- Methylenomycin B
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Methylenomycin B 
2,3-Dimethyl-5-methylene-2-cyclopenten-1-one[1]Identifiers CAS number 52775-77-6 PubChem 3040648 ChemSpider 2303992 
Jmol-3D images Image 1 - O=C/1\C(=C)CC(=C\1C)\C
- InChI=1S/C8H10O/c1-5-4-6(2)8(9)7(5)3/h2,4H2,1,3H3
Key: YDXIEAHUYZKJOH-UHFFFAOYSA-NInChI=1/C8H10O/c1-5-4-6(2)8(9)7(5)3/h2,4H2,1,3H3
Key: YDXIEAHUYZKJOH-UHFFFAOYAN
Properties Molecular formula C8H10O Molar mass 122.16 g mol-1 
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Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Methylenomycin B is a cyclopentanoid antibiotic produced by Streptomyces coelicolor A3(2) that is effective against both Gram-negative and Gram-positive bacteria.[2][3] Methylenomycins are naturally produced in two variants: A and B.
See also
References
- ^ "Methylenomycins". 2009. http://www.druglead.com/cds/Methylenomycins.html. Retrieved 9 February 2010.
- ^ Brian P, Riggle PJ, Santos RA, Champness WC (June 1996). "Global negative regulation of Streptomyces coelicolor antibiotic synthesis mediated by an absA-encoded putative signal transduction system". J. Bacteriol. 178 (11): 3221–31. PMC 178074. PMID 8655502. http://jb.asm.org/cgi/pmidlookup?view=long&pmid=8655502.
- ^ Hobbs G, Obanye AI, Petty J, et al. (March 1992). "An integrated approach to studying regulation of production of the antibiotic methylenomycin by Streptomyces coelicolor A3(2)". J. Bacteriol. 174 (5): 1487–94. PMC 206543. PMID 1537793. http://jb.asm.org/cgi/pmidlookup?view=long&pmid=1537793.
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