H1763
Hippuryl-Gly-Gly
Synonym(s):
N-Benzoyl-Gly-Gly-Gly
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About This Item
Empirical Formula (Hill Notation):
C13H15N3O5
CAS Number:
Molecular Weight:
293.28
UNSPSC Code:
12352204
PubChem Substance ID:
MDL number:
InChI
1S/C13H15N3O5/c17-10(15-8-12(19)20)6-14-11(18)7-16-13(21)9-4-2-1-3-5-9/h1-5H,6-8H2,(H,14,18)(H,15,17)(H,16,21)(H,19,20)
SMILES string
OC(=O)CNC(=O)CNC(=O)CNC(=O)c1ccccc1
InChI key
CYQZRSVDAIOAIY-UHFFFAOYSA-N
assay
≥99% (HPLC)
form
powder
solubility
1 M NH4OH: 50 mg/mL, clear, colorless
storage temp.
−20°C
General description
Substrate for angiotensin converting enzyme (ACE)
Regulatory Information
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Simple radioassay for measuring serum activity of angiotensin-converting enzyme in sarcoidosis.
P K Rohatgi et al.
Chest, 78(1), 69-76 (1980-07-01)
T A Stewart et al.
Peptides, 2(2), 145-152 (1981-01-01)
We purified peptidyl-dipeptidase (converting enzyme, EC 3.4.15.1) to homogeneity from the membrane fraction of human lung and for comparison, from human and hog kidney. The membrane-bound lung enzyme was purified 1800-fold with 19% yield, and the kidney enzyme 640-fold with
L Mor et al.
Journal of pharmacological methods, 23(2), 141-153 (1990-04-01)
We have developed a pressure-dependent isolated lung perfusion system that can be used for the determination of pulmonary enzyme activity and kinetics under physiologic conditions. This development was done using two different artificial radiolabeled substrates, glycine-1-hippuryl-L-histidyl-L-leucine and phenyl-4(n)-hippuryl-glycyl-glycine, for the
J M Jarmey et al.
Insect biochemistry and molecular biology, 25(9), 969-974 (1995-10-01)
A protein, Bm91, which was first identified as a protective vaccine antigen from the tick Boophilus microplus, has regions of very strong amino acid sequence similarity to mammalian carboxydipeptidases or angiotensin converting enzymes (ACE; E.C. 3.4.15.1). This protein is now
H M Neels et al.
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde, 187(2), 129-132 (1983-01-01)
Angiotensin I converting enzyme (ACE) was studied in Vero cells, rabbit corneal fibroblasts, and rabbit corneal endothelial cells. The enzyme activity was determined by means of an assay employing hippuryl-glycyl-glycine as a substrate. The hippuric acid end product was separated
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