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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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Recombinant human adenosine kinase (ADK) is a full-length, tag-free enzyme produced in HEK293 cells for biochemical and enzymatic research. Supplied as a filtered solution with stabilizers, it offers consistent activity and low endotoxin for reliable assay results.
Full-length human sequence (M1-H345).
Expressed in HEK293 mammalian cells for native folding.
Tag free to minimize assay interference.
Purity >95% as determined by reducing SDS-PAGE.
Formulated in 20 mM Tris, 300 mM NaCl, pH 8.0, with stabilizers and 20% glycerol.
Endotoxin <1 EU/μg and measured specific activity for activity-based assays.
Supplied as a frozen solution and shipped on dry ice to preserve activity.
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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).
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Rhodizonic acid disodium (Sodium rhodizonate dibasic) can be used as an indicator in the volumetric determination of barium and sulfates Rhodizonic acid disodium is a kind of biological materials or organic compounds that are widely used in life science research[1]
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Uridine is a nucleoside compound composed of uracil and a ribose ring, connected by a β-N1-glycosidic bond. This compound is used for research purposes and has demonstrated various biological activities.
Inhibits the proliferation of HL-60 leukemia cells
Alleviates CCl4-induced liver fibrosis in mice
Shows anti-ischemic, antioxidant, and anti-arrhythmic effects in rat models
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2'-Deoxyguanosine 5'-monophosphate (dGMP) disodium hydrate is an oxidizable target of pterin (PT) used to evaluate the photosensitizing properties of biopterins. Pterin induces a photosensitive reaction of dGMP under UV-A radiation, leading to DNA damage via two primary mechanisms: electron transfer (type I) and singlet molecular oxygen production (type II).
Oxidizable target of pterin (PT).
Evaluates photosensitizing properties of biopterins.
Induces DNA damage under UV-A radiation.
Functions through Type I (electron transfer) and Type II (singlet molecular oxygen production) mechanisms.
Relevant to cell cycle and DNA damage studies.
Involved in DNA/RNA synthesis research.
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7-Methyl-guanosine-5'-triphosphate (m7GTP) sodium is a guanosine 5'-phosphate. Its phosphorothioate analog is a potent cap-dependent translation inhibitor.
Potent cap-dependent translation inhibitor.
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Glucosamine hydrochloride is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, also used as a dietary supplement. It is a natural constituent of glycosaminoglycans in the cartilage matrix and synovial fluid, exerting pharmacological effects on osteoarthritic cartilage and chondrocytes. This product exhibits dose-dependent DPPH antioxidant activity and inhibits HIF-1α at the protein level.
Exerts pharmacological effects on osteoarthritic cartilage and chondrocytes.
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2'-Deoxyadenosine is an adenine nucleoside used as a research reagent and analytical standard. It inhibits glucose-stimulated insulin release, modulates islet cAMP, activates caspase-3, and has been reported to inhibit S-adenosyl-L-homocysteine hydrolase; it is used in analytical and biochemical studies.
intended for research and analytical applications
inhibits glucose-stimulated insulin release
modulates islet cyclic AMP and activates caspase-3
reported inhibitor of S-adenosyl-L-homocysteine hydrolase
available in labeled and standard variants for analytical use
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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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