (4-(6-methylbenzo[d]oxazol-2-yl)phenyl)methanamine prepared in the Preparation Example 1 (1.06 mmol), EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 2.11 mmol), HOBt (1-hydroxybenzotriazole monohydrate, 2.11 mmol) and DIPEA (N,N-diisopropylethylamine, 3.17 mmol) were dissolved in DMF (dimethylformamide, 4 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was treated with dichloromethane (MC) and hexane (HX) to obtain a white solid. NMR spectrum of N-(4-(6-methylbenzo[d]oxazol-2-yl)benzyl)nicotinamide (hereinafter referred to as “A4276”) prepared as described above is shown in FIG. 1.

¹H NMR (400 MHz, DMSO-d₆): δ 9.36 (t, J=5.6 Hz, 1H), 9.09 (d, J=1.2 Hz, 1H), 8.74 (dd, J=4.6, 1.3 Hz, 1H), 8.27 (d, J=8.0 Hz, 1H), 8.16 (d, J=8.2 Hz, 2H), 7.67 (d, J=8.1 Hz, 1H), 7.62-7.51 (m, 4H), 7.23 (d, J=8.0 Hz, 1H), 4.62 (d, J=5.7 Hz, 2H), 2.47 (s, 3H).

[Synthesis Example 2] Preparation of N-(4-(6-chlorobenzo[d]oxazol-2-yl)benzyl)nicotinamide

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Nicotinic acid (0.77 mmol), (4-(6-chlorobenzo[d]oxazol-2-yl)phenyl)methanamine prepared in the Preparation Example 2 (0.77 mmol), EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 1.54 mmol), HOBt (1-hydroxybenzotriazole monohydrate, 1.54 mmol) and DIPEA (N,N-diisopropylethylamine, 2.31 mmol) were dissolved in DMF (dimethylformamide, 4 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was treated with dichloromethane (MC) and hexane (HX) to obtain a white solid (hereinafter referred to as “A4266”). NMR spectrum of N-(4-(6-chlorobenzo[d]oxazol-2-yl)benzyl)nicotinamide prepared as described above is shown in FIG. 2.

¹H NMR (400 MHz, DMSO-d₆): δ 9.37 (t, J=5.6 Hz, 1H), 9.09 (s, 1H), 8.74 (d, J=4.0 Hz, 1H), 8.27 (d, J=7.9 Hz, 1H), 8.17 (d, J=8.1 Hz, 2H), 8.00 (d, J=1.3 Hz, 1H), 7.82 (d, J=8.5 Hz, 1H), 7.62-7.51 (m, 3H), 7.47 (d, J=8.5 Hz, 1H), 4.62 (d, J=5.6 Hz, 2H).

[Synthesis Example 3] Preparation of N-(4-(naphtho[2,3-d]oxazol-2-yl)benzyl)nicotinamide

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Nicotinic acid (0.73 mmol), (4-(naphtho[2,3-d]oxazol-2-yl)phenyl)methanamine prepared in the Preparation Example 2 (0.73 mmol), EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 1.46 mmol), HOBt (1-hydroxybenzotriazole monohydrate, 1.46 mmol) and DIPEA (N,N-diisopropylethylamine, 2.19 mmol) were dissolved in DMF (dimethylformamide, 4 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was treated with dichloromethane (MC) and hexane (HX) to obtain a white solid (hereinafter referred to as “A4265”). NMR spectrum of N-(4-(naphtho[2,3-d]oxazol-2-yl)benzyl)nicotinamide prepared as described above is shown in FIG. 3.

¹H NMR (400 MHz, DMSO-d₆): δ 9.39 (t, J=5.5 Hz, 1H), 9.10 (s, 1H), 8.75 (d, J=3.4 Hz, 1H), 8.34 (s, 1H), 8.31-8.24 (m, 4H), 8.09 (t, J=8.6 Hz, 2H), 7.62 (d, J=8.1 Hz, 2H), 7.58-7.49 (m, 3H), 4.65 (d, J=5.5 Hz, 2H).

