OA11294A - Branched alkoxy-substituted 2-aminopyridines as nos inhibitors. - Google Patents

Branched alkoxy-substituted 2-aminopyridines as nos inhibitors. Download PDF

Info

Publication number: OA11294A
Authority: OA; OAPI
Prior art keywords: disease; phenyl; alkyl; pyridin; shock
Prior art date: 1997-08-28

Application number

OA1200000053A

Other languages

English (en)

Inventor

Lowe John Adams Iii

Original Assignee

Pfizer Prod Inc

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.)

1997-08-28

Filing date

2000-02-25

Publication date

2003-10-22

2000-02-25 Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc

2003-10-22 Publication of OA11294A publication Critical patent/OA11294A/en

Links

239000003112 inhibitor Substances 0.000 title abstract description 6
150000003930 2-aminopyridines Chemical class 0.000 title description 2
102000008299 Nitric Oxide Synthase Human genes 0.000 claims abstract description 24
108010021487 Nitric Oxide Synthase Proteins 0.000 claims abstract description 24
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 20
239000008194 pharmaceutical composition Substances 0.000 claims abstract description 9
150000001875 compounds Chemical class 0.000 claims description 80
-1 chloro, fluoro, bromo, iodo Chemical group 0.000 claims description 26
125000000217 alkyl group Chemical group 0.000 claims description 18
206010001052 Acute respiratory distress syndrome Diseases 0.000 claims description 16
208000013616 Respiratory Distress Syndrome Diseases 0.000 claims description 16
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
208000002193 Pain Diseases 0.000 claims description 14
230000001154 acute effect Effects 0.000 claims description 14
208000011341 adult acute respiratory distress syndrome Diseases 0.000 claims description 14
201000000028 adult respiratory distress syndrome Diseases 0.000 claims description 14
241000124008 Mammalia Species 0.000 claims description 13
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 13
201000010099 disease Diseases 0.000 claims description 13
125000001424 substituent group Chemical group 0.000 claims description 13
BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 claims description 12
150000003839 salts Chemical class 0.000 claims description 12
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206010040070 Septic Shock Diseases 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 9
239000001257 hydrogen Substances 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
230000036303 septic shock Effects 0.000 claims description 9
230000035939 shock Effects 0.000 claims description 9
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125000003118 aryl group Chemical group 0.000 claims description 7
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125000003710 aryl alkyl group Chemical group 0.000 claims description 5
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125000003545 alkoxy group Chemical group 0.000 claims description 4
125000003282 alkyl amino group Chemical group 0.000 claims description 4
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238000004519 manufacturing process Methods 0.000 claims description 4
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims description 4
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
101100495911 Arabidopsis thaliana CHR10 gene Proteins 0.000 claims description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
125000002837 carbocyclic group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000000719 pyrrolidinyl group Chemical group 0.000 claims description 2
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125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
208000024827 Alzheimer disease Diseases 0.000 claims 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
MNUHYQZBNHDABI-UHFFFAOYSA-N 3-azabicyclo[3.1.0]hexan-6-amine Chemical group C1NCC2C(N)C21 MNUHYQZBNHDABI-UHFFFAOYSA-N 0.000 claims 1
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230000000694 effects Effects 0.000 abstract description 4
210000003169 central nervous system Anatomy 0.000 abstract description 2
XDWUSBKLDNVDDQ-UHFFFAOYSA-N 6-phenylpyridin-2-amine Chemical class NC1=CC=CC(C=2C=CC=CC=2)=N1 XDWUSBKLDNVDDQ-UHFFFAOYSA-N 0.000 abstract 1
230000002265 prevention Effects 0.000 abstract 1
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238000006243 chemical reaction Methods 0.000 description 45
239000000243 solution Substances 0.000 description 38
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LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
PCZOZSATUTWXIC-UHFFFAOYSA-N tetraethylazanium;cyanide Chemical compound N#[C-].CC[N+](CC)(CC)CC PCZOZSATUTWXIC-UHFFFAOYSA-N 0.000 description 1
CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
DSNKGSSXSYPWNC-UHFFFAOYSA-O triethylazanium;cyanide Chemical compound N#[C-].CC[NH+](CC)CC DSNKGSSXSYPWNC-UHFFFAOYSA-O 0.000 description 1
VFJYIHQDILEQNR-UHFFFAOYSA-M trimethylsulfanium;iodide Chemical compound [I-].C[S+](C)C VFJYIHQDILEQNR-UHFFFAOYSA-M 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

