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一个新型α1-去甲肾上腺素受体的光亲和放射性碘探针的母体化合物的合成
引用本文:黄培强,BRouot,RWylde,BCastro.一个新型α1-去甲肾上腺素受体的光亲和放射性碘探针的母体化合物的合成[J].药学学报,1992,27(11):864-866.
作者姓名:黄培强  BRouot  RWylde  BCastro
作者单位:厦门大学化学系,厦门361005;*CentreCNRS-INSERMdePharmacologie-Endocrinologie,RuedelaCatdonille,34094Montpelliercedex-05,France
摘    要:A new and high-yielding procedure was described for the synthesis of 4-amino-6,7-dimethoxy-24-4 (4-aminophenyl) butanoyl]-1-piperazinyl]-quinazoline Ⅶ, the key intermedi-ate for the newly designed potential α1-AR affinity/photoaffinity probes Ⅷa/Ⅸa.

关 键 词:α1-去甲肾上腺素受体  光亲和标记  哌唑嗪
收稿时间:1992-01-03

Synthesis of the key intermediate for a new radioiodinated photoaffinity probe for alpha 1-adrenergic receptor]
PQ Huang,B Rouot,R Wylde,B Castro.Synthesis of the key intermediate for a new radioiodinated photoaffinity probe for alpha 1-adrenergic receptor][J].Acta Pharmaceutica Sinica,1992,27(11):864-866.
Authors:PQ Huang  B Rouot  R Wylde  B Castro
Institution:Department of Chemistry, Xiamen University.
Abstract:A new and high-yielding procedure was described for the synthesis of 4-amino-6,7-dimethoxy-24-4 (4-aminophenyl) butanoyl]-1-piperazinyl]-quinazoline Ⅶ, the key intermedi-ate for the newly designed potential α1-AR affinity/photoaffinity probes Ⅷa/Ⅸa.
Keywords:Photoaffinity label  Prazosin  α1--Adrenergic receptor
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