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// Workers AI · dad joke modeWhat did Methylenomycin B say? "I'm bonded to help

From Wikipedia, the free encyclopedia
Methylenomycin B
Structural formula of methylenomycin B
Ball-and-stick model of the methylenomycin B molecule
Names
IUPAC name
2,3-Dimethyl-5-methylene-2-cyclopenten-1-one
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C8H10O/c1-5-4-6(2)8(9)7(5)3/h2,4H2,1,3H3 checkY
    Key: YDXIEAHUYZKJOH-UHFFFAOYSA-N checkY
  • InChI=1/C8H10O/c1-5-4-6(2)8(9)7(5)3/h2,4H2,1,3H3
    Key: YDXIEAHUYZKJOH-UHFFFAOYAN
  • O=C/1\C(=C)CC(=C\1C)\C
Properties
C8H10O
Molar mass 122.167 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkYX markN ?)

Methylenomycin B is a cyclopentanone derived antibiotic produced by Streptomyces coelicolor A3(2) that is effective against both Gram-negative and Gram-positive bacteria.[1][2] It is the decarboxylated analog of methylenomycin C.

See also

[edit]

References

[edit]
  1. 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. doi:10.1128/jb.178.11.3221-3231.1996. PMC 178074. PMID 8655502.
  2. 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. doi:10.1128/jb.174.5.1487-1494.1992. PMC 206543. PMID 1537793.