DE602004008227D1 - Inhibitoren dernicht-nukleosid-inhibitoren der reversen transkriptase - Google Patents
Inhibitoren dernicht-nukleosid-inhibitoren der reversen transkriptaseInfo
- Publication number
- DE602004008227D1 DE602004008227D1 DE602004008227T DE602004008227T DE602004008227D1 DE 602004008227 D1 DE602004008227 D1 DE 602004008227D1 DE 602004008227 T DE602004008227 T DE 602004008227T DE 602004008227 T DE602004008227 T DE 602004008227T DE 602004008227 D1 DE602004008227 D1 DE 602004008227D1
- Authority
- DE
- Germany
- Prior art keywords
- inhibitors
- reverse transcriptase
- nucleoside
- nucleoside inhibitors
- transcriptase
- 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.)
- Expired - Lifetime
Links
- 239000003112 inhibitor Substances 0.000 title 2
- 102100034343 Integrase Human genes 0.000 title 1
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 title 1
- 239000002777 nucleoside Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
-
- 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
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D409/06—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 carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44797403P | 2003-02-18 | 2003-02-18 | |
US447974P | 2003-02-18 | ||
PCT/EP2004/001477 WO2004074257A1 (en) | 2003-02-18 | 2004-02-17 | Non-nucleoside reverse transcriptase inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
DE602004008227D1 true DE602004008227D1 (de) | 2007-09-27 |
DE602004008227T2 DE602004008227T2 (de) | 2008-05-15 |
Family
ID=32908518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE602004008227T Expired - Lifetime DE602004008227T2 (de) | 2003-02-18 | 2004-02-17 | Inhibitoren dernicht-nukleosid-inhibitoren der reversen transkriptase |
Country Status (17)
Country | Link |
---|---|
US (1) | US7241794B2 (de) |
EP (1) | EP1597235B1 (de) |
JP (1) | JP4608480B2 (de) |
KR (1) | KR100776093B1 (de) |
CN (1) | CN100389109C (de) |
AR (1) | AR043195A1 (de) |
AT (1) | ATE370124T1 (de) |
BR (1) | BRPI0407591A (de) |
CA (1) | CA2515151C (de) |
CL (1) | CL2004000270A1 (de) |
DE (1) | DE602004008227T2 (de) |
ES (1) | ES2291854T3 (de) |
MX (1) | MXPA05008748A (de) |
PL (1) | PL378556A1 (de) |
RU (1) | RU2305680C2 (de) |
TW (1) | TW200423930A (de) |
WO (1) | WO2004074257A1 (de) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA05011922A (es) * | 2003-05-07 | 2006-02-17 | Pfizer Prod Inc | Ligandos del receptor de cannabinoides y sus usos. |
CN1993333B (zh) | 2004-08-04 | 2012-08-01 | 大正制药株式会社 | 三唑衍生物 |
UA87884C2 (uk) * | 2004-12-03 | 2009-08-25 | Мерк Энд Ко., Инк. | Безводна кристалічна калієва сіль інгібітора віл-інтегрази |
US8022091B2 (en) | 2006-02-03 | 2011-09-20 | Taisho Pharmaceutical Co., Ltd. | Triazole derivative |
EP1988081B1 (de) * | 2006-02-06 | 2012-10-17 | Taisho Pharmaceutical Co., Ltd | Bindungsinhibitor von sphingosin-1-phosphat |
US7812175B2 (en) * | 2006-02-14 | 2010-10-12 | Ihara Chemical Industry Co., Ltd. | Process for production of 5-alkoxy-4-hydroxymethylpyrazole compound |
