N-(7H-purin-6-yl)benzamide

Hypoxia and Perfusion Labeling During Photodynamic Therapy

damage as mechanisms of photodynamic effect. The hypoxia markers EF3 [(2-(2-nitroimidazol-1 [H]-yl)-N -(3,3,3-trifluoropropyl)acetamide)] or EF5 [(2-(2-nitroimidazol-1 [H]-yl)-N -(2,2,3,3,3-pentafluoropropyl)acetamide)] can provide a quantitative

Two‐Step, One‐Pot Synthesis of Inosine, Guanosine, and 2′‐Deoxyguanosine O6‐Ethers via Intermediate O6‐(Benzotriazol‐1‐yl) Derivatives

N‐/purin‐6‐yl/pyridinium salts. Nucleic Acids Res. 13:2989‐3003.    Allerson, C.R., Chen, S.L., and Verdine, G.L. 1997. A chemical method for site‐specific modification

Convenient and Efficient Approach to the Permanent or Reversible Conjugation of RNA and DNA Sequences with Functional Groups

with an analytical sample of N ‐(4‐cyanobut‐1‐yl)‐5‐(dimethylamino)naphthalene‐1‐sulfonamide. Conditions: RP‐HPLC analysis is performed under conditions identical to those described for the fluoride‐assisted conversion of S.11 a to uridine in Figure . Abbreviation