PE20070494A1 - COMPUESTOS DERIVADOS DE PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA COMO INHIBIDORES DE LA ENZIMA INTEGRASA DE VIH - Google Patents
COMPUESTOS DERIVADOS DE PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA COMO INHIBIDORES DE LA ENZIMA INTEGRASA DE VIHInfo
- Publication number
- PE20070494A1 PE20070494A1 PE2006001216A PE2006001216A PE20070494A1 PE 20070494 A1 PE20070494 A1 PE 20070494A1 PE 2006001216 A PE2006001216 A PE 2006001216A PE 2006001216 A PE2006001216 A PE 2006001216A PE 20070494 A1 PE20070494 A1 PE 20070494A1
- Authority
- PE
- Peru
- Prior art keywords
- ona
- pirrolo
- naphthyridin
- alkyl
- inhibitors
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- General Chemical & Material Sciences (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE R1 ES H, ALQUILO(C1-C8), ALQUENILO(C2-C8) O HETEROALQUILO(C1-C8) OPCIONALMENTE SUSTITUIDOS CON HALO, CN, ALQUILO(C1-C8), ENTRE OTROS; R2 ES H O ALQUILO(C1-C8); R3 ES ALQUILO(C1-C8), HETEROALQUILO(C1-C8), ARILO(C6-C14), ENTRE OTROS; Z ES -(CR4R4)n- DONDE R4 ES H, HALO, ALQUILO(C1-C8), CICLOALQUILO(C3-C8), ENTRE OTROS; R5 ES H, HETEROALQUILO(C1-C8), ARILO(C6-14), ALQUENILO(C2-C8), ENTRE OTROS; R6 ES H. SON COMPUESTOS PREFERIDOS: 8-BUTIL-3-(4-FLUOROBENCIL)-7-HIDROXI-3,7,8,9-TETRAHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, 3-(4-FLUOROBENCIL)-7-HIDROXI-1-({[(2S)-2-HIDROXIPROPIL]AMINO}METIL)-3,7-DIHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, 1-{[ETIL(METIL)AMINO]METIL}-3-(4-FLUOROBENCIL)-7-HIDROXI-3,7-DIHIDRO-6H-PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA ENZIMA INTEGRASA DEL VIRUS DE INMUNODEFICIENCIA HUMANA (VIH) SIENDO UTILES EN EL TRATAMIENTO DE SIDA
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US72448405P | 2005-10-07 | 2005-10-07 | |
US73070105P | 2005-10-26 | 2005-10-26 | |
US76160506P | 2006-01-24 | 2006-01-24 | |
US82395406P | 2006-08-30 | 2006-08-30 | |
US82637906P | 2006-09-20 | 2006-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20070494A1 true PE20070494A1 (es) | 2007-06-13 |
Family
ID=37684843
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2006001216A PE20070494A1 (es) | 2005-10-07 | 2006-10-05 | COMPUESTOS DERIVADOS DE PIRROLO[2,3-c]-1,7-NAFTIRIDIN-6-ONA COMO INHIBIDORES DE LA ENZIMA INTEGRASA DE VIH |
Country Status (21)
Country | Link |
---|---|
US (1) | US20070099915A1 (es) |
EP (1) | EP1934220A1 (es) |
JP (1) | JP2009511463A (es) |
KR (1) | KR20080042171A (es) |
AP (1) | AP2008004400A0 (es) |
AR (1) | AR061398A1 (es) |
AU (1) | AU2006300926A1 (es) |
BR (1) | BRPI0616657A2 (es) |
CA (1) | CA2623506A1 (es) |
CR (1) | CR9859A (es) |
EA (1) | EA200800758A1 (es) |
IL (1) | IL189939A0 (es) |
MA (1) | MA29855B1 (es) |
NL (1) | NL2000255A1 (es) |
NO (1) | NO20081230L (es) |
PE (1) | PE20070494A1 (es) |
RS (1) | RS20080141A (es) |
SV (1) | SV2009002864A (es) |
TW (1) | TW200800219A (es) |
UY (1) | UY29843A1 (es) |
WO (1) | WO2007042883A1 (es) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005103051A1 (en) * | 2004-04-26 | 2005-11-03 | Pfizer Inc. | Inhibitors of the hiv integrase enzyme |
JP2011517313A (ja) | 2007-12-11 | 2011-06-02 | ビアメト ファーマシューティカルズ,インク. | 金属結合部分を標的化部分と組み合わせて使用する金属酵素阻害剤 |
CN102532021B (zh) * | 2012-01-31 | 2013-10-16 | 天津大学 | 2-烷氧基-3,4-二取代异喹啉-1(2h)-酮类衍生物的制备方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ194747A (en) * | 1979-08-29 | 1988-11-29 | Schering Ag | 9h-pyrido(3,4-b)indol-3-ylcarboxylic acid derivatives |
US5616609A (en) * | 1991-08-08 | 1997-04-01 | Ikekawa; Tetsuro | Carcinostatic compound and production thereof |