CL2007002105A1 (es) * | 2006-07-21 | 2008-02-22 | Hoffmann La Roche | Compuestos derivados de 2-[3-(3-cianofenoxi)(fenoxi o fenilsulfanil)]-n-fenil acetamida, inhibidores de la transcriptasa inversa del vih; procedimiento de preparacion; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar u |
AU2007286345B2 (en) * | 2006-08-16 | 2012-03-08 | F. Hoffmann-La Roche Ag | Non-nucleoside reverse transcriptase inhibitors |
JP2010522706A (ja) | 2007-03-29 | 2010-07-08 | エフ.ホフマン−ラ ロシュ アーゲー | 非ヌクレオシド逆転写酵素阻害剤 |
WO2009017219A1 (ja) | 2007-08-01 | 2009-02-05 | Taisho Pharmaceutical Co., Ltd. | S1p1結合阻害物質 |
MX2010006397A (es) * | 2007-12-21 | 2010-07-05 | Hoffmann La Roche | Compuestos heterociclicos antivirales. |
DE102008015033A1 (de) * | 2008-03-17 | 2009-09-24 | Aicuris Gmbh & Co. Kg | Substituierte (Pyrazolyl-carbonyl)imidazolidinone und ihre Verwendung |
EA024804B1 (ru) * | 2010-03-30 | 2016-10-31 | Мерк Кэнэда Инк. | Ненуклеозидные ингибиторы обратной транскриптазы, композиции, их содержащие, и их применение |
KR101891838B1 (ko) | 2010-07-15 | 2018-09-28 | 다이닛본 스미토모 세이야꾸 가부시끼가이샤 | 피라졸 화합물 |
EP2508511A1 (de) | 2011-04-07 | 2012-10-10 | Laboratoire Biodim | Inhibitoren der Virenreplikation, Verfahren zu deren Herstellung und deren therapeutische Verwendung |
WO2013134562A1 (en) | 2012-03-09 | 2013-09-12 | Inception 2, Inc. | Triazolone compounds and uses thereof |
MX2014014911A (es) | 2012-06-20 | 2015-05-15 | Univ Vanderbilt | Análogos de alcoxi pirazol bicíclico sustituido como moduladores alostéricos de receptores de mglur5. |
CN104736156A (zh) | 2012-06-20 | 2015-06-24 | 范德比尔特大学 | 作为mglur5受体变构调节剂的取代的双环烷氧基吡唑类似物 |
JO3470B1 (ar) | 2012-10-08 | 2020-07-05 | Merck Sharp & Dohme | مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv |
WO2014099503A1 (en) | 2012-12-20 | 2014-06-26 | Inception 2, Inc. | Triazolone compounds and uses thereof |
PE20160880A1 (es) | 2013-09-06 | 2016-09-22 | Inception 2 Inc | Compuestos de triazolona y usos de los mismos |
EP3125894B1 (de) | 2014-04-01 | 2020-09-09 | Merck Sharp & Dohme Corp. | Prodrugs von hiv-umkehrtranskriptasehemmern |
WO2016044445A2 (en) | 2014-09-17 | 2016-03-24 | Ironwood Pharmaceuticals, Inc. | sGC STIMULATORS |
JP2017527604A (ja) | 2014-09-17 | 2017-09-21 | アイアンウッド ファーマシューティカルズ インコーポレイテッド | sGC刺激剤 |
CN107428694A (zh) * | 2015-03-19 | 2017-12-01 | 杜邦公司 | 杀真菌吡唑 |
WO2018001973A1 (en) * | 2016-06-29 | 2018-01-04 | Laboratorios Del Dr. Esteve S.A. | Pyrazole derivatives having activity against pain |
CN110818636A (zh) * | 2019-11-29 | 2020-02-21 | 河北科技大学 | 一种化合物或其盐及其应用和合成方法 |
CN115677585B (zh) * | 2022-10-31 | 2024-03-19 | 上海群力化工有限公司 | 一种甲醛吡唑衍生物的合成工艺 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR9509024A (pt) | 1994-09-26 | 1997-09-30 | Shionogi & Co | Derivados de imidazol |
DE19734664A1 (de) * | 1997-08-11 | 1999-02-18 | Bayer Ag | (Hetero)Aryloxypyrazole |
GB0016787D0 (en) * | 2000-07-07 | 2000-08-30 | Pfizer Ltd | Compounds useful in therapy |
