CO5590958A2 - Inhibidores no nucleosidos de la traqnscriptasa inversa - Google Patents
Inhibidores no nucleosidos de la traqnscriptasa inversaInfo
- Publication number
- CO5590958A2 CO5590958A2 CO05062907A CO05062907A CO5590958A2 CO 5590958 A2 CO5590958 A2 CO 5590958A2 CO 05062907 A CO05062907 A CO 05062907A CO 05062907 A CO05062907 A CO 05062907A CO 5590958 A2 CO5590958 A2 CO 5590958A2
- Authority
- CO
- Colombia
- Prior art keywords
- aryl groups
- carbocycles
- amido
- alkyl
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
-
- 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
-
- 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
- A61K31/4164—1,3-Diazoles
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/4192—1,2,3-Triazoles
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
- C07D233/84—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/28—Sulfur atoms
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
- C07D257/06—Five-membered rings with nitrogen atoms directly attached to the ring carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pain & Pain Management (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Saccharide Compounds (AREA)
- Furan Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1.- Uso de un compuesto de fórmula 1 para fabricar un medicamento para tratar o prevenir una infección del VIH que comprende administrar a un humano infectado una cantidad terapéuticamente eficaz de dicho compuesto de fórmula 1: Ar1-X-W-Ar2 (1)en la que Ar1 es(i) un heterociclo aromático de 5 ó 6 átomos que contiene de 1 a 4 heteroátomos que se seleccionan entre N, O o S; dicho heterociclo está opcionalmente sustituido con alquilo(C1-4), cicloalquilo(C3-7), cicloalquil(C3-7)-alquil(C1-3)-, en el que dicho alquilo, cicloalquilo o cicloalquilalquilo puede estar monosustituido con -OH; y/o fenilo cuando el heterociclo contiene de 1 a 3 átomos de N; en cualquier caso, el citado heterociclo está opcionalmente sustituido con:fenilo, fenilmetilo, heterociclo aromático de 5 ó 6 átomos, fusión fenil(carbociclo saturado o insaturado de 5 ó 6 átomos), fusión fenil-(carbociclo saturado o insaturado de 5 ó 6 átomos)}metilo, o fusión fenil-(heterociclo aromático de 5 ó 6 átomos); cada uno de los mencionados fenilo, fenilmetilo, heterociclo aromático, fusión fenil-carbociclo, fusión fenil-(carbociclo)metilo o fusión fenil-heterociclo aromático está, a su vez, opcionalmente sustituido, con 1 a 3 sustituyentes que se seleccionan independientemente entre:alquilo(C1-6), cicloalquilo(C3-7), cicloalquil(C3-7)-alquilo(C1-3), alquenilo(C2-6), O-alquilo(C1-4), S-alquilo(C1-4), halo, CF3, OCF3, OH, NO2, CN, fenilo opcionalmente sustituido con alquilo(C1-6) o nitro, fenilmetilo opcionalmente sustituido con alquilo(C1-6) o nitro, SO2NH2, SO2-alquilo(C1-4), C(O)NH2, C(O)OR1, NR2R3, morfolino o 1-pirrolilo, en la que R1 es H o alquilo(C1-4), y en la que R2 y R3 cada uno independientemente es H o alquilo(C1-4); en la que dichos sustituyentes son estéricamente compatibles; o(ii) carbociclo saturado o insaturado de 5 ó 6 átomos que está sustituido con fenilo o naftilo, dicho carbociclo saturado o insaturado, o el fenilo o el naftilo opcionalmente sustituidos con los mismos 1 a 3 sustituyentes como se define para los sustituyentes en la sección (i); o (iii) bencimidazol opcionalmente N-sustituido con fenilo o una fusión fenilcarbociclo como se definió más arriba;X es un heteroátomo que se selecciona entre O, S, SO, SO2 o NR4, en el que R4 es H o alquilo(C1-4); o X es un enlace de valencia o CR4AR4B, ...
