2' deoxyadenosine 5' monophosphate

2'-Deoxyadenosine-5'-monophosphate (D-AMP) is a nucleoside comprised of adenine attached to a ribose (ribofuranose) moiety via a -N9-glycosidic bond. Deoxyadenosine monophosphate is a derivative of the common nucleic acid ATP, or adenosine triphosphate, in which the -OH (hydroxyl) group on the 2' carbon on the nucleotide's pentose has been removed (hence the deoxy- part of the name). Additionally, the monophosphate of the name indicates that two of the phosphoryl groups of GTP have been removed, most likely by hydrolysis. Deoxyadenosine monophosphate is abbreviated dAMP.

2'-Deoxyadenosine-5'-monophosphate-D12 dilithium is the deuterium-labeled version of 2'-Deoxyadenosine-5'-monophosphate. This compound, a derivative of nucleic acid AMP, is a deoxyribonucleotide found in DNA. It is utilized in the study of adenosine-based interactions during DNA synthesis and damage processes.

2′-Deoxyadenosine 5′-monophosphate disodium (a nucleic acid AMP derivative) is a deoxyribonucleotide in DNA, used for studying adenosine-based interactions in DNA synthesis and damage analysis.

7-CH-5'-dAMP (5'-dTuMP) is an adenosine monophosphate derivative that serves as a potential substrate, competitive inhibitor, or modulator for enzymes interacting with 2-deoxyadenosine-5'-monophosphate.

2'-Deoxyadenosine 3':5'-cyclic monophosphate sodium is a reagent used in biochemical reactions.