Classifications

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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- 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
- C07D401/02—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 two hetero rings
- C07D401/10—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 two hetero rings linked by a carbon chain containing aromatic rings

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Bioinformatics & Cheminformatics (AREA)
Pharmacology & Pharmacy (AREA)
Engineering & Computer Science (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Neurosurgery (AREA)
Neurology (AREA)
Biomedical Technology (AREA)
Pain & Pain Management (AREA)
Psychiatry (AREA)
Pulmonology (AREA)
Diabetes (AREA)
Ophthalmology & Optometry (AREA)
Hospice & Palliative Care (AREA)
Rheumatology (AREA)
Psychology (AREA)
Cardiology (AREA)
Physical Education & Sports Medicine (AREA)
Addiction (AREA)
Heart & Thoracic Surgery (AREA)
Emergency Medicine (AREA)
Obesity (AREA)
Hematology (AREA)
Immunology (AREA)
Orthopedic Medicine & Surgery (AREA)
Endocrinology (AREA)
Dermatology (AREA)
Otolaryngology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Pyridine Compounds (AREA)

OA1200000053A 1997-08-28 2000-02-25 Branched alkoxy-substituted 2-aminopyridines as nos inhibitors. OA11294A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US5773997P	1997-08-28	1997-08-28

Publications (1)

Publication Number	Publication Date
OA11294A true OA11294A (en)	2003-10-22

Family

ID=22012464

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA1200000053A OA11294A (en)	1997-08-28	2000-02-25	Branched alkoxy-substituted 2-aminopyridines as nos inhibitors.

Country Status (32)

Country	Link
US (2)	US6362195B1 (is)
EP (1)	EP1007512B1 (is)
JP (1)	JP3441714B2 (is)
CN (1)	CN1268122A (is)
AP (1)	AP9801331A0 (is)
AR (1)	AR016644A1 (is)
AT (1)	ATE215532T1 (is)
AU (1)	AU8458698A (is)
BR (1)	BR9811921A (is)
CA (1)	CA2302436C (is)
DE (1)	DE69804635T2 (is)
DK (1)	DK1007512T3 (is)
EA (1)	EA200000165A1 (is)
ES (1)	ES2172173T3 (is)
GT (1)	GT199800135A (is)
HN (1)	HN1998000125A (is)
HR (1)	HRP980476A2 (is)
HU (1)	HUP0002803A2 (is)
ID (1)	ID24318A (is)
IL (1)	IL134302A0 (is)
IS (1)	IS5342A (is)
MA (1)	MA26538A1 (is)
NO (1)	NO20000957L (is)
OA (1)	OA11294A (is)
PA (1)	PA8458301A1 (is)
PE (1)	PE106699A1 (is)
PL (1)	PL339008A1 (is)
PT (1)	PT1007512E (is)
SI (1)	SI1007512T1 (is)
TN (1)	TNSN98157A1 (is)
WO (1)	WO1999011620A1 (is)
ZA (1)	ZA987788B (is)

