Sf. Wnuk et al., Design and biological evaluation of new mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase, NUCLEOS NUC, 18(4-5), 1999, pp. 595-596
Geminal dihalohomovinyl 2 and haloacetylenic 4 analogs derived from adenosi
ne were prepared. These compounds exhibited type II (covalent) mechanism-ba
sed inactivation of S-adenosyl-L-homocysteine hydrolase.