Patent Grant
9908908
This application is a Section 371 of International Application No. PCT/CN2013/079123, filed on Jul. 10, 2013, which was published in the Chinese language on Mar. 6, 2014, under International Publication No. WO 2014/032481 A1, and the disclosure of which is incorporated herein by reference.
The present invention relates to a tenofovir prodrug and a stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof, as well as their medical use.
Hepatitis B virus (HBV) is a kind of DNA virus that causes human acute or chronic hepatitis. As HBV infection is a direct cause of serious liver disease including cirrhosis and hepatocellular carcinoma in humans, hepatitis B is a major threat to human health. HBV-DNA (deoxyribonucleic acid) is the core of HBV and the basis of viral replication. Nucleotides can inhibit viral polymerases by competitive binding to the natural deoxyribose substrate directly, and terminate the DNA chain by inserting DNA. Thus, nucleotides, such as Cidofovir, Adefovir, Lamivudine, and Tenofovir, are the main drugs for treating hepatitis B. Tenofovir is a novel nucleotide reverse transcriptase inhibitor, which is effective against a variety of viruses for the treatment of viral infections. As the phosphate group is a dianion at physiological pH, tenofovir has poor cell membrane permeability, low bioavailability, and dose-dependent renal toxicity, which limits its therapeutic effect. Thus, tenofovir must be prepared into a phosphonate prodrug form via various technical means, such as esterification and salification, for clinical applications. For example, Tenofovir disoproxil fumarate developed by Gilead Sciences Inc. is the first generation oral active tenofovir prodrug for the treatment of HIV infection and hepatitis B.
As Tenofovir disoproxil fumarate is highly sensitive to serum enzyme mediated hydrolysis reactions, its drug concentration cannot be effectively increased at the active site. Moreover, two equivalents of potentially toxic formaldehyde are released upon metabolism, and side effects such as lactic acidosis, severe hepatomegaly and lipodystrophy have been found during clinical use. In order to improve the stability of tenofovir prodrug in plasma and reduce the metabolite-tenofovir concentration to reduce drug toxicity, many pharmaceutical companies are conducting research and development on the next generation of tenofovir prodrugs, and have made some progress. Some new prodrugs have been in phase I/II clinical studies. For example, International Patent Application WO0208241 discloses a kind of natural amino acid (monosubstituted) synthesized tenofovir phosphonamidate prodrug (e.g., GS-7340), and International Patent Application WO2009105513 discloses a kind of novel tenofovir phosphate bisamide prodrug. Compared to tenofovir phosphodiester, these novel prodrugs have improved plasma stability, thereby increasing the cumulative concentration of the active metabolite-tenofovir in peripheral blood mononuclear cells (PBMCs) and the therapeutic effect. For example, the total concentration of the active ingredient produced by GS-7340 in PBMCs is 10 times greater than tenofovir disoproxil, and 30 times greater than tenofovir. However, GS-7340 has certain degradation in plasma and 1-2% of the metabolite-tenofovir can be detected in plasma. So it is inevitable that GS-7340 has toxicity as a side effect generated by tenofovir disoproxil, which results in drug safety problems. Thus, it is important to further develop a tenofovir prodrug with high efficacy and low toxicity. With the purpose of further improving the stability of tenofovir disoproxil in plasma, the present invention synthesizes a series of tenofovir phosphonamidate prodrugs with disubstituted amino acids. This kind of prodrug is proven to be very stable in plasma and no metabolite-tenofovir is found in plasma. On the other hand, the concentration of active metabolite-tenofovir in PBMCs is increased significantly compared with GS-7340. Thus, the present invention makes it possible to provide a new generation of tenofovir prodrugs with high efficacy and low toxicity.
Surprisingly, the inventors found a series of compounds, which have higher efficacy and lower toxicity than the prior art. Compared to GS-7340, the compounds according to the present invention are stable enough in plasma, and the metabolite-tenofovir is completely undetectable in plasma. On the other hand, the concentration of tenofovir is greatly improved in PBMCs. Such a result is totally unexpected for those skilled in the art.
The present invention relates to a compound of general formula (I) and a stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof:
wherein:
R1 and R2 are C1-6 alkyl respectively, or R1 and R2 together with the attached carbon atom form a C3-7 cycloalkyl;
R3 is hydrogen, C1-6 alkyl, substituted or unsubstituted C6-10 aryl or 6- to 10-membered heteroaryl;
Ar is substituted or unsubstituted C6-10 aryl or 6- to 10-membered heteroaryl.
The compound of general formula (I) according to the present invention can be used as a prodrug of tenofovir. This prodrug is stable in plasma and the concentration of active metabolite-tenofovir in PBMCs is improved significantly compared to that of GS-7340.
In the compound of general formula (I) according to the present invention, the phosphorus atom is chiral and the configuration is S or R, or a mixture of R and S.
In an embodiment of the present invention, the compound of general formula (I) or the stereoisomer, pharmaceutically acceptable salt, hydrate or solvate thereof, wherein the stereoisomer comprises a tautomer, cis-trans isomer, conformational isomer, mesomer or enantiomeric or diastereomeric optical isomer.
In a preferred embodiment of the present invention, compounds having the following structures are provided, but the compound of general formula (I) according to the present invention is not limited to the following structures:
In another preferred embodiment of the present invention, chiral compounds with the following structures are disclosed, but the compound of general formula (I) according to the present invention is not limited to the following structures:
The compound of general formula (I) according to the present invention can be prepared according to the following method:
wherein the compound of general formula (II) can be prepared from tenofovir according to the method of Chinese Patent ZL01813161.1 as well as other conventional methods in the art.
Chiral isomer (I1) can be separated from a mixture of isomers (I′) with a reverse phase column or chiral column.
The present invention also provides a pharmaceutical composition comprising a compound of general formula (I) or a stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof and a pharmaceutically acceptable carrier, wherein the pharmaceutically acceptable carrier is selected from the group consisting of water for injection, lyophilized powder excipient, and oral preparation excipient.
