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Merck
모든 사진(1)

문서

H6750

Sigma-Aldrich

Hippuryl-Lys

동의어(들):

N-Benzoyl-Gly-Lys

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About This Item

실험식(Hill 표기법):
C15H21N3O4
CAS Number:
Molecular Weight:
307.34
MDL number:
UNSPSC 코드:
12352204
PubChem Substance ID:
NACRES:
NA.32

분석

≥98% (TLC)

형태

powder

solubility

water: 50 mg/mL, clear, colorless

저장 온도

−20°C

SMILES string

NCCCCC(NC(=O)CNC(=O)c1ccccc1)C(O)=O

InChI

1S/C15H21N3O4/c16-9-5-4-8-12(15(21)22)18-13(19)10-17-14(20)11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10,16H2,(H,17,20)(H,18,19)(H,21,22)

InChI key

LRCZLURYHGISRZ-UHFFFAOYSA-N

기질

Substrate for carboxypeptidase B and carboxypeptidase N.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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문서 라이브러리 방문

A A Lavras et al.
Acta physiologica latino americana, 30(4), 269-274 (1980-01-01)
Evidence is presented to suggest that kininase activity of Bothrops jararaca plasma is due to the presence of at least three distinct enzymes: a carboxypeptidase B type enzyme, similar to that found in human plasma in that its activity is
Andreas Natsch et al.
Chemical research in toxicology, 23(12), 1913-1920 (2010-09-28)
(E)-4-(ethoxymethylene)-2-phenyloxazol-5(4H)-one, commonly referred to as oxazolone, is the most potent skin sensitizer in published databases as determined with the murine local lymph node assay. It has been used very widely in immunological research to induce and elicit skin sensitization reactions
R J Edwards et al.
The Biochemical journal, 221(2), 465-470 (1984-07-15)
The effect of partially purified 'creatine kinase conversion factor' on rabbit muscle creatine kinase is shown to be that of a carboxypeptidase, removing the C-terminal lysine residue from both subunits. These changes fully explain the three-banded electrophoretic patterns of the
F Marceau et al.
Journal of chromatography, 266, 173-177 (1983-08-26)
A rapid and sensitive method for measuring carboxypeptidase N (CPN) activity in human plasma is described. The procedure is based on the hydrolysis of a high-specificity/low-affinity substrate, hippuryl-L-lysine, to its products hippuric acid and lysine. The substrate and product are
Koichi Itakura et al.
Chemistry and physics of lipids, 124(2), 81-88 (2003-06-24)
2-Hydroxyheptanal (2-HH) is one of the major aldehydes derived from peroxidation of polyunsaturated fatty acids. In the present study, to obtain an insight into the contributions of 2-HH to protein modifications during lipid peroxidation, a lysine-containing dipeptide, N(alpha)-hippuryllysine (N-benzoylglycyl-L-lysine, BGL)

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