HUP0300190A2 - Tricyclic compounds as hiv reverse transcriptase inhibitors and pharmaceutical compositions containing them and their preparation - Google Patents
Tricyclic compounds as hiv reverse transcriptase inhibitors and pharmaceutical compositions containing them and their preparationInfo
- Publication number
- HUP0300190A2 HUP0300190A2 HU0300190A HUP0300190A HUP0300190A2 HU P0300190 A2 HUP0300190 A2 HU P0300190A2 HU 0300190 A HU0300190 A HU 0300190A HU P0300190 A HUP0300190 A HU P0300190A HU P0300190 A2 HUP0300190 A2 HU P0300190A2
- Authority
- HU
- Hungary
- Prior art keywords
- group
- optionally substituted
- alkyl
- reverse transcriptase
- atom
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 108010078851 HIV Reverse Transcriptase Proteins 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 239000003419 rna directed dna polymerase inhibitor Substances 0.000 title 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 238000009007 Diagnostic Kit Methods 0.000 abstract 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- 208000036142 Viral infection Diseases 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000005197 alkyl carbonyloxy alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000005002 aryl methyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 239000003153 chemical reaction reagent Substances 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- -1 substituted Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
A találmány (I) általános képletű triciklusos vegyületekre és sóikravonatkozik, amelyek HIV-reverz transzkriptáz gátlására használhatók,továbbá a vegyületeket tartalmazó gyógyászati készítményekre ésdiagnosztikai kitekre, ezek vírusos fertőzés kezelésére vagymeghatározás standardként vagy reagensként való alkalmazásáravonatkozik, ahol a képletben az A gyűrű egy vagy két nitrogénatomottartalmazó, adott esetben B csoporttal helyettesített hattagúheterogyűrű; B jelentése halogénatom, alkil-, hidroxil-, alkoxi-,alkiltio-, trifluormetil-, trifluormetoxi-, nitro-, ciano- és adottesetben helyettesített aminocsoport; W, X, Y és Z jelentésenitrogénatom vagy helyettesített -CH= csoport; R1 jelentése adottesetben halogénatommal helyettesített alkil- vagy ciklopropilcsoport;R2 jelentése adott esetben helyettesített alkil-, alkenil-, alkinil-,cikloalkil-, fenil-, adott esetben helyettesített 3-6-tagú heterociklusos rendszer, amely 1-3 heteroatomot tartalmazaz alábbiak közül választva: oxigén-, nitrogén- vagy kénatom, adottesetben helyettesített hidroxil-, metiltio- vagy aminocsoport;cianocsoport; R8 jelentése hidrogénatom, alkil-, alkoxi-, ariloxi-,arilmetil-, alkilkarboniloxialkoxi-, alkilamino-, fenilamino-,fenilalkoxi- és aminoalkilkarbonilcsoport vagy helyettesítettalkilcsoport; és n értéke 0, 1, 2, 3 vagy 4. Ó
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16032999P | 1999-10-19 | 1999-10-19 | |
US22617100P | 2000-08-17 | 2000-08-17 | |
PCT/US2000/028824 WO2001029037A2 (en) | 1999-10-19 | 2000-10-19 | Condensed naphthyridines as hiv reverse transcriptase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
HUP0300190A2 true HUP0300190A2 (en) | 2003-05-28 |
Family
ID=26856799
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0300190A HUP0300190A2 (en) | 1999-10-19 | 2000-10-19 | Tricyclic compounds as hiv reverse transcriptase inhibitors and pharmaceutical compositions containing them and their preparation |
Country Status (19)
Country | Link |
---|---|
US (2) | US6593337B1 (hu) |
EP (1) | EP1222186A2 (hu) |
JP (1) | JP2003512375A (hu) |
KR (1) | KR20020079729A (hu) |
CN (1) | CN1409711A (hu) |
AU (1) | AU773309B2 (hu) |
BR (1) | BR0015056A (hu) |
CA (1) | CA2387896A1 (hu) |
CZ (1) | CZ20021353A3 (hu) |
EA (1) | EA200200471A1 (hu) |
EE (1) | EE200200202A (hu) |
