IL101960A - 3 -]) hetero (arylmethylamino [- 2 -) di) hetero (arylmethyl (converted quinuclidines and pharmaceutical preparations containing them - Google Patents

3 -]) hetero (arylmethylamino [- 2 -) di) hetero (arylmethyl (converted quinuclidines and pharmaceutical preparations containing them

Info

Publication number
IL101960A
IL101960A IL10196092A IL10196092A IL101960A IL 101960 A IL101960 A IL 101960A IL 10196092 A IL10196092 A IL 10196092A IL 10196092 A IL10196092 A IL 10196092A IL 101960 A IL101960 A IL 101960A
Authority
IL
Israel
Prior art keywords
disorders
compound according
optionally substituted
substituted
alkyl
Prior art date
Application number
IL10196092A
Other languages
English (en)
Hebrew (he)
Other versions
IL101960A0 (en
Original Assignee
Pfizer
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.)
Filing date
Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of IL101960A0 publication Critical patent/IL101960A0/xx
Publication of IL101960A publication Critical patent/IL101960A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
IL10196092A 1991-05-22 1992-05-21 3 -]) hetero (arylmethylamino [- 2 -) di) hetero (arylmethyl (converted quinuclidines and pharmaceutical preparations containing them IL101960A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14682691 1991-05-22

Publications (2)

Publication Number Publication Date
IL101960A0 IL101960A0 (en) 1994-04-12
IL101960A true IL101960A (en) 1999-03-12

Family

ID=15416402

Family Applications (1)

Application Number Title Priority Date Filing Date
IL10196092A IL101960A (en) 1991-05-22 1992-05-21 3 -]) hetero (arylmethylamino [- 2 -) di) hetero (arylmethyl (converted quinuclidines and pharmaceutical preparations containing them

Country Status (25)

Country Link
EP (1) EP0585328B1 (fr)
KR (1) KR100246065B1 (fr)
CN (1) CN1041827C (fr)
AT (1) ATE211743T1 (fr)
AU (1) AU658898B2 (fr)
BR (1) BR9206044A (fr)
CA (1) CA2109415C (fr)
CZ (1) CZ247993A3 (fr)
DE (2) DE9290057U1 (fr)
DK (1) DK0585328T3 (fr)
EG (1) EG20218A (fr)
ES (1) ES2168260T3 (fr)
FI (1) FI935134A (fr)
HU (1) HUT65771A (fr)
IE (1) IE921662A1 (fr)
IL (1) IL101960A (fr)
MX (1) MX9202449A (fr)
NO (1) NO305173B1 (fr)
NZ (2) NZ272941A (fr)
PL (4) PL171921B1 (fr)
PT (1) PT100514B (fr)
RU (1) RU2092486C1 (fr)
UA (1) UA26401C2 (fr)
WO (1) WO1992020676A1 (fr)
ZA (1) ZA923773B (fr)