The present invention also relates to the use of a compound of general formula (I) or a stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof or the pharmaceutical composition in the preparation of a medicament for the treatment of viral infections, preferably hepatitis B or diseases caused by hepatitis B virus.
Unless otherwise stated, the terms in the present invention have the following meanings.
The term “alkyl” means saturated aliphatic hydrocarbon groups comprising a straight or branched chain having 1 to 6 carbon atoms. Examples of alkyl include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, sec-butyl, n-pentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2-methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 2,2-dimethylbutyl, 1,3-dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 2,3-dimethylbutyl and the like. Alkyl can be substituted or unsubstituted. When substituted, the substituent can be substituted at any possible attachment point, and the substituent is preferably one or more groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, thiol, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycloalkylthio, and oxo.
The term “cycloalkyl” means a saturated or partially unsaturated monocycle or polycycle hydrocarbon substituent, which comprises 3 to 7 carbon atoms. Examples of monocyclic cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cyclohexadienyl, cycloheptyl, cycloheptatrienyl and the like. Examples of polycyclic cycloalkyl include, but are not limited to, spiro-ring cycloalkyl, fused-ring cycloalkyl and bridged-ring cycloalkyl. The cycloalkyl can be substituted or unsubstituted. When substituted, the substituent is preferably one or more groups independently selected from the group consisting of alkyl, alkoxy, halogen, hydroxy, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl.
The term “aryl” means a 6 to 10 membered full-carbon monocycle or fused polycycle (i.e., rings which share adjacent pairs of carbon atoms) and polycycle having a conjugated π electron system (i.e., rings having adjacent pairs of carbon atoms), such as phenyl and naphthyl. The aryl can be substituted or unsubstituted. When substituted, the substituent is preferably one or more groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, thiol, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, and heterocycloalkylthio.
The term “heteroaryl” means a heteroaromatic system of 6 to 10 ring atoms, preferably 5 to 6 ring atoms, which comprises one, two, three or four heteroatoms including O, S or N, such as pyridinyl, or pyrimidinyl. “Heteroaryl” can be optionally substituted or unsubstituted. When substituted, the substituent is preferably one or more groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, thiol, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxyl, heterocycloalkoxy, cycloalkylthio, and heterocycloalkylthio.
The present invention will be illustrated by the following examples which enable those skilled in the art to understand the present invention more clearly. The examples are merely for illustrating the technical solutions of the present invention and should not be considered as limiting the scope of the invention.
Step 1:
Trimethylchlorosilane (6.0 g) was added dropwise to a solution of phenol (5 g) and triethylamine (10.1 mL) in dichloromethane (150 mL) at 0° C. After addition, the reaction mixture was stirred for 18 hours after the temperature was raised to 20° C. The white solid was removed and washed with dichloromethane. The filtrate was combined and the solvent was evaporated to give phenoxy trimethylsilane (4.2 g) as a colorless oil.
Step 2:
DMF (0.1 mL) and dichlorosulfoxide (0.73 g) were added to a suspension of tenofovir (1 g, purchased from Suzhou Henderson Pharmaceutical Co., Ltd.) in sulfolane (2.5 mL) at 70° C., and then the temperature was raised to 100° C. The reaction mixture was stirred at 100° C. for 1.5 hours until a clear solution was obtained. Then, phenoxy trimethylsilane (0.70 g) was added rapidly, and the mixture was left to stir at 100° C. for another 1.5 hours. Then, the solvent was evaporated to give a viscous yellow oil. The oil was dissolved in methanol and adjusted to pH 3 with 45% aqueous potassium hydroxide. The precipitate was filtered and dried to give a white powder solid IIa (0.7 g). MS (m/z) 363.96 (MH+).
Step 3:
DMF (0.1 mL) and dichlorosulfoxide (343 mg) were added to a mixture of compound IIa (600 mg) in sulfolane (1 mL) at 60° C. The mixture was then stirred at 60° C. for 30 minutes until a clear solution was obtained. The resulting solution was added to a solution of amino acid ester IIIa (750 mg, purchased from Shanghai Darui Fine Chemicals Co., Ltd.) and diisopropylamine (452 mg) in dichloromethane (7 mL) at 0° C. The mixture was stirred at 20° C. for 2 hour, and then washed with 5% aqueous sodium dihydrogen phosphate and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give a yellow oil crude product, which was purified via column chromatography to give an oil product Ia (150 mg).
1H-NMR (400 MHz, CDCl3) δ 8.34 (m, 1H), 8.05 (m, 1H), 7.36˜6.95 (m, 5H), 6.49 (b, 2H), 6.22˜5.84 (m, 1H), 5.01 (m, 1H), 4.42 (m, 1H), 4.40˜3.60 (m, 3H), 1.52˜1.18 (m, 15H). MS (m/z) 491.13 (MH+).
The Preparation of Chiral Compounds Ia1 and Ia2:
Method 1: Non-Chiral Column Preparation
The crude product Ia (150 mg) was separated via preparative HPLC (preparative column: Waters Symmetry C18, Mobile phase: A: 0.02% aqueous phosphoric acid; B: methanol) to give compound Ia1 (50 mg, retention time: 50.65 min): MS (m/z) 491.17 (MH+) and compound Ia2 (61 mg, retention time: 47.57 min): MS (m/z) 491.10 (MH+).
Method 2: Chiral Column Preparation
The crude product Ia (150 mg) was separated via preparative HPLC (preparative column: Chiralpak AS-H, mobile phase: A: n-hexane; B: ethanol) to give compound Ia1 (62 mg, retention time: 6.53 min) and compound Ia2 (78 mg, retention time: 6.11 min).
DMF (0.1 mL) and dichlorosulfoxide (343 mg) were added to a mixture of compound IIa (600 mg) in sulfolane (1 mL) at 60° C. The mixture was then stirred at 60° C. for 30 minutes until a clear solution was obtained. The resulting solution was added to a solution of amino acid ester IIIb (760 mg, purchased from Shanghai Darui Fine Chemicals Co., Ltd.) and diisopropylamine (452 mg) in dichloromethane (7 mL) at 0° C. The mixture was stirred at 20° C. for 2 hour, and then washed with 5% aqueous sodium dihydrogen phosphate and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give a yellow oil crude product, which was purified via column chromatography to give an oil product Ib (221 mg).
