Patent Grant
8501731
The present invention belongs to the field of materia medica, and particularly relates to a series of novel pyridazinones containing the mother nucleus of 6-[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-one, the preparation method and the use thereof. The above pyridazinones show significant antitumor activities, especially for liver cancer.
Pyridazinones have shown a broad-spectrum biological activity, e.g. as an antidepressant, a vasodilatator, a cardiotonic, an acesodyne/anti-inflammatory agent or an antihypertensive, as acaricide or herbicide in agriculture, and also as inhibitors for acetylcholine esterase, aldose reductase, monoamine oxidase, CDKs, COX-2 and P38MAP kinase, etc. Some pyridazinones have exhibited an antitumor activity to a certain extent. US2007/0072866 A1 reported a series of pyridazinones having a structure formula of
as a GSK-3β inhibitor, which can be used for treating metabolic diseases, neurodegenerative diseases or other related diseases or disorders. CN200380105057 further defines that A is C(O)NHR or NHC(O)R; while in US2007/0072866A1, A is defined as a heterocyclic substituent.
WO 03/059891 and WO 2005/007632 disclose that pyridazinones are useful for treating diseases or conditions caused or exacerbated by unregulated P38 MAP kinase and/or TNF activity. In the above patent literatures, the pyridazinones have a structure formula of
and are useful for treating inflammatory diseases, diabetes, Alzheimer's disease or cancer. Although the described pyridazinones covers almost all substituents, actually, R4 is mainly aryl, R1 is mainly halogen, R2 is various kinds of substituents, and R3 is only H.
The most related literatures of the present application are the patent literatures concerning antitumor activities filed by Aventis Co. under WO2004/046130, WO2005085231, WO2005/111019 and US2007/0173503, which involve a kind of pyridazinone derivatives of formula
as inhibitors of CDK2, wherein, X is C(O)NHR, NHC(O)R or a heterocycle containing N, R2 is H, and R3 is an aromatic ring or heterocycle.
In addition, pyridazinones are described as inhibitors of RAF kinase in WO2006/124874 for treating tumors, and as inhibitors against tumors in European patent publication 0665223. However, such pyridazinones are totally different from the compounds of the present application.
Moreover, various other pyridazinone derivatives are disclosed in other literatures, and they are different from those in the present application in the selection of substituted groups, moieties and/or 6-positioned aromatic ring groups, or in applications of the compounds.
It is well known that liver cancer is the 5th frequent tumor diseases in males, and the 8th frequent tumor diseases in females. In 2007, it was estimated that 80% patients suffered newly from liver cancer were in developing countries, and 55% of all new patients were in China. In developing countries, among the liver cancer patients, 59% were attributed to HBV, and 33% were attributed to HCV. Particularly, there exists a great market demands for drugs against liver cancer due to the severe HBV infection and increasing incidence of liver cancer in Asia-Pacific countries.
One object of the present invention is to disclose a series of novel pyridazinones having the structure of the following formula I.
Another object of the present invention is to disclose a method for preparing the above pyridazinones.
Still another object of the present invention is to disclose a use of the above pyridazinones in manufacturing an antitumor medicament.
The present invention provides a series of novel pyridazinones having the structure of formula I:
wherein,
R is —OH, —SH, substituted or unsubstituted C6-C12 aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C3-C10 cycloalkyl, substituted or unsubstituted heterocyclic group, —ORa, —NHRa, —NRaRb, or —SRa,
wherein, Ra and Rb are each independently substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C3-C10 cycloalkyl, substituted or unsubstituted C6-C12 aryl, substituted or unsubstituted heteroaryl, or substituted or unsubstituted heterocyclic group;
the substituents are selected from the group consisting of halogen, —OH, —NO2, C1-C6 alkyl, carboxyl, C1-C6 alkyloxycarbonyl, C6-C12 aryl, —NH2, C1-C6 alkyl substituted amino, hydroxyl substituted C1-C6 alkyl, hydroxyl substituted C1-C6 alkoxyl group, unsubstituted or C1-C6 alkyl substituted heterocyclic group and —CF3;
the heteroaryl is 5- or 6-membered cyclic ring containing 1 to 3 heteroatoms selected from the group consisting of N, O and S;
the heterocyclic group is 3- to 7-membered monocyclic ring or 8-membered bicyclic ring, which may contain 1 to 3 heteroatoms selected from the group consisting of N, O and S, and the heterocyclic group is optionally oxo substitution or sulfido substitution.
