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194301

6-Acetamidohexanoic acid

Name: 6-Acetamidohexanoic acid
Brand: ALDRICH

99%

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About This Item

Linear Formula:

CH₃CONH(CH₂)₅CO₂H

CAS Number:

57-08-9

Molecular Weight:

173.21

EC Number:

200-310-8

MDL number:

MFCD00004424

UNSPSC Code:

12352200

PubChem Substance ID:

24851643

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assay

99%

mp

102-104 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(=O)NCCCCCC(O)=O

InChI

1S/C8H15NO3/c1-7(10)9-6-4-2-3-5-8(11)12/h2-6H2,1H3,(H,9,10)(H,11,12)

InChI key

WDSCBUNMANHPFH-UHFFFAOYSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Nuclear magnetic resonance (NMR) solution structure, dynamics, and binding properties of the kringle IV type 8 module of apolipoprotein(a).

Seth Chitayat et al.

Biochemistry, 46(7), 1732-1742 (2007-02-01)

The plasma lipoprotein lipoprotein(a) [Lp(a)] comprises a low-density lipoprotein (LDL)-like particle covalently attached to the glycoprotein apolipoprotein(a) [apo(a)]. Apo(a) consists of multiple tandem repeating kringle modules, similar to plasminogen kringle IV (designated KIV1-KIV10), followed by modules homologous to the kringle

[A multicenter clinical trial. Zinc acexamate versus famotidine in the treatment of acute duodenal ulcer. Study Group of Zinc acexamate (new UP doses)].

A García-Plaza et al.

Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva, 88(11), 757-762 (1996-11-01)

A multicentric double-blind trial comparing 600 mg/d of Zinc Acexamate (ACZ) and 40 mg/d of Famotidine (FMT) in the short term treatment of acute duodenal ulcer included 199 patients, diagnosed by endoscopy. One-hundred and five patients received ACZ and 94

Gastrotoxic activity and inhibitory effects on gastric mucosal PGE2 production with different non-steroidal anti-inflammatory drugs: modifications induced by pretreatment with zinc acexamate.

C Navarro et al.

Prostaglandins, leukotrienes, and essential fatty acids, 50(6), 305-310 (1994-06-01)

Gastrotoxic activities of different non-steroidal anti-inflammatory drugs (NSAIDs) (diclofenac, indomethacin, ketoprofen, naproxen and piroxicam) administered per os were compared with their ability to inhibit gastric prostaglandin E2 (PGE2) synthesis in the rat. In a parallel study, effects of pretreatment with

Allergic contact dermatitis to acexamic acid.

Ana Margarida Soares Reis et al.

Contact dermatitis, 58(4), 241-242 (2008-03-21)

Pharmacokinetic interaction between ϵ-acetamidocaproic acid (AACA) and cimetidine in indomethacin-induced acute gastric ulcer and control rats: inhibition of active renal secretion of AACA by cimetidine.

Y H Choi et al.

Xenobiotica; the fate of foreign compounds in biological systems, 41(5), 409-415 (2011-01-22)

After both the intravenous and oral administration of zinc acexamate [ZAC; ion-pairing between zinc and ϵ-acetamidocaproic acid (AACA)] and cimetidine together, the areas under the curve (AUCs) of AACA were significantly greater [by 28.2 and 98.9% after the intravenous and

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