首页> 外国专利> METHOD FOR OBTAINING TREPEPTIDE OF GENERAL FORMULA (I) HPyr-His-TrpOH, APPLIED AS INTERMEDIATE COMPOUND (1-3 FRAGMENT) IN SYNTHESIS OF SYNTHETIC AGONISTS OF GONADOTROPIN-RELEASING-HORMONE (LH-RH), BY METHOD OF LIQUID-PHASE PEPTIDE SYNTHESIS WITHOUT PLACING AND REMOVAL OF PROTECTIVE GROUPS

METHOD FOR OBTAINING TREPEPTIDE OF GENERAL FORMULA (I) HPyr-His-TrpOH, APPLIED AS INTERMEDIATE COMPOUND (1-3 FRAGMENT) IN SYNTHESIS OF SYNTHETIC AGONISTS OF GONADOTROPIN-RELEASING-HORMONE (LH-RH), BY METHOD OF LIQUID-PHASE PEPTIDE SYNTHESIS WITHOUT PLACING AND REMOVAL OF PROTECTIVE GROUPS

机译:通式(I)HPyr-His-TrpOH的中间体的肽的获得方法,通过液相肽法在合成促性腺激素释放激素(LH-RH)的合成激动剂中用作中间化合物(1-3片段)无需放置和移除保护基团即可进行合成

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to method of obtaining HPyr-His-TrpOH applied as main semi-product (1-3 fragment) in synthesis of synthetic antagonists of gonadotropine-releasing-hormone, LH-RH. Tripeptide (I) is obtained by method of liquid-phase peptide synthesis without application of stages of placement and removal of protective groups.;EFFECT: method makes it possible to reduce quantity of synthesis stages, is more economically effective due to absence of placement and removal of protective groups stages and makes it possible to obtain tripeptide with high purity.;1 ex
机译:技术领域本发明涉及获得HPyr-His-TrpOH的方法。<图像文件=“ 00000012.GIF” he =“ 34” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 64” />作为合成促性腺激素释放激素LH-RH拮抗剂的主要半成品(1-3片段)。三肽(I)是通过液相肽合成方法获得的,无需应用放置和去除保护基的阶段。;效果:该方法可以减少合成阶段的数量,由于不存在放置和不存在而更经济有效去除保护基阶段,并有可能获得高纯度的三肽。; 1 ex

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号