HUP0302693A2 - Az alfa4-integrinek által közvetített sejttapadás inhibitoraiként hatásos új fenil-alanin származékok, eljárás elõállításukra és ilyen hatóanyagot tartalmazó gyógyászati készítmények - Google Patents
Az alfa4-integrinek által közvetített sejttapadás inhibitoraiként hatásos új fenil-alanin származékok, eljárás elõállításukra és ilyen hatóanyagot tartalmazó gyógyászati készítményekInfo
- Publication number
- HUP0302693A2 HUP0302693A2 HU0302693A HUP0302693A HUP0302693A2 HU P0302693 A2 HUP0302693 A2 HU P0302693A2 HU 0302693 A HU0302693 A HU 0302693A HU P0302693 A HUP0302693 A HU P0302693A HU P0302693 A2 HUP0302693 A2 HU P0302693A2
- Authority
- HU
- Hungary
- Prior art keywords
- phenylalanin
- alpha4
- derivatives
- preparation
- integrin inhibitors
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 102000006495 integrins Human genes 0.000 title 1
- 108010044426 integrins Proteins 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 150000002993 phenylalanine derivatives Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/81—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/82—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/87—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
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Abstract
A találmány tárgyát az (I) általános képletű fenil-alanin-származékvagy gyógyászatilag elfogadható sója képezi, ahol X1 jelentésehalogénatom, X2 jelentése halogénatom, Q jelentése egy -CH2- vagy egy-(CH2)2 képletű csoport, Y jelentése 1-6 szénatomos alkilcsoport, -CO2R jelentése adott esetben észterezett karboxilcsoport. A találmánykiterjed a vegyületek alkalmazására és előállítási eljárásukra is. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22912800P | 2000-08-31 | 2000-08-31 | |
PCT/US2001/026594 WO2002018320A2 (en) | 2000-08-31 | 2001-08-27 | INHIBITORS OF α4 MEDIATED CELL ADHESION |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP0302693A2 true HUP0302693A2 (hu) | 2003-12-29 |
HUP0302693A3 HUP0302693A3 (en) | 2005-05-30 |
Family
ID=22859926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0302693A HUP0302693A3 (en) | 2000-08-31 | 2001-08-27 | Phenylalanin-derivatives, integrin inhibitors of alpha4, their use and process for their preparation |
Country Status (28)
Country | Link |
---|---|
US (6) | US7026501B2 (hu) |
EP (1) | EP1315694B1 (hu) |
JP (1) | JP3899022B2 (hu) |
KR (1) | KR100528049B1 (hu) |
CN (1) | CN1229334C (hu) |
AR (1) | AR034556A1 (hu) |
AT (1) | ATE292615T1 (hu) |
AU (2) | AU8677801A (hu) |
BR (1) | BR0113629A (hu) |
CA (1) | CA2418054C (hu) |
CZ (1) | CZ303460B6 (hu) |
DE (1) | DE60109943T2 (hu) |
DK (1) | DK1315694T3 (hu) |
ES (1) | ES2240509T3 (hu) |
HK (1) | HK1052684B (hu) |
HU (1) | HUP0302693A3 (hu) |
IL (2) | IL154305A0 (hu) |
MX (1) | MXPA03001837A (hu) |
MY (1) | MY129000A (hu) |
NO (1) | NO327861B1 (hu) |
NZ (1) | NZ524043A (hu) |
PL (1) | PL206656B1 (hu) |
PT (1) | PT1315694E (hu) |
RU (1) | RU2250895C2 (hu) |
SI (1) | SI1315694T1 (hu) |
TW (1) | TWI224587B (hu) |
WO (1) | WO2002018320A2 (hu) |
ZA (1) | ZA200301039B (hu) |
Families Citing this family (40)
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JP3440469B2 (ja) | 2000-08-18 | 2003-08-25 | 味の素株式会社 | 新規フェニルアラニン誘導体 |
TWI312347B (en) | 2001-02-08 | 2009-07-21 | Eisai R&D Man Co Ltd | Bicyclic nitrogen-containing condensed ring compounds |
