IP Library Granted Patent US 9,908,908
Granted Patent B2
US 9,908,908 · App. 14/423,182 · Granted Mar 6, 2018

Tenofovir prodrug and pharmaceutical uses thereof

Inventors: Fuyao Zhang (Shanghai, CN); Dong Wei (Shanghai, CN)
Assignee: Jiangsu Hansoh Pharmaceutical Co., Ltd.
C07F9/65616A61K31/675
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Quick Facts
Patent No.
US 9,908,908
App. No.
14/423,182
Granted
Mar 6, 2018
Kind
B2
Abstract

The invention relates to a tenofovir prodrug and pharmaceutical uses thereof. In particular, the invention relates to a compound as shown in general formula (I): and its isomer, pharmaceutically acceptable salt, hydrate or solvate, as well as their uses in preparing drugs for treating viral infectious diseases, especially HIV infection, hepatitis B, or diseases caused by hepatitis B virus, wherein the definition of each substituent in the general formula (I) is as defined in the specification.

Claims (20)

1. A chiral compound of formula (I) or a stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof:

wherein:

R 1 and R 2 are each methyl, or R 1 and R 2 together with the attached carbon atom form a C 3 cycloalkyl;

R 3 is hydrogen, C 1-6 alkyl, substituted or unsubstituted C 6-10 aryl, or 6- to 10-membered heteroaryl; and

Ar is substituted or unsubstituted C 6-10 aryl, or 6- to 10-membered heteroaryl.

2. The chiral compound of formula (I) according to claim 1 , or the stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof, wherein the stereoisomer is selected from the group consisting of a tautomer, cis-trans isomer, conformational isomer, mesomer, an enantiomeric optical isomer, and a diastereomeric optical isomer.

3. The chiral compound of formula (I) according to claim 1 , or the pharmaceutically acceptable salt thereof, wherein the compound is:

4. A chiral compound of formula (Ia1) or a pharmaceutically acceptable salt thereof:

5. A pharmaceutical composition comprising the chiral compound of formula (I) or the stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof according to claim 1 and a pharmaceutically acceptable carrier.

6. The pharmaceutical composition according to claim 5 , wherein the pharmaceutically acceptable carrier is selected from the group consisting of water for injection, lyophilized powder excipient, and oral preparation excipient.

7. A pharmaceutical composition comprising the chiral compound of formula (Ia1) or the pharmaceutically acceptable salt thereof according to claim 4 and a pharmaceutically acceptable carrier.

8. The pharmaceutical composition according to claim 7 , wherein the pharmaceutically acceptable carrier is selected from the group consisting of water for injection, lyophilized powder excipient, and oral preparation excipient.

9. A pharmaceutical composition comprising the chiral compound of formula (I) or the pharmaceutically acceptable salt thereof according to claim 3 and a pharmaceutically acceptable carrier.

10. A method of treating a viral infection in a subject in need thereof, the method comprising administering to the subject the pharmaceutical composition according to claim 5 .

11. The method according to claim 10 , wherein the viral infection is selected from the group consisting of HIV infection, hepatitis B, and diseases caused by hepatitis B virus.

12. A method of treating a viral infection in a subject in need thereof, the method comprising administering to the subject the pharmaceutical composition according to claim 7 .

13. The method according to claim 12 , wherein the viral infection is selected from the group consisting of HIV infection, hepatitis B, and diseases caused by hepatitis B virus.

14. A method of treating a viral infection in a subject in need thereof, the method comprising administering to the subject the pharmaceutical composition according to claim 9 .

15. The method according to claim 14 , wherein the viral infection is selected from the group consisting of HIV infection, hepatitis B, and diseases caused by hepatitis B virus.

16. The chiral compound according to claim 1 , or the stereoisomer, pharmaceutically acceptable salt, hydrate, or solvate thereof, wherein R 1 and R 2 are each methyl.

Assignments (2)
CHANGE OF NAME Recorded Jun 29, 2018
From: JIANGSU HANSOH PHARMACEUTICAL CO., LTD.
To: JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD.
Reel/Frame 046465/0547 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2015
From: ZHANG, FUYAO; WEI, DONG
To: JIANGSU HANSOH PHARMACEUTICAL CO., LTD.
Reel/Frame 035005/0046 →
Priority Claims (2)
CN 2012 1 0315565 · Aug 30, 2012 · national
CN 2013 1 0041647 · Feb 1, 2013 · national
Continuity (1)
Related Publication 20150225433A1 · Aug 13, 2015