Jump to content

Incensole: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
m task, replaced: J Psychopharmacol. → J. Psychopharmacol.
Line 37: Line 37:


[[Category:Diterpenes]]
[[Category:Diterpenes]]
[[Category:Alcohols]]
[[Category:Secondary alcohols]]
[[Category:Heterocyclic compounds (2 rings)]]
[[Category:Heterocyclic compounds (2 rings)]]
[[Category:Oxygen heterocycles]]
[[Category:Oxygen heterocycles]]

Revision as of 12:34, 6 June 2019

Incensole
Names
IUPAC name
(1R,2R,5E,9Z)-1,5,9-trimethyl-12-propan-2-yl-15-oxabicyclo[10.2.1]pentadeca-5,9-dien-2-ol
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C20H34O2/c1-15(2)20-12-11-17(4)8-6-7-16(3)9-10-18(21)19(5,22-20)13-14-20/h7,11,15,18,21H,6,8-10,12-14H2,1-5H3/b16-7+,17-11-/t18-,19-,20?/m1/s1
    Key: SSBZLMMXFQMHDP-AWBFOCMTSA-N
  • CC1=CCCC(=CCC2(CCC(O2)(C(CC1)O)C)C(C)C)C
Properties
C20H34O2
Molar mass 306.490 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Insensole, an organic compound found as its acetate ester in some frankinsence. It is a diterpene alcohol.[1]

The formula of insensole is C20H34O2[2]

Incensole acetate [3] Its effects on animals have been studied.[4]

References

  1. ^ Corsano, S.; Nicoletti, R. (1967). "The structure of incensole". Tetrahedron. 23 (4): 1977–1984. doi:10.1016/S0040-4020(01)82601-6.
  2. ^ Insensole (at PubChem)
  3. ^ Incensole acetate (@NIST)
  4. ^ Moussaieff, A; Gross, M; Nesher, E; Tikhonov, T; Yadid, G; Pinhasov, A (2012). "Incensole acetate reduces depressive-like behavior and modulates hippocampal BDNF and CRF expression of submissive animals". J. Psychopharmacol. 26 (12): 1584–93. doi:10.1177/0269881112458729. PMID 23015543.