[Synthesis Example 4] Preparation of N-(4-(oxazolo[4,5-c]pyridin-2-yl)benzyl)nicotinamide

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Nicotinic acid (2.44 mmol), (4-(naphtho[2,3-d]oxazol-2-yl)phenyl)methanamine (2.44 mmol), EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 4.87 mmol), HOBt (1-hydroxybenzotriazole monohydrate, 4.87 mmol) and DIPEA (N,N-diisopropylethylamine, 7.31 mmol) were dissolved in DMF (dimethylformamide, 10 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was treated with dichloromethane (MC) and hexane (HX) to obtain a white solid (hereinafter referred to as “B1471”). NMR spectrum of N-(4-(oxazolo[4,5-c]pyridin-2-yl)benzyl)nicotinamide prepared as described above is shown in FIG. 4.

¹H NMR (400 MHz, DMSO-d₆): δ 9.39 (t, 1H, J=5.8 Hz), 9.14-9.08 (m, 2H), 8.74 (dd, 1H, J=4.8, 1.5 Hz), 8.60 (d, 1H, J=5.5 Hz), 8.29-8.25 (m, 1H), 8.22 (d, 2H, J=8.3 Hz), 7.91 (dd, 1H, J=5.5, 0.7 Hz), 7.61 (d, 2H, J=8.3 Hz), 7.55 (dd, 1H, J=7.9, 4.9 Hz), 4.63 (d, 2H, J=5.8 Hz).

Synthesis Example 5 to 33

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According to the above Reaction Scheme 3, acid (2.44 mmol) and amine (2.44 mmol) of the following Table 1, EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 4.87 mmol), HOBt (1-Hydroxybenzotriazole monohydrate, 4.87 mmol) and DIPEA (N,N-diisopropylethylamine, 7.31 mmol) were dissolved in DMF (dimethylformamide, 10 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was purified by flash column chromatography (5% methanol in dichloromethane) and dried in a vacuum pump to produce the final compound shown in Table 2 below.

TABLE 1

Synthesis

Example
acid
Amine

Synthesis Example 5

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Synthesis Example 6

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Synthesis Example 7

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Synthesis Example 8

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Synthesis Example 9

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Synthesis Example 10

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Synthesis Example 11

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Synthesis Example 12

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Synthesis Example 13

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Synthesis Example 14

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Synthesis Example 15

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Synthesis Example 16

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Synthesis Example 17

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Synthesis Example 18

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Synthesis Example 19

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Synthesis Example 20

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Synthesis Example 21

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Synthesis Example 22

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Synthesis Example 23

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Synthesis Example 24

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Synthesis Example 25

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Synthesis Example 26

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Synthesis Example 27

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Synthesis Example 28

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Synthesis Example 29

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Synthesis Example 30

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Synthesis Example 31

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Synthesis Example 32

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TABLE 2

Synthesis
Compound

Example
name
Final Compound

Synthesis Example 5
B1380

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Synthesis Example 6
B1416

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Synthesis Example 7
B1423

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Synthesis Example 8
B1468

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Synthesis Example 9
B1469

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Synthesis Example 10
B1470

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Synthesis Example 11
B1472

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Synthesis Example 12
B1474

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Synthesis Example 13
B1477

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Synthesis Example 14
B1479

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Synthesis Example 15
B1484

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Synthesis Example 16
B1485

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Synthesis Example 17
B1523

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Synthesis Example 18
B1531

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Synthesis Example 19
B1716

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Synthesis Example 20
B1856

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Synthesis Example 21
B1857

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Synthesis Example 22
B1863

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Synthesis Example 23
B1866

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Synthesis Example 24
B1872

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Synthesis Example 25
B1873

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Synthesis Example 26
B1963

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Synthesis Example 27
B1967

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Synthesis Example 28
B1977

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Synthesis Example 29
B1978

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Synthesis Example 30
B1979

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Synthesis Example 31
B1981

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Synthesis Example 32
B1982

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[Synthesis Example 33] Preparation of N-(4-(5-ethylbenzo[d]oxazol-2-yl)benzyl)nicotinamide

