37795-71-4 Usage
Description
2,3-dihydro-3-methyl-9H-isoxazolo[3,2-b]quinazolin-9-one is a complex heterocyclic chemical compound belonging to the isoxazoloquinazolinone class. It features a unique molecular structure that endows it with potential pharmaceutical applications, particularly in the areas of cancer and viral treatment. Its distinctive attributes allow for specific interactions with biological targets, positioning it as a promising candidate for drug development and a valuable tool for researchers in the field of medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
2,3-dihydro-3-methyl-9H-isoxazolo[3,2-b]quinazolin-9-one is used as a potential anticancer agent for its studied properties against cancer cells. It is being investigated for its ability to target and interact with specific biological molecules, which could lead to the development of new cancer therapies.
Additionally, it is used as a potential antiviral agent due to its potential to inhibit viral replication or activity, offering a new avenue for the treatment of viral infections.
Used in Research and Development:
In the field of medicinal chemistry, 2,3-dihydro-3-methyl-9H-isoxazolo[3,2-b]quinazolin-9-one serves as a valuable research tool for studying the structure-activity relationship of similar compounds. This helps in understanding how modifications to the molecular structure can influence the compound's biological activity and therapeutic potential, thereby aiding in the design of more effective drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 37795-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,9 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37795-71:
(7*3)+(6*7)+(5*7)+(4*9)+(3*5)+(2*7)+(1*1)=164
164 % 10 = 4
So 37795-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O2/c1-7-6-15-13-10(7)12-9-5-3-2-4-8(9)11(13)14/h2-5,7H,6H2,1H3
37795-71-4Relevant articles and documents
2,3 Dihydro 9H isoxazolo[3,2 b]quinazolin 9 ones and 3,4 dihydro (1,2) oxazino[3,2 b]quinazolin 10(2H) ones
Reisner,Ludwig,Simon,Dejneka,Sofia
, p. 766 - 770 (2007/10/09)
Two series of compounds, 2,3-dihydro-9H-isoxazolo [3,2-b] quinazolin-9-ones and 3,4-dihydro-(1,2)-oxazino-[3,2-b]quinazolin-10 (2H)-ones, were synthesized and evaluated for anti-inflammatory, antipyretic and analgesic activity. The isoxazolo compounds were generally more active than their oxazino homologs. Three compounds, i.e., 2,3-dihydro 9H isoxazolo [3,2-b]quinazolin-9-one (W-2429) and its 2- and 3-methyl congeners, were the most active of all compounds tested in this study. On the basis of the biological results herein reported, W-2429 is considerably more effective than acetylsalicylic acid in inhibiting carrageenan-induced edema and in reducing brewer's yeast-induced fever in rats. Also, it was found to be more potent than propoxyphene hydrochloride in the Randall-Selitto test for analgesic activity.
