Tigliane
Names
Preferred IUPAC name
(1aS,1bR,3S,4aS,6R,7aR,7bR,8R,9aR)-1,1,3,6,8-pentamethyltetradecahydro-1H-cyclopropa[3,4]benzo[1,2-e]azulene
Other names
Tiglian
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C20H34/c1-11-6-14-7-12(2)9-16-18(15(14)8-11)13(3)10-17-19(16)20(17,4)5/h11-19H,6-10H2,1-5H3/t11-,12+,13-,14+,15-,16-,17-,18-,19+/m1/s1 checkY
    Key: CGVXVPQJMYMMIH-HKDZDBKOSA-N checkY
  • C[C@@H]1C[C@H]2C[C@@H](C[C@@H]3[C@@H]([C@@H]2C1)[C@@H](C[C@@H]4[C@H]3C4(C)C)C)C
Properties
C20H34
Molar mass 274.492 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Tigliane is a diterpene that forms the structural basis for some natural chemical compounds such as phorbol.[1][2]

See also

References

  1. ↑ "Tigliane", Pubchem, retrieved 2022-08-08
  2. ↑ Qi-Run Li, Yung-Yi Cheng, Lei Zhao, Xiao-Lei Huang, Xiao-Gang Jiang, Ya-Dong Cui, Susan L. Morris-Natschke, Masuo Goto, Chin-Ho Chen, Kuo-Hsiung Lee, Dao-Feng Chen, Jian Zhang, New phorbol ester derivatives as potent anti-HIV agents, Bioorganic & Medicinal Chemistry Letters, 50, 2021, doi:10.1016/j.bmcl.2021.128319; ISSN 0960-894X.
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