ECSP066856A - Compuestos novedosos como moduladores del receptor opioide - Google Patents

Compuestos novedosos como moduladores del receptor opioide

Info

Publication number
ECSP066856A
ECSP066856A EC2006006856A ECSP066856A ECSP066856A EC SP066856 A ECSP066856 A EC SP066856A EC 2006006856 A EC2006006856 A EC 2006006856A EC SP066856 A ECSP066856 A EC SP066856A EC SP066856 A ECSP066856 A EC SP066856A
Authority
EC
Ecuador
Prior art keywords
new compounds
opioid
receiver modulators
modulators
opioid receiver
Prior art date
Application number
EC2006006856A
Other languages
English (en)
Inventor
Henry J Breslin
Chaozhong Cai
Wei He
Robert W Kavash
Original Assignee
Janssen Pharmaceutica Nv
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34962827&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ECSP066856(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of ECSP066856A publication Critical patent/ECSP066856A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/417Imidazole-alkylamines, e.g. histamine, phentolamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/4174Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/28Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806Coating materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/10Laxatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/30Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D275/00Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/04Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D275/06Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom

Abstract

La presente invención está dirigida a moduladores del receptor opioide de fórmula (I); la invención además se refiere a métodos para la preparación de dichos compuestos, composiciones farmacéuticas que los contienen, y su uso en el tratamiento de trastornos que se pueden mejorar o tratar mediante la formulación de receptores opioide.
EC2006006856A 2004-03-15 2006-09-15 Compuestos novedosos como moduladores del receptor opioide ECSP066856A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US55334204P 2004-03-15 2004-03-15

Publications (1)

Publication Number Publication Date
ECSP066856A true ECSP066856A (es) 2006-11-24

Family

ID=34962827

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2006006856A ECSP066856A (es) 2004-03-15 2006-09-15 Compuestos novedosos como moduladores del receptor opioide

Country Status (36)

Country Link
US (8) US7741356B2 (es)
EP (5) EP3112352B1 (es)
JP (1) JP4778954B2 (es)
KR (1) KR101166342B1 (es)
CN (2) CN102786476B (es)
AR (2) AR048269A1 (es)
AT (1) ATE516274T1 (es)
AU (1) AU2005224091B2 (es)
BR (1) BRPI0508820B8 (es)
CA (1) CA2560047C (es)
CR (1) CR8655A (es)
CY (3) CY1111927T1 (es)
DK (5) DK2573068T3 (es)
EC (1) ECSP066856A (es)
ES (5) ES2428008T3 (es)
HK (4) HK1099016A1 (es)
HR (4) HRP20110694T1 (es)
HU (2) HUE029852T2 (es)
IL (3) IL178040A (es)
LT (2) LT2653465T (es)
LU (1) LUC00007I2 (es)
ME (3) ME02540B (es)
MX (1) MXPA06010642A (es)
MY (1) MY146972A (es)
NL (1) NL300865I2 (es)
NO (3) NO338203B1 (es)
NZ (1) NZ549842A (es)
PH (1) PH12012501640A1 (es)
PL (4) PL1725537T3 (es)
PT (4) PT1725537E (es)
RS (4) RS51995B (es)
SI (4) SI1725537T1 (es)
TW (1) TWI361069B (es)
UA (1) UA86053C2 (es)
WO (1) WO2005090315A1 (es)
ZA (1) ZA200608587B (es)

