(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL
Compound with spectra: 1 NMR
![(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL](/api/compound/Hu2iqC4n0O6.png?ph=true&h=300&w=458 "(Z)-D-SERINE-[N-BUTYLOXYCARBONYL-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL")
| SpectraBase Compound ID | Hu2iqC4n0O6 |
|---|---|
| InChI | InChI=1S/C29H41Cl3N4O10S/c1-17(2)22(36-23(38)21(14-47-16-33-18(3)37)35-27(42)46-28(4,5)6)25(40)43-13-20(24(39)45-15-29(30,31)32)34-26(41)44-12-19-10-8-7-9-11-19/h7-11,17,20-22H,12-16H2,1-6H3,(H,33,37)(H,34,41)(H,35,42)(H,36,38)/t20-,21+,22+/m1/s1 |
| InChIKey | HCUPPAXIQHIFPT-FSSWDIPSSA-N |
| Mol Weight | 744.1 g/mol |
| Molecular Formula | C29H41Cl3N4O10S |
| Exact Mass | 742.160898 g/mol |
| Enantiomer InChIKey | HCUPPAXIQHIFPT-BHDDXSALSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2R)-2-[[(2R)-3-(benzhydrylthio)-2-(tert-butoxycarbonylamino)propanoyl]amino]-3-methyl-butyric acid benzhydryl ester
Benzyl 5-[(benzyloxy)carbonyl]-11-[(benzylsulfanyl)methyl]-14-isopropyl-3,9,12-trioxo-1-phenyl-2-oxa-4,10,13-triazapentadecan-15-oate
IZKXRHITPSHNLI-MLNNCEHLSA-N
N-[N-(TERT.-BUTOXYCARBONYL)-L-PHENYLALANYL-(BETA-O-ACETYL)-L-SERYL]-O-TERT.-BUTYL-L-VALIN
L-Leucine, N-[N-[N-[N-[N-[(phenylmethoxy)carbonyl]-L-leucyl]-L-isoleucyl]-L-leuc yl]-L-isoleucyl]-, methyl ester
KMWAHPLEKFHROO-UHFFFAOYSA-N
BOC-PHE-CYS((O)ME)-SER(TERT.-BUTYL)-O(TERT.-BUTYL)
L-Leucine, N-[O-(1,1-dimethylethyl)-N-[N-[(phenylmethoxy)carbonyl]-L-.alpha.-glutamyl]-L-seryl]-, 5-(1,1-dimethylethyl) 1-methyl ester
N-{N-[N2-carboxy-N5-(nitroamidino)-L-ornithyl]-L-valyl}tyrosine, N-benzyl ester
N-(ALPHA)-(TERT.-BUTOXYCARBONYL)-O-(TERT.-BUTYL)-GLUTAMYL-O-(BENZYL)-SERYLLEUCINE-TERT.-BUTYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| Solution-Phase Synthesis of Nucleobase-Substituted Analogues of Triostin A | The Journal of Organic Chemistry | 2004 |