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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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The product, 2'-Deoxycytidine-5'-monophosphate (2'-Deoxycytidine-5'-monophosphoric acid), 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.
Appearance: Solid
Color: White to off-white
Shipping: Room temperature in continental US; may vary elsewhere
Storage: -20°C, protect from light, stored under nitrogen
In solvent: -80°C for 6 months; -20°C for 1 month (protect from light, stored under nitrogen)
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2'-Deoxycytidine, a deoxyribonucleoside, can inhibit the biological effects of Bromodeoxyuridine (Brdu). It is essential for the synthesis of nucleic acids and can be used for cancer research.
Deoxyribonucleoside
Inhibits biological effects of bromodeoxyuridine (Brdu)
Essential for the synthesis of nucleic acids
Can be used for cancer research
Inhibits tumor growth in mice
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
2'-Deoxycytidine is a deoxyribonucleoside that can inhibit the biological effects of Bromodeoxyuridine (Brdu). It is essential for the synthesis of nucleic acids and is utilized in cancer research.
Inhibits biological effects of Bromodeoxyuridine (Brdu)
Essential for nucleic acid synthesis
Utilized in cancer research
Acts as a human endogenous metabolite
Functions as a microbial metabolite
Demonstrated to inhibit tumor growth in vivo
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
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
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Isotopically labeled deoxycytidine triphosphate-d14 supplied as the dilithium salt for use in DNA synthesis and analytical workflows. It serves as a deuterium-labeled nucleotide for enzymatic incorporation, tracer studies, and quantitative mass spectrometry.
Isotope-labeled for use as an internal standard and tracer in analytical workflows.
Suitable for enzymatic DNA synthesis, PCR, and cDNA synthesis.
Supplied as the dilithium salt to support aqueous solubility and handling.
High purity consistent with analytical and molecular biology applications.
Available in small-scale quantities for method development and validation.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
2'-Deoxyuridine is a brain-penetrant pyrimidines nucleotide associated with nervous system diseases. It can increase chromosome breakage and decrease thymidylate synthetase activity. It serves as a precursor in the synthesis of Edoxudine and is an analogue of 5-ethynyl-2'-deoxyuridine. Additionally, 2'-deoxyuridine reduces microglial activation and improves oxidative stress damage by modulating glycolytic metabolism on Aβ25-35-induced brain injury, showing promise for Alzheimer's disease (AD) research.
Brain-penetrant pyrimidines nucleotide associated with nervous system diseases.
Increases chromosome breakage.
Decreases thymidylate synthetase activity.
Reduces microglial activation.
Improves oxidative stress damage by modulating glycolytic metabolism on Aβ25-35-induced brain injury.
Promising for Alzheimer's disease (AD) research.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
2-Deoxycytidine, a deoxyribonucleoside, can inhibit biological effects of Bromodeoxyuridine (Brdu). It is essential for the synthesis of nucleic acids and can be used for the research of cancer.
Essential for nucleic acid synthesis.
Used in cancer research.
Deoxyribonucleoside.
Can inhibit biological effects of Bromodeoxyuridine (Brdu).
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
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
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Deoxycytidine triphosphate (trisodium) is provided as a ready-to-use 100 mM aqueous solution of the trisodium salt of dCTP. It functions as a nucleotide substrate for DNA synthesis, polymerase reactions, and enzymatic assays, and is supplied as a high-purity solution intended for molecular biology workflows.
High purity: 99.46% suitable for sensitive assays.
Ready-to-use 100 mM aqueous solution for immediate use.
Trisodium salt form enhances solubility in aqueous buffers.
Colorless to light yellow liquid for easy visual inspection.
Available in small pack sizes (for example, 25 mg) to reduce waste.
Storage-stable when frozen; follow manufacturer storage guidance.
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