13401-38-2 Usage
Description
7-Methyllumizine, a methyl-substituted imidazo[1,2-a]pyrazine derivative, is an oxidative degradation product of Lumazine. It possesses anti-inflammatory, analgesic, and ulcerogenic activities, making it a potential candidate for pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
7-Methyllumizine is used as an active pharmaceutical ingredient for its anti-inflammatory properties, helping to reduce inflammation in various conditions.
7-Methyllumizine is used as an analgesic agent for its pain-relieving capabilities, providing relief from acute and chronic pain.
7-Methyllumizine is used as an ulcerogenic agent for its ability to induce ulcers, which can be useful in research and development of treatments for ulcer-related conditions.
Used in Research and Development:
7-Methyllumizine is used as a research compound for studying its anti-inflammatory, analgesic, and ulcerogenic activities, contributing to the advancement of pharmaceutical sciences and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 13401-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,0 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13401-38:
(7*1)+(6*3)+(5*4)+(4*0)+(3*1)+(2*3)+(1*8)=62
62 % 10 = 2
So 13401-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N4O2/c1-3-2-8-4-5(9-3)10-7(13)11-6(4)12/h2H,1H3,(H2,9,10,11,12,13)
13401-38-2Relevant articles and documents
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Sharefkin,zit. bei Sattler,Zerban
, p. 1401,1403 (1949)
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Solvent-free regioselective synthesis of 6- and 7-substituted pteridines under microwave irradiation
Singh,Geetanjali
, p. 136 - 138 (2007/10/03)
Reactions of 5,6-diaminouracils with α-keto aldehydes over acidic and neutral aluminum oxide under microwave irradiation gave the corresponding 6- and 7-substituted 1,2,3,4-tetrahydropteridine-2,4-diones in 63-79% yield with high regioselectivity. Pleiade
Research on heterocyclic compounds. XXXVII. Synthesis and antiinflammatory activity of methyl-substituted imidazo[1,2-a]pyrazine derivatives
Rimoli,Avallone,De Caprariis,Luraschi,Abignente,Filippelli,Berrino,Rossi
, p. 195 - 203 (2007/10/03)
A series of methyl-substituted imidazo[1,2-a]pyrazines 8 bearing a carboxylic acid group on the imidazole ring were synthesized. The structures of new compounds were confirmed by 1H- and 13C-NMR spectral data; the correct assignment of carbon resonances was made by means of HETCOR and COLOC experiments. Antiinflammatory, analgesic and ulcerogenic activities in vivo were evaluated and compared with those of antiinflammatory imidazopyrazines (2 and 3) and indomethacin. The inhibitory action on cyclooxygenase activity was evaluated in vitro. Compounds 8 were found to be less potent than indomethacin in these assays. SARs are discussed.