Preferably, in the pyridazinones having the structure of formula I,
R is —OH, —SH, substituted or unsubstituted phenyl, substituted or unsubstituted heteroaryl, substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C3-C10 cycloalkyl, substituted or unsubstituted heterocyclic group, —ORa, —NHRa, —NRaRb or —SRa,
wherein, Ra and Rb are each independently substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C3-C10 cycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted heteroaryl or substituted or unsubstituted heterocyclic group;
the substituents are selected from the group consisting of halogen, —OH, —NO2, C1-C6 alkyl, carboxyl, C1-C6 alkoxyl carbonyl, phenyl, —NH2, C1-C6 alkyl substituted amino, hydroxyl substituted C1-C6 alkyl, hydroxyl substituted C1-C6 alkoxyl, unsubstituted or C1-C4 alkyl substituted heterocyclic group and —CF3;
the heteroaryl is 5- or 6-membered cyclic ring containing 1 to 3 nitrogen atoms;
the heterocyclic group is 3- to 7-membered monocyclic ring or 8-membered bicyclic ring, which may contain 1 to 3 nitrogen atoms, and the heterocyclic group is optionally oxo substitution or sulfido substitution. More preferably, the pyridazinones are the following specific compounds:
The above pyridazinones exhibit a high activity against tumors, especially, liver cancer. For example, compound YHHU-646 showed a significant curative effect against liver cancer of animals in vivo. In addition, the pyridazinones showed a significant inhibition activity against the proliferation of vascular endothelial cells, indicating that the series of compounds are inhibitors for the proliferation of the vascular endothelial cells, capable of inhibiting tumor angiogenesis, and suggesting they have potential to treat a variety of cancers.
The above pyridazinones may be prepared by reacting various m-trifluoromethylbenzaldehyde with methyl acrylate through a Setter reaction to give a 1,4-dicarbonyl compound, then directly adding a hydrazine compound into the reaction mixture to perform an “one-pot” reaction to form a ring, and finally, dehydrogenating by CuCl2.2H2O to afford a pyridazinone compound. Alternatively, the desired pyridazinones may be obtained after compounds modified by variously substituted benzene rings were prepared through a coupling reaction.
Specifically, the above pyridazinones may be prepared according to any one of the following methods:
and,
In the above methods, R is —OH, —SH, substituted or unsubstituted C6-C12 aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C3-C10cycloalkyl, substituted or unsubstituted heterocyclic group, —ORa, —NHRa, —NRaRb or —SRa,
wherein, Ra and Rb are each independently substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C3-C10cycloalkyl, substituted or unsubstituted C6-C12 aryl, substituted or unsubstituted heteroaryl or substituted or unsubstituted heterocyclic group;
the substituents are selected from the group consisting of halogen, —OH, —NO2, C1-C6 alkyl, carboxyl, C1-C6 alkoxylcarbonyl, C6-C12 aryl, —NH2, C1-C6 alkyl substituted amino, hydroxyl substituted C1-C6 alkyl, hydroxyl substituted C1-C6 alkoxyl group, unsubstituted or C1-C6 alkyl substituted heterocyclic group and —CF3;
the heteroaryl is 5- or 6-membered cyclic ring containing 1 to 3 heteroatoms selected from the group consisting of N, O and S;
the heterocyclic group is 3- to 7-membered monocyclic ring or 8-membered bicyclic ring, which may contain 1 to 3 heteroatoms selected from the group consisting of N, O and S, and the heterocyclic group is optionally oxo substitution or sulfido substitution.
Another object of the present invention is to disclose a pharmaceutical composition containing the above pyridazinones. The pharmaceutical composition may contain a therapeutically effective amount of one or more of the above pyridazinones and pharmaceutically acceptable adjuvant(s).
The present invention will be further described with reference to the following examples, but the invention is not limited thereto.
NaCN (24.5 mg, 0.5 mmol) was dissolved in 5 ml of dry DMF at 35° C., and under N2, 4-fluoro-3-trifluoromethyl-benzaldehyde (1.03 g, 5 mmol) was dropped thereinto. After the dropping, stirring continued for 30 minutes. Then, methyl acrylate (0.52 g, 6 mmol) was dropped thereinto. After the mixture was reacted for 4 hours, hydrazine hydrate (0.72 g, 12.5 mmol) was added thereinto directly and the reaction mixture was heated to 60° C. and stirred for 8 hours.
