ZQMLIVBQFXSJNR-UGJVRCLBSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 25kiIezngqp |
|---|---|
| InChI | InChI=1S/C41H74N10O11/c1-22(2)31-36(57)49-32(23(3)4)37(58)51-33(25(6)52)38(59)47-28(21-29(42)54)35(56)46-24(5)40(61)62-26(7)34(39(60)50-31)48-30(55)20-27(53)18-16-14-12-10-8-9-11-13-15-17-19-45-41(43)44/h22-28,31-34,52-53H,8-21H2,1-7H3,(H2,42,54)(H,46,56)(H,47,59)(H,48,55)(H,49,57)(H,50,60)(H,51,58)(H4,43,44,45)/t24-,25+,26-,27-,28+,31+,32-,33+,34+/m0/s1 |
| InChIKey | ZQMLIVBQFXSJNR-UGJVRCLBSA-N |
| Mol Weight | 883.1 g/mol |
| Molecular Formula | C41H74N10O11 |
| Exact Mass | 882.553853 g/mol |
| Enantiomer InChIKey | ZQMLIVBQFXSJNR-CSFADBIVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
SUSUITKPVHIIAO-JCDVXJHMSA-N
FUSARICIDIN_B
WRTAZMDZIVBZOD-XUFIUVFQSA-N
BETA-(25-35);GLY-(1)-SER-ASN-LYS-GLY-(5)-ALA-ILE-ILE-GLY-LEU-(10)-MET-(11)
CORDYCOMMUNIN
SCOPULARIDE_A;CYCLO-(3-HYDROXY-4-METHYLDECANOYL-GLY-L-VYL-D-LEU-L-ALA-L-PHE)
Methyl 12,20-diisobutyl-6,9-diisopropyl-2-methyl-4,7,10,15,18-pentaoxo-13,21-bis[(trimethylsilyl)oxy]-17-([(trimethylsilyl)oxy]methyl)-5,8,11,16,19-pentaazatricosan-23-oate
Butanamide, 2-(dimethylamino)-N-[7-[(4-hydroxyphenyl)methyl]-3-(1-methylethyl)-5,8-dioxo-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-10,12,14,15-tetraen-4-yl]-3-methyl-
| Title | Journal or Book | Year |
|---|---|---|
| A macrolactonization approach to the total synthesis of the antimicrobial cyclic depsipeptide LI-F04a and diastereoisomeric analogues | Beilstein Journal of Organic Chemistry | 2012 |
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.