Catalog No.
Product Name
Application
Product Information
Citations
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Nucleoside Metabolite
5-(L-Alanin-3-yl)-2-hydroxy-cis,cis-muconate 6-semialdehyde is a nucleoside metabolite that plays a critical role in metabolic pathways. This compound exhibits notable biological activity related to nucleoside metabolism, making it valuable for research in cellular processes and enzymatic reactions. It is particularly useful for studies focused on nucleoside regulation and metabolism in various biological contexts. -
Purine Nucleoside Analog
1-Amino-7-cyclopropyl methyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl)guanine is a purine nucleoside analog that targets critical pathways in cancer cells. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, through mechanisms such as DNA synthesis inhibition and the induction of apoptosis. Its unique structural features make it a valuable tool in cancer research, particularly for investigating therapeutic strategies in lymphoid cancers. -
Nucleoside Metabolite
(R)-Ureidoisobutyric acid is a nucleoside metabolite that plays a crucial role in various biochemical processes. This compound serves as an important intermediate in nucleotide metabolism and is utilized in research focused on cellular signaling, metabolism, and nucleic acid biochemistry. Its ability to influence metabolic pathways makes it a valuable tool for exploring cellular functions and disease mechanisms. -
Purine Nucleoside Analog
2′-O-Methyl-2-amino-6-chloropurine riboside is a purine nucleoside analog that serves as an important tool in cancer research. It exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, by interfering with DNA synthesis and inducing apoptosis in cancer cells. Its versatile applications in cellular and molecular biology make it a valuable reagent for studying therapeutic strategies against various malignancies. -
Guanosine Analog
2'-C-Methylguanosine is a guanosine analogue that primarily targets and activates Toll-like receptor 7 (TLR7). It exhibits significant immunostimulatory activity and has been shown to induce type I interferons in various animal models, leading to antiviral effects. This compound is valuable for research applications focused on exploring the immune response and antiviral mechanisms. -
Adenosine Analog
3'-β-C-Methyladenosine is an adenosine analog that primarily targets adenosine receptors. This compound exhibits biological activity as a smooth muscle vasodilator and has demonstrated potential in inhibiting cancer progression. It is useful in research applications focused on cardiovascular function and cancer biology. -
Purine Nucleoside Analog
4’-C-Methyl-4-deoxyuridine 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 apoptotic pathways in cancer cells. Its research applications include exploring mechanisms of cancer treatment and evaluating therapeutic efficacy in oncology studies. -
Nucleoside Metabolite
(R)-2-Hydroperoxy-α-linolenic acid is a nucleoside metabolite that plays a crucial role in fatty acid metabolism. It exhibits notable biological activities, including modulation of oxidative stress and cell signaling pathways. This compound is particularly useful in research focused on lipid metabolism, cell function, and the effects of oxidative damage in various biological systems. -
Purine Nucleoside Analog
2'-Deoxy-2'-fluoro-6-S-Methyl-6-thio-ara-guanosine is a purine nucleoside analog that primarily targets nucleotide metabolism. It exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, through mechanisms such as inhibition of DNA synthesis and the induction of apoptosis. This compound serves as a valuable tool in cancer research, facilitating the exploration of therapeutic strategies targeting purine metabolism. -
Purine Nucleoside Analog
5-Hydroxy-2'-O-methyluridine is a purine nucleoside analog that exhibits significant anticancer activity. This compound functions primarily by inhibiting DNA synthesis and inducing apoptosis in cancer cells, making it a valuable tool in research aimed at understanding treatments for indolent lymphoid malignancies. Its biological properties position it as a promising candidate for further investigation in cancer therapy development. -
Purine Nucleoside Analog
6-(2-O-Methyl-beta-D-ribofuranosyl)-3-(2-oxo-propyl)-6H-imidazo[1,2-c]pyrimidin-5-one is a purine nucleoside analog with promising antitumor activity against indolent lymphoid malignancies. Its cytotoxic effects primarily involve the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for cancer research. This compound's unique structure allows for further exploration in the development of targeted therapies for various malignancies. -
Nucleoside Metabolite
4-(2-Amino-3-hydroxyphenyl)-2,4-dioxobutanoic acid is a nucleoside metabolite that plays a significant role in cellular metabolism. This compound is implicated in various biochemical pathways, including those involving nucleobase metabolism. Its biological activities make it valuable for research applications focused on enzymatic reactions related to nucleoside synthesis and regulation. -
