1006-12-8 Usage
Uses
Used in Pharmaceutical Industry:
3,7-Dihydro-3-methyl-6H-purine-6-thione is used as a key intermediate in the synthesis of various pharmaceuticals for the treatment of autoimmune diseases and cancer. Its unique chemical structure allows for the development of drugs with targeted therapeutic effects.
Used in Antiviral and Antifungal Agents:
Thiopurine is used as a precursor in the synthesis of several antiviral and antifungal agents. Its ability to interact with specific biological targets makes it a valuable component in the development of effective treatments against viral and fungal infections.
Used in Neurological Disorder Research:
3,7-Dihydro-3-methyl-6H-purine-6-thione is being studied for its potential use in the treatment of certain neurological disorders. Its unique properties and interactions with biological systems offer promising avenues for the development of novel therapeutic approaches to address neurological conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1006-12-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1006-12:
(6*1)+(5*0)+(4*0)+(3*6)+(2*1)+(1*2)=28
28 % 10 = 8
So 1006-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4S/c1-10-3-9-6(11)4-5(10)8-2-7-4/h2-3H,1H3,(H,7,8)
1006-12-8Relevant academic research and scientific papers
Isolation, synthesis, and biological activity of aphrocallistin, an adenine-substituted bromotyramine metabolite from the hexactinellida sponge Aphrocallistes beatrix
Wright, Amy E.,Roth, Gregory P.,Hoffman, Jennifer K.,Divlianska, Daniela B.,Pechter, Diana,Sennett, Susan H.,Guzman, Esther A.,Linley, Patricia,McCarthy, Peter J.,Pitts, Tara P.,Pomponi, Shirley A.,Reed, John K.
experimental part, p. 1178 - 1183 (2011/02/28)
A new adenine-substituted bromotyrosine-derived metabolite designated as aphrocallistin (1) has been isolated from the deep-water Hexactinellida sponge Aphrocallistes beatrix. Its structure was elucidated on the basis of spectral data and confirmed throug
