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Merck
CN

H4884

Hippuryl-His-Leu acetate salt

≥98% (HPLC), angiotensin converting enzyme substrate, powder

Synonym(s):

N-Benzoyl-Gly-His-Leu

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About This Item

Empirical Formula (Hill Notation):
C21H27N5O5
CAS Number:
Molecular Weight:
429.47
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.32
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Product Name

Hippuryl-His-Leu acetate salt,

assay

≥98% (HPLC)

Quality Level

form

powder

solubility

acetic acid: 50 mg/mL, clear, colorless to very faintly yellow

storage temp.

−20°C

SMILES string

CC(O)=O.CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)CNC(=O)c2ccccc2)C(O)=O

InChI

1S/C21H27N5O5.C2H4O2/c1-13(2)8-17(21(30)31)26-20(29)16(9-15-10-22-12-24-15)25-18(27)11-23-19(28)14-6-4-3-5-7-14;1-2(3)4/h3-7,10,12-13,16-17H,8-9,11H2,1-2H3,(H,22,24)(H,23,28)(H,25,27)(H,26,29)(H,30,31);1H3,(H,3,4)/t16-,17-;/m0./s1

InChI key

NSEVQQKNHZCIKL-QJHJCNPRSA-N

Gene Information

Biochem/physiol Actions

Substrate for angiotensin converting enzyme.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

常规特殊物品

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Lucas Actis-Goretta et al.
FEBS letters, 555(3), 597-600 (2003-12-17)
It was determined that flavan-3-ols and procyanidins have an inhibitory effect on angiotensin I converting enzyme (ACE) activity, and the effect was dependent on the number of epicatechin units forming the procyanidin. The inhibition by flavan-3-ols and procyanidins was competitive
Neha Chaudhary et al.
Journal of food science and technology, 57(4), 1371-1381 (2020-03-18)
Controlled release of Emblicanin rich water soluble extract of Emblica officinalis (EEO) from the inner phase of water-in-oil-in-water type double emulsion (DE), during in vitro digestion and phagocytosis was investigated. It was observed that release of EEO (measured as total polyphenols
Mammalian Genome null



Global Trade Item Number

SKUGTIN
H4884-100MG04061833796405
H4884-1G04061833796412
H4884-25MG04061833796450
H4884-500MG04061833796467