1H-NMR (400 MHz, CDCl3) δ 8.38 (m, 1H), 8.01 (m, 1H), 7.34˜6.95 (m, 5H), 6.48˜6.18 (m, 1H), 5.84 (b, 2H), 5.01˜4.82 (m, 1H), 4.42 (m, 1H), 4.2˜03.60 (m, 5H), 2.68 (m, 1H), 1.41˜1.10 (m, 12H).
The crude product Ib (100 mg) was separated via preparative HPLC (preparative column: Chiralpak AS-H, mobile phase: A: n-hexane; B: ethanol) to give compound Ib1 (35 mg). MS (m/z) 489.26 (MH+).
Step 1:
Trimethylchlorosilane (6.3 g) was added dropwise to a solution of p-chlorophenol (5 g) and triethylamine (10.8 mL) in dichloromethane (150 mL) at 0° C. After addition, the reaction mixture was stirred for 18 hours after the temperature was raised to 20° C. The solvent was evaporated to give p-chlorophenoxy trimethylsilane (5.1 g) as a colorless oil.
Step 2:
DMF (0.1 mL) and dichlorosulfoxide (0.73 g) were added to a suspension of tenofovir (1 g) in sulfolane (2.5 mL) at 70° C., and then the temperature was raised to 100° C. The reaction mixture was stirred at 100° C. for 1.5 hours until a clear solution was obtained. Then, p-chlorophenoxy trimethylsilane (0.77 g) was added rapidly, and the mixture was left to stir at 100° C. for 1.5 hours. The solvent was evaporated to give a viscous yellow oil. The oil was dissolved in methanol and then adjusted to pH 3 with 45% aqueous potassium hydroxide. The precipitate was filtered and dried to give a white powder solid IIc (800 mg). MS (m/z) 398.05 (MH+).
Step 3:
DMF (0.1 mL) and dichlorosulfoxide (343 mg) were added to a mixture of compound IIc (600 mg) in sulfolane (1 mL) at 60° C. The mixture was then stirred at 60° C. for 30 minutes until a clear solution was obtained. The resulting solution was added to a solution of amino acid ester IIIa (731 mg) and diisopropylamine (452 mg) in dichloromethane (7 mL) at 0° C. The mixture was stirred at 20° C. for 2 hours, and then washed with 5% aqueous sodium dihydrogen phosphate and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give a yellow oil crude product which was purified via column chromatography to give an oil product Ic (121 mg).
1H-NMR (400 MHz, CDCl3) δ 8.35 (m, 1H), 8.01 (m, 1H), 7.28 (m, 1H), 7.22 (m, 1H), 7.15˜7.13 (m, 1H), 6.94 (m, 1H), 5.88 (b, 2H), 5.07 (m, 2H), 4.42 (m, 1H), 4.21 (m, 1H), 3.90˜3.81 (m, 2H), 3.71˜3.54 (m, 1H), 1.56˜1.24 (m, 15H).
The crude product Ic (70 mg) was separated by preparative HPLC (preparative column: Chiralpak AS-H, mobile phase: A: n-hexane; B: ethanol) to give compound Ic1 (21 mg). MS (m/z) 525.26 (MH+).
Step 1:
Trimethylchlorosilane (6.3 g) was added dropwise to a solution of p-methoxyphenol (5 g) and triethylamine (10.8 mL) in dichloromethane (150 mL) at 0° C. After addition, the reaction mixture was stirred for 18 hours after the temperature was raised to 20° C. The solvent was evaporated to give p-methoxyphenoxy trimethylsilane (4.7 g) as a colorless oil.
Step 2:
DMF (0.1 mL) and dichlorosulfoxide (0.73 g) were added to a suspension of tenofovir (1 g) in sulfolane (2.5 mL) at 70° C., and then the temperature was raised to 100° C. The reaction mixture was stirred at 100° C. for 1.5 hours until a clear solution was obtained. Then, p-methoxyphenoxy trimethylsilane (0.75 g) was added rapidly and the mixture was left to stir at 100° C. for 1.5 hours. The solvent was evaporated to give a viscous yellow oil. The oil was dissolved in methanol and then adjusted to pH 3 with 45% aqueous potassium hydroxide. The precipitate was filtered and dried to give a white powder solid IId (600 mg). MS (m/z) 394.11 (MH+).
Step 3:
DMF (0.1 mL) and dichlorosulfoxide (181 mg, 1.52 mmol) were added to a mixture of compound IId (300 mg) in sulfolane (1 mL) at 60° C. The mixture was then stirred at 60° C. for 30 minutes until a clear solution was obtained. The resulting solution was added to a solution of amino acid ester IIIa (386 mg) and diisopropylamine (343 mg) in dichloromethane (5 mL) at 0° C. The mixture was stirred at 20° C. for 2 hours, and then washed with 5% aqueous sodium dihydrogen phosphate and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give a yellow oil crude product, and then purified via column chromatography to give an oil product Id (40 mg). 1H-NMR (400 MHz, CDCl3) δ 8.35 (m, 1H), 8.04 (m, 1H), 7.12˜6.85 (m, 4H), 5.86 (b, 2H), 5.06 (m, 1H), 4.42 (m, 1H), 4.18 (m, 1H), 4.08˜3.94 (m, 3H), 3.82 (m, 3H), 3.7˜73.61 (m, 1H), 1.55˜1.17 (m, 15H).
The crude product Id (30 mg) was separated by preparative HPLC (preparative column: Chiralpak AS-H, mobile phase: A: n-hexane; B: ethanol) to give 12 mg compound Id1. MS (m/z) 521.23 (MH+).
Compounds Ie and Ie1 were prepared according to the same preparation method as that of compounds Ic and Ic1.
