A novel dihydroxylated derivative of artemisinin from microbial transformation-Reference-Cited by-同舟云学术

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A novel dihydroxylated derivative of artemisinin from microbial transformation

Published:2017-07 Issue: Volume:120 Page:93-97
ISSN:0367-326X
Container-title:Fitoterapia
language:en
Short-container-title:Fitoterapia

Author:

Zhan Yulian,Wu Yunshan,Xu Fangfang,Bai Yunpeng,Guan Yezhi,Williamson John S.^ORCID,Liu Bo^ORCID

Funder

National Natural Science Foundation of China

Guangdong Provincial Science and Technology Project

Specific Research Fund for TCM Science and Technology of Guangdong Provincial Hospital of Chinese Medicine

Open Funding Project of the State Key Laboratory of Bioreactor Engineering

Guangxi Colleges and Universities Key Laboratory of Biomedical Sensing and Intelligent Instrument

CDC

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,General Medicine

Reference11 articles.

1. Synthesis and structure-activity relationships of peroxidic antimalarials based on artemisinin;Avery;Adv. Med. Chem.,1999

2. Orally active, hydrolytically stable, semisynthetic, antimalarial trioxanes in the artemisinin family;Posner;J. Med. Chem.,1999

3. Biotransformation of artemisinin by Aspergillus niger;Zhan;Appl. Microbiol. Biotechnol.,2015

4. In vitro antimalarial studies of novel artemisinin biotransformed products and its derivatives;Gaur;Phytochemistry,2014

5. Hydroxylation of 10-deoxoartemisinin to 15-hydroxy-10-deoxoartemisinin by Aspergillus niger;Parshikov;Biotechnol. Lett.,2004

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1. New insights into the roles of fungi and bacteria in the development of medicinal plant;Journal of Advanced Research;2023-12

2. A Novel Antimalarial Metabolite in Erythrocyte From the Hydroxylation of Dihydroartemisinin by Cunninghamella elegans;Frontiers in Chemistry;2022-04-26

3. Biotransformation of artemisinin to a novel derivative via ring rearrangement by Aspergillus niger;Applied Microbiology and Biotechnology;2022-03-31

4. Recent Advances in Biotransformation by Cunninghamella Species;Current Drug Metabolism;2021-11

5. UPLC‐PDA coupled HR‐TOF ESI/MS 2 ‐based identification of derivatives produced by whole‐cell biotransformation of epothilone A using Nocardia sp. CS692 and a cytochrome P450 overexpressing strain;Biotechnology and Applied Biochemistry;2021-09-02

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