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Nicotinic acid (2.44 mmol), (4-(5-ethylbenzo[d]oxazol-2-yl)phenyl)methanamine (2.44 mmol), EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 4.87 mmol), HOBt (1-hydroxybenzotriazole monohydrate, 4.87 mmol) and DIPEA (N,N-diisopropylethylamine, 7.31 mmol) were dissolved in DMF (dimethylformamide, 10 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was purified by flash column chromatography (5% methanol in dichloromethane) and then dried in a vacuum pump to prepare a final compound (hereinafter referred to as “Drug 3”). NMR spectrum of N-(4-(5-ethylbenzo[d]oxazol-2-yl)benzyl)nicotinamide prepared as described above is shown in FIG. 5.

Synthesis Example 34 to 39

According to the above Reaction Scheme 3, acid (2.44 mmol) and amine (2.44 mmol) of the following Table 3, EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 4.87 mmol), HOBt (1-Hydroxybenzotriazole monohydrate, 4.87 mmol) and DIPEA (N,N-diisopropylethylamine, 7.31 mmol) were dissolved in DMF (dimethylformamide, 10 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was purified by flash column chromatography (5% methanol in dichloromethane) and dried in a vacuum pump to produce the final compound shown in Table 4 below.

TABLE 3

Synthesis

Example
Acid
Amine

Synthesis Example 34

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Synthesis Example 35

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Synthesis Example 36

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Synthesis Example 37

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Synthesis Example 38

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Synthesis Example 39

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TABLE 4

Synthesis
Compound

¹H NMR spectrum

Example
name
Final Compound
(400 MHz, DMSO-d6):

Synthesis Example 34
A4261

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δ 9.35 (t, J = 5.3 Hz, 1H), 9.05 (s, 1H), 8.70 (d, J = 1.5 Hz, 2H), 8.29 (d, J = 8.7 Hz, 1H), 8.25- 8.17 (m, 3H), 7.97 (d, J = 8.8 Hz, 1H), 7.58 (d, J = 7.9 Hz, 2H), 7.50 (dd, J = 7.2, 5.0 Hz,

1H), 4.60 (d, J =

5.4 Hz, 2H)

Synthesis Example 35
A4262

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δ 9.33 (t, J = 5.5 Hz, 1H), 9.06 (s, 1H), 8.70 (d, J = 3.3 Hz, 1H), 8.23 (d, J = 7.9 Hz, 1H), 8.17 (d, J = 8.1 Hz, 2H), 8.02 (s, 1H), 7.82 (d, J = 8.5 Hz, 1H), 7.73- 7.64 (m, 3H),

7.55 (d, J = 8.0

Hz, 2H), 7.53-

7.41 (m, 3H),

7.35 (t, J = 7.3

Hz, 1H), 4.59

(d, J = 5.5 Hz,

2H)

Synthesis Example 36
A4263

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δ 9.32 (t, J = 5.3 Hz, 1H), 9.05 (s, 1H), 8.70 (d, J = 3.4 Hz, 1H), 8.23 (d, J = 7.9 Hz, 1H), 8.12 (d, J = 8.0 Hz, 2H), 7.74 (s, 1H), 7.66 (d, J = 8.4 Hz, 1H), 7.51 (dd, J = 15.4, 7.9 Hz, 3H), 7.43 (d, J = 8.2

Hz, 1H), 4.57

(d, J = 5.5 Hz,

2H), 1.32 (s,

9H)

Synthesis Example 37
A4275

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δ 9.36 (t, J = 5.5 Hz, 1H), 9.09 (s, 1H), 8.76-8.73 (m, 1H), 8.27 (d, J = 7.9 Hz, 1H), 8.17 (d, J = 8.1 Hz, 2H), 7.65 (d, J = 8.3 Hz, 1H), 7.61- 7.51 (m, 4H),

7.24 (d, J = 8.2

Hz, 1H), 4.62

(d, J = 5.6 Hz,

2H), 2.45 (s,

3H)

