FR16C0031I2 - S-TRIAZOLYL ALPHA-MERCAPTOACETANILIDES AS HIV REVERSE TRANSCRIPTASE INHIBITORS - Google Patents
S-TRIAZOLYL ALPHA-MERCAPTOACETANILIDES AS HIV REVERSE TRANSCRIPTASE INHIBITORSInfo
- Publication number
- FR16C0031I2 FR16C0031I2 FR16C0031C FR16C0031C FR16C0031I2 FR 16C0031 I2 FR16C0031 I2 FR 16C0031I2 FR 16C0031 C FR16C0031 C FR 16C0031C FR 16C0031 C FR16C0031 C FR 16C0031C FR 16C0031 I2 FR16C0031 I2 FR 16C0031I2
- Authority
- FR
- France
- Prior art keywords
- mercaptoacetanilides
- reverse transcriptase
- transcriptase inhibitors
- hiv reverse
- triazolyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
A series of S-triazolyl ±-mercaptoacetanilides having general structure (I) are provided, where Q is CO 2 H, CONR 2 , SO 3 H,or SO 2 NR 2 . The compounds inhibit several variants of the reverse transcriptase of HIV, and are useful in the treatment of HIV infections.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60422004P | 2004-08-25 | 2004-08-25 | |
US60421904P | 2004-08-25 | 2004-08-25 | |
US68635105P | 2005-05-31 | 2005-05-31 | |
EP05790722A EP1789039B1 (en) | 2004-08-25 | 2005-08-25 | S-triazolyl alpha -mercaptoacetanildes as inhibitors of hiv reverse transcriptase |
Publications (2)
Publication Number | Publication Date |
---|---|
FR16C0031I1 FR16C0031I1 (en) | 2016-09-23 |
FR16C0031I2 true FR16C0031I2 (en) | 2017-03-31 |
Family
ID=36000576
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR16C0031C Active FR16C0031I2 (en) | 2004-08-25 | 2016-07-29 | S-TRIAZOLYL ALPHA-MERCAPTOACETANILIDES AS HIV REVERSE TRANSCRIPTASE INHIBITORS |
Country Status (32)
Country | Link |
---|---|
US (8) | US7947721B2 (en) |
EP (5) | EP2433633A1 (en) |
JP (2) | JP4952943B2 (en) |
KR (1) | KR101241716B1 (en) |
CN (2) | CN101817793B (en) |
AT (2) | ATE540677T1 (en) |
AU (2) | AU2005280130C9 (en) |
BR (2) | BRPI0514630B8 (en) |
CA (1) | CA2578068C (en) |
CY (2) | CY1112221T1 (en) |
DK (1) | DK2135608T3 (en) |
EA (2) | EA014737B1 (en) |
EC (1) | ECSP077322A (en) |
ES (2) | ES2380604T3 (en) |
FR (1) | FR16C0031I2 (en) |
HK (1) | HK1133582A1 (en) |
HR (1) | HRP20130075T1 (en) |
HU (1) | HUS1600034I1 (en) |
IL (3) | IL181523A (en) |
IN (1) | IN2014CN03762A (en) |
LT (1) | LTC2135608I2 (en) |
LU (1) | LU93169I2 (en) |
ME (1) | ME01512B (en) |
MX (1) | MX2007002236A (en) |
NL (1) | NL300825I2 (en) |
NZ (2) | NZ581376A (en) |
PL (1) | PL2135608T3 (en) |
PT (1) | PT2135608E (en) |
RS (1) | RS52632B (en) |
SG (2) | SG155246A1 (en) |
SI (1) | SI2135608T1 (en) |
WO (1) | WO2006026356A2 (en) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007050087A1 (en) * | 2004-08-25 | 2007-05-03 | Ardea Biosciences, Inc. | N[S(4-aryl-triazol-3-yl)α -mercaptoacetyl]-p-amino benozoic acids AS HIV REVERSE TRANSCRIPTASE INHIBITORS |
EP2433633A1 (en) * | 2004-08-25 | 2012-03-28 | Ardea Biosciences, Inc. | Triazolyl alpha -mercaptoacetanildes as inhibitors of HIV reverse transcriptase |
MX2009012704A (en) | 2007-05-30 | 2009-12-08 | Hoffmann La Roche | Non-nucleoside reverse transcriptase inhibitors. |
WO2009030996A1 (en) * | 2007-09-05 | 2009-03-12 | Coley Pharmaceutical Group, Inc. | Triazole compounds as toll-like receptor (tlr) agonists |