CA2443802C (en) | 2001-04-27 | 2010-04-13 | Eisai Co., Ltd. | Pyrazolo[1,5-a]pyridines and medicines containing the same |
MY140707A (en) | 2002-02-28 | 2010-01-15 | Mitsubishi Tanabe Pharma Corp | Process for preparing a phenylalanine derivative and intermediates thereof |
US7122580B2 (en) | 2002-08-09 | 2006-10-17 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds and methods to modulate coagulation |
US7176216B2 (en) | 2002-10-22 | 2007-02-13 | Eisai Co., Ltd. | 7-phenylpyrazolopyridine compounds |
EP1555265B1 (en) | 2002-10-22 | 2009-03-25 | Eisai R&D Management Co., Ltd. | 7-phenyl pyrazolopyridine compounds |
JP2007501844A (ja) * | 2003-08-08 | 2007-02-01 | トランス テック ファーマ,インコーポレイテッド | アリール及びヘテロアリール化合物、組成物並びに使用方法 |
WO2005014532A1 (en) * | 2003-08-08 | 2005-02-17 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds, compositions and methods of use |
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US7345049B2 (en) * | 2003-12-22 | 2008-03-18 | Ajinomoto Co., Inc. | Phenylalanine derivatives |
MY140489A (en) | 2003-12-26 | 2009-12-31 | Eisai R&D Man Co Ltd | 1,2-di (cyclic) substituted benzene compounds |
US7419666B1 (en) | 2004-02-23 | 2008-09-02 | Massachusetts Eye And Ear Infirmary | Treatment of ocular disorders |
AU2005320217B2 (en) | 2004-12-20 | 2011-11-10 | Eisai R & D Management Co., Ltd. | Crystal and salt of 1-cyclopropylmethyl-4-[2-(3,3,5,5)-tetramethylcyclohexyl)phenyl]piperazine |
US7410971B2 (en) | 2004-12-24 | 2008-08-12 | Eisai R&D Management Co., Ltd. | 1,2-di(cyclic)substituted benzene compounds |
AR054129A1 (es) | 2005-06-09 | 2007-06-06 | Uc S A | Derivados de 2, 6-quinolinilo, una preparacion farmaceutica que los contiene y su empleo en la fabricacion de medicamentos para el tratamiento de enfermedades dependientes de integrinas alfa4beta1 y/o alfa4beta7 |
EP2091916A2 (en) * | 2005-11-23 | 2009-08-26 | AstraZeneca AB | L-phenylalanine derivatives and their use as integrin antagonists |
US7855291B2 (en) | 2005-12-29 | 2010-12-21 | Lexicon Pharmaceuticals, Inc. | Process for the preparation of substituted phenylalanines |
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IL172896A0 (en) * | 2005-12-29 | 2006-06-11 | Yeda Res & Dev | Cxcr4 inhibition |
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WO2007092471A2 (en) * | 2006-02-03 | 2007-08-16 | The Regents Of The University Of California | Methods for inhibition of lymphangiogenesis and tumor metastasis |
US20090203663A1 (en) * | 2006-02-09 | 2009-08-13 | Astrazeneca Ab | Chemical compounds |
JP2009528359A (ja) | 2006-02-28 | 2009-08-06 | エラン ファーマシューティカルズ,インコーポレイテッド | ナタリズマブを用いて炎症性疾患および自己免疫性疾患を治療する方法 |
JP2009531304A (ja) * | 2006-02-28 | 2009-09-03 | エラン ファーマシューティカルズ,インコーポレイテッド | α−4阻害剤化合物を用いて炎症性疾患および自己免疫疾患を治療する方法 |
SG170058A1 (en) | 2006-03-03 | 2011-04-29 | Elan Pharm Inc | Methods of treating inflammatory and autoimmune diseases with natalizumab |
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WO2018085552A1 (en) * | 2016-11-02 | 2018-05-11 | Saint Louis University | Integrin antagonists |
CN112969687A (zh) | 2018-10-30 | 2021-06-15 | 吉利德科学公司 | 作为α4β7整合素抑制剂的喹啉衍生物 |
KR102641718B1 (ko) | 2018-10-30 | 2024-02-29 | 길리애드 사이언시즈, 인코포레이티드 | 알파4베타7 인테그린 억제제로서의 이미다조피리딘 유도체 |
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