SK63998A3 - Quinoline derivatives, method for the preparation thereof, pharmaceutical composition containing same, and their use - Google Patents

Quinoline derivatives, method for the preparation thereof, pharmaceutical composition containing same, and their use Download PDF

Info

Publication number: SK63998A3
Authority: SK; Slovakia
Prior art keywords: benzo; methyl; quinoline; thiadiazolyl; triazolyl
Prior art date: 1995-11-14

Application number

SK639-98A

Other languages

English (en)

Slovak (sk)

Inventor

Rainer Luond

Villar E Pombo

Original Assignee

Novartis Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-11-14

Filing date

1996-11-13

Publication date

1998-10-07

1996-11-13 Application filed by Novartis Ag filed Critical Novartis Ag

1998-10-07 Publication of SK63998A3 publication Critical patent/SK63998A3/sk

Links

238000000034 method Methods 0.000 title claims abstract description 27
239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 9
238000002360 preparation method Methods 0.000 title claims description 10
229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 title description 4
125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 title 1
-1 benzo[c]furazanyl Chemical group 0.000 claims abstract description 59
238000011282 treatment Methods 0.000 claims abstract description 53
125000001113 thiadiazolyl group Chemical group 0.000 claims abstract description 25
239000002253 acid Substances 0.000 claims abstract description 19
239000003814 drug Substances 0.000 claims abstract description 17
150000003863 ammonium salts Chemical group 0.000 claims abstract description 15
150000001204 N-oxides Chemical class 0.000 claims abstract description 14
125000004076 pyridyl group Chemical group 0.000 claims abstract description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 6
230000008569 process Effects 0.000 claims abstract description 6
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 40
125000005605 benzo group Chemical group 0.000 claims description 29
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 25
201000010099 disease Diseases 0.000 claims description 22
150000003839 salts Chemical class 0.000 claims description 21
230000002757 inflammatory effect Effects 0.000 claims description 15
230000000414 obstructive effect Effects 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
208000027866 inflammatory disease Diseases 0.000 claims description 9
208000023275 Autoimmune disease Diseases 0.000 claims description 7
208000024827 Alzheimer disease Diseases 0.000 claims description 6
208000018737 Parkinson disease Diseases 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000003085 diluting agent Substances 0.000 claims description 6
VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims description 5
208000006011 Stroke Diseases 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
125000001425 triazolyl group Chemical group 0.000 claims description 4
QJKXVPWAXPWTSO-UHFFFAOYSA-N 8-(2-methylbenzotriazol-5-yl)-6-(pyridin-4-ylmethyl)quinoline Chemical compound C=1C2=NN(C)N=C2C=CC=1C(C1=NC=CC=C1C=1)=CC=1CC1=CC=NC=C1 QJKXVPWAXPWTSO-UHFFFAOYSA-N 0.000 claims description 3
KODGCUXGWQLAEK-UHFFFAOYSA-N 3-[6-(pyridin-4-ylmethyl)quinolin-8-yl]-1h-2,1,3-benzoxadiazole Chemical compound C=1C(N2C3=CC=CC=C3NO2)=C2N=CC=CC2=CC=1CC1=CC=NC=C1 KODGCUXGWQLAEK-UHFFFAOYSA-N 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
JKFAIQOWCVVSKC-UHFFFAOYSA-N furazan Chemical compound C=1C=NON=1 JKFAIQOWCVVSKC-UHFFFAOYSA-N 0.000 claims description 2
150000003852 triazoles Chemical class 0.000 claims description 2
DRQNHAXZLIONQV-UHFFFAOYSA-N 4-(6-pyridin-4-ylquinolin-8-yl)-2,1,3-benzoxadiazole Chemical compound C12=NON=C2C=CC=C1C(C1=NC=CC=C1C=1)=CC=1C1=CC=NC=C1 DRQNHAXZLIONQV-UHFFFAOYSA-N 0.000 claims 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract description 46
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229940111121 antirheumatic drug quinolines Drugs 0.000 abstract description 3
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230000002474 noradrenergic effect Effects 0.000 description 1
239000002773 nucleotide Substances 0.000 description 1
125000003729 nucleotide group Chemical group 0.000 description 1
208000007892 occupational asthma Diseases 0.000 description 1
239000002674 ointment Substances 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
239000000162 organ preservation solution Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
238000006053 organic reaction Methods 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
150000003891 oxalate salts Chemical class 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
LXNAVEXFUKBNMK-UHFFFAOYSA-N palladium(II) acetate Substances [Pd].CC(O)=O.CC(O)=O LXNAVEXFUKBNMK-UHFFFAOYSA-N 0.000 description 1
YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
229960001789 papaverine Drugs 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
230000001575 pathological effect Effects 0.000 description 1
230000035515 penetration Effects 0.000 description 1