Ie: 1H-NMR (400 MHz, CDCl3) δ 8.27 (m, 1H), 8.04 (s, 1H), 7.96 (m, 1H), 7.84 (m, 1H), 7.62 (m, 1H), 7.52˜7.33 (m, 4H), 5.78 (b, 2H), 5.04˜4.98 (m, 1H), 4.38˜3.71 (m, 6H), 1.57˜1.06 (m, 15H).
Ie1: MS (m/z) 541.11.
Compounds If and If1 were prepared according to the same preparation method as that of compounds Ic and Ic1.
If: 1H-NMR (400 MHz, CDCl3) δ 8.33 (m, 1H), 8.02 (s, 1H), 7.81˜7.66 (m, 4H), 7.49˜7.41 (m, 2H), 7.31˜7.06 (m, 1H), 5.72 (b, 2H), 5.06˜4.99 (m, 1H), 4.43˜4.35 (m, 1H), 4.19˜3.91 (m, 4H), 3.74˜3.65 (m, 1H), 1.57˜1.20 (m, 15H).
If1: MS (m/z) 541.10.
Compounds Ih and Ih1 were prepared according to the same preparation method as that of compounds Ic and Ic1.
Ih: 1H-NMR (400 MHz, CDCl3) δ 8.33 (m, 1H), 7.95 (m, 1H), 7.00˜6.95 (m, 3H), 5.83 (b, 2H), 5.05˜4.99 (m, 2H), 4.35˜4.31 (m, 1H), 4.23˜4.17 (m, 1H), 4.01˜3.83 (m, 3H), 3.80˜3.77 (m, 1H), 2.35 (s, 3H), 2.31 (s, 3H), 1.33˜1.19 (m, 15H).
Ih1: MS (m/z) 519.15.
Compounds Ii and Ii1 were prepared according to the same preparation method as that of compounds Ic and Ic1.
Ii: 1H-NMR (400 MHz, CDCl3) δ 8.36 (m, 1H), 8.00 (m, 1H), 7.17 (m, 1H), 7.02 (m, 1H), 6.97 (m, 2H), 5.71 (b, 2H), 5.06 (m, 1H), 4.43 (m, 1H), 4.20 (m, 1H), 4.06˜3.84 (m, 3H), 3.72˜3.61 (m, 1H), 1.56˜1.22 (m, 15H).
Ii1: MS (m/z) 509.25.
Compounds Ij and Ij1 were prepared according to the same preparation method as that of compounds Ic and Ic1.
Ij: 1H-NMR (400 MHz, CDCl3) δ 8.32 (m, 1H), 8.06 (s, 1H), 7.58 (m, 2H), 7.52 (m, 2H), 5.89 (b, 2H), 5.02˜4.96 (m, 1H), 4.43˜4.36 (m, 2H), 4.04˜3.91 (m, 4H), 1.58˜1.23 (m, 15H).
Ij1: MS (m/z) 559.08.
Compound Ia1 (480 mg), fumaric acid (120 mg) and acetonitrile were added sequentially to a single-necked flask at 20° C. The mixture was warmed to 60° C. and stirred at this temperature until the solid was completely dissolved. Stirring was continued for another 5 minutes, and then the solution was cooled to 20° C. and filtered to obtain the fumarate of compound Ia1 as a white granular solid (490 mg).
1H NMR (400 MHz, D2O) δ 7.21 (m, 2H), 7.11 (m, 1H), 6.67 (m, 2H), 6.57 (s, 2H), 4.77 (m, 1H), 4.29 (m, 1H), 4.17 (m, 1H), 4.06 (m, 1H), 3.93 (m, 1H), 1.07 (m, 6H), 1.21 (m, 9H).
1. Study of In Vitro Anti-Hepatitis B Virus Activity
HepG 2.2.15 cell was used as the hepatitis B virus (HBV) vehicle to determine the inhibition effect of the compounds on DNA-replication of HBV.
Test method: HepG 2.2.15 cells were seeded into a 96-well culture plate. Various dilutions of test samples and positive control were added, respectively, after 24 hours, in which a cell control well was set. The medium was replaced with culture containing various dilutions of test samples after 72 hours. The supernatants and HepG 2.2.15 cells were collected after 6 days of culture. The HBV DNA-replication was tested via the dot blot method, and IC50 was calculated (the results are shown in Table 1).
2. Cytotoxicity Test
Test method: HepG 2.2.15 cells were seeded into a 96-well culture plate and various dilutions of test samples and positive control were added, respectively. CellTiter-Blue (Promega, Catalog #G8081) was added for 6 days of culture. Fluorescence reading was counted with Flexstation 3 to calculate CC50 (the results were shown in Table 1).
Positive control is GS-7171 and GS-7340, which are disclosed in Examples 2 and 3 of Chinese Patent ZL01813161.1. GS-7171 can be resolved into diastereomers GS-7340 and GS-7339, in which GS7340 has the better efficacy.
3. Conclusion
Experimental results show that the compounds Ia1, Ib1, Ic1, Id1, Ie1, If1, Ih1, and Ij1 have a significant inhibitory effect on HBV-DNA replication without cytotoxicity, in which the inhibitory effects on HBV-DNA replication of compounds Ia1, Ic1, Id1, Ie1, If1, Ih1, Ii1 and Ij1 were better than that of the positive control GS7340.
1. Materials, Reagents and Manufacturers
36%
2. Preparation of Reagents
2.1 Hydrochloric Acid Solution (pH 2.0)
4.5 mL of 36% hydrochloric acid was transferred into a 1 L volumetric flask and diluted with water to 1 L to prepare a stock solution. Then 10 mL of the above solution was transferred into a 50 mL volumetric flask and diluted with water to 50 mL to prepare the hydrochloric acid solution with pH 2.0.
2.2 Simulated Gastric Juice (pH 2.0)
10 ml of the stock solution and 500.0 mg of pepsin were transferred into a 50 mL volumetric flask and diluted with water to 50 ml, which was then subjected to ultrasound to dissolve the pepsin (the solution was not clear now) and then filtered to give a clear solution as simulated gastric juice.
