Thiodiketopiperazines Produced by Penicillium crustosum and Their Activities to Promote Gastrointestinal Motility

Autor: Xin He, Jing Yang, Ling Qiu, Dan Feng, Feng Ju, Lu Tan, Yu-Zhi Li, Yu-Cheng Gu, Zhen Zhang, Da-Le Guo, Yun Deng

Publikováno v: Molecules, Vol 24, Iss 2, p 299 (2019)

Three new thiodiketopiperazines (1–3), along with two known analogues (4 and 5), were isolated from the fermentation broth of Penicillium crustosum. Their structures were elucidated through extensive spectroscopic analysis and the absolute configur

Externí odkaz: https://doaj.org/article/b19e2a92cc734c1fa29d4a35078beaea

Thiodiketopiperazines Produced by Penicillium crustosum and Their Activities to Promote Gastrointestinal Motility

Autor: Yu-Cheng Gu, Jing Yang, Dan Feng, Yuzhi Li, Zhen Zhang, Feng Ju, Da-Le Guo, Yun Deng, Ling Qiu, Lu Tan, Xin He

Publikováno v: Molecules
Volume 24
Issue 2
Molecules, Vol 24, Iss 2, p 299 (2019)

Three new thiodiketopiperazines (1&ndash
3), along with two known analogues (4 and 5), were isolated from the fermentation broth of Penicillium crustosum. Their structures were elucidated through extensive spectroscopic analysis and the absolute

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea89ca961929beb798a29e89d372519e

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Structural and Stereochemical Revision of Isocyanide and Isothiocyanate Amphilectenes from the Caribbean Marine Sponge Cribochalina sp

Autor: Mary J. Garson, Raffaella Puliti, Emiliano Manzo, Carlo Andrea Mattia, Jamie S. Simpson, Lelio Mazzarella, Margherita Gavagnin, Guido Cimino, Maria Letizia Ciavatta

Publikováno v: Tetrahedron (Oxf., Print) 61 (2005): 8049–8053. doi:10.1016/j.tet.2005.05.102
info:cnr-pdr/source/autori:Ciavatta M.L.; Gavagnin M.; Manzo E.; Puliti R.; Mattia C. A.; Mazzarella L.; Cimino G.; Simpson J.S.; Garson M.J./titolo:Structural and stereochemical revision of isocyanide and isothiocyanate amphilectenes from the Caribbean marine sponge Cribochalina sp./doi:10.1016%2Fj.tet.2005.05.102/rivista:Tetrahedron (Oxf., Print)/anno:2005/pagina_da:8049/pagina_a:8053/intervallo_pagine:8049–8053/volume:61

The absolute stereochemistry of amphilectene metabolites from Cribochalina sp. has been revised by a detailed NMR spectroscopic study of the mosher ester derivatives of a related alcohol. The relative stereochemistry of the previously described amphi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e048b78677817e9400af239ffc953aa
https://doi.org/10.1002/chin.200550166