H6750
Hippuryl-Lys
Synonyme(s) :
N-Benzoyl-Gly-Lys
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A propos de cet article
Formule empirique (notation de Hill) :
C15H21N3O4
Numéro CAS:
Poids moléculaire :
307.34
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352204
MDL number:
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≥98% (TLC)
Quality Level
form
powder
solubility
water: 50 mg/mL, clear, colorless
storage temp.
−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
General description
Substrate for carboxypeptidase B and carboxypeptidase N.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| H6750-1G | 04061833801765 |