Elastatinal

Modify Date: 2024-01-02 18:20:34

Elastatinal Structure
Elastatinal structure
Common Name Elastatinal
CAS Number 51798-45-9 Molecular Weight 512.56
Density 1.44 g/cm3 Boiling Point N/A
Molecular Formula C21H36N8O7 Melting Point N/A
MSDS Chinese USA Flash Point N/A

 Use of Elastatinal


Elastatinal is a potent and competitive inhibitor of elastase, with a Ki of 0.21 μM. Elastatinal more potently inhibits pancreatic elastase versus leucocyte elastase. Elastatinal shows no activity on human leucocyte chymotrypsin-like protease[1][2][3][4].

 Names

Name elastatinal
Synonym More Synonyms

 Elastatinal Biological Activity

Description Elastatinal is a potent and competitive inhibitor of elastase, with a Ki of 0.21 μM. Elastatinal more potently inhibits pancreatic elastase versus leucocyte elastase. Elastatinal shows no activity on human leucocyte chymotrypsin-like protease[1][2][3][4].
Related Catalog
In Vitro Elastatinal inhibits the binding of acetyl-alanyl-alanyl-alanine pnitroanilide and acetyl-alanyl-alanyl-alanine methyl ester to elastase, with Kis of 0.24 μM and 0.21 μM, respectively[1]. Elastatinal (5-20 μM) suppresses the enhanced osteoclast differentiation by neutrophils[3].
References

[1]. Umezawa H. Structures and activities of protease inhibitors of microbial origin. Methods Enzymol. 1976;45:678-95.

[2]. Feinstein G, et, al. The inhibition of human leucocyte elastase and chymotrypsin-like protease by elastatinal and chymostatin. Biochim Biophys Acta. 1976 May 13;429(3):925-32.

[3]. Sugisaki R, et, al. Possible involvement of elastase in enhanced osteoclast differentiation by neutrophils through degradation of osteoprotegerin. Bone. 2020 Mar;132:115216.

[4]. Vidhya R, et, al. Anti-inflammatory effects of troxerutin are mediated through elastase inhibition. Immunopharmacol Immunotoxicol. 2020 Oct;42(5):423-435.

 Chemical & Physical Properties

Density 1.44 g/cm3
Molecular Formula C21H36N8O7
Molecular Weight 512.56
Exact Mass 496.27600
PSA 224.47000
LogP 0.62920
Index of Refraction 1.635
Storage condition −20°C
Water Solubility H2O: 20 mg/mL, clear, yellow

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
LZ9600000
CHEMICAL NAME :
L-Glutamamide, L-2-(2-amino-1,4,5,6-tetrahydro-4-pyrimidinyl-N-(((1- carboxy-3-methylbutyl) amino)carbonyl)glycyl-N(sup 1)-(1-methyl-2-oxoethyl)-, stereoisomer
CAS REGISTRY NUMBER :
51798-45-9
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C21-H36-N8-O7
MOLECULAR WEIGHT :
512.65

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>250 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
PPTCBY Proceedings of the International Symposium of the Princess Takamatsu Cancer Research Fund. (Japan Scientific Soc. Press, 6-2-10 Hongo, Bunkyo-ku, Tokyo 113, Japan) 1st- 1971- Volume(issue)/page/year: 6,57,1976

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS LZ9600000

 Preparation

51798-45-9 preparation

 Articles18

More Articles
Elastatinal and leupeptin: effects on u.v.-induced mutation and sister-chromatid exchanges in Chinese hamster cells.

Carcinogenesis 2(4) , 255-9, (1981)

Microbial protease inhibitors elastatinal and leupeptin were tested for cytotoxicity and for effects on spontaneous and u.v.-induced 6-thioguanine-resistant (6TGr) mutation and sister-chromatid exchan...

Reduction of active elastase concentration by means of immobilized inhibitors: a novel therapeutic approach.

Biotechnol. Prog. 20(3) , 968-74, (2004)

The inhibitory power of three different active Nylon membranes, separately loaded with three different protease inhibitors, was studied with the aim of reducing the increased elastase concentration oc...

Effects of inhibitors of membrane signal peptide peptidase on protein translocation into membrane vesicles.

Arch. Microbiol. 153(1) , 90-4, (1989)

The effect of the removal of signal peptides after cleavage of precursor molecules by the signal peptidase I was examined in an in vitro translocation system with Escherichia coli membrane vesicles. T...

 Synonyms

elastatinal from microbial source
Leu-co-cpd-Gln-Ala-h
Elastatinal
EINECS 257-426-7
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