H-GLU-TYR-[SO2C6H4[4-(CO-A)]]-LEU-OBZL
Compound with spectra: 1 NMR
![H-GLU-TYR-[SO2C6H4[4-(CO-A)]]-LEU-OBZL](/api/compound/2hNhvYEn018.png?ph=true&h=300&w=458 "H-GLU-TYR-[SO2C6H4[4-(CO-A)]]-LEU-OBZL")
| SpectraBase Compound ID | 2hNhvYEn018 |
|---|---|
| InChI | InChI=1S/C44H50N8O14S/c1-24(2)18-32(44(60)63-20-26-6-4-3-5-7-26)51-41(58)31(50-40(57)30(45)16-17-34(53)54)19-25-8-12-28(13-9-25)66-67(61,62)29-14-10-27(11-15-29)43(59)64-21-33-36(55)37(56)42(65-33)52-23-49-35-38(46)47-22-48-39(35)52/h3-15,22-24,30-33,36-37,42,55-56H,16-21,45H2,1-2H3,(H,50,57)(H,51,58)(H,53,54)(H2,46,47,48)/t30-,31-,32+,33+,36+,37+,42+/m1/s1 |
| InChIKey | JXNSJXJAKABXRU-FIINVLNPSA-N |
| Mol Weight | 947.0 g/mol |
| Molecular Formula | C44H50N8O14S |
| Exact Mass | 946.316719 g/mol |
| Enantiomer InChIKey | JXNSJXJAKABXRU-RGNLWSJDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
ADENOSINE-5'-PHOSPHORO-AMINOBENZIMIDAZOLIDE
ADENYLYL-(2'->5')-ADENOSINE, ADENYLYL-(2'->5')ADENOSINE
P(1)-(6-HYDROXYMETHYLPTERIN)-P(2)-(5'-ADENOSYL)-DIPHOSPHATE;HP2A
Diphosphopyridine Nucleotide, reduced, disodium tetrahydrate
Benzamide, N-[9-[3-O-benzoyl-5-O-[(4-methoxyphenyl)diphenylmethyl]-.beta.-D-xylo furanosyl]-9H-purin-6-yl]-
N(6)-BENZOYL-5'-O-(4,4'-DIMETHOXYTRITYL)-2'-O-[2-[(N,N-DIMETHYLAMINO)-OXY]-ETHYL]-ADENOSINE
6-N-Benzoyl-9-[2-deoxy-3,5-O-di-p-nitrobenzoyl-.alpha.-d-ribosyl]adenine
ADENOSINE-5'-(7-DEOXY-L-GLYCERO-BETA-D-MANNO-HEPTOPYRANOSYL_DIPHOSPHATE)-BIS-(TRIETHYLAMINE)-SALT
[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3-benzoyloxy-4-[tert-butyl(dimethyl)silyl]oxy-tetrahydrofuran-2-yl]methyl benzoate
ADENOSINE 5'-DIPHOSPHATE, 5' TO 5'-ESTER WITH 3-CARBOXY-1,4-DIHYDRO-1-beta-D-RIBOFURANOSYLPYRIDINE, DISODIUM SALT, TRIHYDRATE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Modified Tripeptides and Tetrapeptides as potential bisubstrate inhibitors of the epidermal growth factor receptor protein tyrosine kinase | Helvetica Chimica Acta | 1997 |