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43079602P | 2002-12-04 | 2002-12-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO5590958A2 true CO5590958A2 (es) | 2005-12-30 |
Family
ID=32469533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO05062907A CO5590958A2 (es) | 2002-12-04 | 2005-06-27 | Inhibidores no nucleosidos de la traqnscriptasa inversa |
Country Status (18)
Country | Link |
---|---|
US (1) | US7642277B2 (es) |
EP (1) | EP1569919B1 (es) |
JP (1) | JP4550584B2 (es) |
KR (1) | KR20050084112A (es) |
CN (1) | CN1720043A (es) |
AT (1) | ATE554077T1 (es) |
AU (1) | AU2003287806A1 (es) |
BR (1) | BR0316385A (es) |
CA (1) | CA2505033C (es) |
CO (1) | CO5590958A2 (es) |
EA (1) | EA200500900A1 (es) |
EC (1) | ECSP055836A (es) |
HR (1) | HRP20050502A2 (es) |
MX (1) | MXPA05005871A (es) |
NO (1) | NO20052712L (es) |
PL (1) | PL378198A1 (es) |
WO (1) | WO2004050643A2 (es) |
ZA (1) | ZA200503960B (es) |
Families Citing this family (62)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2496565C (en) * | 2002-08-23 | 2013-04-02 | Ribapharm Inc. | Non-nucleoside reverse transcriptase inhibitors |
US7563905B2 (en) | 2004-03-12 | 2009-07-21 | Wyeth | Triazole derivatives and method of using the same to treat HIV infections |
WO2005115147A2 (en) * | 2004-05-18 | 2005-12-08 | Merck & Co., Inc. | Hiv reverse transcriptase inhibitors |
US7517998B2 (en) * | 2004-06-01 | 2009-04-14 | Boehringer Ingelheim International Gmbh | Non nucleoside reverse transcriptase inhibitors |
US20060025480A1 (en) | 2004-08-02 | 2006-02-02 | Boehringer Ingelheim International Gmbh | Benzoic acid derivatives as non nucleoside reverse transcriptase inhibitors |
ME01512B (me) * | 2004-08-25 | 2014-04-20 | Ardea Biosciences Inc | S-triazolil alfa-merkaptoacetanilida kao inhibitori HIV reversne transkriptaze |
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 |
KR100940058B1 (ko) * | 2004-08-25 | 2010-02-04 | 아디아 바이오사이언스즈 인크. | HIV 역 전사 효소의 억제제로서 S-트리아졸릴 α-메르캅토아세트아닐리드 |
CA2577144C (en) | 2004-09-30 | 2011-06-21 | Boehringer Ingelheim International Gmbh | Alkynyl compounds as non-nucleoside reverse transcriptase inhibitors |
US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
US8399666B2 (en) | 2005-11-04 | 2013-03-19 | Panmira Pharmaceuticals, Llc | 5-lipoxygenase-activating protein (FLAP) inhibitors |
GB2431927B (en) | 2005-11-04 | 2010-03-17 | Amira Pharmaceuticals Inc | 5-Lipoxygenase-activating protein (FLAP) inhibitors |
JP2009519349A (ja) | 2005-12-15 | 2009-05-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を変調する化合物 |
UA93548C2 (uk) | 2006-05-05 | 2011-02-25 | Айерем Елелсі | Сполуки та композиції як модулятори хеджхогівського сигнального шляху |
WO2008014199A2 (en) | 2006-07-28 | 2008-01-31 | Boehringer Ingelheim International Gmbh | Sulfonyl compounds which modulate the cb2 receptor |
KR20090069318A (ko) | 2006-09-25 | 2009-06-30 | 베링거 인겔하임 인터내셔날 게엠베하 | Cb2 수용체를 조절하는 화합물 |
EP1942104A1 (en) | 2006-12-20 | 2008-07-09 | sanofi-aventis | Heteroarylcyclopropanecarboxamides and their use as pharmaceuticals |
EP2217565B1 (en) | 2007-11-07 | 2013-05-22 | Boehringer Ingelheim International GmbH | Compounds which modulate the cb2 receptor |