Purine Nucleoside Analog
3’-N-Acetyl-3’-amino-3’-deoxyuridine is a purine nucleoside analog primarily involved in inhibiting DNA synthesis. This compound exhibits potent antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include inducing apoptosis and impairing cellular proliferation, making it a valuable reagent for cancer research and therapeutic studies. -
Nucleoside Metabolite
3-Benzylmalic acid is a nucleoside metabolite that serves as a valuable intermediate in biochemical synthesis. It can be produced from 2-Benzylmalic acid via a hydroxyl isomerization reaction catalyzed by HphCD. This compound is utilized in various research applications, particularly in studies related to enzymatic reactions and metabolic pathways involving nucleoside derivatives. -
Purine Nucleoside Analog
5′-O-[Bis(4-methoxyphenyl)phenylmethyl]cytidine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its biological action involves the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool in cancer research. This compound is suitable for studying mechanisms of cancer cell proliferation and developing therapeutic strategies targeting nucleoside metabolism. -
Purine Nucleoside Analog
3’,5’-Di-O-acetyl-2’-deoxy-N3-methyl uridine is a purine nucleoside analog that acts primarily by inhibiting DNA synthesis. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms include induction of apoptosis and disruption of cellular proliferation, making it a valuable reagent for research in oncology and molecular biology. -
Purine Nucleoside Analog
3'-Azido-3'-deoxy-N6-methyladenosine is a purine nucleoside analogue designed for research applications in cancer biology. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, by inhibiting DNA synthesis and inducing apoptosis. Additionally, it serves as a versatile click chemistry reagent, featuring 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 DBCO/BCN-functionalized compounds, facilitating bioconjugation studies. -
Purine Nucleoside Analog
2′-Deoxy-2′-fluoro-N-methyladenosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism of action includes the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound is valuable for researchers investigating therapeutic strategies and mechanisms of action in cancer biology. -
Nucleoside Metabolite
2-Methyl-1-hydroxypropyl-ThPP is a nucleoside metabolite that plays a critical role in nucleoside metabolism. This compound is involved in various biological processes and is essential for studying cellular metabolism pathways. Its applications extend to research on nucleoside-related signaling and metabolic regulation in various biological systems. -
Purine Nucleoside Analog
N4-Ethyl-2’-deoxycytidine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. The compound functions primarily by inhibiting DNA synthesis, leading to the induction of apoptosis in cancer cells. Its applications in research include exploring mechanisms of cancer cell proliferation and evaluating therapeutic strategies targeting nucleosynthesis pathways. -
Quercetin Metabolite
3α,7α,12α,26-Tetrahydroxy-5β-cholestane is a significant metabolite of Quercetin, functioning as a key marker in primary bile acid biosynthesis. This compound plays a crucial role in research related to atherosclerosis, providing insights into lipid metabolism and cardiovascular health. Its biological activities make it a valuable reagent for studying the effects of dietary flavonoids on cellular pathways. -
Nucleoside Metabolite
(S)-Ureidoglycolic acid is a substrate for the enzyme ureidoglycolate dehydrogenase, playing a critical role in purine metabolism pathways. As a member of the n-carbomoyl-α-amino acid class, it is essential for studies focused on nucleotide biosynthesis and related metabolic processes. This compound serves as a valuable research tool for understanding the biochemical intricacies of purine metabolism and its implications in various physiological contexts. -
Nucleoside Metabolite
Phosphonoformyl-CMP is a nucleoside metabolite that serves as an analogue of cytidine monophosphate. This compound is primarily utilized in studies of nucleotide metabolism and enzymatic activity related to nucleoside triphosphate synthesis. Its unique structure allows for exploration of biochemical pathways and interactions involving nucleotides, thereby informing research in molecular biology and pharmacology. -
Purine Nucleoside Analog
2’-Chloro-N6-(4-trifluoromethyl)benzyl adenosine 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, making it a valuable compound for cancer research. This reagent is suitable for studies focused on understanding tumor biology and developing therapeutic strategies targeting nucleoside pathways. -
Purine Nucleoside Analog
