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#1;STEMONATUBERONE-A;(REL)-(3S*,3AS*,6S*,12R*,13R*,13AS*)-13-ETHYL-3-METHYL-6-[(2S*,4S*)-4-METHYL-5-OXO-TETRAHYDROFURAN-2-YL]-DECAHYDRO-2H-7,12-METHANOFURO-[3,

Compound with spectra: 1 NMR

#1;STEMONATUBERONE-A;(REL)-(3S*,3AS*,6S*,12R*,13R*,13AS*)-13-ETHYL-3-METHYL-6-[(2S*,4S*)-4-METHYL-5-OXO-TETRAHYDROFURAN-2-YL]-DECAHYDRO-2H-7,12-METHANOFURO-[3,
SpectraBase Compound ID LoGasr7ouUz
InChI InChI=1S/C22H31NO6/c1-4-13-14-7-5-6-8-23(20(14)25)15(17-9-11(2)21(26)28-17)10-16(24)18-12(3)22(27)29-19(13)18/h11-15,17-19H,4-10H2,1-3H3/t11-,12-,13+,14+,15-,17-,18+,19-/m0/s1
InChIKey CHQGOWAOLJKTQX-GECIJFOUSA-N
Mol Weight 405.49 g/mol
Molecular Formula C22H31NO6
Exact Mass 405.215138 g/mol
Enantiomer InChIKey CHQGOWAOLJKTQX-WGCHMBTQSA-N

View Spectrum of #1;STEMONATUBERONE-A;(REL)-(3S*,3AS*,6S*,12R*,13R*,13AS*)-13-ETHYL-3-METHYL-6-[(2S*,4S*)-4-METHYL-5-OXO-TETRAHYDROFURAN-2-YL]-DECAHYDRO-2H-7,12-METHANOFURO-[3,

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
#2;STEMONATUBERONE-B;(REL)-(3R*,3AR*,6S*,12R*,13R*,13R*)-13-ETHYL-3-METHYL-6-[(2S*,4S*)-4-METHYL-5-OXO-TETRAHYDROFURAN-2-YL]-DECAHYDRO-2H-7,12-METHANOFURO-[3,2
TUBEROSTEMONONE
#3;STEMONATUBERONE-C;(REL)-(3S*,3AR*,6S*,12R*,13R*,13AS*)-13-ETHYL-3-METHYL-6-[(2S*,4S*)-4-METHYL-5-OXO-TETRAHYDROFURAN-2-YL]-DECAHYDRO-2H-7,12-METHANOFURO-[3,
10-(3-bromophenyl)-6-methoxy-9-methyl-8-oxa-10,12-diazatricyclo[7.3.1.0²,⁷]trideca-2,4,6-trien-11-one
17-BETA-HYDROXY-2-(HYDROXYMETHYL)-17-ALPHA-METHYL-ANDROST-1,4-DIEN-3-ONE
methyl 3-benzhydryl-4-oxo-10-oxa-3-azatricyclo[5.2.1.0~1,5~]dec-8-ene-6-carboxylate
4-Methoxy-2,6,8-trimethyl[1,3]oxazolo[5',4':4,5]pyrido[2,3-d]pyrimidine-7,9(6H,8H)-dione
Stanozolol ME II
N-(2',3',5'-TRI-O-BENZOYL-BETA-D-RIBOFURANOSYL)-7-ETHYL-3-FLUORO-10H-PHENOTHIAZINE
3-BETA,12-ALPHA,14,17,25-PENTAHYDROXY-20R,24S-DIEPOXYMALABARICANE
Title Journal or Book Year
New Stemona alkaloids from the roots of Stemona tuberosa Magnetic Resonance in Chemistry 2014
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