ATE541841T1 (de) | 2007-11-15 | 2012-02-15 | Boehringer Ingelheim Int | Inhibitoren der replikation des human immunodeficiency virus |
EP2220046B1 (en) | 2007-11-16 | 2014-06-18 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
SI2217577T1 (sl) | 2007-11-27 | 2014-11-28 | Ardea Biosciences, Inc. | Nove spojine in sestavki ter metode uporabe |
US20110160249A1 (en) | 2008-05-23 | 2011-06-30 | Schaab Kevin Murray | 5-lipoxygenase-activating protein inhibitor |
JP5749162B2 (ja) | 2008-07-10 | 2015-07-15 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を調節するスルホン化合物 |
KR101294872B1 (ko) * | 2008-09-04 | 2013-08-08 | 아디아 바이오사이언스즈 인크. | 요산 수치를 조절하기 위한 화합물, 조성물 및 이들의 사용 방법 |
US8173690B2 (en) | 2008-09-04 | 2012-05-08 | Ardea Biosciences, Inc. | Compounds, compositions and methods of using same 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 |
US20110257177A1 (en) * | 2008-09-22 | 2011-10-20 | Calcimedica, Inc. | Benzylthiotetrazole inhibitors of store operated calcium release |
KR20110063438A (ko) | 2008-09-25 | 2011-06-10 | 베링거 인겔하임 인터내셔날 게엠베하 | Cb2 수용체를 선택적으로 조절하는 설포닐 화합물 |
JP5643290B2 (ja) | 2009-04-09 | 2014-12-17 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Hiv複製の阻害薬 |
CA2760940A1 (en) | 2009-05-20 | 2010-11-25 | Ardea Biosciences, Inc. | Methods of modulating uric acid levels |
US8299103B2 (en) | 2009-06-15 | 2012-10-30 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the CB2 receptor |
WO2010147791A1 (en) | 2009-06-16 | 2010-12-23 | Boehringer Ingelheim International Gmbh | Azetidine 2 -carboxamide derivatives which modulate the cb2 receptor |
JP2013505295A (ja) | 2009-09-22 | 2013-02-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を選択的に調節する化合物 |
EP2523936A1 (en) | 2010-01-15 | 2012-11-21 | Boehringer Ingelheim International GmbH | Compounds which modulate the cb2 receptor |
WO2011109324A1 (en) | 2010-03-05 | 2011-09-09 | Boehringer Ingelheim International Gmbh | Tetrazole compounds which selectively modulate the cb2 receptor |
US8846936B2 (en) | 2010-07-22 | 2014-09-30 | Boehringer Ingelheim International Gmbh | Sulfonyl compounds which modulate the CB2 receptor |
JP6205354B2 (ja) | 2011-07-06 | 2017-09-27 | ギリアード サイエンシーズ, インコーポレイテッド | Hivの処置のための化合物 |
US8754065B2 (en) | 2011-08-16 | 2014-06-17 | Gilead Sciences, Inc. | Tenofovir alafenamide hemifumarate |
RU2014110624A (ru) * | 2011-09-01 | 2015-10-10 | Ф. Хоффманн-Ля Рош Аг | Ингибиторы поли(адф-рибоза)-полимеразы |
US9399645B2 (en) | 2011-12-20 | 2016-07-26 | Boehringer Ingelheim International Gmbh | Inhibitors of HIV replication |
CN102675212B (zh) * | 2012-05-09 | 2014-11-05 | 昆明理工大学 | N-取代苯基-2-((1h-苯并咪唑-2-基)巯基)乙酰胺类衍生物及其用途 |
TW201443037A (zh) * | 2013-01-09 | 2014-11-16 | Gilead Sciences Inc | 治療用化合物 |
PT2943487T (pt) * | 2013-01-09 | 2016-12-15 | Gilead Sciences Inc | Heteroarilos de 5 membros e sua utilização como agentes antivirais |
EP2803668A1 (en) | 2013-05-17 | 2014-11-19 | Boehringer Ingelheim International Gmbh | Novel (cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles |
CN105263913B (zh) * | 2013-06-14 | 2017-12-15 | 广东东阳光药业有限公司 | 硫代1,2,4‑三唑衍生物及其制备方法 |
US10017479B2 (en) | 2013-08-02 | 2018-07-10 | Gregory Rosocha | Process to make non nucleosidal reverse transcriptase inhibitors (NNRTI) for the treatment of HIV |
WO2015130964A1 (en) | 2014-02-28 | 2015-09-03 | Gilead Sciences, Inc. | Therapeutic compounds |