3'-Azido-3'-deoxy-5-trifluoromethyluridine is a purine nucleoside analogue primarily known for its broad antitumor activity against indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis. Additionally, this compound serves as a click chemistry reagent, featuring an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalized compounds. -
Purine Nucleoside Analog
5’-O-TBDPS-2,2’-anhydrouridine is a purine nucleoside analog that acts primarily by inhibiting DNA synthesis. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism also includes the induction of apoptosis, making it a valuable tool for research focused on cancer biology and therapeutic development. -
Purine Nucleoside Analog
3-epi-Azido-3-deoxythymidine is a purine nucleoside analog known for its antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanisms of action include the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for cancer research. This reagent is suitable for studies exploring therapeutic strategies in oncology and the mechanistic understanding of tumor cell behavior. -
Purine Nucleoside Analog
2,3’-Anhydrothymidine is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanism involves the inhibition of DNA synthesis, which leads to subsequent induction of apoptosis. This compound serves as a valuable tool in cancer research, contributing insights into therapeutic strategies for lymphoid cancers. -
Nucleoside Metabolite
20-Hydroxyleukotriene E4 is a nucleoside metabolite that plays a crucial role in the metabolism of leukotrienes. It is involved in various biological processes, including immune response modulation and inflammation. Research applications include investigations of inflammatory diseases and the elucidation of leukotriene signaling pathways. -
Purine Nucleoside Analog
N2-iso-Butyryl-8-azaguanosine is a purine nucleoside analog that demonstrates significant biological activity against indolent lymphoid malignancies. Its anticancer properties are attributed to the inhibition of DNA synthesis and the induction of apoptosis. This compound serves as a valuable tool for research applications in oncology and cancer treatment studies. -
Guanosine Analog
5'-O-DMT-N2-isobutyryl-2'-O-propargylguanosine is a guanosine analog that primarily targets Toll-like receptor 7 (TLR7). This compound exhibits immunostimulatory activity, and in various animal models, it has been shown to induce type I interferons, leading to antiviral effects. Its role in modulating immune responses makes it a valuable tool for research applications focused on viral pathogenesis and immune activation. -
Purine Nucleoside Analog
1-(2,3-Dideoxy-β-D-erythro-hexopyranosyl)cytosine is a purine nucleoside analog that demonstrates significant antitumor 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 tool for cancer research. This compound is suitable for investigations into therapeutic strategies targeting nucleoside metabolism and malignancy treatment. -
Purine Nucleoside Analog
2′-Deoxy-2-thiouridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism of action includes the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool in cancer research. This compound is utilized for exploring therapeutic strategies and understanding the underlying biology of tumor progression. -
Purine Nucleoside Analog
3',5'-Bis-O-benzoyl-2'-deoxy-2'-fluoro-beta-D-arabino-6-azidouridine is a purine nucleoside analog that exhibits broad antitumor activity, particularly against indolent lymphoid malignancies. This compound operates by inhibiting DNA synthesis and inducing apoptosis, making it a valuable tool in cancer research and therapeutic studies. Its unique structural modifications enhance its efficacy as a research reagent in exploring mechanisms of cancer treatment. -
Uridine Analog
N3-[(Tetrahydro-2-furanyl)methyl]uridine is a uridine analog with potential antiepileptic properties. This compound is utilized in research to explore anticonvulsant and anxiolytic activities, making it a valuable tool for the development of new therapies. Additionally, it may contribute to the discovery of novel antihypertensive agents, expanding its application in cardiovascular research. -
Adenosine Analog
9-(2-Deoxy-β-D-threo-pentofuranosyl)-9H-purin-6-amine is an adenosine analog that primarily acts on adenosine receptors. This compound exhibits smooth muscle vasodilatory activity and has demonstrated potential in inhibiting the progression of various cancers. It serves as a valuable tool in biochemical research focusing on vascular biology and oncology. -
Purine Nucleoside Analog
2'-Deoxy-N2-isopropyl guanosine is a purine nucleoside analog that primarily targets DNA synthesis. It exhibits notable antitumor activity, particularly against indolent lymphoid malignancies, through mechanisms such as apoptosis induction and DNA synthesis inhibition. This compound serves as a valuable tool for researchers investigating cancer biology and therapeutic strategies in oncology. -
Thymidine Analog
