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(-)-2-DEOXYORYZALEXIN_S

Compound with spectra: 2 NMR

(-)-2-DEOXYORYZALEXIN_S
SpectraBase Compound ID 2eHQR5WL6tS
InChI InChI=1S/C20H32O/c1-14-11-16-5-6-17-18(2,13-21)8-4-9-19(17,3)20(16)10-7-15(14)12-20/h11,15-17,21H,4-10,12-13H2,1-3H3/t15-,16+,17+,18-,19+,20-/m0/s1
InChIKey TUSCOQSQOOTGAW-BIEDPOGDSA-N
Mol Weight 288.5 g/mol
Molecular Formula C20H32O
Exact Mass 288.245316 g/mol
Enantiomer InChIKey TUSCOQSQOOTGAW-UPQMVPBKSA-N

View Spectrum of (-)-2-DEOXYORYZALEXIN_S

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (-)-2-DEOXYORYZALEXIN_S

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • ENT-STEMARA-13-(14)-EN-19-OL
ENT-STEMARA-13-(14)-EN-18-OL
(+)-2-DEOXYORYZALEXIN_S
ENT-STEMAR-13(14)-EN-19-OL
CJXGXOWASAFJSQ-FACDWMFESA-N
ENT-STEMAR-13-(14)-EN-19-ACETOXY
STEMARIN
13-ALPHA,17,18-TRIHYDROXY-STEMODANE
17-ACETYLOXY-STEMODAN-13-ALPHA-OL
2-ACETOXY-13-METHYLENE-STEMARANE
Cholestan-3-one, 2,2,4,4-tetramethyl-, (5.alpha.)-
Title Journal or Book Year
Regio- and Diastereoselective Synthesis and X-ray Structure Determination of (+)-2-Deoxyoryzalexin S from (+)-Podocarpic Acid. Structural Nonidentity with Its Nominal Natural Isolated Enantiomer Journal of Natural Products 2012
Diterpenes from Calceolaria latifolia Phytochemistry 1990

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