2.3 Preparation of the Sample Solution
2.3.1 Hydrochloric Acid Solution of GS-7340
5.0 mg of GS-7340 were transferred into a 5 mL volumetric flask and mixed with 2.5 mL of isopropyl alcohol to dissolve GS-7340, and then the hydrochloric acid solution (pH 2.0) was added to 5 mL. The solution was shaken well and filtered for using.
2.3.2 Simulated Gastric Juice of GS-7340
5.0 mg of GS-7340 were transferred into a 5 mL volumetric flask and mixed with 2.5 mL of isopropyl alcohol to dissolve GS-7340, and then the simulated gastric juice was added to 5 mL. The solution was shaken well and filtered for using.
2.3.3 Hydrochloric Acid Solution of Compound Ia1
5.0 mg of compound Ia1 were transferred into a 5 mL volumetric flask and mixed with 2.5 mL of isopropyl alcohol to dissolve compound Ia1, and then the hydrochloric acid solution (pH 2.0) was added to 5 mL. The solution was shaken well and filtered for using.
2.3.4 Simulated Gastric Juice of Compound Ia1
5.0 mg of compound Ia1 were transferred into a 5 mL volumetric flask and mixed with 2.5 mL of isopropyl alcohol to dissolve compound Ia1, and then the simulated gastric juice was added to 5 mL. The solution was shaken well and filtered for using.
2.4 Sampling
The prepared sample was filled into the chromatography vial as the initial sample and immediately injected. Meanwhile, the rest of the samples were put into a 37° C. incubator, and were injected into the HPLC system after 6 hours.
The stability results of compound Ia1 and GS-7340 in an acid medium and simulated gastric juice are shown in Table 2.
3. Conclusion
Experimental results show that the stability of tenofovir phosphonamidate prodrug (Ia1) having a disubstituted amino acid is significantly improved compared to tenofovir phosphonamidate prodrug (GS-7340) having a monosubstituted amino acid.
1. Materials
Compound: Ia1 and GS-7340
2. Test Method
Different tenofovir prodrugs were incubated together with fresh human whole blood at 37° C. Plasma and PBMCs were separated, respectively, from the whole blood (Ficoll density gradient centrifugation method) after 1 hour and 2 hours incubation to determine the concentrations of prototype drug and metabolite-tenofovir in plasma and PBMCs. The PBMCs were counted via cell counter and each PBMC was treated as 200 fL to calculate intracellular drug concentration.
3. Plasma/PBMC Sample Treatment
20 μL of internal standard solution (400 ng/mL SN-38 solution), 5.04, methanol-water (50:50, v/v), and 200 μL acetonitrile were added to 100 μL plasma sample or PBMC sample, respectively. The mixture was mixed by vortex for 1 min and centrifuged for 5 min (14000 rpm). 20 μL supernatant and 180 μl mobile phase were mixed by vortex for 1 min, and 10 μL of the above mixture was injected into LC/MS/MS for analysis.
The results of the metabolic stability in fresh human whole blood and the distribution test in PBMCs of tenofovir prodrug are shown in Table 3.
4. Conclusion
As can be seen from Table 3, certain active metabolite-tenofovir was detected in plasma for the positive control GS-7340 after incubation with fresh human whole blood, and the active metabolite-tenofovir released in plasma increased significantly over the incubation time. However, no active metabolite-tenofovir was detected in plasma for the compound Ia1 of the present invention after incubation with fresh human whole blood, and the active metabolite-tenofovir was not always detected over the incubation time, which illustrates that the stability of compound Ia1 in plasma was significantly better than the positive control GS-7340. Therefore, compound Ia1 of the present invention has significant advantages in reducing toxic side effects resulting from tenofovir in plasma compared with the positive control GS-7340.
It also can be seen from Table 3 that the concentration of the active metabolite-tenofovir in peripheral blood mononuclear cells (PBMCs) for compound Ia1 of the present invention increased significantly over the incubation time, while the concentration of the active metabolite-tenofovir in peripheral blood mononuclear cells (PBMCs) for compound GS-7340 was almost the same. The concentration of active metabolite-tenofovir in PBMCs for compound Ia1 was about three times of that for the positive control of GS-7340 after incubation for 2 hours. Thus, compound Ia1 of the present invention has significant advantages in terms of therapeutic effect compared with the positive control GS-7340.
1. Objective: To evaluate anti-HIV activity and cytotoxicity, and EC50 and CC50 value of three compounds.
2. Materials and Method
2.1 Materials
Compound: Compound Ia1, GS-7340, and tenofovir disoproxil
RPMI medium (Invitrogen 21969-035)
DMEM medium (Invitrogen 21969-035)
Glutamic acid 200 mM (Invitrogen 25030)
Fetal bovine serum ((Invitrogen 16000-044)
Penicillin/streptomycin ((Invitrogen 15140-122)
DPBS buffer (Invitrogen 14190-094)
Trypsin-EDTA (Invitrogen 25200)
Trypan blue Sigma T8154
DMSO Sigma D2650
MUG Biochemika 69590
2.2 Test Method
1) MT-2 cells were infected with HIV-1 (IIIb) to form multiplicity of infection (MOI) 0.01 TCID50 per cell.
2) The mixture of virus and cells was incubated in a 384-well plate for 3 days.
3) Cells for the cytotoxic detection were incubated in a 384-well plate for 3 days.
4) The supernatant was transferred to a new plate and incubated with reporter cells (HeLa) for 24 hours.
5) Detecting beta-GAL activity to evaluate anti-HIV activity.
6) Luminescent signal of the cells free of virus was detected to evaluate cytotoxicity after incubation for 3 days.
7) The antiviral activity and cytotoxicity were calculated according to the following equation:
Antiviral activity (%)=100−(Detection value−Maximum value)/(Minimum value−Maximum value)*100
Cytotoxicity (%)=100−(Detection value−Maximum value)/(Minimum value−Maximum value)*100
8) EC50 and CC50 were calculated with Fit Curve of Graphpad Prism 5 (the results are shown in Table 4).
3. Conclusion
The above results show that compound Ia1 has a strong inhibitory effect on HIV virus with no cytotoxicity.
