52333-78-5 Usage
Chemical class
Oxazolo[4,5-b]pyridine
Type of compound
Heterocyclic compound
Structure
Pyridine ring fused to an oxazole ring, with a hydroxyphenyl group attached to the nitrogen atom of the oxazole ring
Biological activities
Potential applications in medicinal chemistry
Uses
Building block for the synthesis of pharmaceuticals, potential therapeutic agent for various medical conditions
Research interest
Unique structure and properties, making it an interesting target for further research and development in pharmaceuticals and medicinal chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 52333-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,3 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52333-78:
(7*5)+(6*2)+(5*3)+(4*3)+(3*3)+(2*7)+(1*8)=105
105 % 10 = 5
So 52333-78-5 is a valid CAS Registry Number.
52333-78-5Relevant articles and documents
Chiral 3-(4,5-dihydrooxazol-2-yl)phenyl alkylcarbamates as novel FAAH inhibitors: Insight into FAAH enantioselectivity by molecular docking and interaction fields
Myllymaeki, Mikko J.,Kaesnaenen, Heikki,Kataja, Antti O.,Lahtela-Kakkonen, Maija,Saario, Susanna M.,Poso, Antti,Koskinen, Ari M.P.
experimental part, p. 4179 - 4191 (2009/12/04)
Fatty acid amide hydrolase (FAAH) and monoglyceride lipase (MGL) are the main enzymes responsible for the hydrolysis of endogenous cannabinoids N-arachidonoylethanolamide (AEA) and 2-arachidonoylglycerol (2-AG), respectively. Phenyl alkylcarbamates are FA
Anti-inflammatory oxazole[4,5-b]pyridines
-
, (2008/06/13)
The various isomers of oxazolo- and thiazolopyridines having utility as antiinflammatory, antipyretic and analgesic agents are prepared by condensation of an appropriate amino-hydroxypyridine or amino-mercaptopyridine with a carboxylic acid, halide or anhydride.
