Aklavinone

TargetMol
Product Code: TAR-T29801
Supplier: TargetMol
CodeSizePrice
TAR-T29801-5mg5mg£850.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

1 / 1

Further Information

Bioactivity:
Aklavinone is a biochemical.
CAS:
16234-96-1
Formula:
C22H20O8
Molecular Weight:
412.394
Purity:
0.98
SMILES:
CC[C@@]1(O)C[C@H](O)c2c(O)c3C(=O)c4c(O)cccc4C(=O)c3cc2[C@H]1C(=O)OC

References

1. Kim E, Song MC, Kim MS, Beom JY, Jung JA, Cho HS, Yoon YJ. One-Pot Combinatorial Biosynthesis of Glycosylated Anthracyclines by Cocultivation of Streptomyces Strains Producing Aglycones and Nucleotide Deoxysugars. ACS Comb Sci. 2017 Apr 10;19(4):262-270. doi: 10.1021/acscombsci.6b00194. Epub 2017 Feb 22. PubMed PMID: 28191923. 2. Kanteev M, Bregman-Cohen A, Deri B, Shahar A, Adir N, Fishman A. A crystal structure of 2-hydroxybiphenyl 3-monooxygenase with bound substrate provides insights into the enzymatic mechanism. Biochim Biophys Acta. 2015 Dec;1854(12):1906-1913. doi: 10.1016/j.bbapap.2015.08.002. Epub 2015 Aug 11. PubMed PMID: 26275805. 3. T?rker L. Tautomerism in 11-hydroxyaklavinone: a DFT study. ScientificWorldJournal. 2012;2012:526289. doi: 10.1100/2012/526289. Epub 2012 May 1. PubMed PMID: 22623911; PubMed Central PMCID: PMC3353482. 4. Lindqvist Y, Koskiniemi H, Jansson A, Sandalova T, Schnell R, Liu Z, M?nts?l? P, Niemi J, Schneider G. Structural basis for substrate recognition and specificity in aklavinone-11-hydroxylase from rhodomycin biosynthesis. J Mol Biol. 2009 Nov 6;393(4):966-77. doi: 10.1016/j.jmb.2009.09.003. Epub 2009 Sep 8. PubMed PMID: 19744497.