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// Workers AI · dad joke modeWhat did varicelin say? I'm feeling a little variant today

From Wikipedia, the free encyclopedia
Variecolin
Names
IUPAC name
(3S,3aS,3bS,5E,6aR,9S,9aS,10aR,12aS)-9,10a,12a-Trimethyl-7-oxo-3-(prop-1-en-2-yl)-1,2,3,3a,3b,4,6a,7,8,9,9a,10,10a,11,12,12a-hexadecahydrobenzo[4,5]cycloocta[1,2-e]indene-6-carbaldehyde
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C25H36O2/c1-15(2)18-8-9-24(4)10-11-25(5)13-19-16(3)12-21(27)22(19)17(14-26)6-7-20(25)23(18)24/h6,14,16,18-20,22-23H,1,7-13H2,2-5H3/b17-6-/t16-,18+,19-,20-,22-,23-,24-,25+/m0/s1
    Key: XAYQASOMEVLRKN-NOJNFTMQSA-N
  • InChI=1/C25H36O2/c1-15(2)18-8-9-24(4)10-11-25(5)13-19-16(3)12-21(27)22(19)17(14-26)6-7-20(25)23(18)24/h6,14,16,18-20,22-23H,1,7-13H2,2-5H3/b17-6-/t16-,18+,19-,20-,22-,23-,24-,25+/m0/s1
    Key: XAYQASOMEVLRKN-NOJNFTMQBM
  • C[C@H]1CC(=O)[C@@H]/2[C@H]1C[C@]3(CC[C@@]4(CC[C@@H]([C@H]4[C@@H]3C/C=C2/C=O)C(=C)C)C)C
Properties
C25H36O2
Molar mass 368.561 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Variecolin is a terpenoid isolated from an ascomycete.[1]

See also

[edit]

References

[edit]
  1. Fujimoto, H.; Nakamura, E.; Okuyama, E.; Ishibashi, M. (2000). "Immunomodulatory constituents from an ascomycete, Emericella aurantio-brunnea". Chemical & Pharmaceutical Bulletin. 48 (10): 1436–1441. doi:10.1248/cpb.48.1436. PMID 11045446.