The reaction was quenched, and the temperature was cooled to room temperature. The reaction mixture was added with 20 ml of water, and extracted with ethyl acetate (20 ml×3). The combined organic layer was washed with saturated saline (10 ml×3), dried with anhydrous Na2SO4, filtrated, and evaporated to dryness in vacuum. The residue was purified by silica gel column chromatography eluting with ethyl acetate-petroleum ether (1:2) to give 6-(4-fluoro-3-trifluoromethyl)phenyl-4,5-dihydro-pyridazin-3(2H)-one as an off-white solid (0.73 g, yield 56%). The solid was dissolved in acetonitrile (10 ml), and CuCl2.2H2O (272 mg, 2.02 mmol) was added thereinto. Then the reaction mixture was refluxed for 1 hour under vigorous agitation. After cooled to room temperature, and the reaction mixture was filtered off the remanent CuCl2, and the filtrate was evaporated to dryness under reduced pressure. The residue was added with ethyl acetate (100 mL), washed with saturated NaHCO3 solution (20 ml) and then with saturated saline (20 ml×2), dried with anhydrous Na2SO4, filtrated, and evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography eluting with ethyl acetate-dichloromethane(1:3) to give the target product 8F (130 mg, yield 50%).
1H NMR (DMSO-d6, 300 MHz): δ 11.50 (1H, bs), 8.17 (3H, m), 7.63 (1H, t, J=9.8 Hz), 7.03 (1H, dd, J=5.6, 1.1 Hz).
To 8F (100 mg, 0.4 mmol) in a 10 ml microwave vial, was added 3 ml of 70% aqueous ethylamine solution, followed by microwave irradiation (80 W, 110, 20 min). After the reaction completed, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified by silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 9a (32.9 mg, yield 30%).
1H NMR (CDCl3, 300 MHz): δ 11.88 (1H, bs), 11.42 (1H, bs), 7.89 (1H, s), 7.80 (1H, s), 7.80 (1H, m), 7.72 (1H, m), 7.05 (1H, d, J=9.6 Hz), 6.79 (1H, d, J=9.6 Hz), 3.28 (2H, q, J=7.2 Hz), 1.34 (3H, t, J=7.2 Hz).
To 8F (100 mg, 0.4 mmol) in a 10 ml microwave vial, was added 3 ml of ethanolamine as a solvent, followed by microwave irradiation (160 W, 180, 20 min). After the reaction was completed, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified by silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 9b.
1H NMR (CDCl3, 300 MHz): δ 8.14 (1H, s), 8.12 (1H, d, J=11.3 Hz), 7.63 (3H, m), 7.38 (1H, bs), 6.83 (1H, d, J=9.4 Hz), 4.00 (2H, t, J=4.0 Hz), 3.57 (2H, m).
To 8F (100 mg, 0.4 mmol) in a 10 ml microwave vial, was added 3 ml of N-methylpiperazine as a solvent, followed by microwave irradiation (100 W, 170, 30 min). After the reaction was completed, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified by silica gel column chromatography eluting with methanol-dichloromethane (1:10) to give the target product 9c.
1H NMR (DMSO-d6, 300 MHz): δ 8.09 (3H, m), 7.59 (1H, d, J=9.5 Hz), 6.98 (1H, d, J=9.8 Hz), 2.90 (4H, t, J=4.0 Hz), 2.44 (4H, m), 2.22 (3H, s).
To 8F (100 mg, 0.4 mmol) in a 10 ml microwave vial, was added an excess amount of sodium methoxide in methanol, followed by microwave irradiation (80 W, 130, 20 min). After the reaction was completed, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified by silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 9d.
1H NMR (CDCl3, 300 MHz): δ 11.43 (1H, bs), 8.01 (1H, s), 7.94 (1H, dd, J=8.8, 1.2 Hz), 7.73 (1H, d, J=9.8 Hz), 7.10 (1H, d, J=8.9 Hz), 7.08 (1H, d, J=10.2 Hz), 3.97 (3H, s).
To a mixture of 100 mg of 3,6-dichloropyridazine (0.67 mmol), 1.2 eq of 5a, 1.5 eq of K2CO3 and 3 mol % of PdCl2 (PPh3)2 in a 25 ml two-necked flask, were added 6 ml of CH3CN and 4 ml of H2O. After purged with N2, the reaction mixture was refluxed and agitated. After the reaction was completed, the mixture was extracted with ethyl acetate, and the organic layer were dried and concentrated. The residue was directly transferred into a 10 ml round necked flask with glacial acetic acid, and refluxed. After the reaction was completed, the reaction mixture was alkalified and extracted with ethyl acetate. The organic layer were dried and concentrated, and the residue was purified through silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 7a.
