Aculeatiols A–G: Lovastatin Derivatives Extracted from <i>Aspergillus aculeatus</i>-Reference-Cited by-同舟云学术

Aculeatiols A–G: Lovastatin Derivatives Extracted from Aspergillus aculeatus

Published:2024-02-19 Issue:4 Volume:87 Page:753-763
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Liu Fei¹,Qiao Xinyi¹,Li Qin¹,Zhou Jiajun¹,Gao Jie¹,He Feng²,Wu Peng²,Chen Chunmei¹,Sun Weiguang¹,Zhu Hucheng¹,Zhang Yonghui¹^ORCID

Affiliation:

1. Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei, People’s Republic of China

2. Hubei Topgene Biotechnology Technical Research Institute Co., Ltd., Wuhan 430030, People’s Republic of China

Funder

National Key Research and Development Program of China

Science and Technology Program of Hubei Province

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.3c00872

Reference24 articles.

1. Monacolin K, a new hypocholesterolemic agent produced by a Monascus species.

2. Monacolin K, a new hypocholesterolemic agent that specifically inhibits 3-hydroxy-3-methylglutaryl coenzyme A reductase.

3. Chemistry and Biology of Biosynthetic Diels–Alder Reactions

4. LovG: The Thioesterase Required for Dihydromonacolin L Release and Lovastatin Nonaketide Synthase Turnover in Lovastatin Biosynthesis

5. Lovastatin Nonaketide Synthase Catalyzes an Intramolecular Diels−Alder Reaction of a Substrate Analogue

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1. Undobolins A–L, Ophiobolin-Type Sesterterpenoids from Aspergillus undulatus;Journal of Natural Products;2024-07-25

2. Aculeatones A and B, epimeric lovastatin derivatives with a 6/6/3-tricyclic carbon skeleton from Aspergillus aculeatus and their chemical transformation;Organic Chemistry Frontiers;2024