CAY10590

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CAS:1101136-50-8
Purity:98% Package:1G;10G;100G Remarks:Phospholipase A2 (PLA2) catalyzes the hydrolysis of fatty acids at the sn-2 position of glycerophospholipids, liberating arachidonic acid for subsequent eicosanoid synthesis. There are three primary t
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CAS:1101136-50-8
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CAS:1101136-50-8
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CAS:1101136-50-8
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
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Products Intro: Product Name:CAY10590
CAS:1101136-50-8
Package:50mg/RMB 19600;10mg/RMB 4950;5mg/RMB 2810
CAY10590 Basic information
Product Name:CAY10590
Synonyms:CAY10590;4-[(1-Oxo-7-phenylheptyl)amino]-(4R)-octanoic acid;ANTPELWBOPVWPH-LJQANCHMSA-N;Octanoic acid, 4-[(1-oxo-7-phenylheptyl)amino]-, (4R)-
CAS:1101136-50-8
MF:C21H33NO3
MW:347.49
EINECS:
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Mol File:1101136-50-8.mol
CAY10590 Structure
CAY10590 Chemical Properties
Melting point 73-75 °C(Solv: ethyl acetate (141-78-6); ligroine (8032-32-4))
Boiling point 567.8±43.0 °C(Predicted)
density 1.028±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMF: 25 mg/ml; DMSO: 20 mg/ml; Ethanol: 30 mg/ml
form A crystalline solid
pka4.60±0.10(Predicted)
color White to off-white
Safety Information
MSDS Information
CAY10590 Usage And Synthesis
DescriptionPhospholipase A2 (PLA2) catalyzes the hydrolysis of fatty acids at the sn-2 position of glycerophospholipids, liberating arachidonic acid for subsequent eicosanoid synthesis.1 Three primary types of PLA2 exist: secretory (sPLA2), calcium-dependent cytosolic (cPLA2), and calcium-independent cytosolic (iPLA2).2 Of these three enzymes, cPLA2 is the rate-limiting stimulus for release of arachidonic acid whereas sPLA2 amplifies the action of cPLA2 and regulates phagocytosis and foam cell formation.3 CAY10590, a simple amide based on (R)-γ-norleucine, is a potent and selective inhibitor of sPLA2. It exhibits 95% inhibition (XI(50) = 0.003) of sPLA2 at 0.091 mole fraction without affecting the activities of cPLA2 or iPLA2.4
References1. Dennis, E.A. Phospholipases The Enzymes XVI,(1983).
2. Dennis, E.A. Diversity of group types, regulation, and function of phospholipase A2 J. Biol. Chem. 269,13057-13060(1994).
3. Balestrieri, B., and Arm, J.P. Group V sPLA2: Classical and novel functions Biochim. Biophys. Acta 1761,1280-1288(2006).
4. Antonopoulou, G., Barbayianni, E., Magrioti, V., et al. Structure-activity relationships of natural and non-natural amino acid-based amide and 2-oxoamide inhibitors of human phospholipase A2 enzymes Bioorg. Med. Chem. 16,10257-10269(2008).
CAY10590 Preparation Products And Raw materials
Raw materialsOctanoic acid, 4-[(1-oxo-7-phenylheptyl)amino]-, ethyl ester, (4R)-
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