1H NMR (CDCl3, 300 MHz): δ 11.38 (1H, bs), 8.02 (1H, d, J=2.1 Hz), 7.90 (1H, dd, J=8.4, 2.4 Hz), 7.75 (1H, d, J=9.9 Hz), 7.36 (1H, d, J=8.8 Hz), 7.08 (1H, d, J=9.9 Hz), 2.90 (4H, t, J=3.3 Hz), 1.72 (4H, m), 1.58 (2H, m).
To a mixture of 100 mg of 3,6-dichloropyridazine (0.67 mmol), 1.2 eq of 5b, 1.5 eq of K2CO3 and 3 mol % of PdCl2(PPh3)2 in a 25 ml two-necked flask, were added 6 ml of CH3CN and 4 ml of H2O. After purged with N2, the reaction mixture was refluxed and stirred. After the reaction was completed, the mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was directly transferred into a 10 ml round necked flask with glacial acetic acid and refluxed. After the reaction was completed, the mixture was alkalified and extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified through silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:1) to give the target product 7b.
1H NMR (CDCl3, 300 MHz): δ 12.00 (1H, bs), 8.08 (1H, d, J=1.8 Hz), 7.96 (1H, dd, J=8.4, 1.8 Hz), 7.76 (1H, d, J=9.9 Hz), 7.42 (1H, d, J=8.6 Hz), 7.11 (1H, d, J=9.9 Hz), 3.86 (4H, t, J=4.4 Hz), 2.99 (4H, t, J=4.6 Hz).
To 8F (100 mg, 0.4 mmol) in a 10 ml microwave vial, was added 3 ml of 2-dimethylaminoethylamine as a solvent, followed by microwave irradiation (80 W, 110, 30 min). After the reaction was completed, the mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified by silica gel column chromatography eluting with methanol-dichloromethane (1:20) to give the target product 9e.
1H NMR (DMSO-d6, 300 MHz): δ 8.03 (1H, d, J=9.8 Hz), 7.93 (2H, m), 6.94 (1H, d, J=10.0 Hz), 6.92 (1H, d, J=8.5 Hz), 5.67 (1H, d, J=4.2 Hz), 3.26 (2H, dd, J=6.3 Hz), 2.50 (2H, m) 2.19 (6H, s).
To 8F (100 mg, 0.4 mmol) in a 10 ml microwave vial, was added an excess amount of cyclohexylamine as a solvent, followed by microwave irradiation (80 W, 140, 30 min). After the reaction was completed, the mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified by silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 9f.
1H NMR (CDCl3, 300 MHz): δ 11.26 (1H, bs), 7.86 (1H, d, J=2.1 Hz), 7.77 (1H, dd, J=8.6, 1.8 Hz), 7.69 (1H, d, J=9.8 Hz), 7.04 (1H, d, J=9.8 Hz), 6.81 (1H, d, J=9.0 Hz), 4.49 (1H, d, J=6.5 Hz), 3.43 (1H, bs), 2.05 (2H, m), 1.77 (2H, m), 1.35 (6H, m).
To 8F (100 mg, 0.4 mmol) in a 10 ml microwave vial, was added an excess amount of 4-hydroxypiperidine (no solvent), followed by microwave irradiation (100 W, 150, 30 min). After the reaction was completed, the mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was purified by silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 9g.
1H NMR (CDCl3, 300 MHz): δ 10.79 (1H, bs), 8.03 (1H, d, J=2.1 Hz), 7.90 (1H, dd, J=8.6, 1.6 Hz), 7.73 (1H, d, J=10.3 Hz), 7.39 (1H, d, J=8.7 Hz), 7.08 (1H, d, J=9.9 Hz), 3.89 (1H, bs), 3.17 (2H, m), 2.84 (2H, m), 2.02 (2H, m), 1.76 (2H, m), 1.45 (1H, d, J=4.0 Hz).
NaCN (24.5 mg, 0.1 eq) was dissolved in 5 ml of dried DMF at 35° C. Under N2, 4-methyl-3-trifluoromethylbenzaldehyde (1.0 eq) was dropped thereinto. After the dropping, the stirring continued for 30 min, and then methyl acrylate (1.1 eq) was dropped thereinto. After the reaction continued for 4 hours, hydrazine hydrate (5.0 eq) was added thereinto directly. The reaction system was heated to 60 and stirred for 8 hours.
