2'-Deoxycytidine 3'-monophosphate (dCMP) is a nucleotide that plays a crucial role in the structure of DNA. It is composed of a deoxyribose sugar, a cytosine base, and a single phosphate group attached to the 3' position of the sugar. This compound is a key building block in the synthesis of DNA, where it pairs with deoxyguanosine in the double helix structure. dCMP is soluble in water and exhibits a neutral pH in solution. It is involved in various biochemical processes, including DNA replication and repair, and serves as a substrate for enzymes such as DNA polymerases. The presence of the deoxyribose sugar distinguishes it from ribonucleotides, which contain ribose. In terms of stability, dCMP can be sensitive to hydrolysis under certain conditions, which can affect its utility in laboratory settings. Overall, 2'-deoxycytidine 3'-monophosphate is essential for genetic information storage and transmission in living organisms.

2'-deoxycytidine 3'-monophosphate

6220-63-9: 2'-Deoxycytidine 3'-monophosphate (dCMP) is a nucleotide that plays a crucial role in the structure of DNA. It is composed of a deoxyribose sugar, a cytosine base, and a single phosphate group attached to the 3' position of the sugar. This compound is a key building block in the synthesis of DNA, where it pairs with deoxyguanosine in the double helix structure. dCMP is soluble in water and exhibits a neutral pH in solution. It is involved in various biochemical processes, including DNA replication and repair, and serves as a substrate for enzymes such as DNA polymerases. The presence of the deoxyribose sugar distinguishes it from ribonucleotides, which contain ribose. In terms of stability, dCMP can be sensitive to hydrolysis under certain conditions, which can affect its utility in laboratory settings. Overall, 2'-deoxycytidine 3'-monophosphate is essential for genetic information storage and transmission in living organisms.

2'-Deoxycytidine-3'-monophosphate free acid is a nucleotide that is synthesized from deoxyadenosine triphosphate and deoxycytidine triphosphate in the presence of ribonucleotide reductase. It is the precursor to DNA synthesis, where it is converted to dCTP by thymidylate synthase. 2'-Deoxycytidine-3'-monophosphate free acid has low energy and vibrational levels, due to its glycosidic bond. This bond can be broken by chromatographic methods. The excised activated product uridine can be used for carcinogenesis studies, as well as for other molecular studies such as electron microscopy and crystallography. 2'-Deoxycytidine-3'-monophosphate free acid is an unstable molecule that can undergo dinucleotide rearrangements, electron transfer, or bond cleavage to form a metastable molecule with

CAS 6220-63-9

2'-deoxycytidine 3'-monophosphate

2'-Deoxycytidine-3'-monophosphate

Ref: 3D-ND46720