Inotodiol

Inotodiol
Names

IUPAC name (3β,22R)-Lanosta-8,24-diene-3,22-diol
Systematic IUPAC name (3β,22R)-Lanosta-8,24-diene-3,22-diol
Identifiers
ChemSpider	23282401
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/s1 Key: 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/s1 Key: KKWJCGCIAHLFNE-KFPHZHIMBI
Jmol-3D images	Image
PubChem	44422314
SMILES C[C@@H]([C@H]1CC[C@@]2([C@@]1(CCC3=C2CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C)[C@@H](CC=C(C)C)O
Properties
Chemical formula	C₃₀H₅₀O₂
Molar mass	442.717
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Inotodiol is an anti-inflammatory sterol isolated from Inonotus obliquus.^[1]

References

↑ 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.