HUP0402282A2 - Triazolo[1,5-a]kinolin-származékok, eljárás az előállításukra, ezeket tartalmazó gyógyszerkészítmények - Google Patents
Triazolo[1,5-a]kinolin-származékok, eljárás az előállításukra, ezeket tartalmazó gyógyszerkészítményekInfo
- Publication number
- HUP0402282A2 HUP0402282A2 HU0402282A HUP0402282A HUP0402282A2 HU P0402282 A2 HUP0402282 A2 HU P0402282A2 HU 0402282 A HU0402282 A HU 0402282A HU P0402282 A HUP0402282 A HU P0402282A HU P0402282 A2 HUP0402282 A2 HU P0402282A2
- Authority
- HU
- Hungary
- Prior art keywords
- branched
- straight
- alkyl
- optionally substituted
- halo
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- OCSVDRXXLBXUJM-UHFFFAOYSA-N triazolo[1,5-a]quinoline Chemical class C1=CC=C2N3N=NC=C3C=CC2=C1 OCSVDRXXLBXUJM-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 6
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- -1 methylenedioxy Chemical group 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- FGLRGMVWMQLOCO-UHFFFAOYSA-N 2h-triazolo[4,5-h]quinoline Chemical class C1=CC2=CC=CN=C2C2=C1N=NN2 FGLRGMVWMQLOCO-UHFFFAOYSA-N 0.000 abstract 2
- 125000002541 furyl group Chemical group 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000001544 thienyl group Chemical group 0.000 abstract 2
- 102000008161 Adenosine A3 Receptor Human genes 0.000 abstract 1
- 108010060261 Adenosine A3 Receptor Proteins 0.000 abstract 1
- 229940123786 Adenosine A3 receptor antagonist Drugs 0.000 abstract 1
- 208000001953 Hypotension Diseases 0.000 abstract 1
- 239000002580 adenosine A3 receptor antagonist Substances 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 230000003042 antagnostic effect Effects 0.000 abstract 1
- 230000003288 anthiarrhythmic effect Effects 0.000 abstract 1
- 230000003266 anti-allergic effect Effects 0.000 abstract 1
- 230000001088 anti-asthma Effects 0.000 abstract 1
- 230000003178 anti-diabetic effect Effects 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000002682 anti-psoriatic effect Effects 0.000 abstract 1
- 230000003356 anti-rheumatic effect Effects 0.000 abstract 1
- 239000003416 antiarrhythmic agent Substances 0.000 abstract 1
- 239000000924 antiasthmatic agent Substances 0.000 abstract 1
- 239000003472 antidiabetic agent Substances 0.000 abstract 1
- 239000003435 antirheumatic agent Substances 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000000824 cytostatic agent Substances 0.000 abstract 1
- 230000001085 cytostatic effect Effects 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 208000021822 hypotensive Diseases 0.000 abstract 1
- 230000001077 hypotensive effect Effects 0.000 abstract 1
- 230000001506 immunosuppresive effect Effects 0.000 abstract 1
- 230000010534 mechanism of action Effects 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P17/06—Antipsoriatics
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- A61P25/00—Drugs for disorders of the nervous system
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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
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- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
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- General Health & Medical Sciences (AREA)
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- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Hematology (AREA)
- Otolaryngology (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Endocrinology (AREA)
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Abstract
