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GHGKPLPBPGYSOO-FBZNIEFRSA-N
SpectraBase Compound ID 8G9mggxOqQt
InChI InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,20-21,23-27,30H,2,7-9,11-18H2,1,3-6H3/t20-,21+,23+,24+,25-,26+,27+,28+,29-/m1/s1
InChIKey GHGKPLPBPGYSOO-FBZNIEFRSA-N
Mol Weight 412.7 g/mol
Molecular Formula C29H48O
Exact Mass 412.370516 g/mol
Enantiomer InChIKey GHGKPLPBPGYSOO-USLLMGQYSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 24-ALPHA-ETHYLCHOLESTA-5,25-DIEN-3-BETA-OL
  • CLEROSTEROL;(3-BETA,24S)-STIGMASTA-5,25-DIENE-3-OL
  • Clerosterol
Title Journal or Book Year
Preparation Antitrypanosomal and Cytotoxic Activities of 22-Hydroxyclerosterol, a New Sterol from Allexis cauliflora (Violaceae) Scientia Pharmaceutica 2011
Steroidal compounds from Teucrium chamaedrys subsp. Chamaedrys Phytochemistry 1994
Sterols from marine green alga Codium decorticatum Phytochemistry 1993
A sterol glycoside from marine green alga Codium iyengarii Phytochemistry 1992

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