Families Citing this family (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5138060A (en) * 1991-01-03 1992-08-11 Pfizer Inc. Process and intermediates for preparing azabicyclo(2.2.2)octan-3-imines
JPH07110850B2 (ja) * 1991-06-20 1995-11-29 フアイザー・インコーポレイテツド 窒素含有複素環化合物のフルオロアルコキシベンジルアミノ誘導体
JP2656702B2 (ja) * 1992-03-23 1997-09-24 ファイザー製薬株式会社 ペプチド性キヌクリジン
JP2909214B2 (ja) * 1992-08-19 1999-06-23 フアイザー・インコーポレイテツド 置換ベンジルアミノ窒素含有非芳香族複素環化合物
JP2656699B2 (ja) * 1992-10-21 1997-09-24 ファイザー製薬株式会社 置換ベンジルアミノキヌクリジン
US5837711A (en) * 1992-10-28 1998-11-17 Pfizer Inc. Substituted quinuclidines as substance P antagonists
JP2656700B2 (ja) * 1992-10-28 1997-09-24 ファイザー製薬株式会社 置換キヌクリジン誘導体
ES2147759T3 (es) * 1992-12-10 2000-10-01 Pfizer Heterociclos no aromaticos sustituidos con aminometileno y uso como antagonistas de la sustancia p.
IL109646A0 (en) * 1993-05-19 1994-08-26 Pfizer Heteroatom substituted alkyl benzylamino-quinuclidines
JP2822274B2 (ja) * 1993-05-19 1998-11-11 ファイザー製薬株式会社 P物質拮抗剤としてのヘテロ原子置換アルキルベンジルアミノキヌクリジン類
US5393762A (en) * 1993-06-04 1995-02-28 Pfizer Inc. Pharmaceutical agents for treatment of emesis
DE69413822T2 (de) * 1993-07-15 1999-02-25 Pfizer Benzyloxychinuclidine als substanz p antagonisten
PT719253E (pt) * 1993-09-17 2004-07-30 Pfizer Piperidinas 3-amino-5-carboxi-substituidas e pirrolidinas 3-amino-4-carboxi-substituidas como antagonistas de taquicinina
US6083943A (en) * 1993-09-17 2000-07-04 Pfizer Inc Substituted azaheterocyclecarboxylic acid
EP0653208A3 (fr) * 1993-11-17 1995-10-11 Pfizer Antagonistes de la substance P pour le traitement et la prévention de l'erythème solaire.
EP0659409A3 (fr) * 1993-11-23 1995-08-09 Pfizer Antagonistes de la substance P pour l'inhibition de l'angiogénése.
EP0655246A1 (fr) * 1993-11-30 1995-05-31 Pfizer Inc. Antagonistes de la substance P pour le traitement des maladies causées par Helicobacter Pylori ou d'autres bacteries spirales, ureare-positives, gram-négatives
FR2728169A1 (fr) 1994-12-19 1996-06-21 Oreal Utilisation d'un antagoniste de substance p pour le traitement des prurits et des dysesthesies oculaires ou palpebrales
FR2728166A1 (fr) 1994-12-19 1996-06-21 Oreal Composition topique contenant un antagoniste de substance p
FR2728165A1 (fr) 1994-12-19 1996-06-21 Oreal Utilisation d'un antagoniste de substance p pour le traitement des rougeurs cutanees d'origine neurogene
PE8798A1 (es) * 1995-07-17 1998-03-02 Pfizer Procedimiento de separacion de los enantiomeros del 1-azabiciclo[2.2.2] octan-3-amina, 2-(difenilmetil) -n- [[2-metoxi-5-(1-metiletil) fenil] metil]
TW458774B (en) 1995-10-20 2001-10-11 Pfizer Antiemetic pharmaceutical compositions
FR2741262B1 (fr) 1995-11-20 1999-03-05 Oreal Utilisation d'un antagoniste de tnf-alpha pour le traitement des rougeurs cutanees d'origine neurogene
MX9706944A (es) * 1996-09-12 1998-08-30 Pfizer Quinuclidinas sustituidas con tetrazolilo como antagonistas de la sustancia p.
