Meso-12-Diphenylethylenediamine 97.0%

2-Deoxyuridine (dU) is frequently halogenated to create thymidine analogues useful for studies of DNA synthesis and degradation mechanisms. Derivatized 2-Deoxyuridines used as labeling substrates include chloro-2-deoxyuridine (CldU) bromodeoxyuridine (BrdU) andor iododeoxyuridine (IdU). Other useful analogues of 2-deoxyuridine include 5-ethynyl-2-deoxyuridine (DdU) and 5-hydroxymethyl-2-deoxyuridine (HmdU).

For R&D use onlynot for drug household or other uses.

Deoxyuridine (dU) is a compound and a nucleoside. It is similar in chemical structure to uridine but without the 2-hydroxyl group. Idoxuridine and Trifluridine are variants of deoxyuridine used as antiviral drugs. They are similar enough to be incorporated as part of DNA replication but they possess side groups on the uracil component (an iodine and a CF3 group respectively) that prevent base pairing.