HUP0303818A2 - HIV reverz transzkriptáz inhibitorként alkalmazható triciklikus vegyületek és ezeket tartalmazó gyógyszerkészítmények - Google Patents
HIV reverz transzkriptáz inhibitorként alkalmazható triciklikus vegyületek és ezeket tartalmazó gyógyszerkészítményekInfo
- Publication number
- HUP0303818A2 HUP0303818A2 HU0303818A HUP0303818A HUP0303818A2 HU P0303818 A2 HUP0303818 A2 HU P0303818A2 HU 0303818 A HU0303818 A HU 0303818A HU P0303818 A HUP0303818 A HU P0303818A HU P0303818 A2 HUP0303818 A2 HU P0303818A2
- Authority
- HU
- Hungary
- Prior art keywords
- tricyclic compounds
- inbitors
- group
- pharmaceutical compositions
- compositions containing
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 229910052731 fluorine Inorganic materials 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- 229910052740 iodine Chemical group 0.000 abstract 2
- 238000009007 Diagnostic Kit Methods 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 108010078851 HIV Reverse Transcriptase Proteins 0.000 abstract 1
- 208000036142 Viral infection Diseases 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003153 chemical reaction reagent Substances 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000009385 viral infection Effects 0.000 abstract 1
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
- C07D471/02—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
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
A találmány tárgyát az általános képletű, HIV-reverz transzkriptázinhibitor hatású triciklusos vegyületek - ahol R1 0-7 halogénatommalszubsztituált 1-3 szénatomos alkilcsoport; R2 -(CH2)OH(CH3)2 csoport;X fluor- , klór-, bróm- vagy jódatom vagy cianocsoport; Y fluor-,klór-, bróm- vagy jódatom, vagy cianocsoport; Z nitrogénatom vagyoxidcsoport - és sztereoizomer formáik, sztereoizomer formáikkeverékei vagy gyógyászatilag elfogadható sóik képezik, továbbá azezeket tartalmazó gyógyszerkészítmények és diagnosztikai készletek. Atalálmány tárgyát képezik továbbá eljárások ezek alkalmazásáravírusfertőzések kezelésére, valamint vizsgáló standardként vagyreagensként. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28481801P | 2001-04-19 | 2001-04-19 | |
PCT/US2002/012208 WO2002085365A1 (en) | 2001-04-19 | 2002-04-17 | Tricyclic compounds useful as hiv reverse transcriptase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
HUP0303818A2 true HUP0303818A2 (hu) | 2004-03-01 |
Family
ID=23091633
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0303818A HUP0303818A2 (hu) | 2001-04-19 | 2002-04-17 | HIV reverz transzkriptáz inhibitorként alkalmazható triciklikus vegyületek és ezeket tartalmazó gyógyszerkészítmények |
Country Status (10)
Country | Link |
---|---|
US (1) | US6825210B2 (hu) |
EP (1) | EP1379248A1 (hu) |
JP (1) | JP2004532224A (hu) |
CN (1) | CN1649591A (hu) |
AR (1) | AR033702A1 (hu) |
BR (1) | BR0208987A (hu) |
CA (1) | CA2444570A1 (hu) |
HU (1) | HUP0303818A2 (hu) |
MX (1) | MXPA03009482A (hu) |
WO (1) | WO2002085365A1 (hu) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69637890D1 (de) * | 1995-06-07 | 2009-05-14 | Progenics Pharm Inc | Monoklonaler antikörper für die inhibierung von hiv-1-hüllgykoprotein-vermittelte membranfusion |
US7118859B2 (en) * | 1996-01-17 | 2006-10-10 | Progenics Pharmaceuticals, Inc. | Methods for inhibiting HIV-1 infection |
US7858298B1 (en) * | 1996-04-01 | 2010-12-28 | Progenics Pharmaceuticals Inc. | Methods of inhibiting human immunodeficiency virus type 1 (HIV-1) infection through the administration of CCR5 chemokine receptor antagonists |
US6344545B1 (en) * | 1996-06-14 | 2002-02-05 | Progenics Pharmaceuticals, Inc. | Method for preventing HIV-1 infection of CD4+ cells |
US20080015348A1 (en) * | 1998-12-16 | 2008-01-17 | Progenics Pharmaceuticals, Inc. | Nucleic acids encoding polypeptides of anti-CCR5 antibodies |
US20040228869A1 (en) * | 1998-12-16 | 2004-11-18 | Progenics Pharmaceuticals, Inc. | Synergistic inhibition of HIV-1 fusion and attachment, compositions and antibodies thereto |
US7138119B2 (en) * | 2000-09-15 | 2006-11-21 | Progenics Pharmaceuticals, Inc. | Compositions and methods for inhibition of HIV-1 infection |
US7060273B2 (en) * | 2001-04-06 | 2006-06-13 | Progenics Pharmaceuticals, Inc. | Methods for inhibiting HIV-1 infection |