A találmány az (I) általános képletű vegyületekre, ahol R1 jelentésehidrogénatom, vagy 1-4 szénatomos egyenes vagy elágazó szénláncúalkilcsoport; R2 jelentése hidrogénatom, vagy 1-4 szénatomos egyenesvagy elágazó szénláncú alkilcsoport; R3 jelentése hidrogénatom, 1-4szénatomos egyenes vagy elágazó szénláncú alkilcsoport, adott esetbenegy vagy több 1-4 szénatomos egyenes, vagy elágazó szénláncúalkilcsoporttal, 1-4 szénatomos egyenes vagy elágazó szénláncúalkoxicsoporttal, vagy halogénatommal szubsztituált fenil-, tienil-,vagy furilcsoport, adott esetben egy vagy több 1-4 szénatomos egyenes,vagy elágazó szénláncú alkilcsoporttal, 1-4 szénatomos egyenes vagyelágazó szénláncú alkoxicsoporttal, vagy halogénatommal szubsztituált,egy vagy két, vagy három nitrogénatomot tartalmazó 5 vagy 6 tagúheteroaromás gyűrű, vagy egy nitrogénatomot és egy oxigénatomot, vagyegy nitrogénatomot és egy kénatomot tartalmazó 5 tagú heteroaromásgyűrű; R4 és R5 jelentése hidrogénatom, vagy együttesen, adott esetbenmetiléndioxicsoporttal, vagy egy vagy több 1-4 szénatomos egyenes vagyelágazó szénláncú alkilcsoporttal, 1-4 szénatomos egyenes vagy elágazószénláncú alkoxicsoporttal, hidroxicsoporttal vagy halogénatommalszubsztituált 1,3-butadienil-csoport; R6 jelentése hidrogénatom,cianocsoport, aminokarbonilcsoport, 1-4 szénatomosalkoxikarbonilcsoport, vagy karboxicsoport; R7 jelentése hidrogénatom,1-4 szénatomos egyenes vagy elágazó szénláncú alkilcsoport, 1-4szénatomos, adott esetben fenilcsoporttal szubsztituáltalkiléncsoport, adott esetben metilén-dioxi-csoporttal, vagy egy vagytöbb 1-4 szénatomos egyenes, vagy elágazó szénláncú alkilcsoporttal,1-4 szénatomos egyenes vagy elágazó szénláncú alkoxicsoporttal,hidroxicsoporttal, trifluormetilcsoporttal, cianocsoporttal,halogénatommal, amino-, mono- vagy adialkil-amino-csoporttalszubsztituált fenil-, benzil-, tienil-, vagy furilcsoport, vagy adottesetben egy vagy több 1-4 szénatomos egyenes vagy elágazó szénláncúalkilcsoporttal, 1-4 szénatomos egyenes vagy elágazó szénláncúalkoxicsoporttal, vagy halogénatommal szubsztituált, egy vagy két vagyhárom nitrogénatomot tartalmazó 5, vagy 6 tagú heteroaromás gyűrű vagyegy nitrogénatomot és egy oxigénatomot, vagy egy nitrogénatomot és egykénatomot tartalmazó 5 tagú heteroaromás gyűrű, X jelentése -CH2-csoport, -NH- csoport, -NR12- csoport, vagy kénatom vagy oxigénatom,vagy szulfocsoport vagy szulfoxicsoport - ahol R12 jelentése 1-4szénatomos egyenes vagy elágazó szénláncú alkilcsoport, vagy 3-6szénatomos cikloalkilcsoport; n értéke nulla, 1 vagy 2 valamintsóikra, szolvátjaikra, optikailag aktív izomerjeikre és ezek sóira ésszolvátjaira, előállítási eljárásukra, alkalmazásukra és az (I)általános képletű vegyületeket tartalmazó gyógyászati készítményekrevonatkozik. Ó
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU0402282A HUP0402282A3 (en) | 2001-12-21 | 2002-12-17 | Triazolo[1,5a] quinoline derivatives, process for their preparation and pharmaceutical compositions containing them |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU0105407A HUP0105407A3 (en) | 2001-12-21 | 2001-12-21 | Triazolo[1,5-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
HU0402282A HUP0402282A3 (en) | 2001-12-21 | 2002-12-17 | Triazolo[1,5a] quinoline derivatives, process for their preparation and pharmaceutical compositions containing them |
HUP0200143 | 2002-12-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP0402282A2 true HUP0402282A2 (hu) | 2005-02-28 |
HUP0402282A3 HUP0402282A3 (en) | 2007-12-28 |
Family
ID=90001529
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0105407A HUP0105407A3 (en) | 2001-12-21 | 2001-12-21 | Triazolo[1,5-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
HU0402282A HUP0402282A3 (en) | 2001-12-21 | 2002-12-17 | Triazolo[1,5a] quinoline derivatives, process for their preparation and pharmaceutical compositions containing them |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0105407A HUP0105407A3 (en) | 2001-12-21 | 2001-12-21 | Triazolo[1,5-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
Country Status (23)
Country | Link |
---|---|
US (2) | US7365089B2 (hu) |
EP (1) | EP1456204A1 (hu) |
JP (2) | JP4724366B2 (hu) |
KR (1) | KR100934796B1 (hu) |
CN (1) | CN1307175C (hu) |
AU (1) | AU2002353240B2 (hu) |
BR (1) | BR0215276A (hu) |
CA (1) | CA2470064C (hu) |
EA (1) | EA007066B1 (hu) |
HR (1) | HRP20040672A2 (hu) |
HU (2) | HUP0105407A3 (hu) |
IL (2) | IL162444A0 (hu) |
