Flavensomycin

Flavensomycin
Names
	IUPAC name [(E)-7,9,11,13,15,17,19,21,23-nonaoxooctatriacont-3-enyl] (E)-4-[(2-hydroxy-5-oxocyclopenten-1-yl)amino]-4-oxobut-2-enoate
Identifiers
CAS Number	29382-82-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	4948761;
PubChem CID	6444925;
	InChI InChI=1S/C47H65NO14/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-19-34(49)26-36(51)28-38(53)30-40(55)32-42(57)33-41(56)31-39(54)29-37(52)27-35(50)20-17-14-15-18-25-62-46(61)24-23-45(60)48-47-43(58)21-22-44(47)59/h14-15,23-24,58H,2-13,16-22,25-33H2,1H3,(H,48,60)/b15-14+,24-23+ Key: ASNAXPLWUAPUIY-ITNOJFFJSA-N;
	SMILES CCCCCCCCCCCCCCCC(=O)CC(=O)CC(=O)CC(=O)CC(=O)CC(=O)CC(=O)CC(=O)CC(=O)CC/C=C/CCOC(=O)/C=C/C(=O)NC1=C(CCC1=O)O;
Properties
Chemical formula	C47H65NO14
Molar mass	868.030 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Flavensomycin is an antibiotic and fungicide with the molecular formula C₄₇H₆₄NO₁₄.^[1]^[2] Flavensomycin has been first isolated in 1957 from a culture of Streptomyces tanashiensis bacteria.^[3]

References edit

^ ^a ^b "Flavensomycin". Pubchem.ncbi.NLM.nih.gov.
^ Gottlieb, David; Inoue, Yukio (October 1967). "Flavensomycin, an Inhibitor of Enzyme Reactions Involving Hydrogen Transfer". Journal of Bacteriology. 94 (4): 844–849. doi:10.1128/jb.94.4.844-849.1967. PMC 276742. PMID 4383133.
^ Gottlieb, David (1967). "Flavensomycin". Mechanism of Action. pp. 617–620. doi:10.1007/978-3-642-46051-7_46. ISBN 978-3-642-46053-1.

Flavensomycin

References edit

Further reading edit