Hinokiol

Inquiry

For Research Use Only.

Category

Diterpenoids

Cat.No.

NP1749

CAS

564-73-8

Product Name

Hinokiol

Structure

Product Details

Description

Hinokiol is extracted from the barks of Cephalotaxus fortunei Hook. f. It inhibits leukotriene B(4) (LTB4) and 5-hydroxy-eicosa-tetra-enoic acid (5-HETE) formations and may have anti-inflammatory activity. It also displays potent activity against clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA).

Synonyms

2,6-Phenanthrenediol, 1,2,3,4,4a,9,10,10a-octahydro-1,1,4a-trimethyl-7-(1-methylethyl)-, (2S,4aS,10aR)-; (2S,4aS,10aR)-1,2,3,4,4a,9,10,10a-Octahydro-1,1,4a-trimethyl-7-(1-methylethyl)-2,6-phenanthrenediol; 2,6-Phenanthrenediol, 1,2,3,4,4a,9,10,10a-octahydro-1,1,4a-trimethyl-7-(1-methylethyl)-, [2S-(2α,4aα,10aβ)]-; Podocarpa-8,11,13-triene-3β,12-diol, 13-isopropyl-; (+)-Hinokiol; NSC 319628

IUPAC Name

(2S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol

Molecular Weight

302.46

Molecular Formula

C20H30O2

Canonical SMILES

CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O

InChI

InChI=1S/C20H30O2/c1-12(2)14-10-13-6-7-17-19(3,4)18(22)8-9-20(17,5)15(13)11-16(14)21/h10-12,17-18,21-22H,6-9H2,1-5H3/t17-,18-,20+/m0/s1

InChIKey

ODFCWXVQZAQDSO-CMKODMSKSA-N