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Merck
CN

A178

醋磺己脲

analytical standard, ≥98% (HPLC)

别名:

4-乙酰基-N-[(环己胺基)羰基]苯磺酰胺

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关于此项目

经验公式(希尔记法):
C15H20N2O4S
化学文摘社编号:
分子量:
324.40
UNSPSC Code:
41116107
PubChem Substance ID:
EC Number:
213-530-4
MDL number:
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InChI key

VGZSUPCWNCWDAN-UHFFFAOYSA-N

InChI

1S/C15H20N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-10,13H,2-6H2,1H3,(H2,16,17,19)

SMILES string

CC(=O)c1ccc(cc1)S(=O)(=O)NC(=O)NC2CCCCC2

grade

analytical standard

assay

≥98% (HPLC)

form

solid

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

color

white

solubility

DMSO: ~45 mg/mL, H2O: insoluble

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

Quality Level

Gene Information

Application

Acetohexamide may be used as a reference standard for the determination of acetohexamide in presence of 1-methylnicotinamide reagent in plasma sample and tablet formulations by spectrofluorimetry method.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem/physiol Actions

口服降血糖药

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Hibah Aldawsari et al.
International journal of pharmaceutics, 453(2), 315-321 (2013-06-26)
A new polymorph of acetohexamide (Form VI) was prepared via the formation of a complex with 2-hydoxybutyl-β-cyclodextrin (HB-β-CD) in aqueous solution. An alkaline solution of acetohexamide and HB-β-CD was adjusted to pH 4.0 by titration with hydrochloric acid. The resulting
Y Imamura et al.
Journal of biochemistry, 121(4), 705-710 (1997-04-01)
The structural requirements of acetohexamide reductases purified from rabbit liver, kidney, and heart for substrates and inhibitors were examined. Acetohexamide, an oral antidiabetic drug with a ketone group, and analogs of it with various alkyl groups instead of the cyclohexyl
H Koyama et al.
Biopharmaceutics & drug disposition, 18(9), 791-801 (1998-01-16)
The binding properties of hypoglycaemic drugs to glycosylated human serum albumin (G-HSA) were investigated using a fluorescence quenching method. Displacement patterns between tolbutamide and Sudlow's-site-specific drugs to G-HSA were also investigated. The order of the binding affinities of these drugs
Hideaki Shimada et al.
Archives of toxicology, 76(1), 8-12 (2002-03-05)
Administration of cadmium (Cd) at a dose of 1.23 mg/kg (2.0 mg/kg as CdCl(2)) markedly decreased the activity of an enzyme (acetohexamide reductase) catalysing the ketone-reduction of acetohexamide, an oral antidiabetic drug, in liver microsomes of male rats. However, the
Zenghan Tong et al.
Journal of chromatography. A, 1218(49), 8915-8924 (2011-05-27)
This study examined the use of frontal analysis and high-performance affinity chromatography for detecting heterogeneous binding in biomolecular interactions, using the binding of acetohexamide with human serum albumin (HSA) as a model. It was found through the use of this

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