CN104016927B (zh) * | 2014-06-19 | 2016-06-22 | 山东大学 | 嘧啶巯乙酰胺类衍生物及其制备方法与应用 |
US10112929B2 (en) | 2015-03-09 | 2018-10-30 | Bristol-Myers Squibb Company | Lactams as inhibitors of rock |
CN104817509B (zh) * | 2015-04-13 | 2019-05-17 | 安徽省逸欣铭医药科技有限公司 | Lesinurad类似物及其制备方法和医药用途 |
MX369307B (es) | 2016-08-19 | 2019-11-05 | Gilead Sciences Inc | Compuestos terapeuticos utiles para tratamiento profilactico o terapeutico de infeccion por virus de inmunodeficiencia humana. |
TW202024061A (zh) | 2017-08-17 | 2020-07-01 | 美商基利科學股份有限公司 | Hiv蛋白質膜抑制劑之固體形式 |
AR112412A1 (es) | 2017-08-17 | 2019-10-23 | Gilead Sciences Inc | Formas de sal de colina de un inhibidor de la cápside del vih |
AU2019221568B2 (en) | 2018-02-15 | 2021-04-22 | Gilead Sciences, Inc. | Pyridine derivatives and their use for treating HIV infection |
EP3752496B1 (en) | 2018-02-16 | 2023-07-05 | Gilead Sciences, Inc. | Methods and intermediates for preparing a therapeutic compound useful in the treatment of retroviridae viral infection |
KR20210033492A (ko) | 2018-07-16 | 2021-03-26 | 길리애드 사이언시즈, 인코포레이티드 | Hiv의 치료를 위한 캡시드 억제제 |
CN114727999A (zh) | 2019-11-26 | 2022-07-08 | 吉利德科学公司 | 用于预防hiv的衣壳抑制剂 |
MX2022006489A (es) * | 2019-11-29 | 2022-07-04 | Jiangsu Hengrui Medicine Co | Derivado de anillo de piridina fusionado, metodo de preparacion y usos farmaceuticos del mismo. |
CN110950816B (zh) * | 2019-12-13 | 2021-07-06 | 山东金城医药化工有限公司 | 1-(2-二甲基氨基乙基)-5-巯基四唑的合成方法 |
CN115996925A (zh) | 2020-06-25 | 2023-04-21 | 吉利德科学公司 | 用于治疗hiv的衣壳抑制剂 |
KR20240117588A (ko) | 2021-12-03 | 2024-08-01 | 길리애드 사이언시즈, 인코포레이티드 | Hiv 바이러스 감염 치료용 화합물 |
EP4440702A1 (en) | 2021-12-03 | 2024-10-09 | Gilead Sciences, Inc. | Therapeutic compounds for hiv virus infection |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4252815A (en) | 1977-04-21 | 1981-02-24 | Mead Johnson & Company | Methods of treating cardiovascular diseases with phenyltetrazolyloxy propanolamines |
US4186131A (en) | 1977-04-21 | 1980-01-29 | Mead Johnson & Company | Phenyltetrazolyloxy propanolamines |
US4663323A (en) | 1978-09-07 | 1987-05-05 | Otsuka Pharmaceutical Co., Ltd. | Tetrazole derivatives, anti-ulcer composition containing the same and method for treating ulcers |
US4766120A (en) | 1978-09-07 | 1988-08-23 | Otsuka Pharmaceutical Company, Limited | Tetrazole derivatives, having a further unsaturated heterocyclic ring anti-ulcer composition containing the same and method for treating ulcers |
JPS5536447A (en) | 1978-09-07 | 1980-03-14 | Otsuka Pharmaceut Co Ltd | Butyramide derivative |
DE2946432A1 (de) | 1979-11-17 | 1981-06-11 | Bayer Ag, 5090 Leverkusen | Tetrazolyloxycarbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
JPH03198048A (ja) | 1989-12-27 | 1991-08-29 | Konica Corp | ハロゲン化銀写真感光材料 |
US5124230A (en) | 1990-02-02 | 1992-06-23 | Fuji Photo Film Co., Ltd. | Silver halide photographic material |
IL99731A0 (en) | 1990-10-18 | 1992-08-18 | Merck & Co Inc | Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them |
CA2156420A1 (en) | 1993-02-24 | 1994-09-01 | Theresa M. Williams | Inhibitors of hiv reverse transcriptase |