NZ329807A (en) * 1997-04-23 2000-07-28 Pfizer NK-1 receptor antagonists and P receptor antagonists 2-Diarylmethyl-3-amino-1-azabicyclo[2.2.2]octane derivatives and amino substituted N-containing rings as agents for treating irritable bowel syndrome
EP1246806B1 (fr) 1999-11-03 2008-02-27 AMR Technology, Inc. Tetrahydroisoquinolines a substitution aryle et heteroaryle et utilisation de ces composes pour bloquer le recaptage de norepinephrine, de dopamine et de serotonine
US7163949B1 (en) 1999-11-03 2007-01-16 Amr Technology, Inc. 4-phenyl substituted tetrahydroisoquinolines and use thereof
AU7334901A (en) 2000-07-11 2002-01-21 Du Pont Pharm Co Novel 4-phenyl substituted tetrahydroisoquinolines and therapeutic use thereof
DOP2002000332A (es) 2001-02-14 2002-08-30 Warner Lambert Co Inhibidores de piridina de metaloproteinasas de la matriz
US6861526B2 (en) * 2002-10-16 2005-03-01 Pfizer Inc. Process for the preparation of (S,S)-cis-2-benzhydryl-3-benzylaminoquinuclidine
WO2006020049A2 (fr) 2004-07-15 2006-02-23 Amr Technology, Inc. Tetrahydroisoquinolines a substitution aryle et heteroaryle et leur utilisation pour bloquer le recaptage de la norepinephrine, la dopamine et la serotonine
ES2382814T3 (es) 2005-05-17 2012-06-13 Merck Sharp & Dohme Ltd. Ácido cis-4-[(4-clorofenil)sulfonil]-4-(2,5-difluorofenil)ciclohexanopropanoico para el tratamiento del cáncer
US7956050B2 (en) 2005-07-15 2011-06-07 Albany Molecular Research, Inc. Aryl- and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin
JP4879988B2 (ja) 2005-09-29 2012-02-22 メルク・シャープ・エンド・ドーム・コーポレイション メラノコルチン−4受容体モジュレーターとしてのアシル化スピロピペリジン誘導体
GB0603041D0 (en) 2006-02-15 2006-03-29 Angeletti P Ist Richerche Bio Therapeutic compounds
CA2770486C (fr) 2006-09-22 2014-07-15 Merck Sharp & Dohme Corp. Utilisation de la platencine et de la platensimycine en tant qu'inhibiteurs de la synthese des acides gras pour traiter l'obesite, lediabete et le cancer
US20110218176A1 (en) 2006-11-01 2011-09-08 Barbara Brooke Jennings-Spring Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
PL2109608T3 (pl) 2007-01-10 2011-08-31 Msd Italia Srl Indazole podstawione grupą amidową jako inhibitory polimerazy poli(ADP-rybozy)-(PARP)
EP2117538A1 (fr) 2007-01-24 2009-11-18 Glaxo Group Limited Compositions pharmaceutiques contenant du 2-méthoxy-5- (5-trifluorométhyl-tétrazol-i-yl-benzyl) - (2s-phényl-pipéridin-3s-yl-)
AU2008233662B2 (en) 2007-04-02 2012-08-23 Msd K.K. Indoledione derivative
JP5501227B2 (ja) 2007-06-27 2014-05-21 メルク・シャープ・アンド・ドーム・コーポレーション ヒストンデアセチラーゼ阻害剤としての4−カルボキシベンジルアミノ誘導体
JP2011515343A (ja) 2008-03-03 2011-05-19 タイガー ファーマテック チロシンキナーゼ阻害薬
US9156812B2 (en) 2008-06-04 2015-10-13 Bristol-Myers Squibb Company Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
UA105182C2 (ru) 2008-07-03 2014-04-25 Ньюрексон, Інк. Бензоксазины, бензотиазины и родственные соединения, которые имеют ингибирующую nos активность
