BG107841A - Имидазолни и бензимидазолни инхибитори на каспази и използването им - Google Patents

Имидазолни и бензимидазолни инхибитори на каспази и използването им Download PDF

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Publication number
BG107841A
BG107841A BG107841A BG10784103A BG107841A BG 107841 A BG107841 A BG 107841A BG 107841 A BG107841 A BG 107841A BG 10784103 A BG10784103 A BG 10784103A BG 107841 A BG107841 A BG 107841A
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Bulgaria
Prior art keywords
disease
hydrogen
amino
ring
fluoro
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BG107841A
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Bulgarian (bg)
English (en)
Inventor
David Kay
Julian Golec
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Vertex Pharmaceuticals Incorporated
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Publication of BG107841A publication Critical patent/BG107841A/bg

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    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
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    • 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
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    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
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    • C07K5/0202Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-X-X-C(=0)-, X being an optionally substituted carbon atom or a heteroatom, e.g. beta-amino acids
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BG107841A 2000-11-21 2003-05-22 Имидазолни и бензимидазолни инхибитори на каспази и използването им BG107841A (bg)

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US25225200P 2000-11-21 2000-11-21

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US (1) US7205327B2 (zh)
EP (1) EP1341767B1 (zh)
JP (2) JP4349802B2 (zh)
KR (1) KR20040020042A (zh)
CN (1) CN1298707C (zh)
AP (1) AP2003002811A0 (zh)
AT (1) ATE359274T1 (zh)
AU (1) AU2002232541A1 (zh)
BG (1) BG107841A (zh)
BR (1) BR0115546A (zh)
CA (1) CA2429630A1 (zh)
CO (1) CO7250442A2 (zh)
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SK (1) SK7792003A3 (zh)
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PE20011350A1 (es) 2000-05-19 2002-01-15 Vertex Pharma PROFARMACO DE UN INHIBIDOR DE ENZIMA CONVERTIDORA DE INTERLEUCINA-1ß (ICE)
AU2003211052A1 (en) * 2002-02-11 2003-09-04 Vertex Pharmaceuticals Incorporated Phospholipids as caspase inhibitor prodrugs
AU2003225088A1 (en) 2002-04-19 2003-11-03 Vertex Pharmaceuticals Incorporated Regulation of tnf-alpha
US20060217299A1 (en) * 2003-02-24 2006-09-28 Hirofumi Doi Degradation inhibitor for hepatitis b virus x interacting protein
AU2003902704A0 (en) * 2003-05-29 2003-06-19 Crc For Waste Management And Pollution Control Limited Of Unsw Process for producing a nanoscale zero-valent metal
US7297714B2 (en) 2003-10-21 2007-11-20 Irm Llc Inhibitors of cathepsin S
US7381827B2 (en) 2004-03-12 2008-06-03 Vertex Pharmaceuticals Incorporated Processes and intermediates
JP4848367B2 (ja) * 2004-05-15 2011-12-28 バーテックス ファーマシューティカルズ インコーポレイテッド Iceインヒビターを使用した発作の処置
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