Synthesis Example 38
A4302

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δ 9.36-9.28 (s, 1H), 9.05 (s, 1H), 8.70 (s, 1H), 8.23 (d, J = 7.9 Hz, 1H), 8.12 (d, J = 7.8 Hz, 2H), 7.65 (d, J = 8.0 Hz, 1H), 7.59 (s, 1H), 7.56- 7.48 (m, 3H),

7.22 (d, J = 8.1

Hz, 1H), 4.57

(d, J = 5.0 Hz,

2H), 2.72 (q, J =

7.4 Hz, 2H),

1.21 (t, J = 7.4

Hz, 3H)

Synthesis Example 39
A4303

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δ 9.13 (t, J = 5.5 Hz, 1H), 8.11 (d, J = 8.0 Hz, 2H), 7.89 (d, J = 7.4 Hz, 2H), 7.62 (d, J = 8.1 Hz, 1H), 7.58-7.42 (m, 5H), 7.19 (d, J = 8.0 Hz, 1H), 4.55 (d, J = 5.7 Hz, 2H), 2.43 (s, 2H)

Synthesis Example 40 to 43

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According to the Reaction Scheme 4, (E)-3-(pyridin-3-yl)acrylic acid (2.44 mmol), amine (2.44 mmol) of the following Table 5, EDC (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 4.87 mmol), HOBt (1-hydroxybenzotriazole monohydrate, 4.87 mmol) and DIPEA (N,N-diisopropylethylamine, 7.31 mmol) were dissolved in DMF (dimethylformamide, 10 ml) and refluxed overnight at room temperature. Thereafter, the reaction mixture was transferred to a separate funnel, followed by the addition of an aqueous solution of NH₄Cl and three extractions with EA (ethyl acetate). The extract was dried with Na₂SO₄and concentrated under reduced pressure. The reaction residue was purified by flash column chromatography (5% methanol in dichloromethane) and then dried in a vacuum pump to prepare the final compound shown in Table 6 below.

TABLE 5

Synthesis Example
Amine

Synthesis Example 40

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Synthesis Example 41

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Synthesis Example 42

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Synthesis Example 43

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TABLE 6

Synthesis

Example
Compound name
Final Compound

Synthesis Example 40
B1964

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Synthesis Example 41
B1975

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Synthesis Example 42
B1976

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Synthesis Example 43
B1983

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[Synthesis Example 44] Preparation of B1386

N-methyl isonicotinamide and 4-(iminomethyl)benzene-1,3-diol represented by the following Chemical Formulae were mixed at a weight ratio of 1:1.

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[Synthesis Example 45] Preparation of B1387

N-methyl isonicotinamide and 4-chloro-2-(iminomethyl) phenol represented by the following Chemical Formulae were mixed at a weight ratio of 1:1.

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[Synthesis Example 46] Preparation of B1467

N,4-dimethylbenzamide and 4-(iminomethyl)benzene-1,3-diol represented by the following Chemical Formulae were mixed at a weight ratio of 1:1.

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[Comparative Example 1] Preparation of N-[4-(1-benzoyl-4-piperidinyl) butyl]-3-(3-pyridinyl)-2E-propenamide

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For comparison of the following effects with the compounds of the present invention, N-[4-(1-benzoyl-4-piperidinyl) butyl]-3-(3-pyridinyl)-2E-propenamide (hereinafter referred to as “FK866”) which is represented by the above Chemical Formula and known as the NamPT inhibitor was prepared.

[Comparative Example 2] Preparation of N-(4-((3,5-difluorophenyl)sulfonyl)benzyl)imidazo[1,2-a]pyridine-6-carboxamide

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[Evaluation Example 1] NamPT Inhibitory Efficacy Evaluation

The effect of the compound prepared in the Synthesis Example 1 to 4 and the FK866 of the Comparative Example 1 on the substrate degradation rate by NAMPT enzyme (Vmax/min) was tested. First, in the step of synthesizing nicotinamide into NAD, the NamPT recombinant protein and the substrates PRPP and nicotinamide were added to the compounds of Synthesis Example 1 to 4 (A4276, A4266, A4265 and B1471) and the compound of Comparative Example 1 at various concentrations and reacted at 30° C. for 30 minutes. The OD value at 450 nm was measured at intervals of 5 minutes for 60 minutes using the conversion from WST-1 to WST-1 formazan by the produced NAD/NADH. The CycLex NAMPT colorimetric assay kit (CY-1251) was used as a measurement apparatus. The results are shown in FIG. 6 to FIG. 10. From these results, Vmax/min was calculated and the results are shown in FIG. 11 to FIG. 15.

