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CAS 5609-91-6

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5-bromo-4-chloro-3-indolyl-N-acetyl-B-D-glucosaminide

Description:
5-Bromo-4-chloro-3-indolyl-N-acetyl-β-D-glucosaminide, with the CAS number 5609-91-6, is a synthetic compound commonly used as a substrate in biochemical assays, particularly in the study of enzyme activity. This compound features an indole ring, which is known for its aromatic properties and biological significance, particularly in the context of tryptophan derivatives. The presence of bromine and chlorine substituents on the indole ring enhances its reactivity and specificity in enzymatic reactions. The N-acetyl-β-D-glucosaminide moiety contributes to its solubility and interaction with glycosyltransferases and other enzymes involved in carbohydrate metabolism. This compound is often utilized in microbiological studies, especially for detecting the activity of specific enzymes in bacterial cultures. Its structural characteristics allow it to serve as a chromogenic or fluorogenic substrate, facilitating the visualization of enzymatic activity through color change or fluorescence. Overall, 5-bromo-4-chloro-3-indolyl-N-acetyl-β-D-glucosaminide is a valuable tool in biochemical research and diagnostics.
Formula:C16H18BrClN2O6
InChI:InChI=1/C16H18BrClN2O6/c1-6(22)20-13-15(24)14(23)12(5-21)26-16(13)25-11-4-19-10-3-9(18)8(17)2-7(10)11/h2-4,12-16,19,21,23-24H,5H2,1H3,(H,20,22)/t12-,13-,14-,15-,16-/m1/s1
SMILES:CC(=N[C@@H]1[C@H]([C@@H]([C@@H](CO)O[C@H]1Oc1c[nH]c2cc(c(cc12)Br)Cl)O)O)O
Synonyms:
  • 5-Bromo-4-chloro-3-indolyl-N-acetyl-beta-D-glucosaminide
  • 5-Bromo-6-chloro-3-indoxyl-N-acetyl-beta-D-glucosaminide
  • 5-bromo-6-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-beta-D-glucopyranoside
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