CN103058944B (en) * | 2007-11-27 | 2015-08-05 | 亚德生化公司 | Regulate the compound of blood uric acid levels |
US8173690B2 (en) | 2008-09-04 | 2012-05-08 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
BRPI0918586A2 (en) * | 2008-09-04 | 2015-12-01 | Ardea Biosciences Inc | compounds, compositions and methods of use thereof for modulating uric acid levels |
US8242154B2 (en) | 2008-09-04 | 2012-08-14 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same for modulating uric acid levels |
WO2010048592A1 (en) * | 2008-10-24 | 2010-04-29 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( 1-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triaz0l-3-ylthi0) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
EP2349258A1 (en) * | 2008-10-24 | 2011-08-03 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( l-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triazol-3-ylthio) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
EP2432468A2 (en) | 2009-05-20 | 2012-03-28 | Ardea Biosciences, Inc. | Methods of modulating uric acid levels |
CN102040546B (en) * | 2009-10-10 | 2014-10-15 | 台州市华南医化有限公司 | Preparation method of 4-cyclopropyl-1-naphthaline isothiocyanate and intermediate 4-cyclopropyl-1-naphthaldehyde oxime/halide |
JP5696346B2 (en) * | 2010-01-08 | 2015-04-08 | アルデア バイオサイエンシーズ インク. | Polymorphism, crystallinity, and mesophase of sodium 2- (5-bromo-4- (4-cyclopropylnaphthalen-1-yl) -4H-1,2,4-triazol-3-ylthio) acetate Form and its use |
US9402827B2 (en) | 2010-03-30 | 2016-08-02 | Ardea Biosciences, Inc. | Treatment of gout |
SI2582683T1 (en) | 2010-06-15 | 2018-07-31 | Ardea Biosciences, Inc. | Treatment of gout and hyperuricemia |
AR081930A1 (en) | 2010-06-16 | 2012-10-31 | Ardea Biosciences Inc | THIOACETATE COMPOUNDS |
TWI499412B (en) | 2010-06-16 | 2015-09-11 | Ardea Biosciences Inc | Phenylthioacetate compositions and methods of use |
CN101899013B (en) * | 2010-07-12 | 2012-07-25 | 山东大学 | 2-(2-substituted aryl-2H-1,2,4-triazole-3-sulfydryl) acetamide derivative and preparation method and application thereof |
WO2012050589A1 (en) * | 2010-10-15 | 2012-04-19 | Ardea Biosciences, Inc. | Methods for treating hyperuricemia and related diseases |
KR101541629B1 (en) | 2010-12-30 | 2015-08-03 | 아디아 바이오사이언스즈 인크. | Polymorphic forms of 2-(5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-ylthio)acetic acid and uses thereof |
DK2776028T3 (en) | 2011-11-03 | 2019-02-04 | Ardea Biosciences Inc | 3,4-DISUBSTITUTED PYRIDIDE COMPOUND, PROCEDURES FOR USING IT AND COMPOSITIONS INCLUDING THIS |
AR091651A1 (en) * | 2012-07-03 | 2015-02-18 | Ardea Biosciences Inc | ACID ELABORATION 2- (5-BROMO-4- (4-CICLOPROPILNAFTALEN-1-IL) -4H-1,2,4-TRIAZOL-3-ILTIO) ACETIC |
WO2014198241A1 (en) * | 2013-06-14 | 2014-12-18 | Sunshine Lake Pharma Co., Ltd. | Thio-1,2,4-triazole derivatives and method for preparing the same |
CN103524440B (en) * | 2013-10-15 | 2015-09-09 | 苏州鹏旭医药科技有限公司 | The preparation method of gout therapertics Lesinurad and Lesinurad intermediate |
EP3071554B1 (en) * | 2013-11-22 | 2018-10-03 | Crystal Pharmatech Co., Ltd. | Crystalline forms of lesinurad |
CN104557748A (en) * | 2014-01-25 | 2015-04-29 | 广东东阳光药业有限公司 | Novel solid form of sulpho-1,2,4-triazole derivative |