Families Citing this family (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080050367A1 (en) 1998-04-07 2008-02-28 Guriq Basi Humanized antibodies that recognize beta amyloid peptide
TWI239847B (en) 1997-12-02 2005-09-21 Elan Pharm Inc N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease
ATE516274T1 (de) 2004-03-15 2011-07-15 Janssen Pharmaceutica Nv Neue verbindungen als modulatoren des opioidrezeptors
CN1984879B (zh) 2004-05-14 2011-07-27 詹森药业有限公司 甲酰胺基阿片样化合物
JP2008523815A (ja) 2004-12-15 2008-07-10 エラン ファーマ インターナショナル リミテッド 認知の改善における使用のためのヒト化アミロイドβ抗体
EP1863764A1 (en) * 2005-03-14 2007-12-12 Janssen Pharmaceutica, N.V. Process for the preparation of opioid modulators
ATE511502T1 (de) * 2005-12-14 2011-06-15 Bristol Myers Squibb Co Arylpropionamid-, arylacrylamid-, arylpropinamid- oder arylmethylharnstoffanaloge als faktor-xia- inhibitoren
JP5473334B2 (ja) * 2005-12-23 2014-04-16 ジーランド ファーマ アクティーゼルスカブ 修飾リジン模倣化合物
RU2473565C2 (ru) 2006-04-07 2013-01-27 Аерпио Терапетикс, Инк. АНТИТЕЛА, СВЯЗЫВАЮЩИЕ ТИРОЗИН ФОСФАТАЗУ БЕТА ЧЕЛОВЕКА (HPTPβ), И ИХ ИСПОЛЬЗОВАНИЕ
US8784810B2 (en) 2006-04-18 2014-07-22 Janssen Alzheimer Immunotherapy Treatment of amyloidogenic diseases
US7622593B2 (en) 2006-06-27 2009-11-24 The Procter & Gamble Company Human protein tyrosine phosphatase inhibitors and methods of use
EP2468724B1 (en) * 2006-12-21 2015-11-18 Zealand Pharma A/S Synthesis of pyrrolidine compounds
JP5702140B2 (ja) * 2007-07-09 2015-04-15 フリエツクス・フアーマシユーテイカルズ・インコーポレーテツド 5−({[2−アミノ−3−(4−カルバモイル−2,6−ジメチル−フェニル)−プロピオニル]−[1−(4−フェニル−1h−イミダゾール−2−イル)−エチル]−アミノ}−メチル)−2−メトキシ−安息香酸の新規な結晶及び製造方法
JP5889529B2 (ja) 2007-07-27 2016-03-22 ヤンセン・サイエンシズ・アイルランド・ユーシー アミロイド原性疾患の処置
JO3076B1 (ar) 2007-10-17 2017-03-15 Janssen Alzheimer Immunotherap نظم العلاج المناعي المعتمد على حالة apoe
TWI468375B (zh) 2008-10-27 2015-01-11 Janssen Pharmaceutica Nv 製備經保護之l-丙胺酸衍生物之方法
US9067981B1 (en) 2008-10-30 2015-06-30 Janssen Sciences Ireland Uc Hybrid amyloid-beta antibodies
JP5198220B2 (ja) * 2008-11-13 2013-05-15 東ソ−・エフテック株式会社 アミノ酸誘導体の製造方法
MY160399A (en) 2009-07-06 2017-03-15 Aerpio Therapeutics Inc Compounds, compositions, and methods for preventing metastasis of cancer cells
EP2524912A1 (en) 2011-05-16 2012-11-21 Bionomics Limited Amine derivatives
JP6254075B2 (ja) 2011-05-16 2017-12-27 バイオノミックス リミテッド カリウムチャネル遮断剤としてのアミン誘導体
WO2013056240A1 (en) 2011-10-13 2013-04-18 Aerpio Therapeutics, Inc. Methods for treating vascular leak syndrome and cancer
US9447079B2 (en) * 2013-03-14 2016-09-20 Epizyme, Inc. PRMT1 inhibitors and uses thereof
US9675587B2 (en) 2013-03-14 2017-06-13 Allergan Holdings Unlimited Company Opioid receptor modulator dosage formulations
DK2970132T3 (da) 2013-03-14 2020-12-21 Epizyme Inc Argininmethyltransferaseinhibitorer og anvendelser deraf
WO2014144659A1 (en) 2013-03-14 2014-09-18 Epizyme, Inc. Pyrazole derivatives as prmt1 inhibitors and uses thereof
US9120757B2 (en) 2013-03-14 2015-09-01 Epizyme, Inc. Arginine methyltransferase inhibitors and uses thereof
US20150050277A1 (en) 2013-03-15 2015-02-19 Aerpio Therapeutics Inc. Compositions and methods for treating ocular diseases
JP6483148B2 (ja) 2014-03-14 2019-03-13 エアーピオ セラピューティクス インコーポレイテッド HPTP−β阻害剤
IS2977B (is) 2015-02-23 2017-07-15 Actavis Group Ptc Ehf. Aðferð til framleiðslu á milliefnum sem eru nytsamleg við nýsmíði á elúxadólíni
US10702498B2 (en) 2015-07-09 2020-07-07 The Regents Of The University Of California MU opioid receptor modulators
US10314819B2 (en) 2015-07-23 2019-06-11 Teva Pharmaceuticals International Gmbh Solid state forms of Eluxadoline
