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IPOMOTAOSIDE_D;(S)-JALAPINOLIC_ACID-11-O-(2-O-TRANS-CINNAMOYL)-[(4-O-N-DODECANOYL)]-ALPHA-L-RHAMNOPYRANOSYL-(1->4)-O-(3-O-N-DECANOYL)-

Compound with spectra: 1 NMR

IPOMOTAOSIDE_D;(S)-JALAPINOLIC_ACID-11-O-(2-O-TRANS-CINNAMOYL)-[(4-O-N-DODECANOYL)]-ALPHA-L-RHAMNOPYRANOSYL-(1->4)-O-(3-O-N-DECANOYL)-
SpectraBase Compound ID C09fp5arceS
InChI InChI=1S/C71H116O21/c1-8-11-14-16-18-19-23-27-34-41-52(72)86-61-47(5)84-71(67(58(61)78)89-55(75)45-44-50-37-31-29-32-38-50)91-63-49(7)82-68(59(79)65(63)88-54(74)42-35-26-21-17-15-12-9-2)90-62-48(6)83-69-60(80)64(62)87-53(73)43-36-28-24-20-22-25-33-40-51(39-30-13-10-3)85-70-66(92-69)57(77)56(76)46(4)81-70/h29,31-32,37-38,44-49,51,56-71,76-80H,8-28,30,33-36,39-43H2,1-7H3/b45-44+/t46-,47+,48+,49+,51+,56+,57+,58-,59-,60-,61+,62+,63+,64+,65+,66-,67-,68+,69+,70+,71+/m1/s1
InChIKey JLXLNASMFJDARQ-FEBORDJLSA-N
Mol Weight 1305.7 g/mol
Molecular Formula C71H116O21
Exact Mass 1304.800911 g/mol
Enantiomer InChIKey JLXLNASMFJDARQ-RUCXKBLPSA-N

View Spectrum of IPOMOTAOSIDE_D;(S)-JALAPINOLIC_ACID-11-O-(2-O-TRANS-CINNAMOYL)-[(4-O-N-DODECANOYL)]-ALPHA-L-RHAMNOPYRANOSYL-(1->4)-O-(3-O-N-DECANOYL)-

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
IPOMOTAOSIDE_C;(S)-JALAPINOLIC_ACID-11-O-(2-O-TRANS-CINNAMOYL)-[(4-O-N-DODECANOYL)]-ALPHA-L-RHAMNOPYRANOSYL-(1->4)-(2-O-N-DECANOYL)-
PESCAPREIN_VI
PESCAPREIN_I
PESCAPREIN_VII
MURUCOIDIN-XII
PESCAPROSIDE_A;(11-S)-HYDROXYHEXADECANOATE_11-O-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-O-[ALPHA-L-RHAMNOPYRANOSYL-(1->4)]-O-[2-O-N-DODECANOYL]-ALPHA-L-RHAM
#2;BATATOSIDE-IV;(S)-JALAPINOLIC-ACID-11-O-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-O-ALPHA-L-RHAMNOPYRANOSYL-(1->4)]-O-[2-O-(S)-2-METHYLBUTYRYL]-(1->2)-ALPHA-L-RHAMNOPY
MURUCOIDIN_I
MURUCIN_4
MURUCIN_5
Title Journal or Book Year
Ipomotaosides A−D, Resin Glycosides from the Aerial Parts of Ipomoea batatas and Their Inhibitory Activity against COX-1 and COX-2 Journal of Natural Products 2010
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