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Nitrogenous bases covalently linked to a sugar with and without phosphate groups; used for synthesis, cell signaling, and as cofactors in enzymatic reactions; includes pyrimidine, purine, pyridine, flavin, pyrrolopyrimidine, and triazole varieties.
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Lamivudine is a nucleoside analog that acts primarily as a reverse transcriptase inhibitor disrupting viral replication by interfering with RNA-dependent DNA polymerase activity It inhibits human immunodeficiency virus type 1 (HIV-1) reverse transcriptase with an IC50 value of approximately 0 316 M Lamivudine also suppresses replication of simian retrovirus (SRV-1 and SRV-2) while exhibiting negligible activity on foamy viruses and amphotropic murine leukemia virus (MLV-A) Due to its antiviral mechanism and dual inhibitory effect against both HIV-1 and hepatitis B virus (HBV) lamivudine is frequently utilized in research involving retroviral infection models particularly HIV-1 and HBV coinfection studies to evaluate viral dynamics antiviral efficacy and biochemical responses
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2'-Deoxyuridine-1'-13C is a stable isotope-labeled compound with the molecular formula C813CH12N2O5 and a molecular weight of 229.19. It appears as a white to off-white solid with an isotopic enrichment of 99%. This product is intended for research use only and has not been fully validated for medical applications.
White to off-white solid appearance
Isotopic enrichment of 99%
Molecular formula C813CH12N2O5
Intended for research use only
Store powder at -20°C for up to 3 years or at 4°C for up to 2 years
Store in solvent at -80°C for 6 months or at -20°C for 1 month
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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
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A thymidine analog that is readily incorporated, following phosphorylation, into newly synthesized DNA in place of thymidine; can be detected immunologically in cells and tissues
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2'-Deoxycytidine-5'-monophosphoric acid (Standard) is the analytical standard of 2'-Deoxycytidine-5'-monophosphoric acid. This product is intended for research and analytical applications. 2'-Deoxycytidine-5'-monophosphate is an endogenous metabolite and a deoxynucleotide building block of DNA. It can be used as a substrate of UMP/CMP kinase to form dCDP upon phosphorylation to dCTP, supporting DNA biosynthesis.
Used as an analytical standard.
Supports DNA biosynthesis.
Suitable for qualitative research experiments.
Suitable for quantitative research experiments.
Suitable for methodological research experiments in HPLC, GC, and MS.
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Deoxycytidine triphosphate-d14 dilithium is a deuterium-labeled nucleoside triphosphate provided as the dilithium salt for use as an isotopic standard or tracer in DNA synthesis workflows, including PCR, sequencing, and analytical method development.
Deuterium-labeled for isotopic tracing and mass-shift detection.
Dilithium salt form, compatible with aqueous buffers.
High purity (~95.7%) suitable for analytical and molecular biology use.
Supplied in a 10 mg vial for small-scale experiments.
Useful as a stable labeled standard for qPCR, sequencing, and method validation.
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2'-Deoxyuridine-1'-13C is a carbon-13 labeled version of 2'-Deoxyuridine. This compound induces chromosome breakage, thereby reducing the synthesis activity of thymidylate. Additionally, it serves as a precursor in the synthesis of Edoxudine.
Carbon-13 labeled version of 2'-Deoxyuridine.
Induces chromosome breakage.
Reduces synthesis activity of thymidylate.
Serves as a precursor in the synthesis of Edoxudine.
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2'-Deoxycytidine-5'-monophosphate is an endogenous metabolite and a deoxynucleotide building block of DNA. It serves as a substrate for UMP/CMP kinase to form dCDP upon phosphorylation to dCTP, supporting DNA biosynthesis. This compound is intended for research use only and is not sold to patients.
Endogenous metabolite
Deoxynucleotide building block of DNA
Supports DNA biosynthesis
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4-Thio-2'-deoxyuridine is a sulfur-substituted deoxyuridine nucleoside analogue used in biochemical and nucleic acid research, including studies of nucleic acid chemistry and incorporation into oligonucleotides. It has molecular formula C9H12N2O4S, molecular weight 244.27 g/mol, and a reported purity of 99.78%.
Sulfur-substituted deoxyuridine analogue useful for nucleic acid studies.
High reported purity (99.8%), suitable for analytical and synthetic applications.
Available in multiple pack sizes for research-scale work.
Provided with certificate of analysis and safety data sheet for quality and handling.
Offered in solid form and as 10 mM DMSO solution for convenient use.
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MW 392.15 Da, Purity >95%. Potent, specific adenosine kinase inhibitor (IC₅₀ = 26 nM). Inhibits platelet aggregation and spreading, and interferes with adenosine and adenine nucleotide metabolism. Additionally inhibits other kinases such as ERK2 (Ki = 525 nM).