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NEUROKININ A ANTAGONISTS

机译:神经激肽拮抗剂

摘要

A procedure for preparing Peptide Derivatives of formula (i), where X is Hydrogen,Alkyl or acyl; A1 is a link or a group composed of 1 to 4 amino acids; A2 is a link or ASP or Glu; A3 is any amino acid; A4 is PHE or N - i - A5 is PHE, Ile, Val, LEU, ala, PHE, Tyr, NLEMet, OR N - i - Val Gly SAR; A6 is or is made; and (ii), where B is a group of Formula - CH2 - RN - CH2 -, - S -, - CH2 -, - ch = CH -, - C or - CH2, CH CH2 (OH) - and - nhcd -Where R is Hydrogen or alkyl or phenyl and the fenilalquileno is replaced or monosustituido alkyl, Hydroxy or alkoxy, halogen; R1 and R2 are isopropyl Isobutyl secbutilo,,,N-butyl and Ethyl 2 - (methylthio), which consists in fixing a attached to a compound ResinFormula (iii) is a butiloxicarbonilo where BOC Protecting Group, and R represents the Circle surrounded by the resin.
机译:制备式(i)肽衍生物的方法,其中X是氢,烷基或酰基; A1是由1至4个氨基酸组成的链或基团; A2是链接或ASP或Glu; A3是任何氨基酸; A4是PHE或N-i-A5是PHE,Ile,Val,LEU,ala,PHE,Tyr,NLEMet或N-i-Val Gly SAR; A6是或制成的; (ii)其中B是下式的基团:-CH2-RN-CH2-,-S-,-CH2-,-ch = CH-,-C或-CH2,CH CH2(OH)-和-nhcd-其中R是氢或烷基或苯基,而苯胺基被取代或单羟基烷基,羟基或烷氧基,卤素; R1和R2是异丙基异丁基仲丁基,N-丁基和乙基2-(甲硫基),其在于固定与化合物树脂连接的通式。(iii)是丁氧羰基,其中BOC保护基,R代表被环包围的环。树脂。

著录项

  • 公开/公告号AR246085A1

    专利类型

  • 公开/公告日1994-03-30

    原文格式PDF

  • 申请/专利权人 MERREL DOW PHARMACEUTICALS INC.;

    申请/专利号AR19890314190

  • 发明设计人

    申请日1989-06-16

  • 分类号C07K1/00;C07K5/02;C07K7/02;A61K37/02;

  • 国家 AR

  • 入库时间 2022-08-22 04:46:45

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