CN108026032B (zh) * 2015-09-11 2020-09-29 株式会社钟化 光学活性4-氨基甲酰基-2,6-二甲基苯基丙氨酸衍生物的制造方法
KR20180054677A (ko) 2015-09-23 2018-05-24 에르피오 세러퓨틱스 인코포레이티드 Tie-2의 활성화제로 안내압을 치료하는 방법
CN105250232B (zh) * 2015-09-29 2018-08-14 江苏汇智知识产权服务有限公司 一种伊卢多啉肠溶片及其制备方法
WO2017114446A1 (zh) * 2015-12-31 2017-07-06 苏州晶云药物科技有限公司 艾沙度林的新晶型及其制备方法
CN107129444B (zh) * 2016-02-29 2018-08-31 尚科生物医药(上海)有限公司 (s)-2-叔丁氧羰基氨基-3-(4-氨甲酰基-2,6-二甲基苯基)丙酸制备方法
EP3272741A1 (en) 2016-07-21 2018-01-24 Euticals S.P.A. New stable solvate crystalline forms of eluxadoline
CN105777584B (zh) * 2016-03-28 2018-01-02 成都伊诺达博医药科技有限公司 丙氨酸衍生物的制备方法
CN105693554B (zh) * 2016-04-06 2017-08-08 成都伊诺达博医药科技有限公司 丙氨酸衍生物的制备方法
WO2017191650A1 (en) * 2016-05-03 2017-11-09 Msn Laboratories Private Limited Process for the preparation of 5-[[[(2s)-2-amino-3-[4-(aminocarbonyl)-2,6-dimethylphenyl]-1-oxopropyl][(1s)-1-(4-phenyl-1h-imidazol-2-yl)ethyl]amino]methyl-2-methoxybenzoic acid and its polymorphs thereof
WO2017208156A1 (en) * 2016-05-30 2017-12-07 Sun Pharmaceutical Industries Limited A process for the preparation of eluxadoline
US10822308B2 (en) * 2016-06-23 2020-11-03 Sun Pharmaceutical Industries Limited Processes for the preparation of eluxadoline
WO2018020450A2 (en) 2016-07-28 2018-02-01 Lupin Limited Process for the preparation of eluxadoline
CZ2016548A3 (cs) 2016-09-07 2018-03-14 Zentiva, K.S. Pevné formy eluxadolinu
WO2018047131A1 (en) * 2016-09-09 2018-03-15 Sun Pharmaceutical Industries Limited Amorphous eluxadoline
EP3515434A4 (en) 2016-09-20 2020-02-26 Sun Pharmaceutical Industries Limited METHOD FOR PRODUCING ELUXADOLIN
EP3573958A1 (en) 2017-01-27 2019-12-04 Quimica Sintetica, S.A. Eluxadoline crystalline forms and processes for their preparation
WO2018138272A1 (en) 2017-01-27 2018-08-02 Quimica Sintetica, S. A. Eluxadoline crystalline form and process for the preparation thereof
CN110709096B (zh) 2017-05-05 2023-10-31 泽兰德制药公司 细胞间隙连接通讯调节剂及其在糖尿病性眼病治疗中的应用
WO2019008604A1 (en) 2017-07-07 2019-01-10 Cipla Limited NEW FORMS OF MU-OPIOID RECEPTOR AGONIST
WO2019144805A1 (zh) * 2018-01-25 2019-08-01 四川科伦博泰生物医药股份有限公司 取代的苯乙胺化合物及其制备方法和用途
WO2019197274A1 (en) 2018-04-09 2019-10-17 Quimica Sintetica, S. A. Process for the preparation of opioid modulators
US20210251964A1 (en) 2018-08-20 2021-08-19 Allergan Holdings Unlimited Company Polymorphs of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1h-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid
WO2020068653A1 (en) 2018-09-24 2020-04-02 Aerpio Pharmaceuticals, Inc. MULTISPECIFIC ANTIBODIES THAT TARGET HPTP - β (VE-PTP) AND VEGF
PL3659433T3 (pl) * 2018-11-30 2021-11-08 Phytobiotics Futterzusatzstoffe Gmbh System analizowania obrazów wydzielin zwierzęcych
CN111377832A (zh) * 2018-12-27 2020-07-07 江苏联昇化学有限公司 一种伊卢多啉中间体制备的新方法
WO2020223209A1 (en) 2019-04-29 2020-11-05 Aerpio Pharmaceuticals, Inc. Tie-2 activators targeting the schlemm's canal
WO2021198780A1 (en) 2020-03-30 2021-10-07 Allergan Holdings Unlimited Company Forms of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1h-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid
IL300110A (en) * 2020-07-28 2023-03-01 Jazz Pharmaceuticals Ireland Ltd Chiral synthesis of RAF inhibitors in compressed cyclics
US11850319B2 (en) 2020-09-29 2023-12-26 Abl Ip Holding Llc Techniques for directing ultraviolet energy towards a moving surface
US20220096676A1 (en) 2020-09-29 2022-03-31 Abl Ip Holding Llc Techniques for Directing Ultraviolet Energy Towards a Moving Surface
CN114163348A (zh) * 2020-11-27 2022-03-11 成都泰蓉生物科技有限公司 一种氨酰基取代的l-苯丙氨酸的合成方法

