PE20020269A1 - Derivados de pirrol como inhibidores de transcriptasa inversa del vih - Google Patents
Derivados de pirrol como inhibidores de transcriptasa inversa del vihInfo
- Publication number
- PE20020269A1 PE20020269A1 PE2001000487A PE2001000487A PE20020269A1 PE 20020269 A1 PE20020269 A1 PE 20020269A1 PE 2001000487 A PE2001000487 A PE 2001000487A PE 2001000487 A PE2001000487 A PE 2001000487A PE 20020269 A1 PE20020269 A1 PE 20020269A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- methyl
- aryl
- inhibitors
- reverse transcriptase
- Prior art date
Links
Classifications
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D207/36—Oxygen or sulfur 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
- C07D401/14—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 three or more hetero rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Immunology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
Abstract
SE REFIERE A DERIVADOS DE PIRROL DE FORMULA I DONDE R1 Y R2 SON ALQUILO, CICLOALQUILO, ARILO, HETEROCICLO; R3 ES H, ALQUILO, CICLOALQUILO, ARILO, HETEROCICLO; R4 ES H, ALQUILO, CARBOXILO, C=OR, CONR'R'", CN, ALQUENILO; R ES H, ALQUILO, ALCOXILO, TRIFLUOROMETILO, METIL-OXI-CARBONILO, ETIL-OXI-CARBONILO; R' Y R" SON H, ALQUILO, ARILO; R5 ES ALQUILO, ARILO, Z-C(=O)R"'; Z ES ENLACE, HC=CH; R2'" ES H, ALQUILO; X ES S, SO, SO2, N-ALQUILO; X-R2 EN CONJUNTO ES CH2-ARILO, CH2-HETEROCICLO; UNO DE R3 Y R4 ES H Y ALQUILO EN R3 NO ES CF3. SON COMPUESTOS PREFERIDOS 5-(3,5-DICLOROFENIL-TIO)-4-ISOPROPIL-2-METIL-1-[(3-PIRIDIL)METIL]-1H-PIRROL-3-METANOL, 4-ISOPROPIL-2-METIL-5-FENILTIO-1-[(4-PIRIDIL)-METIL]-1H-PIRROL-3-METANOL, ENTRE OTROS, TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION Y A COMPUESTOS INTERMEDIOS. LOS COMPUESTOS SON INHIBIDORES DE LA ENZIMA TRANSCRIPTASA INVERSA Y PUEDE SER UTIL PARA EL TRATAMIENTO EL VIH.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0016453.3A GB0016453D0 (en) | 2000-07-04 | 2000-07-04 | Pyrrole derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20020269A1 true PE20020269A1 (es) | 2002-04-08 |
Family
ID=9895031
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2001000487A PE20020269A1 (es) | 2000-07-04 | 2001-05-25 | Derivados de pirrol como inhibidores de transcriptasa inversa del vih |
Country Status (17)
Country | Link |
---|---|
US (1) | US6737429B2 (es) |
EP (1) | EP1301481A1 (es) |
JP (1) | JP2004502674A (es) |
KR (1) | KR100549884B1 (es) |
CN (1) | CN1440385A (es) |
AR (1) | AR028602A1 (es) |
AU (2) | AU2001263874B2 (es) |
BR (1) | BR0112241A (es) |
CA (1) | CA2412270A1 (es) |
EC (1) | ECSP014109A (es) |
GB (1) | GB0016453D0 (es) |
GT (1) | GT200100111A (es) |
MX (1) | MXPA02012409A (es) |
PA (1) | PA8516201A1 (es) |
PE (1) | PE20020269A1 (es) |
UY (1) | UY26720A1 (es) |
WO (1) | WO2002002524A1 (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1405849A1 (en) * | 2002-10-04 | 2004-04-07 | Corning Incorporated | Halogenated styrene compounds and low-absorption-loss polymers obtainable therefrom |
WO2005063293A1 (ja) * | 2003-12-26 | 2005-07-14 | Masatoshi Hagiwara | Sr蛋白質のリン酸化制御方法、および、sr蛋白質の活性制御剤を有効成分とする抗ウイルス剤 |
US8048909B2 (en) | 2004-09-30 | 2011-11-01 | Takeda Pharmaceutical Company Limited | Proton pump inhibitors |
TW200628446A (en) * | 2004-12-14 | 2006-08-16 | Takeda Pharmaceuticals Co | Substituted pyrrole derivative |
