608-09-3 Usage
General Description
(9H-PURIN-6-YLSULFANYL)-ACETIC ACID is a chemical compound that belongs to the class of purine derivatives. It consists of a purine ring with a sulfur atom attached to the 6 position and an acetic acid group attached to the sulfur atom. (9H-PURIN-6-YLSULFANYL)-ACETIC ACID has potential biological activities and has been studied for its potential pharmacological uses. It may also be used as a building block in organic synthesis for the preparation of various other compounds. Overall, (9H-PURIN-6-YLSULFANYL)-ACETIC ACID is a versatile chemical with potential applications in various fields including medicine, biology, and chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 608-09-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 608-09:
(5*6)+(4*0)+(3*8)+(2*0)+(1*9)=63
63 % 10 = 3
So 608-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N4O2S/c12-4(13)1-14-7-5-6(9-2-8-5)10-3-11-7/h2-3,5H,1H2,(H,12,13)
608-09-3Relevant articles and documents
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Skinner et al.
, p. 1223 (1958)
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Synthesis and biological evaluation of some 6-substituted purines
Braga, Fernanda Gambogi,Coimbra, Elaine Soares,de Oliveira Matos, Magnum,Lino Carmo, Arturene Maria,Cancio, Marisa Damato,da Silva, Adilson David
, p. 530 - 537 (2008/02/10)
We report herein the synthesis and the in vitro antileishmanial evaluation of a series of 6-substituted purines. The most active compounds against Leishmania amazonensis promastigotes were 6-(3′-chloropropylthio)purine 2 (D.A. Benson, I. Karsch-Mizrachi, D.J. Lipman, J. Ostell, B.A. Rapp, D.L. Wheeler, Genbank. Nucleic Acids Res. 28 (2000) 15-18; E.V. Aleksandrova, P.M.I.E. Valashek, J. Med. Pharm. Chem. 35 (2001) 172-173), 6-(3′-(thioethylamine)propylthio)purine 5, 6-(α-aceticacidthio)purine 7 and 6-(6′-deoxy-1′-O-methyl-β-d-ribofuranose)purine 14 with an IC50 = 50, 50, 39 and 29 μM, respectively.