As shown in FIG. 6 to FIG. 10, the compounds of the Synthesis Example 1 to 4 according to the present invention showed excellent NamPT inhibitory activity, and thus it is known that the compounds can be effectively used for the treatment of various diseases caused by NamPT, for example, cancer, viral infection, human immunodeficiency virus, hepatitis virus, herpes virus, herpes simplex, inflammatory disorder, irritable bowel syndrome, inflammatory bowel disease, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, osteoarthritis, osteoporosis, dermatitis, atopic dermatitis, psoriasis, systemic lupus erythematosus, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, graft-versus-host disease, Alzheimer's disease, cerebrovascular accident, atherosclerosis, diabetes, glomerulonephritis and metabolic syndrome.

Furthermore, FK866 of Comparative Example 1 showed full inhibition capacity at 20 nM, indicating irreversible inhibition. On the other hand, it was confirmed that NamPT was not inhibited at the concentration of 4 nM diluted 5 times. Namely, it was found that FK866 had an irreversible inhibitory effect on the target enzyme in a narrow concentration range. In contrast, the compounds of the Synthesis Example 1 to 4 according to the present invention all exhibit increased or decreased inhibition capacity within a wide concentration range, and particularly, compounds of Synthesis Example 1 increase or decrease their inhibition capacity within a concentration of 75 times (FIG. 6), and all the compounds have higher slope at the maximum concentration than that of the FK866, indicating that the reversible inhibition was higher.

As shown in FIG. 11 to FIG. 15, it was found that the kinetic properties of the NamPT inhibition of the compounds of the Synthesis Example 1 to 4 according to the present invention contribute to increasing selectivity according to NAPRT expression by inducing a gradual decrease of NAD. It was known that this would be a favorable characteristic in the precise control of the drug dose for the safety margin in clinical practice.

[Evaluation Example 2] Therapeutic Effect of Cancer Cell Line

Various cancer cell lines including H322, H661, H1155, H1993, H1975, H2030, H1299, H2122 and HBEC30 were treated with various concentrations of the compounds of Synthesis Example 1 to 4 at various concentrations to determine the viability of the cell line according to the concentration and the results are shown in FIG. 16 to FIG. 19.

As shown in FIG. 16 to FIG. 19, all the compounds of the Synthesis Examples 1 to 4 have excellent therapeutic effects on various cancer cell lines. In the Synthesis Examples 1 to 4, the difference in LD50 values between the NAPRT positive cell line and the negative cell line was found to be at least 50 to at most 10,000 times. This indicates that the therapeutic window between NAPRT positive cells and negative cancer cells, including normal cells, is at least 5 to at most 1,000 times wider with compared to the FK866 of approximately 10 times difference.

[Evaluation Example 3] Therapeutic Effect of Cancer Cell Line

The H322, H661, H1155, H1299, H1975, H2030, H2122 and HBEC30 cell lines were treated with the compounds of the Synthesis Examples 1 to 46 at various concentrations for and IC₅₀was measured and the results are shown in Table 7 below.