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DD142804A3 (de) * 1977-11-07 1980-07-16 Wagner Guenter Verfahren zur herstellung von na-alkyl-bzw.na-aryl-sulfonylierten omega-amidinophenyl-alpha-aminoalkylcarbonsaeureamiden
US4879398A (en) * 1987-12-31 1989-11-07 Monsanto Company Process for producing 2,6-disubstituted tyrosine
SE9402880D0 (sv) 1994-08-30 1994-08-30 Astra Ab New peptide derivatives
IL116923A (en) 1995-01-27 2000-09-28 Novo Nordisk As Compounds with growth hormone releasing properties and pharmaceutical compositions containing them
US5565568A (en) 1995-04-06 1996-10-15 Eli Lilly And Company 2-acylaminopropanamides as tachykinin receptor antagonists
HUP9802036A3 (en) 1995-04-13 1999-06-28 Aventis Pharmaceuticals Inc Br Novel substituted piperazine derivatives having tachykinin receptor antagonists activity, process for producing them an pharmaceutical compositions containing them
AU6772996A (en) 1995-08-21 1997-03-12 Eli Lilly And Company 2-acylaminopropanamides as growth hormone secretagogues
WO1997019908A1 (en) 1995-11-29 1997-06-05 Nihon Nohyaku Co., Ltd. Phenylalanine derivatives, optically active substances, salts or coordination compounds thereof, and their use as fungicides
US5792760A (en) 1997-04-23 1998-08-11 Eli Lilly And Company Bisindoles as tachykinin receptor antagonists
IT1304898B1 (it) 1998-09-08 2001-04-05 Menarini Ricerche Spa Prodotti con caratteristiche basiche aventi attivita' antagonista sulrecettore nk-1 e loro impiego in preparazioni farmaceutiche
PT1055665E (pt) * 1999-05-28 2004-03-31 Pfizer Prod Inc Derivados da 3-(3-hidroxifenil)-3-amino-propionamida
FR2796643B1 (fr) 1999-07-22 2005-04-29 Sod Conseils Rech Applic Derives de 2-arylimino-2, 3-dihydrothiazoles, leurs procedes de preparation et leur utilisation therapeutique
GB0021419D0 (en) 2000-08-31 2000-10-18 Oxford Glycosciences Uk Ltd Compounds
US20020072017A1 (en) * 2000-10-19 2002-06-13 Hudnall Phillip Montgomery Stabilized p-phenylenediamine-type photographic color developers in free base form
EP1392291B1 (en) 2000-10-30 2007-05-30 Janssen Pharmaceutica N.V. Tripeptidyl peptidase inhibitors
AU2002346994B2 (en) * 2001-10-15 2007-09-06 Janssen Pharmaceutica N.V. Novel substituted 4-phenyl-4-[1H-imidazol-2-yl]-piperidine derivatives and their use as selective non-peptide delta opioid agonists
US7041681B2 (en) 2002-04-29 2006-05-09 Janssen Pharmaceutica N.V. Compounds as opioid receptor modulators
ATE516274T1 (de) * 2004-03-15 2011-07-15 Janssen Pharmaceutica Nv Neue verbindungen als modulatoren des opioidrezeptors
EP1753749B1 (en) * 2004-05-03 2014-07-30 Janssen Pharmaceutica NV Novel indole derivatives as selective androgen receptor modulators (sarms)
EP1863764A1 (en) * 2005-03-14 2007-12-12 Janssen Pharmaceutica, N.V. Process for the preparation of opioid modulators

