Catalog No.
Product Name
Application
Product Information
Citations
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Guanosine Analog
N4-Desmethyl-N5-Methyl wyosine is a guanosine analogue that primarily targets Toll-like receptor 7 (TLR7). It demonstrates notable immunostimulatory activity and has been shown to induce type I interferons in certain animal models, contributing to antiviral effects. This compound is valuable in research focused on innate immunity and the modulation of antiviral responses. -
Purine Nucleoside Analog
3’-Azido-3’-deoxy-3-deazauridine is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. This compound exerts its anticancer effects by inhibiting DNA synthesis and inducing apoptosis. Additionally, it serves as a versatile click chemistry reagent, featuring an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN substrates. -
Adenosine Analog
2'-O-Propargyl A(Bz)-3'-phosphoramidite is an adenosine analog that serves as a versatile reagent in chemical biology. This compound exhibits key biological activities, including vasodilation and potential inhibition of cancer progression. Due to its alkyne group, 2'-O-Propargyl A(Bz)-3'-phosphoramidite is ideal for use in copper-catalyzed azide-alkyne cycloaddition (CuAAc), making it valuable for constructing complex molecular architectures in research applications. -
Purine Nucleoside Analog
8-Chloro-arabinoadenosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include the inhibition of DNA synthesis and the induction of apoptosis. This compound is valuable in cancer research and therapeutic studies focused on lymphoid cancers. -
Purine Nucleoside Analog
2’-Deoxy-2’-fluoro-β-D-arabino-2-thiouridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. This compound's anticancer mechanisms are primarily attributed to its ability to inhibit DNA synthesis and induce apoptosis in tumor cells. It serves as a valuable tool in cancer research, particularly for investigations focused on therapeutic strategies targeting nucleoside metabolism and cancer cell proliferation. -
Uridine Analog
2’-Deoxy-2’-(N-trifluoroacetyl)amino-5’-O-DMTr-uridine 3’-CED phosphoramidite is a uridine analog that serves as a key building block in nucleic acid synthesis. This compound may exhibit potential antiepileptic effects, facilitating research on anticonvulsant and anxiolytic properties. Additionally, it can be utilized in the development of novel antihypertensive agents, making it valuable for various biochemical and therapeutic applications. -
Purine Nucleoside Analog
2’-β-C-Methyl-5-trifluoromethyluridine is a purine nucleoside analog with significant antitumor activity. This compound targets indolent lymphoid malignancies and exhibits its anticancer effects primarily through the inhibition of DNA synthesis and the induction of apoptosis. It is a valuable tool for research into cancer therapeutics and the mechanisms underlying tumor cell proliferation. -
Nucleoside Metabolite
Formylphosphonic acid is a nucleoside metabolite that acts as a potent inhibitor of purine and pyrimidine metabolism. This compound is utilized in research studies focused on understanding nucleoside analogs and their role in cellular biochemistry. Its unique pharmacological properties make it valuable in investigating various metabolic pathways and therapeutic applications in diseases associated with nucleoside metabolism. -
Purine Nucleoside Analog
2’-Fluoro-2’-deoxy-N6,N6-dimethylarabinoadenosine is a purine nucleoside analog known for its potential in cancer research. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for studying tumor biology and therapeutic strategies. -
Thymidine Analog
5-Benzylamino carbonyl-3’-O-acetyl-2’-O-methyluridine is a thymidine analog that exhibits insertional activity into replicated DNA. This compound is valuable for labeling cells and enables the tracking of DNA synthesis, making it useful in various molecular biology applications. Its structural properties facilitate studies in nucleotide metabolism and can aid in researching DNA replication processes. -
Purine Nucleoside Analog
2'-Deoxy-N2-cyclopentyl guanosine is a purine nucleoside analog that exerts its effects primarily through the inhibition of DNA synthesis. This compound exhibits broad antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include the induction of apoptosis and disruption of cellular replication processes, making it a valuable tool for cancer research and therapeutic development. -
Fatty Acid
9,10,18-Trihydroxystearic acid is a fatty acid that features three hydroxyl groups along its carbon chain. This compound is recognized for its ability to influence lipid metabolism and may serve as a crucial intermediate in various biochemical pathways. It is commonly utilized in research related to fatty acid synthesis, lipid signaling, and the study of metabolic disorders. -
Nucleoside Metabolite
L-Metanephrine is a nucleoside metabolite that acts as a key biomarker for catecholamine metabolism. Its primary biological activity includes the regulation of neurotransmitter functions, making it relevant for research in neurobiology and cardiovascular physiology. L-Metanephrine is utilized in studies investigating adrenal function and disorders related to catecholamine synthesis and metabolism. -
Purine Nucleoside Analog
2’-O-Acetyl-N4-benzoyl-5’-O-DMT arabinocytidine 3’-O-phosphoramidite is a purine nucleoside analog that targets DNA synthesis pathways. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, through mechanisms such as the inhibition of DNA synthesis and the induction of apoptosis. It serves as an important tool for research in cancer biology and therapeutic development. -
Purine Nucleoside Analog