HK (1) | HK1049150A1 (hu) |
HU (1) | HUP0300190A2 (hu) |
IL (1) | IL149219A0 (hu) |
MX (1) | MXPA02003958A (hu) |
NO (1) | NO20021835L (hu) |
PL (1) | PL355727A1 (hu) |
SK (1) | SK5342002A3 (hu) |
WO (1) | WO2001029037A2 (hu) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA200300255B (en) | 2000-07-20 | 2004-09-28 | Bristol Myers Squibb Pharma Co | Tricyclic 2-pyridone compounds useful as HIV reverse transcriptase inhibitors. |
US6596729B2 (en) | 2000-07-20 | 2003-07-22 | Bristol-Myers Squibb Company | Tricyclic-2-pyridone compounds useful as HIV reverse transcriptase inhibitors |
US8641644B2 (en) | 2000-11-21 | 2014-02-04 | Sanofi-Aventis Deutschland Gmbh | Blood testing apparatus having a rotatable cartridge with multiple lancing elements and testing means |
MXPA03009482A (es) * | 2001-04-19 | 2004-02-12 | Bristol Myers Squibb Co | Compuestos triciclicos utiles como inhibidores de la transcriptasa inversa del virus de inmunodeficiencia humana (vih). |
US9795747B2 (en) | 2010-06-02 | 2017-10-24 | Sanofi-Aventis Deutschland Gmbh | Methods and apparatus for lancet actuation |
US9427532B2 (en) | 2001-06-12 | 2016-08-30 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US7025774B2 (en) | 2001-06-12 | 2006-04-11 | Pelikan Technologies, Inc. | Tissue penetration device |
US9226699B2 (en) | 2002-04-19 | 2016-01-05 | Sanofi-Aventis Deutschland Gmbh | Body fluid sampling module with a continuous compression tissue interface surface |
TW200306192A (en) | 2002-01-18 | 2003-11-16 | Bristol Myers Squibb Co | Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors |
US9248267B2 (en) | 2002-04-19 | 2016-02-02 | Sanofi-Aventis Deustchland Gmbh | Tissue penetration device |
US7547287B2 (en) | 2002-04-19 | 2009-06-16 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US8702624B2 (en) | 2006-09-29 | 2014-04-22 | Sanofi-Aventis Deutschland Gmbh | Analyte measurement device with a single shot actuator |
US8784335B2 (en) | 2002-04-19 | 2014-07-22 | Sanofi-Aventis Deutschland Gmbh | Body fluid sampling device with a capacitive sensor |
US9795334B2 (en) | 2002-04-19 | 2017-10-24 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US9314194B2 (en) | 2002-04-19 | 2016-04-19 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US8579831B2 (en) | 2002-04-19 | 2013-11-12 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US7708701B2 (en) | 2002-04-19 | 2010-05-04 | Pelikan Technologies, Inc. | Method and apparatus for a multi-use body fluid sampling device |
US6909001B2 (en) | 2002-12-12 | 2005-06-21 | Pharmacia Corporation | Method of making tricyclic aminocyanopyridine compounds |
US8574895B2 (en) | 2002-12-30 | 2013-11-05 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus using optical techniques to measure analyte levels |
WO2006001797A1 (en) | 2004-06-14 | 2006-01-05 | Pelikan Technologies, Inc. | Low pain penetrating |
EP1671096A4 (en) | 2003-09-29 | 2009-09-16 | Pelikan Technologies Inc | METHOD AND APPARATUS FOR PROVIDING IMPROVED SAMPLE CAPTURING DEVICE |
EP1680014A4 (en) | 2003-10-14 | 2009-01-21 | Pelikan Technologies Inc | METHOD AND APPARATUS PROVIDING A VARIABLE USER INTERFACE |
EP1706026B1 (en) | 2003-12-31 | 2017-03-01 | Sanofi-Aventis Deutschland GmbH | Method and apparatus for improving fluidic flow and sample capture |
US8828203B2 (en) | 2004-05-20 | 2014-09-09 | Sanofi-Aventis Deutschland Gmbh | Printable hydrogels for biosensors |
WO2005120365A1 (en) | 2004-06-03 | 2005-12-22 | Pelikan Technologies, Inc. | Method and apparatus for a fluid sampling device |
US9775553B2 (en) | 2004-06-03 | 2017-10-03 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for a fluid sampling device |
US7504969B2 (en) * | 2006-07-11 | 2009-03-17 | Data Domain, Inc. | Locality-based stream segmentation for data deduplication |