WO2010114780A1 (fr) 2009-04-01 2010-10-07 Merck Sharp & Dohme Corp. Inhibiteurs de l'activité akt
KR20120034644A (ko) 2009-05-12 2012-04-12 알바니 몰레큘라 리써치, 인크. 아릴, 헤테로아릴, 및 헤테로사이클 치환된 테트라하이드로이소퀴놀린 및 이의 용도
DK2429296T3 (en) 2009-05-12 2018-03-12 Albany Molecular Res Inc 7 - ([1,2,4,] TRIAZOLO [1,5, -A] PYRIDIN-6-YL) -4- (3,4-DICHLORPHENYL) -1,2,3,4- TETRAHYDROISOQUINOLINE AND USE thereof
JP5739415B2 (ja) 2009-05-12 2015-06-24 ブリストル−マイヤーズ スクウィブ カンパニー (S)−7−([1,2,4]トリアゾロ[1,5−a]ピリジン−6−イル)−4−(3,4−ジクロロフェニル)−1,2,3,4−テトラヒドロイソキノリンの結晶形態およびその使用
US8859776B2 (en) 2009-10-14 2014-10-14 Merck Sharp & Dohme Corp. Substituted piperidines that increase p53 activity and the uses thereof
EP2584903B1 (fr) 2010-06-24 2018-10-24 Merck Sharp & Dohme Corp. Nouveaux composés hétérocycliques utilisés comme inhibiteurs de erk
JP6043285B2 (ja) 2010-08-02 2016-12-14 サーナ・セラピューティクス・インコーポレイテッドSirna Therapeutics,Inc. 低分子干渉核酸(siNA)を用いたカテニン(カドヘリン結合型タンパク質)β1(CTNNB1)遺伝子発現のRNA干渉媒介性阻害
RU2624045C2 (ru) 2010-08-17 2017-06-30 Сирна Терапьютикс,Инк ОПОСРЕДУЕМОЕ РНК-ИНТЕРФЕРЕНЦИЕЙ ИНГИБИРОВАНИЕ ЭКСПРЕССИИ ГЕНОВ ВИРУСА ГЕПАТИТА B (HBV) С ПРИМЕНЕНИЕМ МАЛОЙ ИНТЕРФЕРИРУЮЩЕЙ НУКЛЕИНОВОЙ КИСЛОТЫ (миНК)
US8883801B2 (en) 2010-08-23 2014-11-11 Merck Sharp & Dohme Corp. Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors
EP2613782B1 (fr) 2010-09-01 2016-11-02 Merck Sharp & Dohme Corp. Dérivés d'indazole utilisables en tant qu'inhibiteurs de la voie erk
US9242981B2 (en) 2010-09-16 2016-01-26 Merck Sharp & Dohme Corp. Fused pyrazole derivatives as novel ERK inhibitors
EP2632472B1 (fr) 2010-10-29 2017-12-13 Sirna Therapeutics, Inc. Inhibition facilitée par l'interférence d'arn de l'expression d'un gène au moyen d'acides nucléiques interférents courts (sina)
WO2012087772A1 (fr) 2010-12-21 2012-06-28 Schering Corporation Dérivés d'indazole utiles en tant qu'inhibiteurs de erk
CN103732592A (zh) 2011-04-21 2014-04-16 默沙东公司 胰岛素样生长因子-1受体抑制剂
US9023865B2 (en) 2011-10-27 2015-05-05 Merck Sharp & Dohme Corp. Compounds that are ERK inhibitors
US20150299696A1 (en) 2012-05-02 2015-10-22 Sirna Therapeutics, Inc. SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS
CA2882950A1 (fr) 2012-09-28 2014-04-03 Merck Sharp & Dohme Corp. Nouveaux composes inhibiteurs de erk
RU2660349C2 (ru) 2012-11-28 2018-07-05 Мерк Шарп И Доум Корп. Композиции и способы для лечения злокачественной опухоли
WO2014100065A1 (fr) 2012-12-20 2014-06-26 Merck Sharp & Dohme Corp. Imidazopyridines substituées en tant qu'inhibiteurs de hdm2
WO2014120748A1 (fr) 2013-01-30 2014-08-07 Merck Sharp & Dohme Corp. Purines 2,6,7,8-substituées utilisées en tant qu'inhibiteurs de hdm2
EP3041938A1 (fr) 2013-09-03 2016-07-13 Moderna Therapeutics, Inc. Polynucléotides circulaires
EP3706742B1 (fr) 2017-11-08 2023-03-15 Merck Sharp & Dohme LLC Inhibiteurs de prmt5
WO2020033282A1 (fr) 2018-08-07 2020-02-13 Merck Sharp & Dohme Corp. Inhibiteurs de prmt5
US20210309688A1 (en) 2018-08-07 2021-10-07 Merck Sharp & Dohme Corp. Prmt5 inhibitors