CN105315218A (en) * | 2014-07-17 | 2016-02-10 | 天津药物研究院 | Preparation method of lesinurad intermediate namely 1-naphthyltriazole thioketone |
CN104370841B (en) * | 2014-10-27 | 2016-07-13 | 张远强 | Triazole sulfenyl malonic acid compounds, Preparation Method And The Use |
CN104327000B (en) * | 2014-10-27 | 2016-08-17 | 张远强 | Phenyl substituted triazole sulfenyl malonic acid compounds, Preparation Method And The Use |
CN104341363B (en) * | 2014-10-27 | 2016-08-17 | 张远强 | A kind of nitro substituted triazole sulphonyl malonic acid compounds, Preparation Method And The Use |
CN104341361B (en) * | 2014-10-27 | 2017-01-11 | 张远强 | Cyano-substituted triazolesulfonylmalonic acid compounds as well as preparation method and application thereof |
CN104370842B (en) * | 2014-10-27 | 2016-07-13 | 张远强 | The triazole sulphonyl malonic acid compounds of phenyl replacement, Preparation Method And The Use |
CN104326998B (en) * | 2014-10-27 | 2016-08-17 | 张远强 | Phenyl substituted triazole malonic acid compounds, Preparation Method And The Use |
CN104341362B (en) * | 2014-10-27 | 2016-07-13 | 张远强 | Triazole sulphonyl malonic acid compounds, Preparation Method And The Use |
CN104326993B (en) * | 2014-10-27 | 2016-08-17 | 张远强 | A kind of nitro substituted 1,2,4-triazole sulfenyl malonic acid compounds, Preparation Method And The Use |
CN104311498B (en) * | 2014-10-27 | 2016-04-06 | 张远强 | Triazole sulphonyl propanedioic acid compounds, Preparation Method And The Use that alkoxyl group replaces |
EP3112334A1 (en) | 2015-06-29 | 2017-01-04 | DPx Fine Chemicals Austria GmbH & CoKG | Process for manufacturing 1-cyclopropyl-naphthalenes |
CN104987311A (en) * | 2015-06-30 | 2015-10-21 | 安徽万邦医药科技有限公司 | Preparing method for (4-(4-cyclopropyl-naphthalene-1-yl)-5-nitr-4H-(1, 2, 4) triazole-3-ylsulfanyl)-ethyl acetate and intermediate (5-nitr-4H-(1, 2, 4) triazole-3-sulfenyl)-ethyl acetate thereof |
CN105153056A (en) * | 2015-07-01 | 2015-12-16 | 安徽万邦医药科技有限公司 | New preparation method of [5-bromo-4-(4-cyclopropyl-naphthalene-1-yl)-4H-[1, 2, 4]triazole-3-ylthioalkyl]-methyl acetate |
CN105017168A (en) * | 2015-07-01 | 2015-11-04 | 安徽万邦医药科技有限公司 | New preparation method of [5-bromo-4-(4-cyclopropyl-naphthalene-1-yl)-4H-[1, 2, 4]triazole-3-ylsulfanyl]-methyl acetate |
WO2017036884A1 (en) | 2015-08-28 | 2017-03-09 | Sandoz Ag | A lesinurad, free form / lesinurad ethyl ester co-crystal |
CN105566237B (en) * | 2016-03-01 | 2018-05-18 | 山东大学 | A kind of preparation method for the triazole mercapto phenylacetic acid compound for treating gout |
DK3473617T3 (en) | 2016-06-17 | 2022-11-28 | Medshine Discovery Inc | HALOGENATED COMPOUND AND AXIAL, CHIRAL ISOMERS THEREOF |
EP3281941B1 (en) | 2016-08-11 | 2019-07-24 | Zentiva K.S. | Process for preparing 2-(5-bromo-4-(1-cyclopropylnaphthalen-4-yl)-4h-1,2,4-triazol-3-ylthio)acetic acid |
EP3372592A1 (en) | 2017-03-07 | 2018-09-12 | Zentiva, k.s. | Solid forms of lesinurad amine salts |
US10351537B2 (en) * | 2017-03-10 | 2019-07-16 | Apotex Inc. | Processes for the preparation of lesinurad and intermediates thereof |
EP3315494A1 (en) | 2017-04-19 | 2018-05-02 | Química Sintética, S.A. | Amorphous form of lesinurad and processes for its preparation |