Also Published As

Publication number Publication date
RS52933B (en) 2014-02-28
SI2653465T1 (sl) 2016-10-28
IL178040A (en) 2013-12-31
HUS1700010I1 (hu) 2017-03-28
CR8655A (es) 2008-09-09
RS55122B1 (sr) 2016-12-30
EP2653465A1 (en) 2013-10-23
DK3112352T3 (en) 2019-01-28
PL2653465T3 (pl) 2017-01-31
US20180325870A1 (en) 2018-11-15
EP2573068A1 (en) 2013-03-27
AU2005224091A1 (en) 2005-09-29
EP2573068B9 (en) 2015-08-26
HK1184432A1 (en) 2014-01-24
EP1725537B1 (en) 2011-07-13
UA86053C2 (ru) 2009-03-25
HRP20150305T1 (hr) 2015-04-24
DK1725537T3 (da) 2011-10-31
US10213415B2 (en) 2019-02-26
US8772325B2 (en) 2014-07-08
ES2533176T3 (es) 2015-04-08
US8609709B2 (en) 2013-12-17
EP3112352A1 (en) 2017-01-04
IL178040A0 (en) 2006-12-31
HRP20161331T1 (hr) 2016-12-30
TWI361069B (en) 2012-04-01
US20080096888A1 (en) 2008-04-24
DK2653465T3 (da) 2016-08-22
IL224908A (en) 2015-07-30
NO2017007I1 (no) 2017-02-23
JP2007529527A (ja) 2007-10-25
LTPA2017005I1 (lt) 2017-03-27
CN102786476B (zh) 2017-01-18
IL229444A (en) 2017-03-30
EP1725537A1 (en) 2006-11-29
BRPI0508820B1 (pt) 2018-04-10
NZ549842A (en) 2010-10-29
CA2560047A1 (en) 2005-09-29
US20140256779A1 (en) 2014-09-11
NO2017007I2 (no) 2017-02-23
ES2596434T3 (es) 2017-01-09
RS54199B1 (en) 2015-12-31
PT1725537E (pt) 2011-09-08
CN1950342B (zh) 2012-09-26
AU2005224091B2 (en) 2012-02-02
KR101166342B1 (ko) 2012-07-18
NO20160916A1 (no) 2006-12-14
ES2705077T3 (es) 2019-03-21
NO338203B1 (no) 2016-08-08
ATE516274T1 (de) 2011-07-15
US7786158B2 (en) 2010-08-31
DK2573068T3 (en) 2015-02-16
PH12012501640B1 (en) 2015-10-05
KR20060131983A (ko) 2006-12-20
EP3112352B1 (en) 2018-11-21
MXPA06010642A (es) 2007-03-26
CY2017008I1 (el) 2017-11-14
EP2298744B1 (en) 2013-06-26
US8344011B2 (en) 2013-01-01
PL1725537T3 (pl) 2011-12-30
EP2653465B1 (en) 2016-07-13
NO20064660L (no) 2006-12-14
US7741356B2 (en) 2010-06-22
LUC00007I2 (es) 2017-05-02
PL2573068T3 (pl) 2015-06-30
MY146972A (en) 2012-10-15
US9205076B2 (en) 2015-12-08
HK1155726A1 (en) 2012-05-25
HRP20130800T1 (en) 2013-09-30
HUE029852T2 (en) 2017-04-28
CY1118096T1 (el) 2017-06-28
CN1950342A (zh) 2007-04-18
US20050203143A1 (en) 2005-09-15
SI1725537T1 (sl) 2011-11-30
CN102786476A (zh) 2012-11-21
DK2298744T3 (da) 2013-09-02
CY1111927T1 (el) 2015-11-04
ME02221B (me) 2016-02-20
EP2573068B1 (en) 2014-12-31
US20140039024A1 (en) 2014-02-06
BRPI0508820A (pt) 2007-08-07
LUC00007I1 (es) 2017-03-03
ME01601B (me) 2014-09-20
SI2573068T1 (sl) 2015-03-31
US20160030393A1 (en) 2016-02-04
PT2573068E (pt) 2015-04-27
WO2005090315A1 (en) 2005-09-29
ES2428008T3 (es) 2013-11-05
BRPI0508820B8 (pt) 2022-11-29
IL229444A0 (en) 2013-12-31
PT2653465T (pt) 2016-09-22
SI2298744T1 (sl) 2013-10-30
AR048269A1 (es) 2006-04-12
US9700542B2 (en) 2017-07-11
PT2298744E (pt) 2013-09-12
TW200539876A (en) 2005-12-16
EP2298744A3 (en) 2011-08-10
HK1105967A1 (en) 2008-02-29
HK1099016A1 (en) 2007-08-03
LT2653465T (lt) 2016-09-12
PH12012501640A1 (en) 2015-10-05
ZA200608587B (en) 2008-06-25
AR095848A2 (es) 2015-11-18
PL2298744T3 (pl) 2013-11-29
CA2560047C (en) 2013-12-24
RS51995B (en) 2012-04-30
US20130090478A1 (en) 2013-04-11
US20100324051A1 (en) 2010-12-23
NL300865I1 (nl) 2017-03-14
CY2017008I2 (el) 2017-11-14
ES2367576T3 (es) 2011-11-04
HRP20110694T1 (hr) 2011-12-31
JP4778954B2 (ja) 2011-09-21
ME02540B (me) 2017-02-20
EP2298744A2 (en) 2011-03-23
NL300865I2 (nl) 2020-08-17
LTC1725537I2 (lt) 2018-02-26