TABLE 7

IC₅₀(μM)

H322
H661
H1115
H1299
H1975
H1993
H2030
H2122
HBEC30

NAPRT expression

negative
negative
negative
positive
positive
positive
positive
positive
positive

B1380
6.25
2.5

>12.5

>12.5
>12.5

B1386
1.56
7

>12.5

12.5
>12.5

B1387
6.25
7

>12.5

3.25
>12.5

B1416
<1.56

B1423
0.6
>1
1
>100
>100
>100
>100
>100
>100

B1467
3.125

B1468
<0.024
>1
3.16
>100
>100
>100
>100
>100
>100

B1469
0.06

B1470
0.06

B1471
<0.024
0.7
>1
100
>100
>100
>100
>100
>100

B1472
0.3

B1474
0.05

B1477
<0.024
>1
>1
<100
>100
<100
<100
31.6
>100

B1479
5

B1484
0.05

B1485
0.03

B1523
1.56

B1531
6.25

B1716
12.5

B1856
12.5

B1857
10

B1863
12.5

B1866
10

B1872
10

B1873
5

B1963
0.39

B1964
0.2

B1967
12.5

B1975
1.2

B1976
10

B1977
6.25

B1978
1.2

B1979
0.78

B1981
3.1

B1982
12

B1983
0.3

Drug3
1
<1
<3.1

A4276
<0.03
<0.3
<0.03

A4261
0.03
<0.3
<0.1

A4262
0.03
30
<0.1

A4263
<0.03
1
<0.3

A4265
0.003
<0.03
0.01

A4266
0.03
0.1
0.03

A4275
0.03
<0.3
<0.3

A4302
0.1
0.1
<0.3

A4303
10
10
10

As shown in Table 7, the compounds of Synthesis Examples 1 to 46 showed excellent therapeutic effect on all cancer cell lines, and particularly, the therapeutic effect was more excellent in cancer cells in which NAPRT expression was negative.

[Evaluation Example 4] Toxic Mechanism in Cancer Cell Lines

To investigate the direct effect of the compound according to the present invention on the catalytic activity of NamPT enzyme, after treating H322 cell line with 2.5 μM of the compound of the Synthesis Example 4, the intracellular NAD, ATP and total protein was measured, with the results depicted in FIG. 20.

As shown in FIG. 20, the compound of Synthesis Example 4 of the present invention showed a decrease in the total amount of protein compared to the negative control, and in particular, the amount of ATP which is a NAD and NAD metabolite, was remarkably decreased.

As a result, the compound according to the present invention inhibited NamPT and the biosynthesis product thereof, NAD was decreased.

[Evaluation Example 5] Toxicity Assessment in Normal Cell Line

Primary cardiomyocyte (PromoCell # C-12810, Cardiomyocyte), retinal pigment epithelium cell (Lonza #194987, RPE) which are the normal cell line and liver cell (THLE-2) were cultured and the expression levels of NAPRT and NamPT were measured by Western blot using cell lysate and the results are shown in FIG. 21. In addition, the myocardial cells, retinal pigment epithelial cells and liver cells were treated with the compounds of Synthesis Examples 1 and 2 and Comparative Example 1, and the cell viability was evaluated. The results are shown in FIG. 22 to FIG. 24.

As shown in FIG. 21, normal cell lines normally express NAPRT and NamPT protein, and thus it was predicted that they would be resistant to NamPT inhibition.

As shown in FIG. 22 to FIG. 24, FK866 exhibited unpredictable cytotoxicity in THLE-2, Cardiomyocyte and RPE cells when treated at high concentrations, but the compounds of Synthesis Examples 1 and 2 of the present invention is confirmed not to cause cytotoxicity.

As a result, the compound of the present invention shows a specific killing effect only on cancer cells and does not show toxicity to normal cells.

[Evaluation Example 6] Toxicity Evaluation in Normal Cell Line

The normal liver cell lines THLE-2 and THLE-3 each were treated with the compounds of Synthesis Examples 4, 8 and 13 and Comparative Examples 1 and 2, and the cell viability was evaluated. The results are shown in FIG. 25 and FIG. 26.

As shown in FIG. 25 and FIG. 26, FK866 and GNE617 were toxic with an IC₅₀value of about 0.05 μM, while the compounds of Synthesis Examples 4, 8 and 13 according to the present invention showed little toxicity even at very high concentrations of 50 μM.

As a result, it was found that the compound of the present invention showed a specific killing effect only on cancer cells and did not show toxicity to normal cells.

