Dehydrocurvularin

Dehydrocurvularin
Names
	Preferred IUPAC name (4S,8E)-11,13-Dihydroxy-4-methyl-4,5,6,7-tetrahydro-2H-3-benzoxacyclododecine-2,10(1H)-dione
Identifiers
CAS Number	21178-57-4 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL520014;
ChemSpider	4942635;
PubChem CID	6438143;
UNII	PAU7YA7FF9 ;
CompTox Dashboard (EPA)	DTXSID101017526;
	InChI InChI=1S/C16H18O5/c1-10-5-3-2-4-6-13(18)16-11(8-15(20)21-10)7-12(17)9-14(16)19/h4,6-7,9-10,17,19H,2-3,5,8H2,1H3/b6-4+/t10-/m0/s1 Key: AVIRMQMUBGNCKS-RWCYGVJQSA-N; InChI=1/C16H18O5/c1-10-5-3-2-4-6-13(18)16-11(8-15(20)21-10)7-12(17)9-14(16)19/h4,6-7,9-10,17,19H,2-3,5,8H2,1H3/b6-4+/t10-/m0/s1 Key: AVIRMQMUBGNCKS-RWCYGVJQBB;
	SMILES C[C@H]1CCC/C=C/C(=O)c2c(cc(cc2O)O)CC(=O)O1;
Properties
Chemical formula	C16H18O5
Molar mass	290.315 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

Dehydrocurvularin is an antimicrobial made by Penicillium.^[2]

References

↑ Chambers, Michael. "ChemIDplus - 0021178574 - AVIRMQMUBGNCKS-RWCYGVJQSA-N - Dehydrocurvularin - Similar structures search, synonyms, formulas, resource links, and other chemical information". chem.nlm.nih.gov.
↑ Savchuk, IaI; Zaĭchenko, A. M.; Tsyganenko, E. S. (2012). "Biological activity of Penicillium sp. 10-51 exometabolites". Mikrobiolohichnyi Zhurnal. 74 (4): 52–6. PMID 23088100.

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