108010091212 pepstatin Proteins 0.000 description 1
FAXGPCHRFPCXOO-LXTPJMTPSA-N pepstatin A Chemical compound OC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](C(C)C)NC(=O)[C@H](C(C)C)NC(=O)CC(C)C FAXGPCHRFPCXOO-LXTPJMTPSA-N 0.000 description 1
239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
WRLGYAWRGXKSKG-UHFFFAOYSA-M phenobarbital sodium Chemical compound [Na+].C=1C=CC=CC=1C1(CC)C(=O)NC([O-])=NC1=O WRLGYAWRGXKSKG-UHFFFAOYSA-M 0.000 description 1
YBYRMVIVWMBXKQ-UHFFFAOYSA-N phenylmethanesulfonyl fluoride Chemical compound FS(=O)(=O)CC1=CC=CC=C1 YBYRMVIVWMBXKQ-UHFFFAOYSA-N 0.000 description 1
239000002587 phosphodiesterase IV inhibitor Substances 0.000 description 1
239000002571 phosphodiesterase inhibitor Substances 0.000 description 1
230000001817 pituitary effect Effects 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
235000015497 potassium bicarbonate Nutrition 0.000 description 1
229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
239000011736 potassium bicarbonate Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
230000000069 prophylactic effect Effects 0.000 description 1
238000011321 prophylaxis Methods 0.000 description 1
210000004879 pulmonary tissue Anatomy 0.000 description 1
125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 description 1
ZAHRKKWIAAJSAO-UHFFFAOYSA-N rapamycin Natural products COCC(O)C(=C/C(C)C(=O)CC(OC(=O)C1CCCCN1C(=O)C(=O)C2(O)OC(CC(OC)C(=CC=CC=CC(C)CC(C)C(=O)C)C)CCC2C)C(C)CC3CCC(O)C(C3)OC)C ZAHRKKWIAAJSAO-UHFFFAOYSA-N 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
210000002345 respiratory system Anatomy 0.000 description 1
230000000552 rheumatic effect Effects 0.000 description 1
206010039073 rheumatoid arthritis Diseases 0.000 description 1
201000000306 sarcoidosis Diseases 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
210000001044 sensory neuron Anatomy 0.000 description 1
229940076279 serotonin Drugs 0.000 description 1
230000002295 serotoninergic effect Effects 0.000 description 1
230000035939 shock Effects 0.000 description 1
208000004003 siderosis Diseases 0.000 description 1
QFJCIRLUMZQUOT-HPLJOQBZSA-N sirolimus Chemical compound C1C[C@@H](O)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 QFJCIRLUMZQUOT-HPLJOQBZSA-N 0.000 description 1
229960002930 sirolimus Drugs 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
QGMRQYFBGABWDR-UHFFFAOYSA-N sodium;5-ethyl-5-pentan-2-yl-1,3-diazinane-2,4,6-trione Chemical compound [Na+].CCCC(C)C1(CC)C(=O)NC(=O)NC1=O QGMRQYFBGABWDR-UHFFFAOYSA-N 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003431 steroids Chemical class 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000000829 suppository Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
238000001356 surgical procedure Methods 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
238000002636 symptomatic treatment Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
201000000596 systemic lupus erythematosus Diseases 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
210000001541 thymus gland Anatomy 0.000 description 1
210000001685 thyroid gland Anatomy 0.000 description 1
239000003053 toxin Substances 0.000 description 1
231100000765 toxin Toxicity 0.000 description 1
108700012359 toxins Proteins 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
230000037317 transdermal delivery Effects 0.000 description 1
125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 1
XWNXEWLCHSLQOI-UHFFFAOYSA-K trisodium;triacetate Chemical compound [Na+].[Na+].[Na+].CC([O-])=O.CC([O-])=O.CC([O-])=O XWNXEWLCHSLQOI-UHFFFAOYSA-K 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
239000012588 trypsin Substances 0.000 description 1
102000003390 tumor necrosis factor Human genes 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
229940124549 vasodilator Drugs 0.000 description 1
239000003071 vasodilator agent Substances 0.000 description 1
210000003462 vein Anatomy 0.000 description 1
238000009423 ventilation Methods 0.000 description 1
208000018464 vernal keratoconjunctivitis Diseases 0.000 description 1
230000003612 virological effect Effects 0.000 description 1
238000005303 weighing Methods 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1

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
- C07D401/14—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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- A61P25/16—Anti-Parkinson drugs
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- 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
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
- 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
- C07D417/14—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 three or more hetero rings

Landscapes

Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Biomedical Technology (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Pain & Pain Management (AREA)
Psychiatry (AREA)
Immunology (AREA)
Hospice & Palliative Care (AREA)
Psychology (AREA)
Rheumatology (AREA)
Pulmonology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)

