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#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

Compound with spectra: 1 NMR

#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
SpectraBase Compound ID JrxOYiE2c8e
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-UOVPMPRRSA-N
Mol Weight 405.49 g/mol
Molecular Formula C22H31NO6
Exact Mass 405.215138 g/mol
Enantiomer InChIKey CHQGOWAOLJKTQX-CRHSUSOYSA-N

View Spectrum of #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

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
TUBEROSTEMONONE
#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,
#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,
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
LANCEOCREPIDIASIDE-E
17,21-Cyclo-19-norpregna-1,3,5(10)-triene-20-methanol, 20-(aminomethyl)-3-methoxy-, (20S)-
3-BETA,12-ALPHA,14,17,25-PENTAHYDROXY-20R,24S-DIEPOXYMALABARICANE
11.beta.-methoxy-2,6,6,8.beta.-tetramethyl-5.alpha.-tricyclo(6,3,0,0(1,5))undec-2-en-4-one
Title Journal or Book Year
New Stemona alkaloids from the roots of Stemona tuberosa Magnetic Resonance in Chemistry 2014
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