Catalog No.
Product Name
Application
Product Information
Citations
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Purine Nucleoside Analog
8-Benzyloxy-3'-deoxyguanosine is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include inhibition of DNA synthesis and the induction of apoptosis, making it an essential compound for cancer research. This reagent is valuable for studying cellular responses to nucleoside analogs and their potential therapeutic applications in oncology. -
Purine Nucleoside Analog
8-Hydrazinoadenosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis. This compound is valuable in research focused on understanding and developing treatments for various cancer types. -
Cytidine Analog
N4,N4-Dimethylcytidine is a cytidine nucleoside analog that acts primarily by inhibiting DNA methyltransferases. This compound exhibits potential anti-metabolic and anti-tumor activities, making it a valuable tool in cancer research. Its ability to modulate DNA methylation patterns can assist in understanding epigenetic regulation and the mechanisms of tumorigenesis. -
Adenosine Analog
N6,N6-Dimethyl-2’-β-C-methyladenosine is an adenosine analog that primarily targets adenosine receptors. This compound exhibits significant vasodilatory effects on smooth muscle and has been implicated in inhibiting cancer progression. It serves as a valuable tool for research in cardiovascular studies and cancer biology, providing insights into the modulation of adenosine signaling pathways. -
Nucleoside Metabolite
S-Inosyl-L-homocysteine is a nucleoside metabolite that plays a significant role in cellular metabolism. It is involved in the regulation of homocysteine levels and can influence various biochemical pathways associated with nucleotide synthesis. This compound is primarily utilized in research related to metabolic disorders, cardiovascular diseases, and the study of cellular signaling mechanisms. -
Coenzyme A Analog
3α,7α-Dihydroxy-24-oxo-5β-cholestan-26-oyl-CoA is a coenzyme A (CoA) analog that plays a crucial role in bile acid biosynthesis. This compound serves as a substrate in enzymatic reactions involved in the metabolic pathway of bile acids, facilitating important biological processes. Its applications extend to biochemical studies focused on cholesterol metabolism and liver function, offering insights into lipid homeostasis and related disorders. -
Purine Nucleoside Analog
2’,3’,5’-Tri-O-acetyl-5-methoxycarbonylmethyl-2-thiouridine is a purine nucleoside analog that exhibits notable antitumor activity, particularly against indolent lymphoid malignancies. Its biological action involves the inhibition of DNA synthesis and the induction of apoptosis, making it a useful tool in cancer research. This compound is valuable for studies exploring nucleoside analog mechanisms and therapeutic applications in oncology. -
Uridine Analog
5-Fluoro-4’-C-methyluridine is a uridine analogue that serves as a valuable tool in neurological research. It exhibits potential antiepileptic properties and is utilized to investigate anticonvulsant and anxiolytic activities. Additionally, this compound can aid in the development of novel antihypertensive agents. -
Cytidine Analog
5-Methyl-2'-O,4'-C-methylenecytidine is a cytidine nucleoside analog that functions primarily as an inhibitor of DNA methyltransferases. This compound exhibits notable anti-metabolic and anti-tumor properties, making it valuable for research applications in cancer biology and epigenetic regulation. Its ability to modulate DNA methylation provides a useful tool for studying gene expression and potential therapeutic strategies in various malignancies. -
Purine Nucleoside Analog
6-Ethoxy-9-beta-D-(2-C-methyl-ribofuranosyl)purine is a purine nucleoside analog that primarily inhibits DNA synthesis. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, through mechanisms such as the induction of apoptosis. It is a valuable tool for research in cancer biology and therapeutic development. -
Purine Nucleoside Analog
2-Amino-7-propargyl-7,8-dihydro-8-oxo-9-(beta-D-xylofuranosyl)purine is a purine nucleoside analog that exhibits significant antitumor activity, particularly in indolent lymphoid malignancies. Its anticancer mechanisms primarily involve the inhibition of DNA synthesis and the induction of apoptosis. Additionally, this compound functions as a click chemistry reagent, featuring an alkyne group that allows it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with azide-containing molecules. This versatility makes it a valuable tool for biochemical research and therapeutic applications. -
Purine Nucleoside Analog
3'-Azido-3'-deoxy-5-methoxyuridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. Additionally, this compound serves as a versatile click chemistry reagent, containing an azide group that enables it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules or those featuring DBCO or BCN groups. -
Adenosine Analog
5’-O-(4,4’-Dimethoxytrityl)-2’-O-t-butyldimethylsilyl adenosine is an adenosine analog that serves as a smooth muscle vasodilator and exhibits potential in inhibiting cancer progression. This compound is utilized in various research applications, including studies on vasodilation mechanisms and cancer therapies. Its structural modifications enhance stability and bioavailability, making it a valuable tool for investigating adenosine-related biochemical pathways. -