2-Amino-6-chloropurine-3’,5’-di-O-acetyl-2’-deoxyriboside is a purine nucleoside analog with notable antitumor activity. This compound is primarily utilized in research related to indolent lymphoid malignancies, where it functions by inhibiting DNA synthesis and inducing apoptosis. Its mechanism of action positions it as a valuable tool in cancer research, offering insights into therapeutic strategies for treating various forms of malignancies. -
Nucleoside Metabolite
3-Methoxy-4-hydroxyphenylglycolaldehyde is a nucleoside metabolite known for its involvement in biochemical pathways related to nucleic acid synthesis and metabolism. This compound exhibits potential activity in modulating nucleoside signaling and may serve as an important tool in studies of cellular metabolism and nucleotide regulation. Its applications span various fields of research, including pharmacology, biochemistry, and molecular biology, where it aids in the exploration of nucleoside-related processes. -
Nucleoside Metabolite
1-Pyrroline-4-hydroxy-2-carboxylate is a nucleoside metabolite that plays a significant role in cellular metabolism. It is involved in various biochemical pathways, particularly in the synthesis and degradation of nucleotides. This compound is relevant in research applications exploring metabolic disorders and enzymatic activities related to nucleotide metabolism. Its structural features make it a valuable tool in studying nucleoside-related biochemical processes. -
Thymidine Analog
5-Azidomethyl-2’,3’,5’-tri-O-benzoyl uridine is a thymidine analog designed for applications in DNA research. This compound exhibits insertional activity towards replicated DNA, facilitating the labeling of cells and tracking of DNA synthesis. As a versatile click chemistry reagent, it features an azide group that engages in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions, making it suitable for bioconjugation strategies involving alkyne, DBCO, or BCN functionalized molecules. -
Purine Nucleoside Analog
2′-β-C-Methyl-beta-D-6-methylpurine riboside is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound is useful for research applications focused on cancer biology and therapeutics, offering insights into treatment strategies for lymphoid malignancies. -
Purine Nucleoside Analog
3’-Deoxy-3’-fluoro-N6-methyladenosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. This compound primarily functions by inhibiting DNA synthesis and inducing apoptosis in cancer cells, making it a valuable tool for research in cancer biology and therapeutic development. Its unique properties contribute to a deeper understanding of nucleoside metabolism and potential intervention strategies in oncology. -
Purine Nucleoside Analog
2',3'-O-Isopropylidene-5-pyrrolidinomethyl-2-thiouridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for cancer research. This compound can be utilized to explore therapeutic strategies and the biochemical pathways involved in cancer cell proliferation and survival. -
Adenosine Analog
2-Cyanomethylthioadenosine is an adenosine analog that primarily targets adenosine receptors. This compound demonstrates potent vasodilatory effects on smooth muscle tissue and has shown potential in inhibiting cancer progression. It serves as a valuable tool in research applications focusing on vascular biology and cancer therapeutics. -
Adenosine Analog
3’-β-C-Ethynyladenosine is an adenosine analog that primarily targets adenosine receptors. It exhibits smooth muscle vasodilatory effects and has been implicated in the inhibition of cancer progression. Additionally, this compound serves as a click chemistry reagent, featuring an alkyne group that allows it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules, facilitating bioconjugation applications in chemical biology and drug development. -
Nucleoside Metabolite
3-Deoxy-D-arabino-heptulosonate 7-phosphate is a key nucleoside metabolite synthesized through the condensation of D-erythrose 4-phosphate with phosphoenolpyruvate, catalyzed by DAH 7-P synthase. This compound plays a crucial role in the shikimic acid pathway, serving as an intermediate in the biosynthesis of aromatic amino acids. Its study is essential for understanding metabolic processes in various organisms and can be applied in research focused on plant biochemistry and microbial metabolism. -
Nucleoside Metabolite
Ciliatocholate, a nucleoside metabolite, acts as a potent modulator of cellular signaling pathways. This compound has demonstrated biological activity in various research applications, including studies related to nucleic acid metabolism and cellular functions. Its role in cellular processes makes it a valuable tool for investigating the mechanisms underlying nucleoside metabolism and related biological phenomena. -
Nucleoside Metabolite
N-Formyl-L-glutamate is a nucleoside metabolite and a structural derivative of L-glutamate. It plays a role in amino acid metabolism, being a precursor to L-glutamate through enzymatic degradation processes. This compound is useful in biochemical studies focused on amino acid synthesis and metabolism, as well as in research exploring metabolic pathways in various organisms. -
Purine Nucleoside Analog
3'-Amino-3'-deoxyuridine is a purine nucleoside analog that exhibits broad antitumor activity, particularly against indolent lymphoid malignancies. Its efficacy is attributed to mechanisms such as the inhibition of DNA synthesis and the induction of apoptosis. This compound is valuable for research focused on cancer biology and could serve as a potential therapeutic agent in the development of treatments for various malignancies. -
Adenosine Analog
7'-O-DMT-morpholino thymine is an adenosine analog primarily known for its role in modulating adenosine receptors. It exhibits biological activities such as smooth muscle vasodilation and may play a role in inhibiting cancer progression. This compound is valuable for research applications in cardiovascular studies and cancer biology, providing insights into cellular signaling pathways and therapeutic strategies. -
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.