WO2009126900A1 (en) | 2008-04-11 | 2009-10-15 | Pelikan Technologies, Inc. | Method and apparatus for analyte detecting device |
US9375169B2 (en) | 2009-01-30 | 2016-06-28 | Sanofi-Aventis Deutschland Gmbh | Cam drive for managing disposable penetrating member actions with a single motor and motor and control system |
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 |
US8965476B2 (en) | 2010-04-16 | 2015-02-24 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
WO2012092367A1 (en) * | 2010-12-28 | 2012-07-05 | University Of Rochester | Nucleic acid binding compounds, methods of making, and use thereof |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3262294D1 (en) | 1981-05-13 | 1985-03-28 | Ici Plc | Pharmaceutical compositions containing spiro succinimide derivatives |
DD204480A1 (de) | 1982-04-13 | 1983-11-30 | Meisel | Verfahren zur herstellung von in 10-stellung basisch substituierten 5,5-dimethyl-5,10-dihydro-benzo(b)(1,8)naphthyridinen |
EP0393604B1 (en) | 1989-04-20 | 1997-12-29 | Boehringer Ingelheim Pharmaceuticals Inc. | 6,11-Dihydro-5H-pyrido(2,3-b)(1,5,)benzodiazepin-5-ones and thiones and their use in the prevention or treatment of AIDS |
ATE116320T1 (de) | 1989-04-20 | 1995-01-15 | Boehringer Ingelheim Pharma | 5,11-dihydro-6h-pyrido(2,3-b)(1,4)benzodiazepin 6-one und -thione und deren verwendung bei der vorbeugung und und behandlung von aids. |
US5171745A (en) | 1990-07-13 | 1992-12-15 | Du Pont Merck Pharmaceutical Company | Method of treating neurological dysfunction using neutrotransmitter enhancers |
US5087625A (en) | 1990-10-19 | 1992-02-11 | Boehringer Ingelheim Pharmaceuticals, Inc. | Pyridodiazepines and their use in the prevention or treatment of HIV infection |
IL102764A0 (en) | 1991-08-16 | 1993-01-31 | Merck & Co Inc | Quinazoline derivatives,and pharmaceutical compositions containing them |
WO1993004047A1 (en) | 1991-08-16 | 1993-03-04 | Merck & Co., Inc. | Quinazoline derivatives as inhibitors of hiv reverse transcriptase |
US5527819A (en) * | 1991-09-06 | 1996-06-18 | Merck & Co., Inc. | 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 |
CA2145407C (en) | 1992-09-28 | 2009-09-22 | Louis A. Carpino | 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 |
DE4344452A1 (de) | 1993-12-24 | 1995-06-29 | Hoechst Ag | Aza-4-iminochinoline, Verfahren zu ihrer Herstellung und ihre Verwendung |
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 |
-
2000
- 2000-10-18 US US09/691,249 patent/US6593337B1/en not_active Expired - Lifetime
- 2000-10-19 AU AU12137/01A patent/AU773309B2/en not_active Ceased
- 2000-10-19 HU HU0300190A patent/HUP0300190A2/hu unknown
- 2000-10-19 CZ CZ20021353A patent/CZ20021353A3/cs unknown
- 2000-10-19 WO PCT/US2000/028824 patent/WO2001029037A2/en not_active Application Discontinuation
- 2000-10-19 PL PL00355727A patent/PL355727A1/xx not_active Application Discontinuation
- 2000-10-19 EA EA200200471A patent/EA200200471A1/ru unknown
- 2000-10-19 EP EP00973644A patent/EP1222186A2/en not_active Withdrawn
- 2000-10-19 CA CA002387896A patent/CA2387896A1/en not_active Abandoned
- 2000-10-19 BR BR0015056-8A patent/BR0015056A/pt not_active IP Right Cessation
- 2000-10-19 MX MXPA02003958A patent/MXPA02003958A/es unknown
- 2000-10-19 CN CN00817018A patent/CN1409711A/zh active Pending
- 2000-10-19 IL IL14921900A patent/IL149219A0/xx unknown
- 2000-10-19 KR KR1020027005054A patent/KR20020079729A/ko not_active Application Discontinuation
- 2000-10-19 JP JP2001531836A patent/JP2003512375A/ja active Pending
- 2000-10-19 SK SK534-2002A patent/SK5342002A3/sk unknown
- 2000-10-19 EE EEP200200202A patent/EE200200202A/xx unknown
-
2002
- 2002-04-18 NO NO20021835A patent/NO20021835L/no not_active Application Discontinuation
- 2002-11-07 HK HK02108077.7A patent/HK1049150A1/zh unknown
-