Cytidine Analog
N4-Benzoyl-5-methyl-2’-O,4’-C-methylenecytidine is a cytidine analog that acts as an inhibitor of DNA methyltransferases. This compound demonstrates significant anti-metabolic and anti-tumor activities, making it a valuable tool in cancer research. It offers potential applications in studying epigenetic modifications and therapeutic strategies targeting aberrant DNA methylation patterns. -
Purine Nucleoside Analog
N6-Dimethylaminomethylidene isoguanosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. It functions primarily through the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for cancer research. Its unique mechanism of action positions it as a potential candidate for therapeutic applications in oncology. -
Purine Nucleoside Analog
3'-O-(2-Methoxyethyl)-2-thiouridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound is valuable for research applications focused on cancer therapeutics and the study of nucleoside analogs in cellular biology. -
Guanosine Analog
N2-Phenoxyacetyl-3′,5′-O-(tetraisopropyldisiloxane-1,3-diyl)guanosine functions as a guanosine analog, exhibiting immunostimulatory activity. This compound has been shown to induce type I interferons in various animal models, thereby contributing to antiviral responses. Its biological activity is mediated through the activation of Toll-like receptor 7 (TLR7), making it a valuable tool for research into immune modulation and antiviral mechanisms. -
Glucosinolate Metabolism
Indolylmethyl-desulfoglucosinolate is a compound involved in glucosinolate metabolism, primarily targeting the metabolic pathways of these bioactive compounds. This reagent exhibits biological activity related to the modulation of plant secondary metabolites, particularly in the context of stress responses and defense mechanisms. It serves as a useful tool for researchers studying plant biochemistry, stress physiology, and metabolic engineering in crops. -
Purine Nucleoside Analog
2’-Azido-2’-deoxy-5’-O-(4,4’-dimethoxytrityl)-5-methyluridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound serves as a valuable tool in cancer research, facilitating investigations into therapeutic strategies targeting nucleoside metabolism and cell proliferation. -
Phosphagen
N-Phosphotaurocyamine, a phosphagen, serves as a critical energy reservoir in Arenicola species for the rapid regeneration of ATP. This compound plays a key role in energy metabolism and is essential for sustaining high-energy activities in organisms. Its ability to effectively replenish ATP makes it valuable for research in bioenergetics and cellular metabolism studies. -
Purine Nucleoside Analog
3'-Deoxy-3'-fluoro-xyloguanosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly in the treatment of indolent lymphoid malignancies. Its mechanism of action primarily involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound serves as a valuable tool for researchers investigating therapeutic strategies in cancer biology, especially for lymphoid tumors. -
Purine Nucleoside Analog
3'-Deoxy-5-methycytidine is a purine nucleoside analog that exerts its biological effects primarily through inhibition of DNA synthesis. It demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies. This compound is valuable in cancer research for exploring mechanisms of apoptosis induction and evaluating therapeutic strategies targeting nucleoside metabolism. -
Purine Nucleoside Analog
2-Chloro-2’-β-C-methyl-6-N,N-dimethyladenosine is a purine nucleoside analog that primarily targets DNA synthesis pathways. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, by inducing apoptosis and inhibiting cellular proliferation. Its use in research includes exploring mechanisms of cancer therapy and elucidating pathways involved in nucleoside metabolism. -
Guanosine Analog
3′-C-Methylguanosine is a guanosine analog that acts primarily as an immunostimulatory agent. This compound has been shown to induce the production of type I interferons in animal models, demonstrating notable antiviral effects. Its functional activity largely relies on the activation of Toll-like receptor 7 (TLR7), making it a valuable tool for research into immune response and antiviral therapies. -
Purine Nucleoside Analog
3’-Deoxy-2’,5’-di-O-acetyl-8-hydroxyguanosine is a purine nucleoside analog that interferes with nucleotide metabolism and DNA synthesis. This compound demonstrates significant antitumor activity and is particularly effective against indolent lymphoid malignancies. Its mechanisms of action include the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for cancer research and therapeutic development. -
Purine Nucleoside Analog
2'-O-Phthalimidopropyl cytidine is a purine nucleoside analog that primarily targets DNA synthesis pathways. Its notable biological activity includes inducing apoptosis in cancer cells, making it valuable for research focused on antitumor mechanisms. This compound is particularly relevant for studies involving indolent lymphoid malignancies and contributes to understanding cancer cell proliferation and survival. -