After the reaction was quenched, the reaction system was cooled to room temperature, added with 20 ml of water, and extracted with ethyl acetate (20 ml×3). The combined organic layer was washed with saturated saline (10 ml×3), dried by anhydrous Na2SO4, filtrated, and evaporated to dryness in vacuum. The residue was purified by silica gel column chromatography eluting with ethyl acetate-petroleum ether (1:2) to give 6-(4-methyl-3-trifluoromethyl)phenyl-4,5-dihydro-pyridazin-3(2H)-one as an off-white solid. The resulted solid was dissolved in acetonitrile (10 ml), followed by addition of CuCl2.2H2O (1.5 eq). The reaction mixture was refluxed for 1 hour under vigorous agitation, cooled to room temperature, and filtrated off the remaining CuCl2. The filtrate was evaporated to dryness under reduced pressure and the residue was added with ethyl acetate (100 ml), washed with saturated NaHCO3 solution (20 ml) and then with saturated saline (20 ml×2), dried by anhydrous Na2SO4, filtrated and evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 4a.
1H NMR (CDCl3, 300 MHz): δ 11.03 (1H, bs), 8.01 (1H, s), 7.94 (1H, dd, J=8.6, 1.2 Hz), 7.73 (1H, d, J=9.8 Hz), 7.10 (1H, d, J=8.7 Hz), 7.08 (1H, d, J=9.9 Hz), 1.97 (3H, s).
NaCN (24.5 mg, 0.1 eq) was dissolved in 5 ml of dry DMF at 35° C. Under N2, 4-(N-t-butyloxycarbonylpiperazinyl)-3-trifluoromethylbenzaldehyde (1.0 eq) was dropped thereinto. After the dropping, the stirring continued for 30 min, and then methyl acrylate (1.1 eq) was dropped therein. After the reaction continued for 4 hours, hydrazine hydrate (5.0 eq) was added thereinto directly. The reaction system was heated to 60° C. and stirred for 8 hours The reaction was ceased, and the reaction system was cooled to room temperature, added with 20 ml of water, and extracted with ethyl acetate (20 ml×3). The combined organic layer was washed with saturated saline (10 ml×3), dried by anhydrous Na2SO4, filtrated and evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography eluting with ethyl acetate-petroleum ether (1:2) to give 6-(4-(N-t-butyloxycarbonylpiperazinyl)-3-trifluoromethyl)phenyl-4,5-dihydro-pyridazin-3(2H)-one. The resultant solid was dissolved in acetonitrile (10 ml), followed by addition of CuCl2.2H2O (1.5 eq). The reaction was refluxed for 1 hour under vigorous agitation. After cooled to room temperature, the reaction mixture was filtrated off the remaining CuCl2, and the filtrate was evaporated to dryness under reduced pressure. The residue was added with ethyl acetate (100 ml). The solution was washed with saturated NaHCO3 solution (20 ml) and then with saturated saline (20 ml×2), dried by anhydrous Na2SO4, filtrated and evaporated to dryness under reduced pressure. The residue was separated by silica gel column chromatography eluting with ethyl acetate-dichloromethane (1:2) to give the target product 4b.
1H NMR (DMSO-d6, 300 MHz): δ 13.27 (1H, bs), 8.12 (3H, m), 7.65 (1H, d, J=8.8 Hz), 7.01 (1H, dd, J=1.9, 9.9 Hz), 3.45 (4H, m), 2.87 (4H, m), 1.43 (9H, s).
To a mixture of 8Br (50 mg, 0.18 mmol), 5 mol % PdCl2(PPh3)2 and 5 mol % CuI in a dry two-necked flask under N2, were added 5 eq of EtN(i-Pr)2 and 1.2 eq of p-trifluoromethylphenylacetylene, followed by addition of redistilled dry DMF. After the reaction at 30 was finished, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was separated by silica gel column chromatography eluting with ethyl acetate-petroleum ether (1:2) to give the target product 9h.
1H NMR(CDCl3, 300 MHz): δ 12.05 (1H, bs), 8.04 (1H, s), 8.17 (2H, m), 7.58 (1H, d, J=7.6 Hz), 7.32 (2H, d, J=8.9 Hz), 7.40 (2H, d, J=8.9 Hz), 7.08 (1H, d, J=7.6 Hz).
