2-Chloro-4-nitrophenyl-α-D-glucopyranoside

For research use only. Not for therapeutic Use.

  • CAT Number: R000811
  • CAS Number: 119047-14-2
  • Molecular Formula: C12H14ClNO8
  • Molecular Weight: 335.693
  • Purity: ≥95%
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Carbohydrates conjugated with 2-<wbr></wbr>chloro-<wbr></wbr>4-<wbr></wbr>nitrophenyl (CNP) serve as chromogenic substrates in assays for enzymes that release CNP from the conjugated carbohydrate. For example, CNP-<wbr></wbr>β-<wbr></wbr>D-<wbr></wbr>maltoheptaoside and CNP-α-<wbr></wbr>maltotrioside are chromogenic substrates for α-<wbr></wbr>amylase. 2-<wbr></wbr>Chloro-<wbr></wbr>4-<wbr></wbr>nitrophenyl-<wbr></wbr>α-<wbr></wbr>D-<wbr></wbr>glucopyranoside is a conjugate of CNP and α-<wbr></wbr>D-<wbr></wbr>glucose. The related conjugate between CNP and β-<wbr></wbr>D-<wbr></wbr>glucose, 2-<wbr></wbr>chloro-<wbr></wbr>4-<wbr></wbr>nitrophenyl β-<wbr></wbr>D-<wbr></wbr>glucopyranoside, is used as a chromogenic substrate for glycosyltransferases. This product is a chromogenic substrate for enzymes that target the linkage between CNP and α-<wbr></wbr>D-<wbr></wbr>glucose.


Catalog Number R000811
CAS Number 119047-14-2
Synonyms

CNP-α-D-glucopyranoside

Molecular Formula C12H14ClNO8
Purity ≥95%
Storage -20°C
IUPAC Name (2R,3R,4S,5S,6R)-2-(2-chloro-4-nitrophenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
InChI InChI=1S/C12H14ClNO8/c13-6-3-5(14(19)20)1-2-7(6)21-12-11(18)10(17)9(16)8(4-15)22-12/h1-3,8-12,15-18H,4H2/t8-,9-,10+,11-,12+/m1/s1
InChIKey PJCVBKZRKNFZOD-ZIQFBCGOSA-N
SMILES C1=CC(=C(C=C1[N+](=O)[O-])Cl)OC2C(C(C(C(O2)CO)O)O)O

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