Hyperforin

Hyperforin
Clinical data
Dependence; liability	None
Routes of; administration	Oral
ATC code	none;
Legal status
Legal status	UK: General sales list (GSL, OTC); US: OTC; unscheduled in most countries, with the notable exception of Ireland (Rx-only);
Pharmacokinetic data
Metabolism	Hepatic and CYP3A & CYP2B
Identifiers
	IUPAC name (1R,5S,6R,7S)-4-Hydroxy-6-methyl-1,3,7-tris(3-methylbut-2-en-1-yl)-6-(4-methylpent-3-en-1-yl)-5-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dion;
CAS Number	11079-53-1;
PubChem CID	114787;
IUPHAR/BPS	2764;
DrugBank	DB01892 ;
ChemSpider	16736597 ;
UNII	RM741E34FP;
KEGG	C07608 ;
ChEBI	CHEBI:5834 ;
CompTox Dashboard (EPA)	DTXSID90891409 ;
ECHA InfoCard	100.112.565
Chemical and physical data
Formula	C35H52O4
Molar mass	536.797 g·mol−1
3D model (JSmol)	Interactive image;
Melting point	79–80 °C (174–176 °F)
Solubility in water	0.66 mg/mL (20 °C)
	SMILES CC(C)C(=O)[C@@]21C(=O)[C@@](C[C@H](C\C=C(/C)C)[C@@]1(C)CC\C=C(/C)C)(C\C=C(/C)C)C(=O)C(\C\C=C(/C)C)=C2\O;
	InChI InChI=1S/C35H52O4/c1-22(2)13-12-19-33(11)27(16-14-23(3)4)21-34(20-18-25(7)8)30(37)28(17-15-24(5)6)31(38)35(33,32(34)39)29(36)26(9)10/h13-15,18,26-27,38H,12,16-17,19-21H2,1-11H3/t27-,33+,34+,35-/m0/s1 ; Key:IWBJJCOKGLUQIZ-HQKKAZOISA-N ;
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Hyperforin is a phytochemical produced by some of the members of the plant genus Hypericum, notably Hypericum perforatum (St John's wort). Hyperforin may be involved in the pharmacological effects of St. John's wort, specifically in its antidepressant effects.

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