Pyrimidine nucleosides
Chem-Impex International, Inc. (E)-5-(2-Bromovinyl)-2'-deoxyuridine | MFCD00058585 | 1G
(E)-5-(2-Bromovinyl)-2'-deoxyuridine, MFCD00058585, 1G
Cayman Chemical 5-Formyl-2-deoxyurIdIn 10mg
A nucleoside derivative; inhibits the proliferation of BHK-21 cells and Ehrlich ascites tumor cells (IC50s = 4 and 6 µM, respectively); reduces virus yield in psuedorabies-infected BHK-21 cells at 1 mM; a product of oxidative DNA damage in vitro
Cayman Chemical 2-DeoxyurIdIn 500mg
A pyrimidine nucleoside; has been used as a precursor in the synthesis of antiviral deoxyuridine derivatives, including idoxuridine
Apexbio Technology LLC 2-Deoxyuridine 951-78-0 100mg
2-Deoxyuridine (CAS 951-78-0) is a pyrimidine nucleoside analog in which the 2 -hydroxyl group of uridine is absent In biological systems it can be incorporated into DNA in place of thymidine thereby influencing DNA structure and metabolism The compound serves as a precursor for halogenated nucleoside analogues widely utilized in studies examining DNA replication and degradation pathways 2-Deoxyuridine is frequently employed in molecular biology research to investigate DNA synthesis mechanisms and to facilitate the development of labeled nucleic acid probes
Cayman Chemical 5-Formyl-2-deoxyurIdIn 250mg
A nucleoside derivative; inhibits the proliferation of BHK-21 cells and Ehrlich ascites tumor cells (IC50s = 4 and 6 µM, respectively); reduces virus yield in psuedorabies-infected BHK-21 cells at 1 mM; a product of oxidative DNA damage in vitro
Chem-Impex International, Inc. 5-Trifluorothymidine | MFCD00006534 | 100MG
5-Trifluorothymidine, MFCD00006534, 100MG
eMolecules 2'-Bromo-2'-deoxyuridine | 4753-02-0 | MFCD06658226 | 1g
Combi-Blocks, Inc. | 2'-Bromo-2'-deoxyuridine | 1g | 586079399 | QB-1791 | 95.000 | 4753-02-0 | MFCD06658226 | 307.100 | C9H11BrN2O5
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eMolecules Building Block Tool
Medchemexpress LLC 2'-Deoxycytidine-5'-monophosphate | 1032-65-1 | 99.9% | 307.20 | 5 G
2'-Deoxycytidine-5'-monophosphate is an endogenous metabolite and a deoxynucleotide building block of DNA. It can serve as a substrate for UMP/CMP kinase to form dCDP upon phosphorylation to dCTP, thereby supporting DNA biosynthesis.
- Endogenous metabolite
- Deoxynucleotide building block of DNA
- Substrate for UMP/CMP kinase
- Supports DNA biosynthesis
Medchemexpress LLC 2'-Deoxycytidine-5'-monophosphoric acid-13C9,15N3 dilithium | 1032-65-1 | 99.8% | 330.98 | 10 MG
2'-Deoxycytidine-5'-monophosphoric acid-13C9,15N3 dilithium is a 13C and 15N-labeled version of 2'-Deoxycytidine-5'-monophosphoric acid, which is an endogenous metabolite.
- 13C and 15N-labeled compound.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Endogenous metabolite.
- Stable heavy isotopes of hydrogen, carbon, and other elements can be incorporated into drug molecules for quantitation during drug development.
- Deuteration can affect the pharmacokinetic and metabolic profiles of drugs.
Medchemexpress LLC 2'-Deoxycytidine-5'-monophosphate | 1032-65-1 | MFCD00006546 | 99.99% | 307.20 | 25MG
2'-Deoxycytidine-5'-monophosphate is an endogenous metabolite and a deoxynucleotide building block of which DNA is made. It can serve as a substrate for UMP/CMP kinase to form dCDP upon phosphorylation to dCTP, thereby supporting DNA biosynthesis.
- Endogenous metabolite
- Deoxynucleotide building block for DNA
- Supports DNA biosynthesis
- For research use only
- Available in various quantities
- High purity (99.99%)
Medchemexpress LLC 2'-Deoxycytidine-5'-monophosphate | 1032-65-1 | 99.99% | 307.20 | 5 MG
2'-Deoxycytidine-5'-monophosphate (2'-Deoxycytidine-5'-monophosphoric acid) is an endogenous metabolite and a deoxynucleotide building block of DNA. It acts as a substrate of UMP/CMP kinase to form dCDP upon phosphorylation to dCTP, thereby supporting DNA biosynthesis.
- Endogenous metabolite
- Deoxynucleotide building block for DNA
- Substrate for UMP/CMP kinase
- Supports DNA biosynthesis
Selleck Chemical LLC 2-deoxyuridine
2 -deoxyuridine (dU 2 -dU) is frequently halogenated to create thymidine analogues useful for studies of DNA synthesis and degradation mechanisms