US20030008841A1 (en) * | 2000-08-30 | 2003-01-09 | Rene Devos | Anti-HCV nucleoside derivatives |
GB0024795D0 (en) * | 2000-10-10 | 2000-11-22 | Hoffmann La Roche | Pyrazole derivatives for the treatment of viral diseases |
GB0028484D0 (en) * | 2000-11-22 | 2001-01-10 | Hoffmann La Roche | Imidazolone derivatives for the treatment of viral diseases |
CZ305099B6 (cs) * | 2001-04-10 | 2015-05-06 | Pfizer Inc. | Derivát pyrazolu, způsoby a meziprodukty pro výrobu, farmaceutická kompozice s jeho obsahem a jeho lékařské aplikace, zejména k léčení infekcí HIV |
GB0113524D0 (en) * | 2001-06-04 | 2001-07-25 | Hoffmann La Roche | Pyrazole derivatives |
-
2004
- 2004-02-12 TW TW093103358A patent/TW200423930A/zh unknown
- 2004-02-16 CL CL200400270A patent/CL2004000270A1/es unknown
- 2004-02-17 DE DE602004008227T patent/DE602004008227T2/de not_active Expired - Lifetime
- 2004-02-17 JP JP2006500034A patent/JP4608480B2/ja not_active Expired - Fee Related
- 2004-02-17 AR ARP040100477A patent/AR043195A1/es not_active Application Discontinuation
- 2004-02-17 WO PCT/EP2004/001477 patent/WO2004074257A1/en active IP Right Grant
- 2004-02-17 CA CA2515151A patent/CA2515151C/en not_active Expired - Fee Related
- 2004-02-17 RU RU2005128832/04A patent/RU2305680C2/ru active
- 2004-02-17 AT AT04711607T patent/ATE370124T1/de not_active IP Right Cessation
- 2004-02-17 KR KR1020057015085A patent/KR100776093B1/ko not_active IP Right Cessation
- 2004-02-17 PL PL378556A patent/PL378556A1/pl not_active Application Discontinuation
- 2004-02-17 EP EP04711607A patent/EP1597235B1/de not_active Expired - Lifetime
- 2004-02-17 CN CNB2004800044061A patent/CN100389109C/zh not_active Expired - Fee Related
- 2004-02-17 BR BRPI0407591-9A patent/BRPI0407591A/pt not_active IP Right Cessation
- 2004-02-17 ES ES04711607T patent/ES2291854T3/es not_active Expired - Lifetime
- 2004-02-17 MX MXPA05008748A patent/MXPA05008748A/es active IP Right Grant
- 2004-02-18 US US10/781,373 patent/US7241794B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP1597235B1 (de) | 2007-08-15 |
CN1751028A (zh) | 2006-03-22 |
JP4608480B2 (ja) | 2011-01-12 |
PL378556A1 (pl) | 2006-05-02 |
DE602004008227T2 (de) | 2008-05-15 |
ATE370124T1 (de) | 2007-09-15 |
KR100776093B1 (ko) | 2007-11-15 |
US7241794B2 (en) | 2007-07-10 |
ES2291854T3 (es) | 2008-03-01 |
CA2515151A1 (en) | 2004-09-02 |
CA2515151C (en) | 2010-11-30 |
KR20050105471A (ko) | 2005-11-04 |
US20040192666A1 (en) | 2004-09-30 |
RU2305680C2 (ru) | 2007-09-10 |
JP2006515339A (ja) | 2006-05-25 |
CL2004000270A1 (es) | 2005-02-04 |
BRPI0407591A (pt) | 2006-02-14 |
CN100389109C (zh) | 2008-05-21 |
EP1597235A1 (de) | 2005-11-23 |
WO2004074257A1 (en) | 2004-09-02 |
MXPA05008748A (es) | 2005-09-20 |
TW200423930A (en) | 2004-11-16 |
AR043195A1 (es) | 2005-07-20 |
AU2004213134A1 (en) | 2004-09-02 |
RU2005128832A (ru) | 2006-04-27 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8364 | No opposition during term of opposition |