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US20010049379A1 (en)	1997-08-27	2001-12-06	Lowe John Adams	2-aminopyridines containing fused ring substituents
SK1702001A3 (en) *	1998-08-11	2003-02-04	Pfizer Prod Inc	New pharmaceutical uses for NOS inhibitors
CN1341099A (zh) *	1999-02-25	2002-03-20	辉瑞产品公司	含有稠合环取代基的2－氨基吡啶
WO2001009307A2 (en) *	1999-07-30	2001-02-08	University College London	Screen for nitric oxide synthase modulators
EP1203098A2 (en) *	1999-07-30	2002-05-08	University College London	Inducible screen for drug discovery
GB0004153D0 (en) *	2000-02-23	2000-04-12	Astrazeneca Uk Ltd	Novel use
GB0004152D0 (en)	2000-02-23	2000-04-12	Astrazeneca Uk Ltd	Novel compounds
GB0004151D0 (en)	2000-02-23	2000-04-12	Astrazeneca Uk Ltd	Novel use
GB0004149D0 (en) *	2000-02-23	2000-04-12	Astrazeneca Uk Ltd	Novel compounds
US6469172B2 (en) *	2000-03-08	2002-10-22	Merck & Co., Inc.	Process for the preparation of chemical compounds
SE0102640D0 (sv)	2001-07-31	2001-07-31	Astrazeneca Ab	Novel compounds
US20040077853A1 (en) *	2001-10-10	2004-04-22	Pfizer Inc.	2-amino-6-(2,4,5-substituted-phenyl)-pyridines
EP1501511A4 (en) *	2002-05-06	2006-06-07	Univ Washington	METHODS OF TREATING GLAUCOMA AND OTHER CONDITIONS INDUCED BY EXPRESSION OF NOS-2 BY INHIBITING THE EGFR PATHWAY
WO2005007627A1 (ja) *	2003-07-18	2005-01-27	Nihon Nohyaku Co., Ltd.	フェニルピリジン誘導体、その中間体及びこれを有効成分とする除草剤
WO2006053109A1 (en) *	2004-11-10	2006-05-18	Synta Pharmaceuticals Corp.	Heteroaryl compounds
US8604031B2 (en) *	2006-05-18	2013-12-10	Mannkind Corporation	Intracellular kinase inhibitors
UA105182C2 (ru)	2008-07-03	2014-04-25	Ньюрексон, Інк.	Бензоксазины, бензотиазины и родственные соединения, которые имеют ингибирующую nos активность
EP3002279A1 (de)	2014-10-02	2016-04-06	Bayer CropScience AG	Verfahren zur Herstellung von 3-(5-Aminotriazolyl)-Sulfid-Derivaten

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US5892112A (en) *	1990-11-21	1999-04-06	Glycomed Incorporated	Process for preparing synthetic matrix metalloprotease inhibitors
WO1996018616A1 (en) *	1994-12-12	1996-06-20	Merck & Co., Inc.	Substituted 2-aminopyridines as inhibitors of nitric oxide synthase
US5972975A (en) *	1995-12-08	1999-10-26	Merck & Co., Inc.	Substituted 2-aminopyridines as inhibitors of nitric oxide synthase
JP4431638B2 (ja) *	1996-01-29	2010-03-17	アメリカ合衆国	ジヒドロピリジン―、ピリジン―、ベンゾピラン―オン―およびトリアゾロキナゾリン誘導体、それらの製造およびそれらのアデノシン受容体アンタゴニストとしての用途
PT891332E (pt)	1996-03-29	2004-07-30	Pfizer	Derivados de 6-fenilpiridil-2-amina
HN1997000027A (es) *	1996-12-06	1997-06-05	Pfizer Prod Inc	Derivados de 6-fenil piridil - 2 amina

