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N-[[2-(LACTOBIONAMIDO)-ETHYL]-N-[2-[2,3-(DITETRADECANAMIDO)-PROPIONAMIDO]-ETHYL]]-LACTOBIONAMIDE;BISLAC

Compound with spectra: 1 NMR

N-[[2-(LACTOBIONAMIDO)-ETHYL]-N-[2-[2,3-(DITETRADECANAMIDO)-PROPIONAMIDO]-ETHYL]]-LACTOBIONAMIDE;BISLAC
SpectraBase Compound ID E0BuneQwtsh
InChI InChI=1S/C61H116N6O25/c1-3-5-7-9-11-13-15-17-19-21-23-25-43(74)65-33-38(66-44(75)26-24-22-20-18-16-14-12-10-8-6-4-2)57(86)62-27-30-67(31-28-63-58(87)51(82)49(80)55(39(72)34-68)91-60-53(84)47(78)45(76)41(36-70)89-60)32-29-64-59(88)52(83)50(81)56(40(73)35-69)92-61-54(85)48(79)46(77)42(37-71)90-61/h38-42,45-56,60-61,68-73,76-85H,3-37H2,1-2H3,(H,62,86)(H,63,87)(H,64,88)(H,65,74)(H,66,75)/t38?,39?,40?,41-,42-,45+,46+,47+,48+,49?,50?,51?,52?,53-,54-,55?,56?,60+,61+/m0/s1
InChIKey RMDCZJIDKXDQMB-SKMNOAOXSA-N
Mol Weight 1333.6 g/mol
Molecular Formula C61H116N6O25
Exact Mass 1332.799013 g/mol
Enantiomer InChIKey RMDCZJIDKXDQMB-LFHJRQQGSA-N

View Spectrum of N-[[2-(LACTOBIONAMIDO)-ETHYL]-N-[2-[2,3-(DITETRADECANAMIDO)-PROPIONAMIDO]-ETHYL]]-LACTOBIONAMIDE;BISLAC

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3:CD3OD
N-[2-[2,3-(DITETRADECANAMIDO)-PROPIONAMIDO]-ETHYL]-LACTOBIONAMIDE;MONOLAC
(3R,4R,5R,6S)-HEXAHYDRO-3,5,6-TRIHYDROXY-1H-AZEPINE-4-YL-TRIS-[O-ALPHA-D-GLUCOPYRANOSYL-(1->4)]-ALPHA-D-GLUCOPYRANOSIDE
(3R,4R,5R,6S)-HEXAHYDRO-3,5,6-TRIHYDROXY-1H-AZEPINE-4-YL-BIS-[O-ALPHA-D-GLUCOPYRANOSYL-(1->4)]-ALPHA-D-GLUCOPYRANOSIDE
(3R,4R,5R,6S)-HEXAHYDRO-3,5,6-TRIHYDROXY-1H-AZEPINE-4-YL-O-ALPHA-D-GLUCOPYRANOSYL-(1->4)-ALPHA-D-GLUCOPYRANOSIDE
3,3'-O-(1,16-HEXADECAMETHYLENE)-2,2'-DI-O-[(R)-3,7-DIMETHYLOCTYL]-1-O-(BETA-D-GALACTOFURANOSYL)-1'-O-(BETA-LACTOSYL)-SN-DIGLYCEROL
BIS-[O-ALPHA-D-GLUCOPYRANOSYL-(1->4)]-6-AZIDO-6-DEOXY-D-GLUCOPYRANOSIDE
TETRAKIS-[O-ALPHA-D-GLUCOPYRANOSYL-(1->4)]-6-AZIDO-6-DEOXY-D-GLUCOPYRANOSIDE
Nebramycin factor 12
MONO-6'-DEOXY-6'-AMIDOSUCCINYL-CYCLOMALTOHEPTAOSE
4-NITROPHENYL-BETA-D-GALACTOPYRANOSYL-(1->4)-BETA-D-CELLOBIOSIDE
Title Journal or Book Year
Amphiphilic Anionic Analogues of Galactosylceramide:  Synthesis, Anti-HIV-1 Activity, and gp120 Binding Journal of Medicinal Chemistry 2001
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