Phellinstatin

Phellinstatin
Names
	Preferred IUPAC name (22S,23S,3E,7E)-22-(3,4-Dihydroxyphenyl)-14,54,55,64,93,94-hexahydroxy-22,23-dihydro-16H,24H,66H-2(3,6)-furo[3,2-c]pyrana-1(2),6(5,2)-dipyrana-5(1,2),9(1)-dibenzenanonaphane-3,7-diene-16,24,66-trione
Identifiers
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL1682259;
ChemSpider	26385089;
PubChem CID	54728876;
	InChI InChI=1S/C39H26O15/c40-20-12-31(53-33(48)13-20)35-36-32(54-37(35)19-4-8-25(42)27(44)11-19)15-22(52-39(36)50)6-3-18-10-28(45)29(46)16-23(18)34-30(47)14-21(51-38(34)49)5-1-17-2-7-24(41)26(43)9-17/h1-16,35,37,40-47H/b5-1+,6-3+/t35-,37+/m0/s1 Key: KAEWYNFUJFCGQA-UPSVAIHWSA-N;
	SMILES C1=CC(=C(C=C1/C=C/C2=CC(=C(C(=O)O2)C3=CC(=C(C=C3/C=C/C4=CC5=C([C@@H]([C@H](O5)C6=CC(=C(C=C6)O)O)C7=CC(=CC(=O)O7)O)C(=O)O4)O)O)O)O)O;
Properties
Chemical formula	C39H26O15
Molar mass	734.622 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

Phellinstatin is an enoyl-ACP reductase inhibitor isolated from the fungus Phellinus linteus.^[1]

References[edit]

^ Cho, JY; Kwon, YJ; Sohn, MJ; Seok, SJ; Kim, WG (2011). "Phellinstatin, a new inhibitor of enoyl-ACP reductase produced by the medicinal fungus Phellinus linteus". Bioorganic & Medicinal Chemistry Letters. 21 (6): 1716–8. doi:10.1016/j.bmcl.2011.01.080. PMID 21316961.

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