WO2006072833A1 (en) * | 2005-01-06 | 2006-07-13 | Pfizer Limited | Imidazole derivatives as enzyme reverse transcriptase modulators |
JP4035559B1 (ja) | 2005-08-30 | 2008-01-23 | 武田薬品工業株式会社 | 酸分泌抑制薬としての1−ヘテロシクリルスルホニル、2−アミノメチル、5−(ヘテロ−)アリール置換1−h−ピロール誘導体 |
US20100113421A1 (en) * | 2006-10-06 | 2010-05-06 | Williams Theresa M | Non-nucleoside reverse transcriptase inhibitors |
CA2669675A1 (en) * | 2006-11-10 | 2008-05-15 | Syndax Pharmaceuticals, Inc. | Combination of er.alpha.+ ligands and histone deacetylase inhibitors for the treatment of cancer |
US8933105B2 (en) | 2007-02-28 | 2015-01-13 | Takeda Pharmaceutical Company Limited | Pyrrole compounds |
WO2009015180A2 (en) * | 2007-07-23 | 2009-01-29 | Syndax Pharmaceuticals, Inc. | Novel compounds and methods of using them |
KR101546987B1 (ko) * | 2007-10-16 | 2015-08-24 | 가부시키가이샤 니콘 | 조명 광학 시스템, 노광 장치 및 디바이스 제조 방법 |
WO2009067453A1 (en) * | 2007-11-19 | 2009-05-28 | Syndax Pharmaceuticals, Inc. | Combinations of hdac inhibitors and proteasome inhibitors |
MY152008A (en) | 2008-08-27 | 2014-08-15 | Takeda Pharmaceutical | Pyrrole compounds |
GB0823001D0 (en) * | 2008-12-17 | 2009-01-28 | Syngenta Participations Ag | Thiophene,furan and pyrrole derivatives with plant growth regulating properties |
CN101775011B (zh) * | 2009-01-13 | 2013-07-31 | 中国人民解放军军事医学科学院毒物药物研究所 | N-取代苯基-3-甲烯杂环芳烃-2,5-二甲基吡咯类化合物及其抗hiv/aids的应用 |
JP2023503062A (ja) * | 2019-11-19 | 2023-01-26 | ニューヨーク ブラッド センター インコーポレイテッド | Hivにおける治療活性を有する置換複素環 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3644631A (en) * | 1969-05-13 | 1972-02-22 | Endo Lab | Therapeutic methods utilizing aryl pyrrol-3-yl ketones |
US4282242A (en) * | 1980-03-07 | 1981-08-04 | Pfizer Inc. | Antidiabetic pyrrolecarboxylic acids |
US4347186A (en) * | 1980-10-20 | 1982-08-31 | Syntex (U.S.A.) Inc. | Process for preparing 5-aroyl 1,2-dihydro-3-H pyrrolo[1,2-a]pyrrole-1-carboxylic acids and novel intermediates therein |
DK0674631T3 (da) * | 1992-12-17 | 2000-04-10 | Pfizer | Substituerede pyrazoler som CRF-antogonister |
EP0764153A1 (en) * | 1994-06-06 | 1997-03-26 | Pfizer Inc. | Substituted pyrazoles having corticotropin-releasing factor (crf) antagonist activity |
TW406075B (en) * | 1994-12-13 | 2000-09-21 | Upjohn Co | Alkyl substituted piperidinyl and piperazinyl anti-AIDS compounds |
AU3044197A (en) * | 1996-07-11 | 1998-02-09 | Pfizer Inc. | Pyridylpyrrole compounds useful as interleukin- and tnf antagonists |
DE19963174A1 (de) * | 1999-12-27 | 2001-07-12 | Gruenenthal Gmbh | Substituierte Pyrrol-Mannichbasen |
-
2000
- 2000-07-04 GB GBGB0016453.3A patent/GB0016453D0/en not_active Ceased
-
2001
- 2001-04-30 AU AU2001263874A patent/AU2001263874B2/en not_active Ceased
- 2001-04-30 CA CA002412270A patent/CA2412270A1/en not_active Abandoned
- 2001-04-30 KR KR1020037000138A patent/KR100549884B1/ko not_active IP Right Cessation
- 2001-04-30 MX MXPA02012409A patent/MXPA02012409A/es active IP Right Grant
- 2001-04-30 BR BR0112241-0A patent/BR0112241A/pt not_active Withdrawn
- 2001-04-30 AU AU6387401A patent/AU6387401A/xx active Pending
- 2001-04-30 CN CN01812290A patent/CN1440385A/zh active Pending
- 2001-04-30 JP JP2002507781A patent/JP2004502674A/ja active Pending
- 2001-04-30 WO PCT/EP2001/004832 patent/WO2002002524A1/en not_active Application Discontinuation
- 2001-04-30 EP EP01938137A patent/EP1301481A1/en not_active Withdrawn
- 2001-05-04 PA PA20018516201A patent/PA8516201A1/es unknown
