sPLA2 inhibitor 1

Modify Date: 2024-01-13 14:10:32

sPLA2 inhibitor 1 Structure
sPLA2 inhibitor 1 structure
Common Name sPLA2 inhibitor 1
CAS Number 393569-31-8 Molecular Weight 487.63
Density 1.1±0.1 g/cm3 Boiling Point 720.9±60.0 °C at 760 mmHg
Molecular Formula C31H37NO4 Melting Point N/A
MSDS USA Flash Point 389.8±32.9 °C

 Use of sPLA2 inhibitor 1


sPLA2 inhibitor 1, a D-tyrosine derivative, is an orally active, potent secretory phospholipase A2 (sPLA2) inhibitor with an IC50 of 29 nM for human nonpancreatic secretory PLA2 isoform IIa (hnpsPLA2-IIa). sPLA2 inhibitor 1 has anti-inflammatory activity[1].

 Names

Name KH064
Synonym More Synonyms

 sPLA2 inhibitor 1 Biological Activity

Description sPLA2 inhibitor 1, a D-tyrosine derivative, is an orally active, potent secretory phospholipase A2 (sPLA2) inhibitor with an IC50 of 29 nM for human nonpancreatic secretory PLA2 isoform IIa (hnpsPLA2-IIa). sPLA2 inhibitor 1 has anti-inflammatory activity[1].
Related Catalog
Target

sPLA2:29 nM (IC50)

In Vivo sPLA2 inhibitor 1 (compound 2b; oral; 5 mg/kg/day; on Days 10-13 after inoculation with arthritogen) shows substantial inhibition of the oedema. Drug-treated rats shows mild capsular oedema and minimal infiltration of macrophages into the red pulp[1].
References

[1]. Karl A Hansford, et al. D-Tyrosine as a chiral precusor to potent inhibitors of human nonpancreatic secretory phospholipase A2 (IIa) with antiinflammatory activity. Chembiochem. 2003 Mar 3;4(2-3):181-5.

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 720.9±60.0 °C at 760 mmHg
Molecular Formula C31H37NO4
Molecular Weight 487.63
Flash Point 389.8±32.9 °C
Exact Mass 487.272247
LogP 6.16
Vapour Pressure 0.0±2.4 mmHg at 25°C
Index of Refraction 1.573
Storage condition 2-8°C

 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

 Articles7

More Articles
Inhibitors of secretory phospholipase A2 group IIA.

Curr. Med. Chem. 12(25) , 3011-26, (2005)

Phospholipases A2 cleave membrane phospholipids to release arachidonic acid, the precursor to a large family of pro-inflammatory eicosanoids including prostaglandins and leukotrienes that have been pr...

Antifibrotic activity of an inhibitor of group IIA secretory phospholipase A2 in young spontaneously hypertensive rats.

J. Immunol. 176(11) , 7000-7, (2006)

The development of fibrosis in the chronically hypertensive heart is associated with infiltration of inflammatory cells and cardiac hypertrophy. In this study, an inhibitor of the proinflammatory enzy...

Group IIa secretory phospholipase expression correlates with group IIa secretory phospholipase inhibition-mediated cell death in K-ras mutant lung cancer cells.

J. Thorac. Cardiovasc. Surg. 144(6) , 1479-85, (2012)

There are currently no targeted therapies against lung tumors with oncogenic K-ras mutations that are found in 25% to -40% of lung cancers and are characterized by their resistance to epidermal growth...

 Synonyms

KH064
Benzenepentanoic acid, γ-[(1-oxo-7-phenylheptyl)amino]-4-(phenylmethoxy)-, (γS)-
MFCD06411576
sPLA2 inhibitor
(4S)-5-[4-(Benzyloxy)phenyl]-4-[(7-phenylheptanoyl)amino]pentanoic acid
5-(4-Benzyloxyphenyl)-4S-(7-phenylheptanoylamino)pentanoic acid
Top Suppliers:I want be here
  • DC Chemicals Limited
  • China
  • Product Name: KH064
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/500mg
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao


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