IS (1) | IS7318A (hu) |
MA (1) | MA27094A1 (hu) |
MX (1) | MXPA04006113A (hu) |
NO (1) | NO329757B1 (hu) |
NZ (1) | NZ534016A (hu) |
PL (1) | PL370747A1 (hu) |
RS (1) | RS56004A (hu) |
TN (1) | TNSN04106A1 (hu) |
UA (1) | UA79955C2 (hu) |
WO (1) | WO2003053968A1 (hu) |
ZA (1) | ZA200404802B (hu) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HUP0105407A3 (en) * | 2001-12-21 | 2004-04-28 | Sanofi Aventis | Triazolo[1,5-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
HUP0203976A3 (en) | 2002-11-15 | 2004-08-30 | Sanofi Aventis | Adenozine a3 receptors, process for their preparation and pharmaceutical compositions containing them |
HUP0400812A2 (en) * | 2004-04-19 | 2006-02-28 | Sanofi Aventis | Crystalline forms of 2-amino-3-cyano-quinoline derivatives, process for their preparation and pharmaceutical compositions containing them |
US20050288502A1 (en) * | 2004-06-25 | 2005-12-29 | Andersen Denise L | Substituted heterocyclic compounds and methods of use |
CN102702314A (zh) * | 2006-11-30 | 2012-10-03 | 首都医科大学 | 具有靶向抗血栓活性的rgdfyigsr、制备和应用 |
CN102702312A (zh) * | 2006-11-30 | 2012-10-03 | 首都医科大学 | 具有靶向抗血栓活性的rgdvyigsk、制备和应用 |
CN102702315A (zh) * | 2006-11-30 | 2012-10-03 | 首都医科大学 | 具有靶向抗血栓活性的rgdsyigsk、制备和应用 |
CN102702313A (zh) * | 2006-11-30 | 2012-10-03 | 首都医科大学 | 具有靶向抗血栓活性的rgdvyigsr、制备和应用 |
CN102702316A (zh) * | 2006-11-30 | 2012-10-03 | 首都医科大学 | 具有靶向抗血栓活性的rgdfyigsk、制备和应用 |
HUP0700395A2 (en) * | 2007-06-07 | 2009-03-02 | Sanofi Aventis | Substituted [1,2,4] triazolo [1,5-a] quinolines, process for their preparation, pharmaceutical compositions thereof, and intermediates |
DE102007061763A1 (de) * | 2007-12-20 | 2009-06-25 | Bayer Healthcare Ag | Substituierte azabicyclische Verbindungen und ihre Verwendung |
DK2950649T3 (da) | 2013-02-01 | 2020-05-04 | Wellstat Therapeutics Corp | Aminforbindelser med antiinflammations-, antisvampe-, antiparasit- og anticanceraktivitet |
CN108358927B (zh) * | 2018-01-26 | 2020-09-01 | 郑州大学 | 1,4-二取代1,2,3-三氮唑核苷类似物及其制备方法和应用 |
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Publication number | Priority date | Publication date | Assignee | Title |
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DE280110C (hu) | ||||
DE280109C (hu) | ||||
GB1479759A (en) * | 1974-11-23 | 1977-07-13 | Lepetit Spa | Heterocyclic fused derivatives of indole and quinoline |
DD280110A1 (de) * | 1989-02-22 | 1990-06-27 | Univ Berlin Humboldt | Verfahren zur herstellung von 1.2.4-triazolo/1.5-a/-pyridin-8-carbonitrilen |
DD280109A1 (de) * | 1989-02-22 | 1990-06-27 | Univ Berlin Humboldt | Verfahren zur herstellung substituierter 1.2.4-triazolo/1.5-a/-pyridine |
DE3926770A1 (de) | 1989-08-12 | 1991-02-14 | Basf Ag | (1,2,4)triazolo(1,5-a)pyridine |
US6066642A (en) * | 1996-01-29 | 2000-05-23 | The United States Of America As Represented By The Department Of Health And Human Services | Dihydropyridine-, pyridine-, benzopyran-4-one- and triazoloquinazoline derivative, their preparation and their use as adenosine receptor antagonists |
US5780481A (en) * | 1996-08-08 | 1998-07-14 | Merck & Co., Inc. | Method for inhibiting activation of the human A3 adenosine receptor to treat asthma |
US6448253B1 (en) * | 1998-09-16 | 2002-09-10 | King Pharmaceuticals Research And Development, Inc. | Adenosine A3 receptor modulators |
US6355653B1 (en) * | 1999-09-06 | 2002-03-12 | Hoffmann-La Roche Inc. | Amino-triazolopyridine derivatives |
HUP0105407A3 (en) * | 2001-12-21 | 2004-04-28 | Sanofi Aventis | Triazolo[1,5-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
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2001
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2002
- 2002-12-17 UA UA20040706067A patent/UA79955C2/uk unknown
- 2002-12-17 EP EP02788260A patent/EP1456204A1/en not_active Withdrawn
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- 2002-12-17 AU AU2002353240A patent/AU2002353240B2/en not_active Ceased
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