The present invention has been described and illustrated by specific embodiments. Certain modifications and equivalent variations are apparent for those skilled in this art and are included within the scope of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2012 1 0315565 | Aug 2012 | CN | national |
| 2013 1 0041647 | Feb 2013 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2013/079123 | 7/10/2013 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2014/032481 | 3/6/2014 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 5278153 | Biller | Jan 1994 | A |
| 5545750 | Kempf et al. | Aug 1996 | A |
| 5670675 | Kempf et al. | Sep 1997 | A |
| 5717095 | Arimilli et al. | Feb 1998 | A |
| 5731432 | Edon et al. | Mar 1998 | A |
| 5733788 | Bischofberger | Mar 1998 | A |
| 5789394 | Nguyen-Ba et al. | Aug 1998 | A |
| 5798340 | Bischofberger et al. | Aug 1998 | A |
| 5854228 | Webb, II et al. | Dec 1998 | A |
| 5874577 | Chen et al. | Feb 1999 | A |
| 5886179 | Arimilli et al. | Mar 1999 | A |
| 5977061 | Holy et al. | Nov 1999 | A |
| 6005107 | Nguyen-Ba et al. | Dec 1999 | A |
| 6228861 | Nagarathnam et al. | May 2001 | B1 |
| 6331543 | Garvey et al. | Dec 2001 | B1 |
| 6455513 | McGuigan et al. | Sep 2002 | B1 |
| 6465649 | Gutierrez et al. | Oct 2002 | B1 |
| 6489476 | Dang et al. | Dec 2002 | B1 |
| 6653296 | Holy et al. | Nov 2003 | B1 |
| 6756360 | Erion et al. | Jun 2004 | B1 |
| 7300924 | Boojamra et al. | Nov 2007 | B2 |
| 7390791 | Becker et al. | Jun 2008 | B2 |
| 7439350 | Bischofberger et al. | Oct 2008 | B2 |
| 7951787 | McGuigan | May 2011 | B2 |
| 8835630 | Hostetler et al. | Sep 2014 | B1 |
| 8946243 | Margolis et al. | Feb 2015 | B2 |
| 20020035155 | Kaddurah-Daouk | Mar 2002 | A1 |
| 20030050251 | Semple et al. | Mar 2003 | A1 |
| 20030144283 | Coleman et al. | Jul 2003 | A1 |
| 20030236227 | Druzgala et al. | Dec 2003 | A1 |
| 20040002475 | Hakimelahi | Jan 2004 | A1 |
| 20050080078 | Aquila et al. | Apr 2005 | A1 |
| 20050148623 | DeGoey et al. | Jul 2005 | A1 |
| 20050215612 | Kuo et al. | Sep 2005 | A1 |
| 20060030545 | Cheng et al. | Feb 2006 | A1 |
| 20060046981 | Shibata | Mar 2006 | A1 |
| 20090163712 | Guo et al. | Jun 2009 | A1 |
| 20130210757 | Huang et al. | Aug 2013 | A1 |
| 20140256684 | Beard et al. | Sep 2014 | A1 |
| 20140256685 | Beard et al. | Sep 2014 | A1 |
| 20140288025 | Milne et al. | Sep 2014 | A1 |
| 20140315790 | Bushell et al. | Oct 2014 | A1 |
| Number | Date | Country |
|---|---|---|
| 1425680 | Jun 2003 | CN |
| 1465582 | Jan 2004 | CN |
| 1523028 | Aug 2004 | CN |
| 1583769 | Feb 2005 | CN |
| 1634943 | Jul 2005 | CN |
| 1796393 | Jul 2006 | CN |
| 1810816 | Aug 2006 | CN |
| 1966514 | May 2007 | CN |
| 1984640 | Jun 2007 | CN |
| 1986553 | Jun 2007 | CN |
| 101003550 | Jul 2007 | CN |
| 101066980 | Nov 2007 | CN |
| 101066981 | Nov 2007 | CN |
| 101085785 | Dec 2007 | CN |
| 101089004 | Dec 2007 | CN |
| 101143879 | Mar 2008 | CN |
| 101190927 | Jun 2008 | CN |
| 101190935 | Jun 2008 | CN |
| 101230065 | Jul 2008 | CN |
| 101278938 | Oct 2008 | CN |
| 101279987 | Oct 2008 | CN |
| 101307076 | Nov 2008 | CN |
| 101418017 | Apr 2009 | CN |
| 101450954 | Jun 2009 | CN |
| 101463045 | Jun 2009 | CN |
| 101475594 | Jul 2009 | CN |
| 101531679 | Sep 2009 | CN |
| 101531680 | Sep 2009 | CN |
| 101574356 | Nov 2009 | CN |
| 101585854 | Nov 2009 | CN |
| 101591357 | Dec 2009 | CN |
| 101648974 | Feb 2010 | CN |
| 101659676 | Mar 2010 | CN |
| 101712692 | May 2010 | CN |
| 101759722 | Jun 2010 | CN |
| 101781334 | Jul 2010 | CN |
| 101781335 | Jul 2010 | CN |
| 101870713 | Oct 2010 | CN |
| 1947796 | Nov 2010 | CN |
| 101906119 | Dec 2010 | CN |
| 101928302 | Dec 2010 | CN |
| 101948485 | Jan 2011 | CN |
| 101985454 | Mar 2011 | CN |
| 102040626 | May 2011 | CN |
| 102060876 | May 2011 | CN |
| 102070670 | May 2011 | CN |
| 102093417 | Jun 2011 | CN |
| 102276667 | Dec 2011 | CN |
| 102485229 | Jun 2012 | CN |
| 103845345 | Jun 2014 | CN |
| 103923124 | Jul 2014 | CN |
| 104072539 | Oct 2014 | CN |
| 104558035 | Apr 2015 | CN |
| 104628773 | May 2015 | CN |
