Taraxerol

Taraxerol
Names

IUPAC name (3S,4aR,6aR,6aS,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol
Identifiers
3D model (JSmol)	Interactive image
ChemSpider	83146
PubChem CID	92097
InChI InChI=1S/C30H50O/c1-25(2)17-18-27(5)13-9-21-29(7)14-10-20-26(3,4)24(31)12-16-28(20,6)22(29)11-15-30(21,8)23(27)19-25/h9,20,22-24,31H,10-19H2,1-8H3/t20-,22+,23+,24-,27-,28-,29-,30+/m0/s1 Key: GGGUGZHBAOMSFJ-GADYQYKKSA-N InChI=1/C30H50O/c1-25(2)17-18-27(5)13-9-21-29(7)14-10-20-26(3,4)24(31)12-16-28(20,6)22(29)11-15-30(21,8)23(27)19-25/h9,20,22-24,31H,10-19H2,1-8H3/t20-,22+,23+,24-,27-,28-,29-,30+/m0/s1 Key: GGGUGZHBAOMSFJ-GADYQYKKBI
SMILES C[C@]12CCC(C[C@H]1C3(CC[C@@H]4[C@]5(CC[C@@H](C([C@@H]5CC[C@]4(C3=CC2)C)(C)C)O)C)C)(C)C
Properties
Chemical formula	C₃₀H₅₀O
Molar mass	426.73 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

Taraxerol is an anti-inflammatory triterpenoid.^[1]

See also

Taraxerol synthase

References

↑ Yao, X; Li, G; Bai, Q; Xu, H; Lü, C (2013). "Taraxerol inhibits LPS-induced inflammatory responses through suppression of TAK1 and Akt activation". International immunopharmacology. 15 (2): 316–24. PMID 23333629. doi:10.1016/j.intimp.2012.12.032.

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