FR2759369B1 (fr) | 1997-02-13 | 1999-04-02 | Essilor Int | Nouveaux monomeres mono(thio)(meth)acrylates, composes intermediaires pour la synthese de ces monomeres, compositions polymerisables et polymeres obtenus et leurs applications optiques et ophtalmiques |
US6245817B1 (en) | 1997-02-14 | 2001-06-12 | Bayer Corporation | NPY5 receptor antagonists and methods for using same |
AU6267198A (en) * | 1997-02-14 | 1998-09-08 | Bayer Corporation | Amides as npy5 receptor antagonists |
DE69809827D1 (de) | 1997-03-31 | 2003-01-16 | Korea Res Inst Chem Tech | Chinolinische Sulfid-Derivate als NMDA Rezeptor-Antagonisten und Verfahren zu ihrer Herstellung |
US6124306A (en) | 1997-09-25 | 2000-09-26 | Pharmacia & Upjohn Company | Thioalkyl alpha substituted pyrimidine compounds |
US5998411A (en) * | 1998-03-17 | 1999-12-07 | Hughes Institute | Heterocyclic nonnucleoside inhibitors of reverse transcriptase |
NZ508297A (en) | 1998-04-27 | 2002-12-20 | Centre Nat Rech Scient | 3-(amino- or aminoalkyl)pyridinone derivatives and their use for the treatment of HIV related diseases |
IT1305313B1 (it) | 1998-07-17 | 2001-05-04 | Colla Paolo | 3,4 - diidro- 6- benzil-4-oxopirimidine sostituite e relativo processodi produzione e impiego nella terapia delle infezioni da hiv-1. |
US6124324A (en) | 1999-06-23 | 2000-09-26 | Hughes Institute | Thiophene-ethyl thiourea compounds and use |
EP1206568A2 (en) | 1999-08-30 | 2002-05-22 | K.U. Leuven Research & Development | Target for antiparasitic agents and inhibitors thereof |
US6221573B1 (en) | 1999-10-27 | 2001-04-24 | Eastman Kodak Company | Yellow coupler, photographic element, and process |
TWI270547B (en) | 2000-06-16 | 2007-01-11 | Boehringer Ingelheim Ca Ltd | Non-nucleoside reverse transcriptase inhibitors |
AU2001221154A1 (en) | 2000-10-19 | 2002-04-29 | Parker Hughes Institute | Aromatic and heterocyclic thiazolyl thiourea compounds and use |
US6995283B2 (en) | 2001-03-02 | 2006-02-07 | Smithkline Beecham Corporation | Benzophenones as inhibitors of reverse transcriptase |
CA2496565C (en) * | 2002-08-23 | 2013-04-02 | Ribapharm Inc. | Non-nucleoside reverse transcriptase inhibitors |
-
2003
- 2003-11-21 US US10/719,369 patent/US7642277B2/en active Active
- 2003-12-01 MX MXPA05005871A patent/MXPA05005871A/es not_active Application Discontinuation
- 2003-12-01 CA CA2505033A patent/CA2505033C/en not_active Expired - Fee Related
- 2003-12-01 CN CNA2003801051640A patent/CN1720043A/zh active Pending
- 2003-12-01 PL PL378198A patent/PL378198A1/pl not_active Application Discontinuation
- 2003-12-01 AT AT03779603T patent/ATE554077T1/de active
- 2003-12-01 EP EP03779603A patent/EP1569919B1/en not_active Expired - Lifetime
- 2003-12-01 KR KR1020057009999A patent/KR20050084112A/ko not_active Application Discontinuation
- 2003-12-01 BR BR0316385-7A patent/BR0316385A/pt not_active IP Right Cessation
- 2003-12-01 AU AU2003287806A patent/AU2003287806A1/en not_active Abandoned
- 2003-12-01 WO PCT/CA2003/001870 patent/WO2004050643A2/en active Application Filing
- 2003-12-01 JP JP2004555920A patent/JP4550584B2/ja not_active Expired - Fee Related
- 2003-12-01 EA EA200500900A patent/EA200500900A1/ru unknown
-
2005
- 2005-05-17 ZA ZA200503960A patent/ZA200503960B/en unknown
- 2005-06-03 EC EC2005005836A patent/ECSP055836A/es unknown
- 2005-06-03 HR HR20050502A patent/HRP20050502A2/xx not_active Application Discontinuation
