#4;4-[5-[[2-[2-(4-AMINO-4-CARBOXYBUTANOYLAMINO)-2-(CARBOXYMETHYLCARBAMOYL)-ETHYLSULFANYL]-ETHYL]-(2-HYDROXYETHYL)-AMINO]-1-METHYL-1H-BENZOIMIDAZOL-2-YL]
Compound with spectra: 1 NMR
![#4;4-[5-[[2-[2-(4-AMINO-4-CARBOXYBUTANOYLAMINO)-2-(CARBOXYMETHYLCARBAMOYL)-ETHYLSULFANYL]-ETHYL]-(2-HYDROXYETHYL)-AMINO]-1-METHYL-1H-BENZOIMIDAZOL-2-YL]](/api/compound/EthJTnRaySD.png?ph=true&h=300&w=458 "#4;4-[5-[[2-[2-(4-AMINO-4-CARBOXYBUTANOYLAMINO)-2-(CARBOXYMETHYLCARBAMOYL)-ETHYLSULFANYL]-ETHYL]-(2-HYDROXYETHYL)-AMINO]-1-METHYL-1H-BENZOIMIDAZOL-2-YL]")
| SpectraBase Compound ID | EthJTnRaySD |
|---|---|
| InChI | InChI=1S/C26H38N6O9S/c1-31-20-7-5-16(13-18(20)29-21(31)3-2-4-23(35)36)32(9-11-33)10-12-42-15-19(25(39)28-14-24(37)38)30-22(34)8-6-17(27)26(40)41/h5,7,13,17,19,33H,2-4,6,8-12,14-15,27H2,1H3,(H,28,39)(H,30,34)(H,35,36)(H,37,38)(H,40,41)/t17-,19-/m0/s1 |
| InChIKey | DIAHDZATTOUFDG-HKUYNNGSSA-N |
| Mol Weight | 610.7 g/mol |
| Molecular Formula | C26H38N6O9S |
| Exact Mass | 610.242098 g/mol |
| Enantiomer InChIKey | DIAHDZATTOUFDG-IEBWSBKVSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
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#3;4-[5-[BIS-[2-[2-(4-AMINO-4-CARBOXYBUTANOYLAMINO)-2-(CARBOXYMETHYLCARBAMOYL)-ETHYLSULFANYL]-ETHYL]-AMINO]-1-METHYL-1H-BENZOIMIDAZOL-2-YL]-BUTANOIC-ACI
benzamide, 3,4,5-trimethoxy-N-[1-methyl-2-(4-morpholinylmethyl)-1H-benzimidazol-5-yl]-
benzamide, 3,4-dimethoxy-N-[1-methyl-2-(4-morpholinylmethyl)-1H-benzimidazol-5-yl]-
benzamide, 3,4,5-trimethoxy-N-[1-methyl-2-(1-piperidinylmethyl)-1H-benzimidazol-5-yl]-
benzamide, 3,4-dimethoxy-N-[1-methyl-2-(1-piperidinylmethyl)-1H-benzimidazol-5-yl]-
N-Pyrrolidino protonitazene
sec-Butonitazene
N-[1-[2-(Diethylamino)ethyl]-2-(4-ethoxybenzyl)-1H-benzimidazol-5-yl]acetamide
Clonitazene
N-(2-benzyl-1,2,3,4-tetrahydropyrazino[1,2-a]benzimidazol-8-yl)acetamide
| Title | Journal or Book | Year |
|---|---|---|
| Identification and Quantitation of theN-Acetyl-L-cysteineS-Conjugates of Bendamustine and Its Sulfoxides in Human Bile after Administration of Bendamustine Hydrochloride | Drug Metabolism and Disposition | 2008 |