3'-O-Methyl-5-methyluridine is a thymidine analog that exhibits insertional activity towards replicated DNA. This reagent is utilized for labeling cells and monitoring DNA synthesis, making it valuable for studies in molecular biology and genetic research. Its unique properties allow for enhanced tracking of nucleic acid dynamics in various cellular contexts. -
5'-dIMP Analogue
5'-dIMPS is an analogue of 5'-dIMP that serves as a potential substrate, competitive inhibitor, or regulator of enzymes that interact with 5'-dIMP. Its structural similarity allows it to modulate enzymatic activities involved in nucleotide biosynthesis pathways. This compound can be utilized in biochemical studies to explore enzyme mechanisms and regulatory processes within cellular metabolism. -
Purine Nucleoside Analog
2-Amino-6-chloropurine-9-beta-D-(2'-deoxy-3',5'-di-O-benzoyl-2'-fluoro)arabinoriboside is a purine nucleoside analog that exerts its biological activity by inhibiting DNA synthesis and inducing apoptosis. This compound demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies. Its role as a nucleoside analog makes it a valuable tool for research in cancer biology and therapeutic development. -
Adenosine Analog
2-Amino-2′-O-(2-methoxy-2-oxoethyl)adenosine is an adenosine analogue targeting adenosine receptors. It exhibits smooth muscle vasodilatory effects and has demonstrated potential in inhibiting cancer progression. This compound is valuable for research applications focusing on vascular biology and cancer therapeutics. -
Purine Nucleoside Analog
N6-(4-Methoxybenzyl)-2’-C-methyl adenosine 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, making it a valuable tool for cancer research. This compound is particularly useful for studying the effects of purine analogs on tumor progression and therapeutic responses. -
Purine Nucleoside Analog
1,2-Di-O-acetyl-3,5-di-O-benzoyl-3-beta-C-methyl-D-ribofuranose serves as a purine nucleoside analog, primarily targeting DNA synthesis inhibition. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include the induction of apoptosis and disruption of cellular proliferation, making it a valuable reagent for cancer research applications. -
Uridine Analog
4′-C-2-Propen-1-yluridine serves as a uridine analog, targeting pathways involved in neurological function. This compound exhibits potential antiepileptic properties and is instrumental in exploring anticonvulsant and anxiolytic activities. Additionally, it holds promise for the development of novel antihypertensive agents, making it a valuable tool in biomedical research. -
Purine Nucleoside Analog
4-Hydroxy-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinone is a purine nucleoside analog primarily targeting DNA synthesis pathways. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer effects are attributed to mechanisms such as the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable reagent for research in cancer biology and therapeutic development. -
5'-dGMP Analogue
5'-dGMPS is a 5'-dGMP analogue that serves as a potential substrate, competitive inhibitor, or regulator of enzymes that interact with 5'-dGMP. This reagent can be utilized in enzymatic assays to study the kinetics and mechanisms of nucleotide metabolism and signaling pathways. Research applications include investigating the role of 5'-dGMP in cellular processes and the development of therapeutic interventions targeting nucleotide-related pathways. -
Guanosine Analog
2'-F-2'-ara-N2-ibu-dG Phosphoramidite is a guanosine analog that targets Toll-like receptor 7 (TLR7) to exhibit immunostimulatory activity. It has been shown to induce type I interferons in certain animal models, resulting in antiviral effects. This compound is valuable for research applications focused on antiviral mechanisms and immune response modulation. -
Thymidine Analog
2'-Deoxy-2'-fluoro-5-hydroxymethyl arabinouridine is a thymidine analog that incorporates into DNA during replication. This compound demonstrates insertional activity, allowing for effective labeling of cells and monitoring of DNA synthesis. It serves as a valuable tool in molecular biology research, particularly for studies involving DNA dynamics and cellular proliferation. -
Purine Nucleoside Analog
2-Chloro-3'-deoxy-3'-fluoroadenosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms include the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for cancer research. This compound can be utilized in studies aiming to understand nucleoside analog effects and therapeutic strategies for hematological cancers. -
Purine Nucleoside Analog
3'-O-(t-Butyldimethylsilyl)-2'-deoxy-2'-fluorouridine is a purine nucleoside analog that exhibits significant antitumor activities. It primarily functions by inhibiting DNA synthesis and promoting apoptosis in various cancer cell types, making it especially relevant for research involving indolent lymphoid malignancies. This compound serves as a valuable tool for studying cancer biology and the development of targeted therapeutics.
