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20-HYDROXYECDISONE
SpectraBase Compound ID 9dhiIK0qEQ1
InChI InChI=1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15?,17-,19+,20-,21-,22+,24+,25+,26?,27+/m0/s1
InChIKey NKDFYOWSKOHCCO-KCJGERRASA-N
Mol Weight 480.6 g/mol
Molecular Formula C27H44O7
Exact Mass 480.308704 g/mol
Enantiomer InChIKey NKDFYOWSKOHCCO-PGBMQTGCSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
  • 20-HYDROXY-ECDYDONE
  • 20-Hydroxyecdysone
Title Journal or Book Year
Ecdysteroids of Vitex scabra Stem Bark Journal of Natural Products 2002
Ecdysteroids from a Zoanthus sp. Journal of Natural Products 2002
Ecdysteroid xylosides from Limnanthes douglasii Phytochemistry 1997
Synthesis and biological activity of side-chain analogues of ecdysone and 20-hydroxyecdysone Journal of the Chemical Society, Perkin Transactions 1 1997
Ecdysteroids from Vitex canescens Phytochemistry 1995
Ecdysteroids from Vitex pinnata Phytochemistry 1993

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