2003
- 2003-04-24 US US10/422,202 patent/US20040002498A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
NO20021835L (no) | 2002-06-18 |
WO2001029037A2 (en) | 2001-04-26 |
US20040002498A1 (en) | 2004-01-01 |
KR20020079729A (ko) | 2002-10-19 |
CZ20021353A3 (cs) | 2002-09-11 |
NO20021835D0 (no) | 2002-04-18 |
PL355727A1 (en) | 2004-05-17 |
WO2001029037A3 (en) | 2002-01-24 |
AU1213701A (en) | 2001-04-30 |
SK5342002A3 (en) | 2003-04-01 |
EP1222186A2 (en) | 2002-07-17 |
MXPA02003958A (es) | 2002-12-10 |
CN1409711A (zh) | 2003-04-09 |
IL149219A0 (en) | 2002-11-10 |
EA200200471A1 (ru) | 2003-04-24 |
HK1049150A1 (zh) | 2003-05-02 |
EE200200202A (et) | 2003-06-16 |
JP2003512375A (ja) | 2003-04-02 |
AU773309B2 (en) | 2004-05-20 |
BR0015056A (pt) | 2003-06-10 |
CA2387896A1 (en) | 2001-04-26 |
US6593337B1 (en) | 2003-07-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HUP0300190A2 (en) | Tricyclic compounds as hiv reverse transcriptase inhibitors and pharmaceutical compositions containing them and their preparation | |
CY1107532T1 (el) | Παραγωγα ναφθυριδινης, παρασκευη και χρηση τους ως αναστολεις του ισοενζυμου 4 της φωσφοδιεστepασης (pde4) | |
HUP0004845A2 (hu) | PPAR-gamma agonista aktivitással rendelkező szubsztituált 4-hidroxi-fenil-alkánsav-származékok és ezeket tartalmazó gyógyszerkészítmények | |
HUP0303729A2 (hu) | Akridinszármazékok és azok gyógyszerként történő alkalmazása és eljárás az előállításukra | |
HUP0300416A2 (hu) | Antibiotikus hatású oxazolidinon-származékok, eljárás az előállításukra, alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények | |
HUP0104646A2 (hu) | Fuzionált 1,2,4-tiadiazin-származékok, azok előállítása és felhasználása | |
EP1381366A4 (en) | INDOL, AZAINDOL AND RELATED HETEROCYCLIC AMIDOPIPERAZINE DERIVATIVES | |
HUP9802822A2 (hu) | Halogén-benzimidazol-származékok, intermedierjeik, előállításuk és a vegyületeket hatóanyagként tartalmazó mikrobicid készítmények | |
HUP0203450A2 (hu) | Pirazolo[4,3-d]pirimidin-származékok, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk | |
TW200512208A (en) | Piperazine derivatives | |
HUP0204101A2 (hu) | 3-Amino-kinazolin-2,4-dion antibakteriális hatóanyagok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk | |
HUP0101031A2 (hu) | Biciklo[2.2.1]heptán-származékok és rokon vegyületek | |
HUP0105081A2 (hu) | Triazolo[4,5-d]pirimidin-származékok, eljárás előállításukra, alkalmazásuk és az ezeket tartalmazó gyógyszerkészítmények | |
HUP0201789A2 (hu) | A légzőrendszerre ható szinciciális vírus replikációját gátló vegyületek | |
HUP0203438A2 (hu) | Foszfodiészteráz gátló hatású 5-(2-helyettesített-5-heterociklilszulfonilpirid-3-il)-dihidropirazolo[4,3-d]-pirimidin-7-on-származékok, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények | |
HUP0400370A2 (hu) | Antibakteriális hatású oxazolidinonszármazékok, előállításukra szolgáló eljárás, azokat hatóanyagként tartalmazó gyógyászati készítmények, alkalmazásuk és intermedierek | |
DK0759027T3 (da) | Bicykliske amidinderivater som inhibitorer af nitrogenoxidsynthetase | |
SE9701304D0 (sv) | Compounds | |
HUP0202191A2 (hu) | A koagulációs kaszkád szelektív gátlására alkalmas helyettesített policiklusos aril- és heteroaril-pirazinonok, valamint az ezeket tartalmazó gyógyszerkészítmények | |
WO2003008412A3 (en) | Hetero-bicyclic crf antagonists | |
HUP0400317A2 (hu) | Béta-karbolin származékok, eljárás az előállításukra, alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények | |
BR0308759A (pt) | Derivados de fenil amidas siliconadas utilizáveis como microbiocida | |
DE60201089D1 (de) | 6-(2-chlor-6-fluor-phenyl)-triazolpyrimidine | |
TR199801648T2 (xx) | Herbisid olarak pirazol-4-il-hetaroil t�revleri | |
ATE259359T1 (de) | Benzoxazol-derivate zur verwendung als integrin- inhibitoren |