CAS 3395-37-7

3-[[2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl]oxy]-7-bromo-N-(2-methoxyphenyl)-2-naphthalenecarboxamide

Description:

The chemical substance known as 3-[[2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl]oxy]-7-bromo-N-(2-methoxyphenyl)-2-naphthalenecarboxamide, with the CAS number 3395-37-7, is a complex organic compound characterized by its multi-functional structure. It features a naphthalene core substituted with a bromine atom and an amide group, which contributes to its potential biological activity. The presence of a glucopyranosyl moiety indicates that it is a glycoside, which may influence its solubility and interaction with biological systems. The acetylamino group enhances its stability and may affect its pharmacokinetic properties. This compound is likely to exhibit specific interactions with biological targets, making it of interest in medicinal chemistry and drug development. Its structural complexity suggests potential applications in areas such as cancer research or as an antimicrobial agent, although specific biological activities would require empirical investigation. Overall, the unique combination of functional groups and structural features positions this compound as a candidate for further study in pharmaceutical applications.

Formula: C₂₆H₂₇BrN₂O₈

InChI: InChI=1S/C26H27BrN2O8/c1-13(31)28-22-24(33)23(32)21(12-30)37-26(22)36-20-11-14-7-8-16(27)9-15(14)10-17(20)25(34)29-18-5-3-4-6-19(18)35-2/h3-11,21-24,26,30,32-33H,12H2,1-2H3,(H,28,31)(H,29,34)/t21-,22-,23-,24-,26-/m1/s1

InChI key: InChIKey=DMLKUPXKUQREOC-CFXNPWLASA-N

SMILES: C(NC1=C(OC)C=CC=C1)(=O)C=2C(O[C@H]3[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](CO)O3)=CC4=C(C2)C=C(Br)C=C4

Synonyms:

• 2-Naphth-o-anisidide, 3-[(2-acetamido-2-deoxy-β-<span class="text-smallcaps">D</span>-glucopyranosyl)oxy]-7-bromo-
• 2-Naphthalenecarboxamide, 3-[[2-(acetylamino)-2-deoxy-β-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]-7-bromo-N-(2-methoxyphenyl)-
• 3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-7-bromo-N-(2-methoxyphenyl)naphthalene-2-carboxamide
• 3-[[2-(Acetylamino)-2-deoxy-β-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]-7-bromo-N-(2-methoxyphenyl)-2-naphthalenecarboxamide
• Glucopyranoside, 6-bromo-3-[(o-methoxyphenyl)carbamoyl]-2-naphthyl 2-acetamido-2-deoxy-+, β-<span class="text-smallcaps">D</span>-
• 2-Naphthalenecarboxamide, 3-[[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]oxy]-7-bromo-N-(2-methoxyphenyl)-
• Glucopyranoside, 6-bromo-3-[(o-methoxyphenyl)carbamoyl]-2-naphthyl 2-acetamido-2-deoxy-+, β-D-
• 3-[[2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl]oxy]-7-bromo-N-(2-methoxyphenyl)-2-naphthalenecarboxamide
• 2-Naphth-o-anisidide, 3-[(2-acetamido-2-deoxy-β-D-glucopyranosyl)oxy]-7-bromo-

Naphthol AS-BI N-acetyl-β-D-glucosaminide

CAS: 3395-37-7

Formula: C₂₆H₂₇BrN₂O₈

Purity: 97%

Molecular weight: 575.4052

Ref: IN-DA00C8SL

Naphthol AS-BI N-acetyl-β-D-glucosaminide

CAS: 3395-37-7

Ref: 7W-GC1035

Naphthol AS-BI N-acetyl-beta-D-glucosaminide

CAS: 3395-37-7

Naphthol AS-BI N-acetyl-beta-D-glucosaminide is a fluorogenic substrate for the pararosaniline-glyoxalase (PG) reaction. This substrate is used to study enzymatic activity in two human isoenzymes of PG, PG I and PG II. The conversion of this substrate by PG I or PG II results in a color change from yellow to red. Naphthol AS-BI N-acetyl-beta-D-glucosaminide may be used as an experimental tool to measure the activity of these enzymes and to study the effect of inhibitors on their activity. It can also be used as a marker for studying enzyme transfer between cells.

Formula: C₂₆H₂₇BrN₂O₈

Purity: Min. 97.0 Area-%

Molecular weight: 575.42 g/mol

Ref: 3D-N-2001

Naphthol AS-BI N-acetyl-β-D-glucosaminide

Controlled Product

CAS: 3395-37-7

Formula: C₂₆H₂₇BrN₂O₈

Color and Shape: Neat

Molecular weight: 575.40

Ref: TR-N339530