Nucleoside Metabolite
2-Methoxyestradiol-17beta 3-sulfate is a nucleoside metabolite that modulates various biological pathways through its interactions with estrogen receptors. This compound exhibits significant anti-proliferative and anti-angiogenic properties, making it a valuable tool in cancer research. Its role in cell signaling and metabolism supports its use in studies related to endocrine function and tumor biology. -
Purine Nucleoside Analog
5’-Azido-5’-deoxy-2’-O,4’-C-methyleneuridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms primarily involve the inhibition of DNA synthesis and the induction of apoptosis. Additionally, this compound functions as a click chemistry reagent, featuring an azide group that allows it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. It is also capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) functionalized compounds, making it a valuable tool for chemical biology applications. -
Purine Nucleoside Analog
3’-O-Acetyl-N2-iso-Butyroyl-2’-deoxy-guanosine is a purine nucleoside analog that serves as a potent inhibitor of DNA synthesis. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, by inducing apoptosis and disrupting cellular proliferation. Its versatile applications in cancer research make it a valuable tool for studying mechanisms of tumor growth and treatment strategies. -
Purine Nucleoside Analog
5'-Homocytidine is a purine nucleoside analog that exerts its effects primarily through the inhibition of DNA synthesis. This compound displays significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include the induction of apoptosis and interference with cellular replication processes, making it a valuable tool for cancer research and therapeutic studies. -
Hydrocinnamic acid Metabolite
cis-3-(3-Carboxyethenyl)-3,5-cyclohexadiene-1,2-diol is a metabolite involved in the dioxygenolytic catabolism of hydrocinnamic acid (3-phenylpropionic acid). This compound plays a crucial role in the degradation pathway of hydrocinnamic acid and is valuable for research into metabolic processes and enzymatic activity related to phenolic compounds. Its characterization can aid in understanding metabolic pathways and the environmental fate of hydrocinnamic acid derivatives. -
Purine Nucleoside Analog
8-Chloroguanosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanism involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound is valuable for research applications focused on cancer biology and treatment strategies targeting nucleoside metabolic pathways. -
Purine Nucleoside Analog
1,2-Di-O-acetyl-3-deoxy-3-fluoro-5-O-(4-methyl)benzoyl-D-ribofuranose is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. This compound functions by inhibiting DNA synthesis and inducing apoptosis, making it a valuable tool in cancer research. Its ability to interfere with nucleic acid metabolism facilitates exploration into therapeutic strategies for hematological cancers. -
Glutathione-spermidine Conjugate
Bis(glutathionyl)spermine is a glutathione-spermidine conjugate that primarily targets oxidative stress and cellular redox balance. This compound demonstrates significant biological activity in modulating intracellular levels of reactive oxygen species (ROS) and enhancing cellular antioxidant capacity. It is utilized in research applications focused on cellular signaling, apoptosis, and the protective mechanisms of glutathione in various biological contexts. -
Nucleoside Metabolite
(3S)-2,3-Oxidosqualene acts as a nucleoside metabolite with significant biological relevance. This compound is involved in various biosynthetic pathways, particularly in sterol synthesis and cellular signaling. Research applications include investigations into cholesterol metabolism and the exploration of potential therapeutic targets in lipid-related diseases. -
Nucleoside Metabolite
2'-Deoxyinosine 5'-diphosphate (dIDP) is a nucleoside metabolite that serves as an intermediate in the synthesis of deoxyribonucleotides. It plays a crucial role in nucleic acid metabolism and is involved in various biochemical pathways related to DNA replication and repair. dIDP is valuable for research applications concerning nucleotide metabolism, enzymatic assays, and studies of cellular processes involving deoxynucleotides. -
Cytidine Analog
5-Bromo-2'-deoxy-2'-fluoro-beta-D-arabinocytidine is a cytidine nucleoside analog that functions primarily by inhibiting DNA methyltransferases. This compound exhibits notable anti-metabolic and anti-tumor properties, making it a valuable tool in cancer research. Its unique structure and mechanism provide insights into nucleoside metabolism and potential therapeutic strategies for malignancies. -
Guanosine Analog
N2-iso-Butyroyl-3’-O-(methoxyethyl)guanosine is a guanosine analog that exhibits immunostimulatory properties. This compound has been shown to induce type I interferons in animal models, leading to antiviral effects. Its functional activity is linked to the activation of Toll-like receptor 7 (TLR7), making it a valuable tool for investigating immune responses and antiviral mechanisms in research. -