SK639-98A 1995-11-14 1996-11-13 Quinoline derivatives, method for the preparation thereof, pharmaceutical composition containing same, and their use SK63998A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GBGB9523267.4A GB9523267D0 (en)	1995-11-14	1995-11-14	Organic compounds
PCT/EP1996/004978 WO1997018208A1 (en)	1995-11-14	1996-11-13	Quinoline derivatives as type iv phosphodiesterase inhibitors

Publications (1)

Publication Number	Publication Date
SK63998A3 true SK63998A3 (en)	1998-10-07

Family

ID=10783856

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK639-98A SK63998A3 (en)	1995-11-14	1996-11-13	Quinoline derivatives, method for the preparation thereof, pharmaceutical composition containing same, and their use

Country Status (17)

Country	Link
EP (1)	EP0873338A1 (cs)
JP (1)	JPH11515000A (cs)
KR (1)	KR19990067574A (cs)
CN (1)	CN1202170A (cs)
AU (1)	AU7570996A (cs)
BR (1)	BR9611504A (cs)
CA (1)	CA2235126A1 (cs)
CO (1)	CO4770973A1 (cs)
CZ (1)	CZ149498A3 (cs)
GB (1)	GB9523267D0 (cs)
HU (1)	HUP9903492A3 (cs)
MX (1)	MX9803839A (cs)
PE (1)	PE17598A1 (cs)
PL (1)	PL326636A1 (cs)
SK (1)	SK63998A3 (cs)
TR (1)	TR199800851T2 (cs)
WO (1)	WO1997018208A1 (cs)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA2715683A1 (en)	1999-08-21	2001-03-01	Nycomed Gmbh	Synergistic combination
WO2002094321A1 (en)	2001-05-23	2002-11-28	Tanabe Seiyaku Co., Ltd.	Compositions for promoting healing of bone fracture
WO2002094320A1 (en)	2001-05-23	2002-11-28	Tanabe Seiyaku Co., Ltd.	Therapeutic compositions for repairing chondropathy
EA200501548A1 (ru)	2003-04-01	2006-02-24	Апплайд Резеч Системз Арс Холдинг Н.В.	Ингибиторы фосфодиэстераз при бесплодии
JP4932495B2 (ja) *	2004-01-23	2012-05-16	アムゲンインコーポレイテッド	化合物及び使用方法
JP2006347936A (ja) *	2005-06-15	2006-12-28	Bayer Cropscience Ag	殺虫性ベンズアニリド類
NZ603136A (en)	2010-05-10	2014-11-28	Gilead Sciences Inc	Bifunctional quinoline derivatives
WO2011143106A1 (en)	2010-05-10	2011-11-17	Gilead Sciences, Inc.	Bi - functional pyrazolopyridine compounds
US9309222B2 (en)	2012-10-16	2016-04-12	Janssen Pharmaceutica Nv	Phenyl linked quinolinyl modulators of RORγt
JP6466335B2 (ja)	2012-10-16	2019-02-06	ヤンセンファーマシューティカエヌ．ベー．	ＲＯＲ−γ−Ｔのメチレン連結キノリニルモジュレーター
CN104884448A (zh)	2012-10-16	2015-09-02	詹森药业有限公司	Rorγt的杂芳基连接的喹啉基调节剂
US9221804B2 (en)	2013-10-15	2015-12-29	Janssen Pharmaceutica Nv	Secondary alcohol quinolinyl modulators of RORγt
US9328095B2 (en)	2013-10-15	2016-05-03	Janssen Pharmaceutica Nv	Heteroaryl linked quinolinyl modulators of RORgammat
US10555941B2 (en)	2013-10-15	2020-02-11	Janssen Pharmaceutica Nv	Alkyl linked quinolinyl modulators of RORγt
CN105873439A (zh)	2013-10-15	2016-08-17	詹森药业有限公司	RORγt的烷基连接的喹啉基调节剂
US9403816B2 (en)	2013-10-15	2016-08-02	Janssen Pharmaceutica Nv	Phenyl linked quinolinyl modulators of RORγt
US9284308B2 (en)	2013-10-15	2016-03-15	Janssen Pharmaceutica Nv	Methylene linked quinolinyl modulators of RORγt
KR20160068956A (ko)	2013-10-15	2016-06-15	얀센 파마슈티카 엔.브이.	RORyT의 퀴놀리닐 조절제
US11427545B2 (en) *	2018-06-24	2022-08-30	Adama Agan Ltd.	Process for the preparation of Quinmerac

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9027055D0 (en) *	1990-12-13	1991-02-06	Sandoz Ltd	Organic compounds
US5455252A (en) *	1993-03-31	1995-10-03	Syntex (U.S.A.) Inc.	Optionally substituted 6,8-quinolines

