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ISORHIZOPODIN;(Z)-ISOMER

Compound with spectra: 1 NMR

ISORHIZOPODIN;(Z)-ISOMER
SpectraBase Compound ID SDXA3Cx35C
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)43-69(89)77(5,6)72-46-74-80-60(48-102-74)66(98-16)30-24-20-22-27-57(93-11)39-55(85)41-75(91)103-71(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)45-73-79-59(47-101-73)65(97-15)29-23-19-21-28-58(94-12)40-56(86)42-76(92)104-72/h19-28,37-38,47-58,63-72,85-86,89-90H,29-36,39-46H2,1-18H3/b23-19+,24-20+,27-22+,28-21+,37-25-,38-26-
InChIKey MEWISJWGMKBQQA-HJBRPPLBSA-N
Mol Weight 1469.9 g/mol
Molecular Formula C78H124N4O22
Exact Mass 1468.870722 g/mol

View Spectrum of ISORHIZOPODIN;(Z)-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
ISORHIZOPODIN;(E)-ISOMER
SECOHALICHONDRAMIDE;MAJOR-ISOMER
HALISHIGAMIDE-B
SODBQKXNADUHHH-DZFDLWGFSA-N
Benzyl-dehydro-ascorbic acid, methyl glucoside
6108-D
ANKARAHOLIDE-B
2-.beta.-tert-Butoxyclovan-9.alpha.-ol
No Name
8.alpha.-Hydroxy-15-oxo-5,7.alpha.-H,6,11.beta.-H-elema-1,3-diene-12,6-olide
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

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