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#12A;(Z)-D-SERINE-[(Z)-D-SERINE-[BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL

Compound with spectra: 1 NMR

#12A;(Z)-D-SERINE-[(Z)-D-SERINE-[BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL
SpectraBase Compound ID D058FXc2qiJ
InChI InChI=1S/C55H80N10O19S2/c1-30(2)42(64-48(72)41(27-86-29-57-35(8)67)61-45(69)33(6)59-54(79)84-55(9,10)11)50(75)80-24-38(62-52(77)82-22-36-18-14-12-15-19-36)46(70)58-32(5)44(68)60-40(26-85-28-56-34(7)66)47(71)65-43(31(3)4)51(76)81-25-39(49(73)74)63-53(78)83-23-37-20-16-13-17-21-37/h12-21,30-33,38-43H,22-29H2,1-11H3,(H,56,66)(H,57,67)(H,58,70)(H,59,79)(H,60,68)(H,61,69)(H,62,77)(H,63,78)(H,64,72)(H,65,71)(H,73,74)/t32-,33+,38+,39+,40-,41+,42+,43-/m0/s1
InChIKey TXIIBVPZBQTLIP-GMGNKKTLSA-N
Mol Weight 1249.4 g/mol
Molecular Formula C55H80N10O19S2
Exact Mass 1248.504263 g/mol
Enantiomer InChIKey TXIIBVPZBQTLIP-CBEGLJEKSA-N

View Spectrum of #12A;(Z)-D-SERINE-[(Z)-D-SERINE-[BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
(Z)-D-SERINE-[(Z)-D-SERINE-[BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-L-VALINE]-L-ALANINE-L-CYSTEINE-L-VALINE]-OH-DISULFIDE
Cbz-Thr(rprenyl)-Ser(rprenyl)-Lle-OMe
Hexapeptide boc-leu-tyr(bzl)-leu-val-cys(set)-gly-04
N-TERT.-BUTYLOXYCARBONYL-GLYCYL-(S-PALMITOYL)-L-CYSTEYL-L-THREONYL-L-LEUCYL-L-SERYL-L-ALANINE-CHOLINE-ESTER-BROMIDE;BOC-GLY-CYS(PAL)-THR-LEU-SER-A
N-(TERT.-BUTOXYCARBONYL)-4-BENZYL-L-ASPARTYL-5-BENZYL-L-GLUTAMYL-O-BENZYL-L-THREONINE-METHYLESTER
BEAUVEROLIDE-LA;CYCLO-[3-HYDROXY-4-METHYLDECANOYL-L-PHENYL-ALANYL-D-ALLO-ISOLEUCYL]
ISO-ISARIIN_B;CYCLO-[3-HYDROXY-4-METHYLOCTANOYL-GLY-(2)-VAL-(3)-LEU-(4)-ALA-(5)-VAL-(6)]
BOC-PHE-CYS((O)ME)-CYS(TRT)-OME
CBZ-D-val-ser(TBDMS)-D-phe-ser(TBDMS)-ome
CBZ-val-ser(TBDMS)-D-phe-ser(TBDMS)-ome
Title Journal or Book Year
Solution-Phase Synthesis of Nucleobase-Substituted Analogues of Triostin A The Journal of Organic Chemistry 2004
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