RHIZOPODIN;(E)-ISOMER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 802Yw5kMqjx |
|---|---|
| InChI | InChI=1S/C78H124N4O22/c1-51(33-35-61(87)53(3)63(95-13)31-25-37-81(9)49-83)67(99-17)43-71-77(5,6)69(89)45-73-79-59(47-101-73)65(97-15)29-23-20-22-28-58(94-12)40-56(86)42-76(92)104-72(44-68(100-18)52(2)34-36-62(88)54(4)64(96-14)32-26-38-82(10)50-84)78(7,8)70(90)46-74-80-60(48-102-74)66(98-16)30-24-19-21-27-57(93-11)39-55(85)41-75(91)103-71/h19-28,37-38,47-58,63-72,85-86,89-90H,29-36,39-46H2,1-18H3/b23-20+,24-19+,27-21+,28-22+,37-25+,38-26+/t51-,52-,53-,54-,55-,56-,57-,58-,63+,64+,65-,66-,67-,68-,69-,70-,71-,72-/m0/s1 |
| InChIKey | MWDPPGCTEBRUNT-IKBNIWNCSA-N |
| Mol Weight | 1469.9 g/mol |
| Molecular Formula | C78H124N4O22 |
| Exact Mass | 1468.870722 g/mol |
| Enantiomer InChIKey | MWDPPGCTEBRUNT-PDSCCFHKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
BISISORHIZOPODIN;(E)-ISOMER
19-O-DEMETHYLSCYTOPHYCIN_C;MAJOR_ISOMER
LASONOLIDE-A
.beta.-9-O-Chloroleuconolide A3 Acetoxyacetal
(1S,3S,7S,10R,11S,12S,16R)-3-[(E)-1-Methyl-2-(2-methyl-1,3-thiazol-4-yl)-1-ethenyl]-11-hydroxy-7-(4-methoxybenzyloxy)-8,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadecane-5,9-dione
LASONOLIDE_E
(1R,5R)-4-(R)-O-ACETYL-7-(R),8-(R)-O-ISOPROPYLIDENE-2-OXABICYCLO-[3.3.0]-OCT-3-ONE
LASONOLIDE_F
2,4-Diacetoxy-1,7,7-trimethyl-bicyclo(2.2.1)heptane
| Title | Journal or Book | Year |
|---|---|---|
| Two New Ring-Contracted Congeners of Rhizopodin Illustrate Significance of the Ring Moiety of Macrolide Toxins on the Actin Disassembly-Mediated Cytotoxicity | Chemical and Pharmaceutical Bulletin | 2014 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.