T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes-Reference-Cited by-同舟云学术

T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes

Published:2008-12-10 Issue:1 Volume:72 Page:99-101
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Ding Ling¹,Pfoh Roland¹,Rühl Stephan¹,Qin Song¹,Laatsch Hartmut¹

Affiliation:

1. Department of Organic and Biomolecular Chemistry, University of Göttingen, Tammannstrasse 2, D-37077 Göttingen, Germany, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, 266071 Qingdao, People’s Republic of China, Graduate School of the Chinese Academy of Sciences, Yuquan Road 19A, 100039 Beijing, People’s Republic of China, and Department of Inorganic Chemistry, University of Göttingen, Tammannstrasse 4, D-37077 Göttingen, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/np8006843

Reference12 articles.

1. Article No. XXXVIII on Marine Bacteria. For part XXXVII, see:

2. Amorphane Sesquiterpenes from a Marine Streptomyces sp.,1

3. Extractive components from the wood of taiwania cryptomerioides hayata: Three new sesquiterpene alcohols, muurolane-3-ene-9β-ol-2-one, muurolane-2δ,9β-diol-3-ene, and muurolane-2β,9β-diol-3-ene

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