Similar Documents

Publication Publication Date Title
ECSP066856A (es) Compuestos novedosos como moduladores del receptor opioide
CO6450612A2 (es) Compuestos 1-cianoetilheterociclilcarboxamida sustituidos 750
UY28752A1 (es) Agentes terapeuticos
BRPI0910182B8 (pt) composto de fórmula (i), composição farmacêutica e uso de um composto
CR10243A (es) "bencimidazoles 2-sustituidos como modulares de receptor de androgeno selectivos"
UY29058A1 (es) Compuestos de isoindolona y su uso como potenciadores del receptor metabotropico de glutamato
DOP2009000133A (es) Derivados de indol como agonistas de los receptores s1p1
CL2011001263A1 (es) Compuestos derivados de pirimidinonas opcionalmente sustituidas; composicion farmaceutica que los comprende; y su uso como inhibidores de fosfodiesterasa 1 (pde1) para el tratamiento de enfermedades que involucran trastornos de la trayectoria intracelular del receptor de dopamina d1 como parkinson, alzheimer, depresion, enfermedad bipolar, hipertension, glaucoma.
AR054786A1 (es) (6-fluor-benzol(1,3) dioxolil)-morfolin-4-il-metanomas, moduladoras del receptor cb1
UY32648A (es) Nuevos derivados de pirimidina y su uso en el tratamiento de enfermedades
ECSP109903A (es) Derivados de pirazinona y su uso en el tratamiento de enfermedades pulmonares
CL2011002837A1 (es) Compuestos derivados de 1,2,4-triazolo[4,3-a]piridina, moduladores alostericos positivos de receptores mglur2; composicion farmaceutica; proceso para prepararla; y su uso en el tratamiento o la prevencion de un trastorno del sistema nervioso central tal como la ansiedad, esquizofrenia y migraña, entre otros.
CL2011002103A1 (es) Compuestos derivados de indazol; procedimiento de preparacion; compuesto intermediario; composicion farmaceutica y combinacion que los comprende; y uso para tratar una afeccion para la que esta indicado un antagonista del receptor ccr4.
EA200970967A1 (ru) Оксадиазол замещенные производные индазола для применения в качестве агонистов сфингозин 1-фосфата (sip)
EA201070327A1 (ru) Катехоламиновые производные и их пролекарства
CR10497A (es) Derivados de piperazinilo utiles en el tratamiento de enfermedades mediadas por el receptor gpr38
CR10682A (es) Compuestos de tiazol pirazolopirimidina
UY30572A1 (es) N-(1-ftalazin-1-il-piperidin-4-il)-amidas como moduladores del receptor ep2
UY31922A (es) Compuestos
EA201190017A1 (ru) Аминоэфирные производные алкалоидов и их медицинские композиции
EA201100161A1 (ru) Производные хинуклидина карбоната и их медицинские композиции
UY29798A1 (es) Derivados de carboxamida como antagonistas del receptor muscarínico
UY28839A1 (es) Agentes terapeuticos
ECSP088584A (es) Nuevos derivados de benzimidazol como inhibidores del receptor vanilloide 1 (vrl)
CO6351723A2 (es) Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de crf1