Purine Nucleoside Analog
7-Cyclopropylmethyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl) guanine acts as a purine nucleoside analog with significant antitumor activity, primarily targeting indolent lymphoid malignancies. Its anticancer effects are attributed to the inhibition of DNA synthesis and the induction of apoptosis. This compound is valuable for research applications focused on understanding the mechanisms of action in cancer therapeutics. -
Purine Nucleoside Analog
2′-Amino-2′-deoxycytidine is a purine nucleoside analog that exhibits significant antitumor activity against indolent lymphoid malignancies. Its primary mechanism involves the inhibition of DNA synthesis, leading to the induction of apoptosis in cancer cells. This compound is primarily utilized in research applications focused on cancer biology and therapeutic development. -
Purine Nucleoside Analog
9-(2’-O-Acetyl-5’-O-benzoyl-3’-O-methyl-beta-D-ribofuranosyl)-2,6-dichloropurine is a purine nucleoside analog that inhibits DNA synthesis. This compound exhibits significant antitumor activity against indolent lymphoid malignancies, with mechanisms that include the induction of apoptosis. It serves as a valuable tool in cancer research for understanding the effects of nucleoside modifications on tumor progression and treatment response. -
Adenosine Analog
N6-(3-Methoxybenzyl)-2’-C-methyl adenosine is an adenosine analog that primarily targets adenosine receptors. This compound exhibits significant biological activity as a smooth muscle vasodilator and demonstrates potential anti-cancer properties. It is suitable for research applications focused on vascular biology and cancer therapeutics. -
Purine Nucleoside Analog
1-(alpha-L-Threofuranosyl)thymine is a purine nucleoside analog that demonstrates significant antitumor activity, especially in the treatment of indolent lymphoid malignancies. Its mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells, making it a valuable tool for studying cancer biology and therapeutic strategies. This compound is useful in the development of treatments targeting specific malignancies and contributes to advancing understanding in the field of oncology research. -
Adenosine Analog
N-(3-Methylbutyl)adenosine is an adenosine analog that functions primarily as a smooth muscle vasodilator. This compound has been shown to possess inhibitory effects on cancer progression, making it valuable for research in both cardiovascular and oncology studies. Its application in various biological assays highlights its potential as a therapeutic agent in the treatment of vascular and cancer-related diseases. -
Purine Nucleoside Analog
5’-Azido-5’-deoxy-2'-O-methyluridine is a purine nucleoside analog that demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms involve the inhibition of DNA synthesis and induction of apoptosis. Additionally, this compound functions as a versatile click chemistry reagent, featuring an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups. This unique combination of biological activity and reactivity makes it valuable for various research applications in chemical biology. -
Adenosine Analog
N6-Methyl-2’-β-C-methyladenosine is an adenosine analog that primarily targets adenosine receptors. This compound has demonstrated vasodilatory effects on smooth muscle and exhibits potential in inhibiting cancer progression. Its unique structure allows for various research applications related to adenosine signaling pathways and therapeutic interventions. -
Purine Nucleoside Analog
1-(3-Deoxy-3-fluoro-β-D-xylofuranosyl)-2,4(1H,3H)-pyrimidinedione is a purine nucleoside analog that exhibits significant anti-tumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable compound for cancer research. This reagent is suited for studies aimed at understanding the molecular pathways involved in tumorigenesis and potential therapeutic interventions. -
Purine Nucleoside Analog
9-(3-Deoxy-3-fluoro-β-D-ribofuranosyl)-6-[6-(4-methylpiperazinyl)pyridin-3-yl]purine acts as a purine nucleoside analog with significant implications for cancer research. This compound exhibits broad antitumor activity, particularly against indolent lymphoid malignancies, by inhibiting DNA synthesis and inducing apoptosis. It is a valuable tool for studying cancer mechanisms and developing therapeutic strategies in oncology. -
Adenosine Analog
5’-O-(4,4’-Dimethoxytrityl)-N6-phenoxyacetyl adenosine is an adenosine analog that primarily targets adenosine receptors. This compound exhibits significant smooth muscle vasodilatory effects and has been implicated in the inhibition of cancer progression. It is a valuable reagent for research focused on vascular biology, immunology, and oncology, facilitating investigations into the therapeutic potential of nucleotide derivatives. -
Purine Nucleoside Analog
2′,3′-Didehydro-2′,3′-dideoxy-5-fluorouridine is a purine nucleoside analog that exhibits potent antitumor activity, particularly against indolent lymphoid malignancies. This compound primarily functions through the inhibition of DNA synthesis and the induction of apoptosis. It serves as an important tool for research in cancer biology and therapeutic development.
