1992
DOI: 10.7164/antibiotics.45.914
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Herboxidiene, a new herbicidal substance from Streptomyces chromofuscus A7847. Taxonomy, fermentation, isolation, physico-chemical and biological properties.

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Cited by 74 publications
(46 citation statements)
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“…The analogs described here (7,8,9,12,13, and 14) helped elucidate the biosynthetic route to hemiketal formation as well as confirmed the positive contributions of the C-4 hydroxy and epoxide groups for cytotoxic potency. Because compounds 2 and 3 are desirable drug leads, the dioxygenase mutant generated in this study sets the stage for further strain development.…”
Section: Discussionmentioning
confidence: 55%
“…The analogs described here (7,8,9,12,13, and 14) helped elucidate the biosynthetic route to hemiketal formation as well as confirmed the positive contributions of the C-4 hydroxy and epoxide groups for cytotoxic potency. Because compounds 2 and 3 are desirable drug leads, the dioxygenase mutant generated in this study sets the stage for further strain development.…”
Section: Discussionmentioning
confidence: 55%
“…Recently, three bacterial natural products, pladienolides [1214], FR901464 [1517], and herboxidiene [18, 19] (Figure 2), have all been shown to modulate the function of the spliceosome (Figure 1) [2022]. Since pladienolide B and FR901464 are structurally distinct, and derived from distantly related bacterial genera ( Streptomyces and Pseudomonas , respectively), convergent evolution has led to divergent prokaryotes producing spliceosome modulators that share a common pharmacophore.…”
Section: Natural Product Spliceosome Modulatorsmentioning
confidence: 99%
“…Herboxidiene (compound 1, Fig. 1A) was isolated from Streptomyces chromofuscus A7847 (ATCC 49982) as a novel polyketide which selectively and effectively controls several annual weed species (10,16). Later, compound 1 was found to effectively reduce plasma cholesterol and possess stronger low-density lipoprotein receptor upregulation activity than tricholstatin A and TMC-49A, representing a new type of anticholesterol molecule (13).…”
mentioning
confidence: 99%