发明名称 NEUROTENSIN ANTAGONIST PEPTIDES
摘要 <p>Compounds of formula (I) in which R is a hydroxy, alkoxy, phenylalkyloxy radical or -NH-CH2-COOH, R1 is a hydrogen atom, an adamantylacetyl, adamantylcarbonyl, norbornylacetyl, norbornylphenoxycarbonyl, benzoyl, nicotinoyl, 4-phenylbenzoyl, 4-tert-butylbenzoyl, 2-pyrrolidinecarbonyl radical or a protective group of an amine function, R2 is an Arg or Lys residue, R3 is an Arg or Lys residue, R4 is a Pro, m, n and p residue, which are the same or different and are a number equal to 0 or 1, given that when R1 is a hydrogen atom, the sum m+n+p is at least equal to 1, R5 and R6 are the same and are a hydroxy or methoxy radical and R7 is a hydrogen, chlorine, bromine or iodine atom or a nitro radical, the equivalents of the compounds of formula (I) in which one or more peptide bonds (CO-NH) between two amino acid residues are replaced by -CH2-NH bonds and/or the peptide bond (CO-NH) between the amino acid residues R2 and R3 is replaced by a CH=CH bond. The invention also concerns the salts of said compounds, the preparation thereof and drugs containing same.</p>
申请公布号 WO9532218(A1) 申请公布日期 1995.11.30
申请号 WO1995FR00643 申请日期 1995.05.17
申请人 RHONE-POULENC RORER S.A.;CLERC, FRANCOIS-FREDERIC;DUBROEUCQ, MARIE-CHRISTINE;HELYNCK, GERARD;LEBOUL, JEAN;MARTIN, JEAN-PAUL 发明人 CLERC, FRANCOIS-FREDERIC;DUBROEUCQ, MARIE-CHRISTINE;HELYNCK, GERARD;LEBOUL, JEAN;MARTIN, JEAN-PAUL
分类号 C12P21/02;A61K38/00;A61P1/00;A61P1/04;A61P9/00;A61P11/00;A61P25/00;A61P25/18;A61P25/28;A61P35/00;A61P37/08;C07C27/22;C07K5/10;C07K7/02;C07K7/06;C07K7/08;C07K7/18;C07K14/655;C12R1/04;(IPC1-7):C07K7/08;A61K38/08 主分类号 C12P21/02
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