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5'-Uridylic acid, 2'-azido-2'-deoxy-5-methyl- is a chemical compound with the molecular formula C10H13N3O6. It is a modified nucleoside, derived from the naturally occurring uridine, which is a component of RNA. The compound features a 2'-azido group, which replaces the hydroxyl group at the 2' position of the sugar moiety, and a 5-methyl group, which is attached to the uracil base. This modification can potentially alter the properties and interactions of the molecule in biological systems, making it a subject of interest for research in fields such as molecular biology and drug development. The compound's unique structure may be used to study the effects of these modifications on molecular recognition and stability, as well as to develop new therapeutic strategies.

488099-47-4

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488099-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 488099-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,0,9 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 488099-47:
(8*4)+(7*8)+(6*8)+(5*0)+(4*9)+(3*9)+(2*4)+(1*7)=214
214 % 10 = 4
So 488099-47-4 is a valid CAS Registry Number.

488099-47-4Downstream Products

488099-47-4Relevant academic research and scientific papers

Synthesis and evaluation of thymidine-5′-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase

Vanheusden, Veerle,Munier-Lehmann, Helene,Pochet, Sylvie,Herdewijn, Piet,Van Calenbergh, Serge

, p. 2695 - 2698 (2002)

A number of 2′- and 3′-modified thymidine 5′-O-monophosphate analogues were synthesized as potential leads for new anti-mycobacterial drugs. Evaluation of their affinity for Mycobacterium tuberculosis thymidine monophosphate kinase showed that a 2′-halogeno substituent and a 3′-azido function are the most favorable leads for further development of potent inhibitors of this enzyme.

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