[Evaluation Example 7] Microsome Stability Evaluation

Metabolic stability was assessed using human liver microsomes and mouse liver microsomes. Specifically, pooled male mouse liver microsomes (in-house preparation per SOP), pooled human liver microsomes (XENOTECH; Batch No-H0630-1110189) were used. 100 μl reaction was performed with 1 μM of the compound prepared in the Synthesis Example 1 to 3 (A4276, A4266 or A4265) or the compound of Comparative Example 1 (FK866), 0.3 mg/ml microsomal protein and cofactor in the buffer (1 mM NADPH) and in addition, the mixture was incubated at different time points (0, 15, 30, 45, 60, and 90 minutes). The reaction was stopped by addition of acetonitrile (Telmesartin) containing the same volume of internal standard. The precipitated proteins were removed by centrifugation and the supernatant was analyzed by LC/MS-MS method. The percentage of the parent compound remaining after 30 minutes of reaction was quantified by the analysis using the equation, and the results are shown in Table 8 below.

Residual % parent compound=(peak area at time x/peak area at TO)×100.

The intrinsic clearance was calculated by the following equation.

TABLE 8

Compound
Human(%)
Mouse(%)

A4265
81.11 ± 4.76
78.24 ± 6.49

A4276
71.99 ± 3.86
60.69 ± 1.04

A4266
>99
89.3 ± 3.12

FK866
25.48 ± 1.45
10.26 ± 0.91

positive control
0.101 ± 0.028
3.189 ± 1.078

(Buspirone)

As shown in Table 8, when the compounds of the Synthesis Example 1 to 3 according to the present invention were treated, it was confirmed that the stability in human and mouse liver microsomes was remarkably superior to that of FK866 of Comparative Example 1.

[Evaluation Example 8] Evaluation of Cardiac Toxicity (hERG)

The hERG screening was performed by measuring the fluorescence polarization of the compound of Synthesis Example 1 to 3 and E4031 compound as a positive control using the high affinity red fluorescent hERG channel ligand tracer of the Korea Research Institute of Chemical Technology. The results are shown in Table 9 below. However, in this test method, when the inhibition rate by the 10 μM compound was at least 50, it was judged to be a substance which needs attention to hERG channel binding.

In addition, as the hERG K+ channel activity evaluation, the potential risk of log QT prolongation according to the dose used was evaluated by measuring the current inhibition according to the drug using a patch clamp technique and evaluating the IC₅₀. The results are shown in Table 10 below. However, IC₅₀values for the hERG K+ channel by the patch fixation test method were not measured within the maximum concentration of 100 μM. In this test method, when the IC₅₀value for hERG K+ channel was at least 10 μM, it was judged to be safe against cardiac toxicity.

TABLE 9

Concentration
% inhibition

Treatment

(μM)
capacity

positive control
E4031
10
87.7 ± 5.41

compound
A4265
10
7.44 ± 3.12

A4266
10
<1

A4276
10
12.0 ± 5.04

(However, % inhibition capacity in the Table 9 is expressed as mean±standard deviation.)

TABLE 10

Compound
Concentration (μM)
IC₅₀(μM)

A4265
0.001, 0.01, 0.1, 1, 10, 100
Predicted above 100

μM

A4266
0.001, 0.01, 0.1, 1, 10, 100
Predicted above 100

μM

A4276
0.001, 0.01, 0.1, 1, 10, 100
Predicted above 100

μM

As shown in Table 9, it was confirmed that all the compounds of the Synthesis Example 1 to 3 according to the present invention were safe against inhibition of hERG channel activity due to protein binding.

In addition, as shown in Table 10, all the compounds of the Synthesis Example 1 to 3 according to the present invention had an IC₅₀value of at least 100 μM and thus were safe for cardiac toxicity.

INDUSTRIAL APPLICABILITY

The compound of the present invention can be used as a nicotinamide phosphoribosyltransferase (NamPT) inhibitor, and further, a therapeutic agent for NamPT disease or cancer.

NOVEL COMPOUND FOR INHIBITING NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE AND COMPOSITION CONTAINING SAME

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Abstract

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