US7122185B2 (en) * | 2002-02-22 | 2006-10-17 | Progenics Pharmaceuticals, Inc. | Anti-CCR5 antibody |
CA2516642C (en) * | 2003-02-21 | 2010-11-23 | Jarrow Formulas, Inc. | Methods for treatment of hiv or malaria using combinations of chloroquine and protease inhibitors |
US20070026441A1 (en) * | 2005-07-22 | 2007-02-01 | Olson William C | Methods for reducing viral load in HIV-1-infected patients |
KR20100102087A (ko) * | 2007-07-13 | 2010-09-20 | 인터몰레큘러 인코퍼레이티드 | 로우-k 유전체 재료의 표면 개질 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3262294D1 (en) | 1981-05-13 | 1985-03-28 | Ici Plc | Pharmaceutical compositions containing spiro succinimide derivatives |
US5171745A (en) | 1990-07-13 | 1992-12-15 | Du Pont Merck Pharmaceutical Company | Method of treating neurological dysfunction using neutrotransmitter enhancers |
IL102764A0 (en) | 1991-08-16 | 1993-01-31 | Merck & Co Inc | Quinazoline derivatives,and pharmaceutical compositions containing them |
AU2436792A (en) | 1991-08-16 | 1993-03-16 | Merck & Co., Inc. | Quinazoline derivatives as inhibitors of hiv reverse transcriptase |
HUT71132A (en) | 1992-03-27 | 1995-11-28 | Schering Corp | Bis-aryl-carbinol derivatives, pharmaceutical compositions containing them and process for producing |
US5665720A (en) | 1992-08-07 | 1997-09-09 | Merck & Co., Inc. | Benzoxazinones as inhibitors of HIV reverse transcriptase |
WO1994007910A1 (en) | 1992-09-28 | 1994-04-14 | Research Corporation Technologies, Inc. | New reagents for peptide couplings |
US5594001A (en) | 1993-04-08 | 1997-01-14 | The Dupont Merck Pharmaceutical Company | Polycyclic systems, and derivatives thereof, as neurotransmitter release enhancers useful in the treatment of cognitive disorders |
DE4320347A1 (de) | 1993-06-19 | 1994-12-22 | Boehringer Mannheim Gmbh | Quinazolin-Derivate und diese enthaltende Arzneimittel |
WO1995012583A1 (en) | 1993-11-05 | 1995-05-11 | Merck & Co., Inc. | New quinazolines as inhibitors of hiv reverse transcriptase |
US5750528A (en) | 1995-02-01 | 1998-05-12 | The Dupont Merck Pharmaceutical Company | Blockade of neuronal m-channels as a therapeutic approach to the treatment of neurological disease |
WO1996031469A1 (en) | 1995-04-07 | 1996-10-10 | Novo Nordisk A/S | N-substituted azaheterocyclic carboxylic acids and esters thereof |
US5874430A (en) | 1996-10-02 | 1999-02-23 | Dupont Pharmaceuticals Company | 4,4-disubstitued-1,4-dihydro-2H-3,1-benzoxazin-2-ones useful as HIV reverse transcriptase inhibitors and intermediates and processes for making the same |
US6124302A (en) | 1997-04-09 | 2000-09-26 | Dupont Pharmaceuticals | 4,4-disubstituted-3,4-dihydro-2(1H)-quinazolinones useful as HIV reverse transcriptase inhibitors |
AU4719799A (en) | 1998-06-30 | 2000-01-17 | Du Pont Pharmaceuticals Company | Substituted quinolin-2(1h)-ones useful as hiv reverse transcriptase inhibitors |
US6593337B1 (en) * | 1999-10-19 | 2003-07-15 | Bristol-Myers Squibb Pharma Company | Tricyclic compounds useful as HIV reverse transcriptase inhibitors |
-
2002
- 2002-04-17 CN CNA028119665A patent/CN1649591A/zh active Pending
- 2002-04-17 CA CA002444570A patent/CA2444570A1/en not_active Abandoned
- 2002-04-17 US US10/124,105 patent/US6825210B2/en not_active Expired - Lifetime
- 2002-04-17 HU HU0303818A patent/HUP0303818A2/hu unknown
- 2002-04-17 JP JP2002582938A patent/JP2004532224A/ja active Pending
- 2002-04-17 MX MXPA03009482A patent/MXPA03009482A/es unknown
- 2002-04-17 EP EP02723891A patent/EP1379248A1/en not_active Withdrawn
- 2002-04-17 BR BR0208987-4A patent/BR0208987A/pt not_active Application Discontinuation
- 2002-04-17 WO PCT/US2002/012208 patent/WO2002085365A1/en not_active Application Discontinuation
- 2002-04-19 AR ARP020101445A patent/AR033702A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
US6825210B2 (en) | 2004-11-30 |
MXPA03009482A (es) | 2004-02-12 |
EP1379248A1 (en) | 2004-01-14 |
AR033702A1 (es) | 2004-01-07 |
CN1649591A (zh) | 2005-08-03 |
WO2002085365A1 (en) | 2002-10-31 |
JP2004532224A (ja) | 2004-10-21 |
BR0208987A (pt) | 2004-04-27 |
US20020177603A1 (en) | 2002-11-28 |
CA2444570A1 (en) | 2002-10-31 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD9A | Lapse of provisional protection due to non-payment of fees |