CAS 97143-65-2

Formule : C17H22N2O2

InChI : InChI=1S/C17H22N2O2/c1-17(15-9-5-4-6-10-15,16-11-7-8-12-18-16)21-14-13-19(2,3)20/h4-12H,13-14H2,1-3H3

Code InChI : SSGKPGKMFJONCR-UHFFFAOYSA-N

SMILES : CC(C1=CC=CC=C1)(C2=CC=CC=N2)OCC[N+](C)(C)[O-]

Doxylamine N-Oxide

CAS : 97143-65-2

Compounds containing an unfused pyridine ring in the structure, nesoi

Formule : C₁₇H₂₂N₂O₂

Couleur et forme : Yellow Semi-Solid

Masse moléculaire : 286.16813

Ref: 45-1A07790

Doxylamine Aliphatic N-Oxide

CAS : 97143-65-2

Formule : C₁₇H₂₂N₂O₂

Couleur et forme : Pale Yellow Solid

Masse moléculaire : 286.38

Ref: 4Z-D-383

Doxylamine N-Oxide

CAS : 97143-65-2

Formule : C₁₇H₂₂N₂O₂

Masse moléculaire : 286.4

Ref: ST-EA-CP-D27005

Doxylamine N-Oxide

Produit contrôlé

CAS : 97143-65-2

Stability Hygroscopic
Applications A metabolite of Doxylamine (D562000).
References Luo, H., et al.: Xenobiotica, 21, 1281 (1991),

Formule : C₁₇H₂₂N₂O₂

Couleur et forme : Neat

Masse moléculaire : 286.369

Ref: TR-D562015

Doxylamine N-oxide

Produit contrôlé

CAS : 97143-65-2

Doxylamine N-oxide is a chemical compound that is synthetically derived from doxylamine and n-oxide. This drug has been shown to be highly active against gram-positive bacteria, such as Clostridium difficile. Doxylamine N-oxide appears to inhibit bacterial growth by binding to the bacterial enzyme dihydropteroate synthase, which is involved in folate synthesis. Doxylamine N-oxide also inhibits intestinal microflora and chloroformate profiles, which may be due to its effects on metabolic enzymes in the intestine. The chemical ionization mass technique was used in this study to show that doxylamine N-oxide binds to bacterial dna gyrase and dna topoisomerase I.

Formule : C₁₇H₂₂N₂O₂

Degré de pureté : Min. 95%

Masse moléculaire : 286.37 g/mol

Ref: 3D-FD22612