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(S)-4-benzyl-3-((2S,3R)-3-hydroxy-2-vinylpentanoyl)oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

287398-70-3

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287398-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287398-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,3,9 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 287398-70:
(8*2)+(7*8)+(6*7)+(5*3)+(4*9)+(3*8)+(2*7)+(1*0)=203
203 % 10 = 3
So 287398-70-3 is a valid CAS Registry Number.

287398-70-3Downstream Products

287398-70-3Relevant academic research and scientific papers

Macrodiolide formation by the thioesterase of a modular polyketide synthase

Zhou, Yongjun,Prediger, Patrícia,Dias, Luiz Carlos,Murphy, Annabel C.,Leadlay, Peter F.

, p. 5232 - 5235 (2015)

Elaiophylin is an unusual C2-symmetric antibiotic macrodiolide produced on a bacterial modular polyketide synthase assembly line. To probe the mechanism and selectivity of diolide formation, we sought to reconstitute ring formation in vitro by using a non-natural substrate. Incubation of recombinant elaiophylin thioesterase/cyclase with a synthetic pentaketide analogue of the presumed monomeric polyketide precursor of elaiophylin, specifically its N-acetylcysteamine thioester, produced a novel 16-membered C2-symmetric macrodiolide. A linear dimeric thioester is an intermediate in ring formation, which indicates iterative use of the thioesterase active site in ligation and subsequent cyclization. Furthermore, the elaiophylin thioesterase acts on a mixture of pentaketide and tetraketide thioesters to give both the symmetric decaketide diolide and the novel asymmetric hybrid nonaketide diolide. Such thioesterases have potential as tools for the in vitro construction of novel diolides. Think again: The thioesterase/cyclase enzyme of the elaiophylin polyketide synthase catalyzes symmetric diolide formation in vitro from a synthetic pentaketide substrate by an iterative mechanism. Unexpectedly, a tetraketide that is not itself a substrate can be co-opted in the presence of the pentaketide to produce an asymmetric macrodiolide.

Racemic thioesters for production of polyketides

-

, (2008/06/13)

Facile methods for preparing diketide and triketide thioesters are disclosed. The resulting thioesters may be used as intermediates in the synthesis of desired polyketides, and may contain functional groups which ultimately reside in side chains on the resulting polyketide and thus can be used further to manipulate the polyketide so as form derivatives. The polyketides produced may also be tailored by glycosylation, hydroxylation and the like. New polyketides and their derivatives and tailored forms are thereby produced.

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