CN108947919B (en) | 2017-05-17 | 2023-05-02 | 上海奥博生物医药股份有限公司 | Novel preparation method of anti-gout drug Lesinurad and key intermediate thereof |
WO2019001325A1 (en) * | 2017-06-28 | 2019-01-03 | 苏州科睿思制药有限公司 | Crystal form xv of lesinurad and preparation method therefor |
EP3498697A1 (en) | 2017-12-12 | 2019-06-19 | Química Sintética, S.A. | Novel salts and polymorphs of lesinurad |
DE112022002825T5 (en) | 2021-05-28 | 2024-03-14 | Sumitomo Chemical Company, Limited | Process for the preparation of cycloalkyl bromide |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US226186A (en) | 1880-04-06 | Car-coupling | ||
US2008A (en) * | 1841-03-18 | Gas-lamp eok conducting gas pkom ah elevated buhner to one below it | ||
US2006A (en) * | 1841-03-16 | Clamp for crimping leather | ||
US2009A (en) * | 1841-03-18 | Improvement in machines for boring war-rockets | ||
JPS5641637B2 (en) | 1973-11-26 | 1981-09-29 | ||
US6832996B2 (en) * | 1995-06-07 | 2004-12-21 | Arthrocare Corporation | Electrosurgical systems and methods for treating tissue |
JPH07215940A (en) | 1994-01-27 | 1995-08-15 | Torii Yakuhin Kk | Compound having antiviral activity |
US6245817B1 (en) * | 1997-02-14 | 2001-06-12 | Bayer Corporation | NPY5 receptor antagonists and methods for using same |
EP0910565A1 (en) | 1997-02-14 | 1999-04-28 | Bayer Corporation | Amide derivatives as selective neuropeptide y receptor antagonists |
JPH10243033A (en) * | 1997-02-28 | 1998-09-11 | Oki Electric Ind Co Ltd | Demodulator |
DE69943247D1 (en) * | 1998-03-27 | 2011-04-14 | Janssen Pharmaceutica Nv | HIV-inhibiting pyrimidine derivatives |
IL143105A0 (en) | 1998-11-12 | 2002-04-21 | Neurocrine Biosciences Inc | Fused polycyclic heterocyclic compounds and pharmaceutical compositions containing the same |
US6414147B1 (en) * | 1998-12-23 | 2002-07-02 | Neurogen Corporation | 2-amino-9-alkylpurines: GABA brain receptor ligands |
NZ512184A (en) * | 1998-12-25 | 2003-08-29 | Shionogi & Co | Aromatic heterocycle compounds having HIV integrase inhibiting activities |
US6593077B2 (en) * | 1999-03-22 | 2003-07-15 | Special Materials Research And Technology, Inc. | Method of making thin films dielectrics using a process for room temperature wet chemical growth of SiO based oxides on a substrate |
NZ527864A (en) | 2001-03-02 | 2004-05-28 | Smithkline Beecham Corp | Benzophenones as inhibitors of reverse transcriptase |
JO3429B1 (en) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | Hiv inhibiting pyrimidines derivatives |
WO2003097047A1 (en) | 2002-05-13 | 2003-11-27 | Eli Lilly And Company | Multicyclic compounds for use as melanin concentrating hormone antagonists in the treatment of obesity and diabetes |
EA009478B1 (en) * | 2002-08-23 | 2008-02-28 | Ардеа Байосайенсиз, Инк. | Non-nucleoside reverse transcriptase inhibitors |
US7642277B2 (en) * | 2002-12-04 | 2010-01-05 | Boehringer Ingelheim International Gmbh | Non-nucleoside reverse transcriptase inhibitors |
KR20110132482A (en) | 2003-02-07 | 2011-12-07 | 얀센 파마슈티카 엔.브이. | Pyrimidine derivatives for the prevention of hiv infection |
WO2005028479A2 (en) | 2003-09-25 | 2005-03-31 | Janssen Pharmaceutica N.V. | Hiv replication inhibiting purine derivatives |