- 2001-05-18 UY UY26720A patent/UY26720A1/es not_active Application Discontinuation
- 2001-05-22 AR ARP010102414A patent/AR028602A1/es not_active Application Discontinuation
- 2001-05-25 PE PE2001000487A patent/PE20020269A1/es not_active Application Discontinuation
- 2001-06-12 GT GT200100111A patent/GT200100111A/es unknown
- 2001-06-13 US US09/880,534 patent/US6737429B2/en not_active Expired - Fee Related
- 2001-07-04 EC EC2001004109A patent/ECSP014109A/es unknown
Also Published As
Publication number | Publication date |
---|---|
WO2002002524A1 (en) | 2002-01-10 |
CA2412270A1 (en) | 2002-01-10 |
GT200100111A (es) | 2002-03-18 |
KR20030014321A (ko) | 2003-02-15 |
MXPA02012409A (es) | 2003-04-25 |
AR028602A1 (es) | 2003-05-14 |
GB0016453D0 (en) | 2000-08-23 |
US6737429B2 (en) | 2004-05-18 |
US20020032221A1 (en) | 2002-03-14 |
PA8516201A1 (es) | 2002-07-30 |
EP1301481A1 (en) | 2003-04-16 |
KR100549884B1 (ko) | 2006-02-06 |
ECSP014109A (es) | 2002-02-25 |
BR0112241A (pt) | 2003-06-24 |
AU2001263874B2 (en) | 2006-10-19 |
JP2004502674A (ja) | 2004-01-29 |
AU6387401A (en) | 2002-01-14 |
CN1440385A (zh) | 2003-09-03 |
UY26720A1 (es) | 2001-11-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20020269A1 (es) | Derivados de pirrol como inhibidores de transcriptasa inversa del vih | |
PE20020753A1 (es) | Heteroaromaticos fusionados como activadores de la glucoquinasa | |
NO20061107L (no) | CRF-antagonister og heterobrcykliske forbindelser | |
PE20090709A1 (es) | Compuestos heterociclico de 5 miembros | |
PE20040581A1 (es) | Inhibidores heterociclicos de cinasas | |
NO178067C (no) | Analogifremgangsmåte til fremstilling av terapautisk aktive heterocykliske forbindelser | |
PE20080404A1 (es) | Derivados bencil-amino-piperidina como inhibidores de cetp | |
PE20090641A1 (es) | Amidas heterociclicas | |
TR200201752T2 (tr) | Dipeptid nitril katepsin K inhibitörleri. | |
PE20020509A1 (es) | Aza y poliaza-naftalenil carboxamidas utiles como inhibidores de la integrasa del vih | |
PE20080843A1 (es) | Inhibidores de renina y metodo para su utilizacion | |
TW200800949A (en) | Macrocylic inhibitors of hepatitis C virus | |
EA200401381A1 (ru) | 3-гетероарилзамещённые изоксазолины | |
TR200102805T2 (tr) | Glikokinaz aktivatörleri | |
KR950704304A (ko) | 이환식 헤테로환 함유 술폰아미드 및 술폰산 에스테르 유도체(bicyclic heterocyclic sulfonamide and sulfonic ester derivatives) | |
EA200800477A1 (ru) | Макроциклические ингибиторы вируса гепатита с | |
PE20080706A1 (es) | Arilmidazolonas y ariltriazolonas sustituidas como inhibidores de receptores de vasopresina | |
PE20110294A1 (es) | Compuestos heterociclicos como inhibidores de enzimas de senal especifica | |
PE20070189A1 (es) | COMPUESTO DE AMINO-5-HETEROARILO (5 MIEMBROS) IMIDAZOLONA Y SU USO PARA MODULACION DE LA ß-SECRETASA | |
DK200001556A (da) | Substituerede thiazolidindionderivater | |
RU2008107726A (ru) | Макроциклические ингибиторы вируса гепатита с | |
PE20030007A1 (es) | Inhibidores de aldosa reductasa del grupo de las piridazinonas | |
PE20090610A1 (es) | Derivados de pirazol sustituidos | |
PE20121157A1 (es) | Compuestos heterociclicos como inhibidores de proteasas serinas | |
AR029301A1 (es) | Compuestos derivados de biarilo, metodos para su preparacion composiciones que los contienen, su uso como agonistas en receptores beta-adreno-receptores atipicos |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |