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UROSPERMAL A,11-B,13-DIHYDRO+TAI

Compound with spectra: 1 NMR

UROSPERMAL A,11-B,13-DIHYDRO+TAI
SpectraBase Compound ID 29yUmRuWcQq
InChI InChI=1S/C20H21Cl3N2O9.C2H3Cl3/c1-10-16-13(33-19(10)31)6-12(9-32-24-15(28)8-27)4-2-3-11(7-26)5-14(16)34-25-18(30)17(29)20(21,22)23;1-2(3,4)5/h3,6-8,10,13-14,16H,2,4-5,9H2,1H3,(H,24,28)(H,25,30);1H3/b11-3+,12-6-;/t10-,13+,14-,16-;/m0./s1
InChIKey IHOLTUYXIDKPRJ-ZYXNLMSASA-N
Mol Weight 673.16 g/mol
Molecular Formula C22H24Cl6N2O9
Exact Mass 669.961297 g/mol
Enantiomer InChIKey IHOLTUYXIDKPRJ-IMTBXNNKSA-N

View Spectrum of UROSPERMAL A,11-B,13-DIHYDRO+TAI

13C NMR Spectrum
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Solvent Chloroform
15-O-BETA-D-GLUCOPYRANOSYL-11-BETA,13-DIHYDROUROSPERMAL-A
UROSPERMAL-A+TAI
8-ALPHA-O-(4-ACETOXY-5-HYDROXYANGELOYL)-11-BETA,13-DIHYDROCNICIN
11-BETA,13-DIHYDROCNICIN
11-B-H-GERMACRA-4E,10(14)-DIEN-12,6-A-OLIDE,8-A-ANGELOYLOXY-1-OXO
8.beta.-(Acetoxy)-15-[angeloyloxy]-14-oxo-(4Z)-acanthospermolide
ACANTHOSPERMOLIDE,15-HYDROXY-8-B-METHYLBUTYRYLOXY-14-OXO
LECOCARPINOLIDE_C
(6-S,7-R,8-S)-8,15-DI-ACETOXY-14-OXO-MELAMPA-1-(10),4,11-(13)-TRIEN-12,6-OLIDE
8-BETA-(4'-ACETOXY-TIGLOYLOXY)-14-AL-COSTUNOLIDE
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