To a mixture of 8Br (50 mg, 0.18 mmol), 1.2 eq of phenylboric acid, 1.5 mol % of Pd2(dba)3, 3.0 mol % of Xantphos(4,5-bi(diphenylphosphino)-9,9-dimethylxanthene) and 3 eq of K2CO3 in a 10 ml microwave vial, were added 1.5 ml of CH3CN and 1.0 ml of H2O. After purged with N2, the reaction mixture was subjected to a microwave treatment (65 W, 120, 20 min). After the reaction was completed, the mixture was extracted with ethyl acetate, and the organic layer was dried and concentrated. The residue was separated by silica gel column chromatography eluting with ethyl acetate-petroleum ether (1:2) to give the target product 9i.
1H NMR(CDCl3, 300 MHz): δ 13.00 (1H, bs), 8.04 (1H, s), 7.90 (2H, m), 7.58 (1H, d, J=7.9 Hz), 7.35 (5H, m), 7.08 (1H, d, J=7.9 Hz).
Protocol: the antineoplasmic activities in vitro of the compounds were assayed by a Sulforhodamine B (SRB) protocol. Tumor cells were cultivated at 37 under 5% CO2 in a RPMI 1640 medium or a DMEM medium (Gibco) containing 10% fetal bovine serum. Tumor cells were inoculated on a 96-well plate with a concentration of 0.4-1.0×104 cells per well according to the cell types. 24 hours later, the target compounds diluted 10 times were added, each compound having at least 5 concentrations. After treated by the compounds for 72 hours, the culture media were discarded, and the cells were fixed by 10% cold trichloroacetic acid, and then stained by Sulforhodamine B (SRB) solution. The uncombined SRB was washed off, and the SRB combined with protein was dissolved with Tris. OD values were recorded at 515 nm on an ELISA Reader, and the cell growth inhibition rate was calculated according to following equation:
Inhibition rate=(ODcontrol−ODexperimental)/ODcontrol×100%
IC50 (50% inhibitory concentration) was calculated by using Logit method based on the inhibition rates at various concentration, and the results are shown in tables 1 and 2.
The above experimental results confirm that the novel pyridazinones of the present invention, which comprise 6-[3-(trifluoromethyl)phenyl]pyridazin-3(3H)-one as the mother nucleus and a electron-donating substitutents containing N, O, S or C at 4-position of aryl, have significant antitumor activities.
1. Experimental Compounds
Name and lot number: YHHU-744, a white powder, lot No.: No. c001471-106; YHHU-755, a white powder, lot No.: No. c001471-102; YHHU-756, a white powder, lot No.: No. c00147-106; YHHU-759, a white powder, lot No.: No. c001471-102; YHHU-776, a white powder, lot No.: No. c001471-107. Sorafenib was used as a positive control.
Formulation: YHHU-744, YHHU-755, YHHU-756, YHHU-759, YHHU-776 and the positive control were each diluted with 0.1% Tween-80 and distilled water to a desired concentration.
2. Laboratory Animal:
BALB/cA nude mice, 6-7 weeks old, ♀, were purchased from Shanghai SLAC Laboratory Animal Co. LTD. Certificate No.: SCXK (Shanghai) 2007-0005. Habitat: SPF level.
3. Experimental Procedure:
Human liver cancer cells Bel-7402 were inoculated on nude mice subcutaneously. After the tumor grew up to 300-450 mm3, animals were grouped randomly (d0). Dosage and dosage regimen were shown in table 3. The tumor volume was measured 2-3 times each week and the weights of mice were recorded. The tumor volume was calculated according to as the following equation.
V=½×a×b2 wherein, a and b are length and width, respectively.
4. Result:
Mice bearing cancer were consecutively administered with compounds YHHU-744, YHHU-755, YHHU-756, YHHU-759 or YHHU-776 intragastrically once a day for 11 days, and observation was continued to the 17th day. After administration, all tumors diminished significantly. At the 11th day, except for the group of compound YHHU-744 (4/5 vanished), all tumors vanished in the other groups (5/5), and no recrudescence was observed at the end of the experiment (results were shown in table 3 and
Table 3 The therapeutic effect of compounds YHHU-744, YHHU-755, YHHU-756, YHHU-759, YHHU-776 and Sorafenib on human liver cancer cells Bel-7402 transplanted tumor on nude mice
| Number | Date | Country | Kind |
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| 2008 1 0034796 | Mar 2008 | CN | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CN2009/000295 | 3/18/2009 | WO | 00 | 11/17/2010 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2009/114993 | 9/24/2009 | WO | A |
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| 20110112061 A1 | May 2011 | US |