US20080031901A1 (en) * | 2004-09-24 | 2008-02-07 | Abbott Laboratories | Sustained release monoeximic formulations of opioid and nonopioid analgesics |
US7517998B2 (en) | 2004-06-01 | 2009-04-14 | Boehringer Ingelheim International Gmbh | Non nucleoside reverse transcriptase inhibitors |
EP2433633A1 (en) | 2004-08-25 | 2012-03-28 | Ardea Biosciences, Inc. | Triazolyl alpha -mercaptoacetanildes as inhibitors of HIV reverse transcriptase |
WO2007050087A1 (en) * | 2004-08-25 | 2007-05-03 | Ardea Biosciences, Inc. | N[S(4-aryl-triazol-3-yl)α -mercaptoacetyl]-p-amino benozoic acids AS HIV REVERSE TRANSCRIPTASE INHIBITORS |
CN103058944B (en) * | 2007-11-27 | 2015-08-05 | 亚德生化公司 | Regulate the compound of blood uric acid levels |
EP2349258A1 (en) | 2008-10-24 | 2011-08-03 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( l-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triazol-3-ylthio) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
WO2010048592A1 (en) | 2008-10-24 | 2010-04-29 | Ardea Biosciences, Inc. | Compositions comprising 4- (2- ( 5-br0m0-4- ( 1-cyclopropylnaphthalen-4-yl) -4h-1, 2, 4-triaz0l-3-ylthi0) acetamido -3-chlorobenzoic acid and pharmaceutically acceptable salts thereof |
TWM377707U (en) * | 2009-09-16 | 2010-04-01 | Nat Energy Technology Co Ltd | Assembly of power supply |
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2005
- 2005-08-25 EP EP11184025A patent/EP2433633A1/en not_active Withdrawn
- 2005-08-25 EP EP05790722A patent/EP1789039B1/en active Active
- 2005-08-25 JP JP2007530127A patent/JP4952943B2/en active Active
- 2005-08-25 EP EP12187096.8A patent/EP2609917A1/en not_active Withdrawn
- 2005-08-25 CA CA2578068A patent/CA2578068C/en active Active
- 2005-08-25 SG SG200905668-0A patent/SG155246A1/en unknown
- 2005-08-25 RS RS20130029A patent/RS52632B/en unknown
- 2005-08-25 EA EA200700488A patent/EA014737B1/en not_active IP Right Cessation
- 2005-08-25 CN CN200910205213.7A patent/CN101817793B/en active Active
- 2005-08-25 SG SG2012083366A patent/SG185992A1/en unknown
- 2005-08-25 BR BRPI0514630A patent/BRPI0514630B8/en active IP Right Grant
- 2005-08-25 ES ES05790722T patent/ES2380604T3/en active Active
- 2005-08-25 ES ES09170772T patent/ES2374773T3/en active Active
- 2005-08-25 ME MEP-2013-18A patent/ME01512B/en unknown
- 2005-08-25 EP EP11177941A patent/EP2402011B1/en active Active
- 2005-08-25 PT PT09170772T patent/PT2135608E/en unknown
- 2005-08-25 AT AT05790722T patent/ATE540677T1/en active
- 2005-08-25 NZ NZ581376A patent/NZ581376A/en not_active IP Right Cessation
- 2005-08-25 AT AT09170772T patent/ATE528001T1/en active
- 2005-08-25 EP EP09170772A patent/EP2135608B8/en active Active
- 2005-08-25 SI SI200531426T patent/SI2135608T1/en unknown
- 2005-08-25 AU AU2005280130A patent/AU2005280130C9/en active Active
- 2005-08-25 MX MX2007002236A patent/MX2007002236A/en active IP Right Grant
- 2005-08-25 KR KR1020077006746A patent/KR101241716B1/en active IP Right Grant
- 2005-08-25 EA EA200901186A patent/EA015846B1/en not_active IP Right Cessation
- 2005-08-25 DK DK09170772.9T patent/DK2135608T3/en active
- 2005-08-25 WO PCT/US2005/030259 patent/WO2006026356A2/en active Application Filing
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