H-GLU-TYR-[SO2C6H3(3-OH)[4-(CO-A)]]-LEU-OBZL
Compound with spectra: 1 NMR
![H-GLU-TYR-[SO2C6H3(3-OH)[4-(CO-A)]]-LEU-OBZL](/api/compound/BrzROsDu2L6.png?ph=true&h=300&w=458 "H-GLU-TYR-[SO2C6H3(3-OH)[4-(CO-A)]]-LEU-OBZL")
| SpectraBase Compound ID | BrzROsDu2L6 |
|---|---|
| InChI | InChI=1S/C44H50N8O15S/c1-23(2)16-31(44(61)64-19-25-6-4-3-5-7-25)51-41(59)30(50-40(58)29(45)14-15-34(54)55)17-24-8-10-26(11-9-24)67-68(62,63)27-12-13-28(32(53)18-27)43(60)65-20-33-36(56)37(57)42(66-33)52-22-49-35-38(46)47-21-48-39(35)52/h3-13,18,21-23,29-31,33,36-37,42,53,56-57H,14-17,19-20,45H2,1-2H3,(H,50,58)(H,51,59)(H,54,55)(H2,46,47,48)/t29-,30-,31+,33+,36+,37+,42+/m1/s1 |
| InChIKey | BITXXFHNBUMJRQ-RGCWJYPFSA-N |
| Mol Weight | 963.0 g/mol |
| Molecular Formula | C44H50N8O15S |
| Exact Mass | 962.311634 g/mol |
| Enantiomer InChIKey | BITXXFHNBUMJRQ-GWNKUZHYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
IYEVZTRKGVWIIK-IQZMFCRQSA-N
DIHYDRONICOTINAMIDE-ADENIN-DINUCLEOTIDE
NICOTINAMIDE-ADENIN-DINUCLEOTIDE;NADH
6-N-ACETYL-6-N-ALLYL-2',3',5'-TRIS-O-(tert-BUTYL-DIMETHYLSILYL)-ADENOSINE
2'-O-TERT.-BUTYL-DIMETHYLSILYL-5'-O-PARA-METHOXYTRITYL-ADENOSINE-DIETHYL-3'-PHOSPHATE
(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(6-(furan-3-ylmethylamino)-9H-purin-9-yl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
4-[[(1S,3R,6R,8R,9R)-8-(6-aminopurin-9-yl)-9-hydroxy-3-keto-2,4,7-trioxa-3$l^{5}-phosphabicyclo[4.3.0]nonan-3-yl]oxymethyl]-6-methoxy-coumarin
6-N-BENZOYL-2',3',5'-TRIS-O-tert-BUTYL-DIMETHYLSILYL-6-N-METHYL-ADENOSINE
2-AMINO-9-[5_DIASTEREOMER2,3-DI-O-METHANESULFONYL-BETA-D-RIBOFURANOSYL]-6-METHOXYPURINE
2',3',5'-TRIS-O-tert-BUTYL-DIMETHYLSILYL-6-N-(2,2,2-TRICHLORO-1,1-DIMETHYL-ETHOXYCARBONYL)-6-N-METHYL-ADENOSINE
| 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 |