» Articles » PMID: 3429338

Biosynthesis of Napyradiomycins

Overview
Date 1987 Dec 1
PMID 3429338
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Biosynthetic studies on napyradiomycins were carried out based on the incorporation of [2-13C]acetate and [1,2-13C]acetate. The alignment of acetate units suggested that the B and C rings of napyradiomycins are derived from a pentaketide, while ring A and the side chain may be synthesized from mevalonate.

Citing Articles

MAR4 : A Unique Resource for Natural Product Discovery.

Sweeney D, Chase A, Bogdanov A, Jensen P J Nat Prod. 2024; 87(2):439-452.

PMID: 38353658 PMC: 10897937. DOI: 10.1021/acs.jnatprod.3c01007.


Bacterial terpenome.

Rudolf J, Alsup T, Xu B, Li Z Nat Prod Rep. 2020; 38(5):905-980.

PMID: 33169126 PMC: 8107197. DOI: 10.1039/d0np00066c.


Asymmetric Alkene and Arene Halofunctionalization Reactions in Meroterpenoid Biosynthesis.

Moore B Synlett. 2019; 29(4):401-409.

PMID: 31031546 PMC: 6483395. DOI: 10.1055/s-0036-1590919.


Total Enzyme Syntheses of Napyradiomycins A1 and B1.

McKinnie S, Miles Z, Jordan P, Awakawa T, Pepper H, Murray L J Am Chem Soc. 2018; 140(51):17840-17845.

PMID: 30525563 PMC: 6491662. DOI: 10.1021/jacs.8b10134.


Natural products as inspiration for the development of new synthetic methods.

Ma Z, Chen C J Chin Chem Soc. 2018; 65(1):43-59.

PMID: 29430058 PMC: 5800783. DOI: 10.1002/jccs.201700134.