04304
9-(Hydroxymethyl)-10-carbamoylacridan
analytical standard
别名:
9-HMCA, 9-OH-CBZ, 9-(Hydroxymethyl)-10(9H)-acridinecarboxamide
等级
analytical standard
质量水平
方案
≥98.0% (HPLC)
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
应用
pharmaceutical
包装形式
neat
储存温度
2-8°C
SMILES字符串
NC(N1C2=CC=CC=C2C(CO)C3=C1C=CC=C3)=O
InChI
1S/C15H14N2O2/c16-15(19)17-13-7-3-1-5-10(13)12(9-18)11-6-2-4-8-14(11)17/h1-5,7-8,18H,6,9H2,(H2,16,19)
InChI key
UMRKOEWAECPINL-UHFFFAOYSA-N
其他说明
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
9-Hydroxymethyl-10-carbamoylacridan in human serum is one of the major metabolites of carbamazepine
Seiji ETO, et al.
Biological & Pharmaceutical Bulletin, 18(6), 926-928 (1995)
The metabolism of carbamazepine in humans: steric course of the enzymic hydrolysis of the 10, 11-epoxide
Bellucci G, et al.
Journal of Medicinal Chemistry, 30(5), 768-773 (1987)
Arnold Bahlmann et al.
Water research, 57, 104-114 (2014-04-08)
The occurrence of carbamazepine (CBZ) and its metabolites in German and Portuguese wastewater was investigated. A total of 46 samples from influent and effluent wastewater were analyzed by liquid-chromatography (LC) tandem mass spectrometry. The five metabolites 10,11-dihydro-10,11-dihydroxy-CBZ (DiOH-CBZ), 10,11-dihydro-10-hydroxy-CBZ (10-OH-CBZ)
G Bellucci et al.
Journal of medicinal chemistry, 30(5), 768-773 (1987-05-01)
Carbamazepine 10,11-oxide (1a,10b-dihydro-6H-dibenzo[b,f]oxireno[d]azepine-6-carboxamide), a key intermediate in carbamazepine metabolism, was found to be unusually resistant to enzymatic hydrolysis when incubated with microsomal and cytosolic fractions from rabbit, rat, and guinea pig livers. However, its hydrolysis product, trans-10,11-dihydro-10,11-dihydroxy-5H-dibenzo[b,f]azepine-5-carboxamide , was excreted
Carbamazepine: detection of another metabolite in serum, 9 hydroxymethyl-10-carbamoyl acridan
Wad N, et al.
Therapeutic Drug Monitoring, 19(3), 314-317 (1997)
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