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Methylenomycin A
Names
	Preferred IUPAC name (1S,2R,5S)-1,5-Dimethyl-3-methylidene-4-oxo-6-oxabicyclo[3.1.0]hexane-2-carboxylic acid
Identifiers
CAS Number	52775-76-5 ;
3D model (JSmol)	Interactive image;
ChemSpider	9074545 ;
PubChem CID	10899285;
UNII	X902U0148F ;
CompTox Dashboard (EPA)	DTXSID40967224 ;
	InChI InChI=1S/C9H10O4/c1-4-5(7(11)12)8(2)9(3,13-8)6(4)10/h5H,1H2,2-3H3,(H,11,12)/t5-,8-,9+/m0/s1 Key: HBECYYFDLZZMPL-WLGLDCGKSA-N ; InChI=1/C9H10O4/c1-4-5(7(11)12)8(2)9(3,13-8)6(4)10/h5H,1H2,2-3H3,(H,11,12)/t5-,8-,9+/m0/s1 Key: HBECYYFDLZZMPL-WLGLDCGKBO;
	SMILES O=C1C(=C)[C@@H](C(=O)O)[C@@]2(O[C@]12C)C;
Properties
Chemical formula	C9H10O4
Molar mass	182.175 g·mol−1
Boiling point	341.2 °C (646.2 °F; 614.3 K)
Hazards
Flash point	141.2 °C (286.2 °F; 414.3 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Methylenomycin A is a cyclopentanone derived antibiotic produced by Streptomyces coelicolor A3(2) that is effective against both Gram-negative and Gram-positive bacteria.^[1]^[2] The last step of its biosynthesis is epoxidation of the alkene of methylenomycin C.^[3]

References

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