97345-82-9Relevant academic research and scientific papers
The effect of absolute configuration on activity, subtype selectivity (M3/M2) of 3α-acyloxy-6β-acetoxyltropane derivatives as muscarinic M3 receptor antagonists
Wang, Zhi-Peng,Liu, Hui-Zhong,Zhu, Liang,Hu, You-Min,Cui, Yong-Yao,Niu, Yin-Yao,Lu, Yang,Chen, Hong-Zhuan
, p. 1234 - 1239 (2013/03/14)
Both enantiomers of 3α-acyloxy-6β-acetoxyltropane derivatives 1-4 were prepared respectively and underwent functional studies and radioreceptor binding assays. 6S Enantiomers showed obvious muscarinic M3, M2 antagonistic activity, while the 6R ones elicit
Alkaloids of the Genus Erythroxylum. Part 5. E. hypericifolium Lam. Root-bark
Al-Said, Mansour S.,Evans, William C.,Grout, Raymond J.
, p. 957 - 960 (2007/10/02)
The root-bark of Erythroxylum hypericifolium contains the new bases tropan-3α-yl 3-hydroxyphenylacetate, (+)-tropane-3α,6β-diol 3-phenylacetate, tropane-3α,6β-diol 3-phenylacetate 6-acetate, tropane-3α,6β,7β-triol 3-phenylacetate, and nortropan-3-yl phenylacetate; tropan-3α-yl phenylacetate was also isolated.Chemotaxonomic implications are discussed.