- 2005-06-06 NO NO20052712A patent/NO20052712L/no not_active Application Discontinuation
- 2005-06-27 CO CO05062907A patent/CO5590958A2/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JP2006514936A (ja) | 2006-05-18 |
ATE554077T1 (de) | 2012-05-15 |
PL378198A1 (pl) | 2006-03-06 |
EA200500900A1 (ru) | 2005-12-29 |
HRP20050502A2 (en) | 2006-07-31 |
WO2004050643A3 (en) | 2004-09-10 |
AU2003287806A1 (en) | 2004-06-23 |
JP4550584B2 (ja) | 2010-09-22 |
CA2505033A1 (en) | 2004-06-17 |
BR0316385A (pt) | 2005-10-04 |
CA2505033C (en) | 2011-09-20 |
MXPA05005871A (es) | 2005-08-29 |
EP1569919A2 (en) | 2005-09-07 |
US7642277B2 (en) | 2010-01-05 |
NO20052712L (no) | 2005-06-27 |
CN1720043A (zh) | 2006-01-11 |
ECSP055836A (es) | 2005-08-11 |
NO20052712D0 (no) | 2005-06-06 |
ZA200503960B (en) | 2006-11-29 |
US20050054639A1 (en) | 2005-03-10 |
WO2004050643A2 (en) | 2004-06-17 |
KR20050084112A (ko) | 2005-08-26 |
EP1569919B1 (en) | 2012-04-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CO5590958A2 (es) | Inhibidores no nucleosidos de la traqnscriptasa inversa | |
NO20090541L (no) | Prodrug av cinnamidforbindelse | |
DE69829875D1 (de) | Piperazin-verbindungen und ihre medizinische verwendung | |
DK0705254T3 (da) | Phenylheterocykliske forbindelser som cyclooxygenase-2-inhibitorer | |
NO20081930L (no) | Oksazolforbindelser og farmasoytiske blandinger | |
NO20070368L (no) | Virale polymeraseinhibitorer | |
MY143245A (en) | 4- 2-(cycloalkylamino)pyrimidin-4-yl-(phenyl)-imidazolin-2-one derivatives as p38 map-kinase inhibitors for the treatment of inflammatory diseases | |
NO20082562L (no) | Heterocyklisk forbindelse med inhiberende aktivitet pa 11- -hydroksysteroid-dehydrogenase type 1 | |
NO950533D0 (no) | Hydroksyetylaminosulfonamider som er nyttige som retrovirale proteasehemmere | |
AR055112A1 (es) | Fungicidas n-(2-(haloalcoxi) fenil) heteroaril carboxamidas | |
DE602004028907D1 (de) | Als kinaseinhibitoren geeignete verbindungen auf thiazolylbasis | |
WO2004083177A3 (en) | Linear chain substituted monocyclic and bicyclic derivatives as factor xa inhibitors | |
NO20062892L (no) | 7-fenylalkyl-substituert 2-kinolinoner og 2-kinoksalinoner som poly(adp-ribose)-polymeraseinhibitorer | |
NO20051600L (no) | 1,4-disubstituerte piperidinderivater og anvendelse derav som 11-betaHSD1 inhibitorer | |
WO2006014282A3 (en) | Prodrugs of hiv protease inhibitors | |
NO20061789L (no) | Aminopyridinderivater som induserbare NO-syntaseinhibitorer | |
SE0103710D0 (sv) | Compounds | |
BRPI0910761A2 (pt) | compostos tendo atividade antagonista de receptores npy y5 e composições farmacêuticas compreendendo os mesmos | |
DK1706414T3 (da) | Fremgangsmåde til fluorcytidinderivater | |
WO2008136378A1 (ja) | 新規なスルホンアミド誘導体またはその塩 | |
WO2005058841A3 (en) | Hiv protease inhibiting compounds | |
DE602004023873D1 (de) | Verwendung davon | |
WO2004066952A3 (en) | Benzoxazole, benzothiazole, and benzimidazole derivatives for the treatment of cancer and other diseases | |
DK1628968T3 (da) | 4-imidazolin-2-on-forbindelser | |
BR0013409B1 (pt) | compostos fungicidas possuindo uma porção flúorvinil ou fluorpropenil-oxifeniloxima e processo para preparação dos mesmos. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Application refused |