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990005525A1 (fr) * 1988-11-23 1990-05-31 Pfizer Inc. Derives de quinuclidine en tant qu'antagonsites de substance p

Also Published As

Publication number Publication date
AU658898B2 (en) 1995-05-04
WO1992020676A1 (fr) 1992-11-26
DK0585328T3 (da) 2002-02-11
ES2168260T3 (es) 2002-06-16
PL170513B1 (en) 1996-12-31
HU9303307D0 (en) 1994-03-28
CZ247993A3 (en) 1994-07-13
ATE211743T1 (de) 2002-01-15
PL172069B1 (pl) 1997-07-31
CN1041827C (zh) 1999-01-27
PL170525B1 (en) 1996-12-31
EG20218A (en) 1997-11-30
FI935134A0 (fi) 1993-11-19
FI935134A (fi) 1993-11-19
CA2109415C (fr) 1998-12-29
UA26401C2 (uk) 1999-08-30
BR9206044A (pt) 1995-03-01
EP0585328B1 (fr) 2002-01-09
PT100514A (pt) 1993-09-30
HUT65771A (en) 1994-07-28
RU2092486C1 (ru) 1997-10-10
CN1068571A (zh) 1993-02-03
AU1927592A (en) 1992-12-30
PL171921B1 (pl) 1997-06-30
EP0585328A1 (fr) 1994-03-09
NZ272941A (en) 1997-05-26
DE9290057U1 (de) 1994-01-05
IL101960A0 (en) 1994-04-12
MX9202449A (es) 1993-03-01
NO934195D0 (no) 1993-11-19
ZA923773B (en) 1993-11-22
NO305173B1 (no) 1999-04-12
DE69232334D1 (de) 2002-02-14
CA2109415A1 (fr) 1992-11-23
NO934195L (no) 1993-11-19
PT100514B (pt) 1999-06-30
KR100246065B1 (en) 2000-04-01
NZ242880A (en) 1995-10-26
IE921662A1 (en) 1992-12-02
DE69232334T2 (de) 2002-11-14

Similar Documents

Publication Publication Date Title
IL101960A (en) 3 -]) hetero (arylmethylamino [- 2 -) di) hetero (arylmethyl (converted quinuclidines and pharmaceutical preparations containing them
IE83327B1 (en) Substituted 3-aminoquinuclidines
CA2123403C (fr) Derives ethylenediamine acycliques utilises comme antagonistes des recepteurs de la substance p
EP0699199B1 (fr) Alkyle benzylaminoquinuclidines a substitution heteroatomique utilisees comme antagonistes de substances p
EP0632809B1 (fr) Derives de quinuclidine utiles comme antagonistes de la substance p
EP0665844B1 (fr) Benzylaminoquinuclidines substituees utilisees comme antagonistes de substance p
JPH0578354A (ja) アザ二環式化合物、これを含有する医薬組成物及び治療のための使用方法
US20100267766A1 (en) Derivatives of pyrrolizine, indolizine and quinolizine, preparation thereof and therapeutic use thereof
US5852038A (en) Substituted 3-aminoquinuclidines
US5569662A (en) Quinuclidine derivatives as substance P antagonists
US5604241A (en) Substituted benzylaminoquinuclidines as substance P antagonists
JP2719063B2 (ja) 置換3−アミノキヌクリジンp物質拮抗剤
JP3172461B2 (ja) サブスタンスpアンタゴニストとしての3−[(5−置換ベンジル)アミノ]−2−フェニルピペリジン

Legal Events

Date Code Title Description
FF Patent granted
KB Patent renewed
MM9K Patent not in force due to non-payment of renewal fees