| 00206459 | Dec 1986 | EP |
| 269947 | Jun 1988 | EP |
| 270885 | Jun 1988 | EP |
| 402646 | Dec 1990 | EP |
| 481214 | Apr 1992 | EP |
| 745893 | Dec 1996 | EP |
| 829493 | Mar 1998 | EP |
| 853084 | Jul 1998 | EP |
| 989122 | Mar 2000 | EP |
| 0996430 | May 2000 | EP |
| 1065207 | Jan 2001 | EP |
| 1627902 | Feb 2006 | EP |
| 2001031690 | Feb 2001 | JP |
| 2001031691 | Feb 2001 | JP |
| 2012025678 | Mar 2012 | KR |
| 9119721 | Dec 1991 | WO |
| 9209611 | Jun 1992 | WO |
| 9319075 | Sep 1993 | WO |
| 9403467 | Feb 1994 | WO |
| 9404143 | Mar 1994 | WO |
| 9418200 | Aug 1994 | WO |
| 9507920 | Mar 1995 | WO |
| 9623801 | Aug 1996 | WO |
| 9629336 | Sep 1996 | WO |
| 9633200 | Oct 1996 | WO |
| 9713507 | Apr 1997 | WO |
| 9717969 | May 1997 | WO |
| 9724361 | Jul 1997 | WO |
| 9735855 | Oct 1997 | WO |
| 9735990 | Oct 1997 | WO |
| 98004569 | Feb 1998 | WO |
| 9811121 | Mar 1998 | WO |
| 9842758 | Oct 1998 | WO |
| 1999005150 | Feb 1999 | WO |
| 9941277 | Aug 1999 | WO |
| 9945016 | Sep 1999 | WO |
| 9962871 | Dec 1999 | WO |
| 2000014095 | Mar 2000 | WO |
| 2000018775 | Apr 2000 | WO |
| 2000038666 | Jul 2000 | WO |
| 2000075236 | Dec 2000 | WO |
| 2000076505 | Dec 2000 | WO |
| 2001032636 | May 2001 | WO |
| 2001049688 | Jul 2001 | WO |
| 2001066553 | Sep 2001 | WO |
| 2001098344 | Dec 2001 | WO |
| 0208241 | Jan 2002 | WO |
| 200204475 | Jan 2002 | WO |
| 2002003978 | Jan 2002 | WO |
| 2002008241 | Jan 2002 | WO |
| 2002012366 | Feb 2002 | WO |
| 2002020475 | Mar 2002 | WO |
| 2002022572 | Mar 2002 | WO |
| 2002094185 | Nov 2002 | WO |
| 2002096892 | Dec 2002 | WO |
| 2003006628 | Jan 2003 | WO |
| 2003016274 | Feb 2003 | WO |
| 2003020773 | Mar 2003 | WO |
| 2003024943 | Mar 2003 | WO |
| 03053989 | Jul 2003 | WO |
| 2003087298 | Oct 2003 | WO |
| 2003091264 | Nov 2003 | WO |
| 2003095665 | Nov 2003 | WO |
| 2004024681 | Mar 2004 | WO |
| 2004029064 | Apr 2004 | WO |
| 2004037161 | May 2004 | WO |
| 2004041167 | May 2004 | WO |
| 2004064845 | Aug 2004 | WO |
| 2004096285 | Nov 2004 | WO |
| 2004101579 | Nov 2004 | WO |
| 2005012324 | Feb 2005 | WO |
| 2005016942 | Feb 2005 | WO |
| 2005044279 | May 2005 | WO |
| 2005044757 | May 2005 | WO |
| 2005058330 | Jun 2005 | WO |
| 2005066189 | Jul 2005 | WO |
| 2005079812 | Sep 2005 | WO |
| 2005085183 | Sep 2005 | WO |
| 2005087788 | Sep 2005 | WO |
| 2005123729 | Dec 2005 | WO |
| 2006013203 | Feb 2006 | WO |
| 2006017044 | Feb 2006 | WO |
| 2006059357 | Jun 2006 | WO |
| 2006102594 | Sep 2006 | WO |
| 2006114064 | Nov 2006 | WO |
| 2006114065 | Nov 2006 | WO |
| 2006114492 | Nov 2006 | WO |
| 2006130217 | Dec 2006 | WO |
| 2006133632 | Dec 2006 | WO |
| 2007002808 | Jan 2007 | WO |
| 2007002912 | Jan 2007 | WO |
| 2007009236 | Jan 2007 | WO |
| 2007013085 | Feb 2007 | WO |
| 2007013086 | Feb 2007 | WO |
| 2007014352 | Feb 2007 | WO |
| 2007044565 | Apr 2007 | WO |
| 2002057288 | May 2007 | WO |
| 2007084157 | Jul 2007 | WO |
| 2007095269 | Aug 2007 | WO |
| 2007101371 | Sep 2007 | WO |
| 2007111994 | Oct 2007 | WO |
| 2007128815 | Nov 2007 | WO |
| 2007130783 | Nov 2007 | WO |
| 2007134457 | Nov 2007 | WO |
| 2007136650 | Nov 2007 | WO |
| 2007143823 | Dec 2007 | WO |
| 2007143824 | Dec 2007 | WO |
| 2008005555 | Jan 2008 | WO |
| 2008007392 | Jan 2008 | WO |
| 2008010985 | Jan 2008 | WO |
| 2008047345 | Apr 2008 | WO |
| 2008056264 | May 2008 | WO |
| 2008082601 | Jul 2008 | WO |
| 2008088147 | Jul 2008 | WO |
| 2008093173 | Aug 2008 | WO |
| 2008096369 | Aug 2008 | WO |
| 2008104408 | Sep 2008 | WO |
| 2008134578 | Nov 2008 | WO |
| 2008140302 | Nov 2008 | WO |
| 2008143500 | Nov 2008 | WO |
| 2008157657 | Dec 2008 | WO |
| 2009005693 | Jan 2009 | WO |
| 2009023718 | Feb 2009 | WO |
| 2009052050 | Apr 2009 | WO |
| 2009046573 | Apr 2009 | WO |
| 2009055289 | Apr 2009 | WO |
| 2009064174 | May 2009 | WO |
| 2009074351 | Jun 2009 | WO |
| 2009077671 | Jun 2009 | WO |
| 2009094190 | Jul 2009 | WO |
| 2009105513 | Aug 2009 | WO |
| 2009130437 | Oct 2009 | WO |
| 2010026603 | Mar 2010 | WO |
| 2010068708 | Jun 2010 | WO |
| 2010081082 | Jul 2010 | WO |
| 2010091386 | Aug 2010 | WO |