WO1995003311A1 (fr) * | 1993-07-19 | 1995-02-02 | Xuande Luo | Derives de qinghaosu utilises pour lutter contre le sida |
US6057297A (en) * | 1996-08-06 | 2000-05-02 | Polifarma S.P.A. | Inhibitor compounds of zinc-dependent metalloproteinases associated with pathological conditions, and therapeutic use thereof |
FR2754262B1 (fr) * | 1996-10-08 | 1998-10-30 | Synthelabo | Derives de 1h-pyrido[3,4-b]indole-4-carboxamide, leur preparation et leur application en therapeutique |
US6403347B1 (en) * | 1998-02-03 | 2002-06-11 | Merck & Co., Inc. | HIV integrase inhibitors |
AU8009900A (en) * | 1999-10-13 | 2001-04-23 | Merck & Co., Inc. | Hiv integrase inhibitors |
WO2001098248A2 (en) * | 2000-06-16 | 2001-12-27 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
PA8586801A1 (es) * | 2002-10-31 | 2005-02-04 | Pfizer | Inhibidores de hiv-integrasa, composiciones farmaceuticas y metodos para su uso |
CA2513141A1 (en) * | 2003-01-27 | 2004-08-12 | Pfizer Inc. | Hiv-integrase inhibitors, pharmaceutical compositions, and methods for their use |
WO2005103051A1 (en) * | 2004-04-26 | 2005-11-03 | Pfizer Inc. | Inhibitors of the hiv integrase enzyme |
WO2006027694A1 (en) * | 2004-09-07 | 2006-03-16 | Pfizer Inc. | Inhibitors of the hiv integrase enzyme |
-
2006
- 2006-09-25 EA EA200800758A patent/EA200800758A1/ru unknown
- 2006-09-25 JP JP2008534098A patent/JP2009511463A/ja not_active Withdrawn
- 2006-09-25 RS RSP-2008/0141A patent/RS20080141A/sr unknown
- 2006-09-25 AP AP2008004400A patent/AP2008004400A0/xx unknown
- 2006-09-25 KR KR1020087008162A patent/KR20080042171A/ko not_active Application Discontinuation
- 2006-09-25 WO PCT/IB2006/002735 patent/WO2007042883A1/en active Application Filing
- 2006-09-25 BR BRPI0616657-1A patent/BRPI0616657A2/pt not_active Application Discontinuation
- 2006-09-25 CA CA002623506A patent/CA2623506A1/en not_active Abandoned
- 2006-09-25 AU AU2006300926A patent/AU2006300926A1/en not_active Abandoned
- 2006-09-25 EP EP06808923A patent/EP1934220A1/en not_active Withdrawn
- 2006-10-03 NL NL2000255A patent/NL2000255A1/nl active Search and Examination
- 2006-10-04 AR ARP060104374A patent/AR061398A1/es not_active Application Discontinuation
- 2006-10-05 TW TW095137139A patent/TW200800219A/zh unknown
- 2006-10-05 PE PE2006001216A patent/PE20070494A1/es not_active Application Discontinuation
- 2006-10-06 UY UY29843A patent/UY29843A1/es not_active Application Discontinuation
- 2006-10-06 US US11/539,205 patent/US20070099915A1/en not_active Abandoned
-
2008
- 2008-02-04 CR CR9859A patent/CR9859A/es not_active Application Discontinuation
- 2008-03-04 IL IL189939A patent/IL189939A0/en unknown
- 2008-03-07 NO NO20081230A patent/NO20081230L/no not_active Application Discontinuation
- 2008-04-07 SV SV2008002864A patent/SV2009002864A/es not_active Application Discontinuation
- 2008-04-07 MA MA30821A patent/MA29855B1/fr unknown
Also Published As
Publication number | Publication date |
---|---|
US20070099915A1 (en) | 2007-05-03 |
TW200800219A (en) | 2008-01-01 |
IL189939A0 (en) | 2008-08-07 |
EA200800758A1 (ru) | 2008-08-29 |
EP1934220A1 (en) | 2008-06-25 |
MA29855B1 (fr) | 2008-10-03 |
BRPI0616657A2 (pt) | 2011-06-28 |
CR9859A (es) | 2008-06-20 |
RS20080141A (en) | 2009-07-15 |
JP2009511463A (ja) | 2009-03-19 |
NL2000255A1 (nl) | 2007-04-11 |
NO20081230L (no) | 2008-04-08 |
AU2006300926A1 (en) | 2007-04-19 |
WO2007042883A1 (en) | 2007-04-19 |
AP2008004400A0 (en) | 2008-04-30 |
AR061398A1 (es) | 2008-08-27 |
SV2009002864A (es) | 2009-02-19 |
CA2623506A1 (en) | 2007-04-19 |
KR20080042171A (ko) | 2008-05-14 |
UY29843A1 (es) | 2007-05-31 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |