Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Xin Zhao Deng"'
Autor:
Zhi-Kai Guo, Yi-Qin Zhou, Hao Han, Wen Wang, Lang Xiang, Xin-Zhao Deng, Hui-Ming Ge, Rui-Hua Jiao
Publikováno v:
Marine Drugs, Vol 16, Iss 2, p 45 (2018)
Marine fungi are a promising source of novel bioactive natural products with diverse structure. In our search for new bioactive natural products from marine fungi, three new phenone derivatives, asperphenone A–C (1–3), have been isolated from the
Externí odkaz:
https://doaj.org/article/a784dfad40e84a99afcd63a3fdb550bf
Autor:
Rui Hua Jiao, Wei Li, Bo Zhang, Yi Shuang Wang, Mei Zhang, Yong Sheng Xiao, Jing Shi, Li Yang, Hui Ming Ge, Xin Zhao Deng, Ren-Xiang Tan, Cheng Long Yang
Publikováno v:
The Journal of Antibiotics. 70:853-855
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f846cb710a14bf8863c59509d01564
https://doi.org/10.1038/ja.2017.50
https://doi.org/10.1038/ja.2017.50
Autor:
Ye Shen, Ren-Xiang Tan, Hui-Min Wu, Xin-Zhao Deng, Yong-Sheng Xiao, Xuan Zhang, Rui-Hua Jiao, Qin-Lan Xu, Ting Ting Wang, Hui Ming Ge, Wei Li
Publikováno v:
Journal of Asian natural products research. 20(3)
Chaetospirolactone (1), a novel spiro-lactone bearing a rare 1-oxaspiro [4.4] non-7-ene-2,6-dione skeleton, and orsellide F (2), together with six known compounds (3–8), were isolated from an endophytic fungus Chaetomium sp. NF00754. Their structur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cc68462e46e7b86e777c76729c392e3
https://pubmed.ncbi.nlm.nih.gov/28478698
https://pubmed.ncbi.nlm.nih.gov/28478698
Autor:
Mei Zhang, Hui Ming Ge, Jing Shi, Ren-Xiang Tan, Bo Zhang, Xin Zhao Deng, Rui Hua Jiao, Yong Sheng Xiao, Zhi-Kai Guo, Wei Li
Publikováno v:
Organicbiomolecular chemistry. 15(18)
Cultivation of locust associated rare actinobacteria, Amycolatopsis sp. HCa4, has provided five unusual macrolactams rifamorpholines A-E. Their structures were determined by interpretation of spectroscopic and crystallographic data. Rifamorpholines A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a21f3e8460491bd9b64e37c9546026e
https://pubmed.ncbi.nlm.nih.gov/28422262
https://pubmed.ncbi.nlm.nih.gov/28422262
Publikováno v:
Organicbiomolecular chemistry. 14(44)
An isocyanide insertion reaction promoted by the combination of an amide and a photoredox is now presented. By using visible light, 6-amidophenanthridine derivatives can be prepared in good chemical yields under mild and eco-friendly reaction conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5e203c5424307e908cbecf177cb479
https://pubmed.ncbi.nlm.nih.gov/27752696
https://pubmed.ncbi.nlm.nih.gov/27752696
Publikováno v:
Planta medica. 82(11-12)
Herpecaudin (3), a xanthine oxidase inhibitor with an unprecedented scaffold, was discovered from Herpetospermum caudigerum seeds. The structure was determined by spectroscopic and X-ray single crystallographic methods. A possible biogenetic pathway
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a285459883cb5d8f43e561620f233371
https://pubmed.ncbi.nlm.nih.gov/27272398
https://pubmed.ncbi.nlm.nih.gov/27272398
Publikováno v:
Organic letters. 18(8)
Curvularia sp. IFB-Z10, a white croaker-associated fungus, generates a skeletally unprecedented indolizine alkaloid named curindolizine (1), which displays an anti-inflammatory action in lipopolyssacharide (LPS)-induced RAW 264.7 macrophages with an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31051fda1e8f208dc2b1102b50c83d20
https://pubmed.ncbi.nlm.nih.gov/27046459
https://pubmed.ncbi.nlm.nih.gov/27046459
Autor:
Ren-Xiang Tan, Xin Zhao Deng, Chao Jun Chen, Yuan Tian, Nan Jiang, Wen Jing Zhang, Ai Hua Zhang
Publikováno v:
Organic letters. 17(6)
A mutasynthetic strategy is introduced for the mycosynthesis of naphthalene-based molecules (mutadalesols A–F) with directed substitution patterns and new frameworks by generating and using the ΔpksTL mutant strain of Daldinia eschscholzii. (±)-M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::222e358d5d84206d4d09fcd9a983e954
https://pubmed.ncbi.nlm.nih.gov/25746213
https://pubmed.ncbi.nlm.nih.gov/25746213
Autor:
Bo Zhang, Kai Biao Wang, Wen Wang, Shu Feng Bi, Ya Ning Mei, Xin Zhao Deng, Rui Hua Jiao, Ren Xiang Tan, Hui Ming Ge
Publikováno v:
Organic Letters; 5/18/2018, Vol. 20 Issue 10, p2967-2971, 5p
Publikováno v:
Organic Letters; Apr2016, Vol. 18 Issue 8, p1816-1819, 4p