| 2010108995 | Sep 2010 | WO |
| 2010125200 | Nov 2010 | WO |
| 2010142761 | Dec 2010 | WO |
| 2011005672 | Jan 2011 | WO |
| 2011017253 | Feb 2011 | WO |
| 2011031628 | Mar 2011 | WO |
| 2011038207 | Mar 2011 | WO |
| 2011053812 | May 2011 | WO |
| 2011069688 | Jun 2011 | WO |
| 2011100698 | Aug 2011 | WO |
| 2011111074 | Sep 2011 | WO |
| 2011128374 | Oct 2011 | WO |
| 2011130557 | Oct 2011 | WO |
| 2011133963 | Oct 2011 | WO |
| 2011150360 | Dec 2011 | WO |
| 2012079035 | Jun 2012 | WO |
| 2012098255 | Jul 2012 | WO |
| 2012116050 | Aug 2012 | WO |
| 2012117219 | Sep 2012 | WO |
| 2012142671 | Oct 2012 | WO |
| 2012149236 | Nov 2012 | WO |
| 2012149567 | Nov 2012 | WO |
| 2012154698 | Nov 2012 | WO |
| 2013019874 | Feb 2013 | WO |
| 2013052094 | Apr 2013 | WO |
| 2013078277 | May 2013 | WO |
| 2013078288 | May 2013 | WO |
| 2013090420 | Jun 2013 | WO |
| 2013095684 | Jun 2013 | WO |
| 2013115916 | Aug 2013 | WO |
| 2013116720 | Aug 2013 | WO |
| 2013116730 | Aug 2013 | WO |
| 2013167743 | Nov 2013 | WO |
| 2013175231 | Nov 2013 | WO |
| 2013187978 | Dec 2013 | WO |
| 2014032481 | Mar 2014 | WO |
| 2014033688 | Mar 2014 | WO |
| 2014068265 | May 2014 | WO |
| 2014070771 | May 2014 | WO |
| 2014088923 | Jun 2014 | WO |
| 2014099578 | Jun 2014 | WO |
| 2014177464 | Nov 2014 | WO |
| 2014183462 | Nov 2014 | WO |
| 2015040640 | Mar 2015 | WO |
| 2015079240 | Jun 2015 | WO |
| 2015079241 | Jun 2015 | WO |
| Entry |
|---|
| Cihlar, Tomas “Amidate Prodrugs of Nucleotide Phosphonates: From Design to In vivo Proof of Concept” Collect. Symp. Series (2008), 10: pp. 45-53. |
| Lee, W., G. He, E. Eisenberg, T. Cihlar, S. Swaminathan, A. Mulato, and K. Cundy “Selective Intracellular Activation of a Novel Prodrug of the Human Immunodeficiency Virus Reverse Transcriptase Inhibitor Tenofovir leads to Preferential Distribution and Accumulation in Lymphatic Tissue” Antimicro. Agents Chemother. (2005), 49 (5), pp. 1898-1906. |
| Birkus, G., N. Kutty, G. He, A. Mulato, W. Lee, M. McDermott, and T. Cihlar “Activation of 9-[(R)-2-[[(S)-[[(S)-1(Isopropoxycarbonyl)ethyl]amino]phenoxyphosphinyl]-methoxy]propyl]adenine (GS-7340) and Other Tenofovir Phosphonoamidate Prodrugs by Human Proteases” Mol. Pharmacol. (2008), 74(1), pp. 92-100. |
| Int'l Search Report dated Oct. 17, 2013 in Int'l Application No. PCT/CN2013/079123. |
| Journal of Medicinal Chemistry (2011), 54(16), 5680-5693 (Tyrosine-based 1-(S)-[3-hydroxy-2-(phosphonomethoxy) propyl]cytosine and -adenine ((S)-HPMPC and (S)-HPMPA) prodrugs: Synthesis, stability, antiviral activity, and in vivo transport studies) (Abstract Only). |
| Nucleosides, Nucleotides & Nucleic Acids (2001), 20(4-7), 621-628 (Practical synthesis, separation, and stereochemical assignment of the PMPA pro-drug GS-7340) (Abstract Only). |
| Bioorganic & Medicinal Chemistry Letters (2001), 11(8), 1053-1056 (Synthesis and evaluation of novel amidate prodrugs of PMEA and PMPA) (Abstract Only). |
| International Journal of Antimicrobial Agents (1999), 12(1), 53-61 (Inhibition of the in vitro growth of Plasmodium falciparum by acyclic nucleoside phosphonates) (Abstract Only). |
| Drug Metabolism and Disposition (1997), 25(3), 362-366 (Pharmacokinetics and metabolism of selected prodrugs of PMEA in rats). |
| Nucleosides & Nucleotides (1995), 14(3-5), 767-70 (In vivo antiretroviral efficacy of oral bis(POM)-PMEA, the bis(pivaloyloxymethyl)prodrug of 9-(2-phosphonylmethoxyethyl)adenine (PMEA)) (Abstract Only). |
| Journal of Medicinal Chemistry (1994), 37(12), 1857-64 (Synthesis, Oral Bioavailability Determination, and in vitro Evaluation of Prodrugs of the Antiviral Agent 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA)) (Abstract Only). |
| Balzarini et al. Federation of European Biochemical Societies, 410 (1997) 324-328. |
| Perrone et al. J. Med. Chem. (2007) 50, 1840-1849. |
| Cahard et al. Mini-Reviews in Medicinal Chemistry (2004) 4, 371-381. |
| Pertusati et al. Antiviral Chem and Chemotherapy (2012) 22, 181-203. |
| Number | Date | Country | |
|---|---|---|---|
| 20150225433 A1 | Aug 2015 | US |