1995
- 1995-11-14 GB GBGB9523267.4A patent/GB9523267D0/en active Pending
1996
- 1996-11-12 PE PE1996000810A patent/PE17598A1/es not_active Application Discontinuation
- 1996-11-13 BR BR9611504A patent/BR9611504A/pt not_active Application Discontinuation
- 1996-11-13 CZ CZ981494A patent/CZ149498A3/cs unknown
- 1996-11-13 SK SK639-98A patent/SK63998A3/sk unknown
- 1996-11-13 WO PCT/EP1996/004978 patent/WO1997018208A1/en not_active Ceased
- 1996-11-13 CO CO96059775A patent/CO4770973A1/es unknown
- 1996-11-13 CN CN96198305A patent/CN1202170A/zh active Pending
- 1996-11-13 JP JP9515313A patent/JPH11515000A/ja not_active Withdrawn
- 1996-11-13 KR KR1019980703597A patent/KR19990067574A/ko not_active Withdrawn
- 1996-11-13 CA CA002235126A patent/CA2235126A1/en not_active Abandoned
- 1996-11-13 EP EP96938196A patent/EP0873338A1/en not_active Withdrawn
- 1996-11-13 HU HU9903492A patent/HUP9903492A3/hu unknown
- 1996-11-13 TR TR1998/00851T patent/TR199800851T2/xx unknown
- 1996-11-13 PL PL96326636A patent/PL326636A1/xx unknown
- 1996-11-13 AU AU75709/96A patent/AU7570996A/en not_active Abandoned
1998
- 1998-05-14 MX MX9803839A patent/MX9803839A/es unknown

Also Published As

Publication number	Publication date
WO1997018208A1 (en)	1997-05-22
CO4770973A1 (es)	1999-04-30
PL326636A1 (en)	1998-10-12
KR19990067574A (ko)	1999-08-25
JPH11515000A (ja)	1999-12-21
EP0873338A1 (en)	1998-10-28
CN1202170A (zh)	1998-12-16
AU7570996A (en)	1997-06-05
TR199800851T2 (xx)	1998-08-21
CA2235126A1 (en)	1997-05-22
CZ149498A3 (cs)	1998-08-12
MX9803839A (es)	1998-09-30
BR9611504A (pt)	1999-03-02
HUP9903492A3 (en)	2000-08-28
HUP9903492A2 (en)	2000-07-28
GB9523267D0 (en)	1996-01-17
PE17598A1 (es)	1998-04-06

Publication	Publication Date	Title
CZ149498A3 (cs)	1998-08-12	Deriváty chinolinu, způsob jejich přípravy, farmaceutický prostředek, který je obsahuje, a jejich použití
US5177085A (en)	1993-01-05	Dihydro-isoquinoline derivatives, processes for their production, pharmaceutical compositions containing them, and their use in treating asthma
US5747506A (en)	1998-05-05	Isoquinoline compounds, compositions containing them and their pharmaceutical uses
US6136821A (en)	2000-10-24	Naphthyridine derivatives
KR100484045B1 (ko)	2005-04-20	기관지 치료용 벤조나프티리딘
US4980359A (en)	1990-12-25	Isoquinoline derivatives and their use
KR20070043968A (ko)	2007-04-26	Ｐａｒｐ 저해제로서의 치환 ２-알킬 퀴나졸리논 유도체
EP1332147A1 (en)	2003-08-06	Thieno[2,3-c isoquinolines for use as inhibitors of parp
JPWO1997019078A1 (ja)	1998-12-22	ピリド［２，３−ｄ］ピリミジン誘導体及びその医薬組成物
JP2006506414A (ja)	2006-02-23	抗炎症性３−アリールチオ−３−チアゾリル−アルキルアミン
EP1142881A1 (en)	2001-10-10	Poly(adp-ribose) polymerase inhibitors consisting of pyrimidine derivatives
SU1395140A3 (ru)	1988-05-07	Способ получени карбостирильных производных
SK170299A3 (en)	2000-08-14	Aminospiro piperidine quinazoline derivatives, process and intermediates to their preparation, pharmaceutical compositions them containing and their use
JP2007507463A (ja)	2007-03-29	誘導性ＮＯシンターゼ阻害剤としてのイミダゾ［４，５−ｂ］ピリジン誘導体
US20200361902A1 (en)	2020-11-19	Crystal form i of a 5-aminopyrazole carboxamide compound as btk inhibitor
NO178430B (no)	1995-12-18	Nye dihydroisokinolinderivater og deres anvendelse som terapeutikum
HK1022305B (en)	2004-02-06	Naphthyridine derivatives