1998
- 1998-08-10 HN HN1998000125A patent/HN1998000125A/es unknown
- 1998-08-11 PL PL98339008A patent/PL339008A1/xx unknown
- 1998-08-11 DE DE69804635T patent/DE69804635T2/de not_active Expired - Fee Related
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- 1998-08-11 AU AU84586/98A patent/AU8458698A/en not_active Abandoned
- 1998-08-11 CA CA002302436A patent/CA2302436C/en not_active Expired - Fee Related
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- 1998-08-11 HU HU0002803A patent/HUP0002803A2/hu unknown
- 1998-08-11 EA EA200000165A patent/EA200000165A1/ru unknown
- 1998-08-11 PT PT98935247T patent/PT1007512E/pt unknown
- 1998-08-11 AT AT98935247T patent/ATE215532T1/de not_active IP Right Cessation
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- 1998-08-11 IL IL13430298A patent/IL134302A0/xx unknown
- 1998-08-11 BR BR9811921-4A patent/BR9811921A/pt not_active Application Discontinuation
- 1998-08-11 US US09/381,887 patent/US6362195B1/en not_active Expired - Fee Related
- 1998-08-11 EP EP98935247A patent/EP1007512B1/en not_active Expired - Lifetime
- 1998-08-11 WO PCT/IB1998/001223 patent/WO1999011620A1/en not_active Ceased
- 1998-08-17 GT GT199800135A patent/GT199800135A/es unknown
- 1998-08-24 PE PE1998000770A patent/PE106699A1/es not_active Application Discontinuation
- 1998-08-26 MA MA25230A patent/MA26538A1/fr unknown
- 1998-08-26 PA PA19988458301A patent/PA8458301A1/es unknown
- 1998-08-26 AR ARP980104258A patent/AR016644A1/es unknown
- 1998-08-26 TN TNTNSN98157A patent/TNSN98157A1/fr unknown
- 1998-08-27 AP APAP/P/1998/001331A patent/AP9801331A0/en unknown
- 1998-08-27 ZA ZA9807788A patent/ZA987788B/xx unknown
- 1998-08-28 HR HR60/057,739A patent/HRP980476A2/hr not_active Application Discontinuation
2000
- 2000-01-14 IS IS5342A patent/IS5342A/is unknown
- 2000-02-25 OA OA1200000053A patent/OA11294A/en unknown
- 2000-02-25 NO NO20000957A patent/NO20000957L/no not_active Application Discontinuation
2001
- 2001-09-20 US US09/957,398 patent/US20020022642A1/en not_active Abandoned

Also Published As

Publication number	Publication date
TNSN98157A1 (fr)	2005-03-15
BR9811921A (pt)	2000-08-15
ZA987788B (en)	2000-02-28
NO20000957D0 (no)	2000-02-25
AU8458698A (en)	1999-03-22
HUP0002803A2 (hu)	2001-06-28
ES2172173T3 (es)	2002-09-16
HN1998000125A (es)	1999-02-09
DE69804635T2 (de)	2002-07-18
GT199800135A (es)	2000-02-08
AP9801331A0 (en)	2000-02-27
PT1007512E (pt)	2002-07-31
PE106699A1 (es)	1999-11-02
AR016644A1 (es)	2001-07-25
ID24318A (id)	2000-07-13
HRP980476A2 (en)	1999-06-30
PA8458301A1 (es)	2000-05-24
EP1007512A1 (en)	2000-06-14
EP1007512B1 (en)	2002-04-03
US6362195B1 (en)	2002-03-26
WO1999011620A1 (en)	1999-03-11
US20020022642A1 (en)	2002-02-21
CN1268122A (zh)	2000-09-27
SI1007512T1 (en)	2002-10-31
EA200000165A1 (ru)	2000-10-30
IL134302A0 (en)	2001-04-30
NO20000957L (no)	2000-02-25
PL339008A1 (en)	2000-12-04
DE69804635D1 (de)	2002-05-08
CA2302436A1 (en)	1999-03-11
IS5342A (is)	2000-01-14
JP2001514252A (ja)	2001-09-11
ATE215532T1 (de)	2002-04-15
MA26538A1 (fr)	2004-12-20
CA2302436C (en)	2003-10-07
JP3441714B2 (ja)	2003-09-02
DK1007512T3 (da)	2002-07-08

Publication	Publication Date	Title
ES2206691T3 (es)	2004-05-16	Derivados de 6-fenilpiridil-2-amina utiles como inhibidores de nos.
OA11294A (en)	2003-10-22	Branched alkoxy-substituted 2-aminopyridines as nos inhibitors.
ES2200813T3 (es)	2004-03-16	2-aminopiridinas que contienen sustituyentes de anillo condesado.
EP1084109B1 (en)	2005-01-26	2-aminopyridines containing fused ring substituents as nitric oxide synthase inhibitors
OA11595A (en)	2004-08-19	New pharmaceutical uses for NOS inhibitors.
OA12664A (en)	2006-06-19	2-Amino-6-(2,4,5-substituted-phenyl)-pyridines foruse as nitric oxide synthase inhibitors.
MXPA00002028A (en)	2001-05-17	Branched alkoxy-subsituted 2-aminopyridines as nos inhibitors
US20040142924A1 (en)	2004-07-22	6-Phenylpyridyl-2-amine derivatives useful as NOS inhibitors