Misplaced Pages

Inotodiol

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Inotodiol
Names
IUPAC name (22R)-Lanosta-8,24-diene-3β,22-diol
Systematic IUPAC name (1R,3aR,5aR,7S,9aS,11aR)-1--3a,6,6,9a,11a-pentamethyl-2,3,3a,4,5,5a,6,7,8,9,9a,10,11,11a-tetradecahydro-1H-cyclopentaphenanthren-7-ol
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C30H50O2/c1-19(2)9-11-24(31)20(3)21-13-17-30(8)23-10-12-25-27(4,5)26(32)15-16-28(25,6)22(23)14-18-29(21,30)7/h9,20-21,24-26,31-32H,10-18H2,1-8H3/t20-,21+,24+,25-,26-,28+,29+,30-/m0/s1Key: KKWJCGCIAHLFNE-KFPHZHIMSA-N
  • InChI=1/C30H50O2/c1-19(2)9-11-24(31)20(3)21-13-17-30(8)23-10-12-25-27(4,5)26(32)15-16-28(25,6)22(23)14-18-29(21,30)7/h9,20-21,24-26,31-32H,10-18H2,1-8H3/t20-,21+,24+,25-,26-,28+,29+,30-/m0/s1Key: KKWJCGCIAHLFNE-KFPHZHIMBI
SMILES
  • C(1CC2(1(CCC3=C2CC43(CC(C4(C)C)O)C)C)C)(CC=C(C)C)O
Properties
Chemical formula C30H50O2
Molar mass 442.717
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Inotodiol is an anti-inflammatory sterol isolated from Inonotus obliquus.

References

  1. Ma, L; Chen, H; Dong, P; Lu, X (2013). "Anti-inflammatory and anticancer activities of extracts and compounds from the mushroom Inonotus obliquus". Food Chemistry. 139 (1–4): 503–8. doi:10.1016/j.foodchem.2013.01.030. PMID 23561137.


Stub icon

This article about a steroid is a stub. You can help Misplaced Pages by expanding it.

Categories: