Catalog No.
Product Name
Application
Product Information
Citations
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Pyrimidine Nucleoside Analog
4,6-Diamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine is a pyrimidine nucleoside analog targeting nucleic acid metabolism. This compound demonstrates significant biological activities, including inhibition of DNA and RNA synthesis, antiviral properties, and immunomodulatory effects. It is a valuable research tool for studying molecular mechanisms in cancer biology, virology, and immunology. -
Nucleoside Metabolite
3-Oxo-3-ureidoisobutyrate is a nucleoside metabolite involved in various biochemical pathways. It plays a crucial role in the metabolism of nucleotides, influencing nucleobase synthesis and cellular energy homeostasis. This compound is useful in research applications related to nucleotide metabolism and can aid in understanding the regulatory mechanisms of nucleoside derivatives in cellular processes. -
Purine Nucleoside Analog
5'-Deoxy-5'-N,N-diethylamino thymidine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include inhibition of DNA synthesis and the induction of apoptosis, making it a valuable compound for cancer research and therapeutic studies focused on lymphoid neoplasms. This compound is instrumental in understanding the role of nucleoside analogs in cancer treatment and their potential effects on cell proliferation and viability. -
Purine Nucleoside Analog
3’-Azido-3’-deoxy-5-methyluridine is a purine nucleoside analog primarily effective in inhibiting DNA synthesis, which promotes apoptosis in cancer cells. Its broad antitumor activity is particularly relevant for indolent lymphoid malignancies. Additionally, this compound serves as a 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) reactions with DBCO or BCN groups, facilitating various biochemical applications in research. -
Purine Nucleoside Analog
2’-dG (iBu)-2’-phosphoramidite is a purine nucleoside analog that selectively targets DNA synthesis pathways. It exhibits significant antitumor activity against indolent lymphoid malignancies through mechanisms such as the inhibition of DNA replication and the induction of apoptosis. This reagent is essential for research applications focused on cancer biology and nucleic acid synthesis. -
Purine Nucleoside Analog
8-Methyl-2’-deoxyguanosine 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, making it a valuable tool in cancer research and therapeutic studies. This compound is instrumental in investigating mechanisms of action and developing targeted treatments for various malignancies. -
Thymidine Analog
5-Hydroxymethyl-arauridine is a thymidine analogue that exhibits insertional activity towards replicated DNA. This compound is particularly valuable for labeling cells and monitoring DNA synthesis in various research applications. Its ability to mimic natural nucleotides makes it an effective tool for investigating cellular proliferation and the dynamics of DNA replication. -
Purine Nucleoside Analog
5-Hydroxymethyl-2',3'-O-isopropylidene-2-thiouridine is a purine nucleoside analog that exhibits notable antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanisms include the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound serves as a valuable research tool for investigating therapeutic strategies in cancer treatment and understanding the molecular pathways involved in tumor progression. -
Guanosine Analog
7-Cyano-7-deaza-2'-deoxy guanosine is a guanosine analog with significant immunostimulatory properties. It has been demonstrated to induce type I interferons in various animal models, thereby exerting antiviral effects. The biological activity of this compound is closely linked to the activation of Toll-like receptor 7 (TLR7), making it a valuable tool for research in immunology and antiviral therapies. -
Adenosine Analog
N6-Benzoyl-7'-O-DMT-morpholino adenine is an adenosine analog that primarily targets adenosine receptors. This compound exhibits notable biological activities, including smooth muscle vasodilation and the potential inhibition of cancer progression. It is commonly utilized in research applications related to cardiovascular studies and cancer therapeutics, contributing valuable insights into adenosine signaling and its effects on physiological processes. -
Purine Nucleoside Analog
5-Difluoromethyluridine 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 reagent is valuable for research applications focused on cancer biology and the development of therapeutic strategies targeting tumor cell proliferation. -
Purine Nucleoside Analog
1-(2-Deoxy-β-D-erythro-pentofuranosyl)-4(1H)-pyrimidinone is a purine nucleoside analog known for its potential anticancer activity. It exhibits efficacy against indolent lymphoid malignancies primarily through mechanisms that inhibit DNA synthesis and induce apoptosis. This compound is valuable for research in cancer biology and drug development focused on targeted therapies for lymphoid-related tumors. -
5'-dAMP Analogue
5'-dAMPS is an analogue of 5'-deoxyadenosine monophosphate (5'-dAMP) that serves as a potential substrate, competitive inhibitor, or regulator of enzymes that interact with dAMP. This compound is valuable in biochemical research for studying nucleotide metabolism and enzyme kinetics, particularly in the context of adenine nucleotide chemistry. Its ability to modulate enzyme activity makes it a useful tool for exploring the roles of dAMP-related pathways in cellular processes. -
Purine Nucleoside Analog
N4-Amino-2'-C-methylcytidine 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 is relevant for studies investigating nucleoside metabolism and the development of therapeutic strategies in oncology. -
Purine Nucleoside Analog
Methyl 4-C-hydroxymethyl-2,3-O-isopropylidene-beta-D-ribofuranoside 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 in cancer cells. Its unique properties make it a valuable tool for researchers investigating therapeutic approaches to cancer treatment. -
Cytidine Analog
Xylocytidine is a cytidine analog that primarily inhibits DNA methyltransferases, which are crucial enzymes involved in DNA epigenetic regulation. This compound exhibits potential anti-metabolic and anti-tumor activities, making it a valuable tool for cancer research and studies focused on gene expression regulation. Its role in modulating DNA methylation offers promising applications in understanding epigenetic alterations in various diseases. -
Purine Nucleoside Analog
N6-Ethyl-2’-C-methyladenosine is a purine nucleoside analog that exerts significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound serves as a useful tool for research into cancer biology, drug development, and therapeutic applications in hematological malignancies. -
Purine Nucleoside Analog
N4-Benzoyl-2’-deoxy-2’,2’-difluorocytidine is a purine nucleoside analog known for its potent antitumor activity. This compound primarily targets indolent lymphoid malignancies by interfering with DNA synthesis and promoting apoptosis in cancer cells. It serves as a valuable tool for researchers investigating the mechanisms of cancer treatment and exploring therapeutic strategies in oncology. -
Purine Nucleoside Analog
4-Amino-1-(2-C-methyl-β-D-ribofuranosyl)-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile is a purine nucleoside analog that exhibits significant biological activity against indolent lymphoid malignancies. Its anticancer mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis. This compound is valuable for research applications focused on cancer therapeutics and the study of nucleoside analog effects on cellular processes. -
Purine Nucleoside Analog
2,6-Dichloro-2',3',5'-triacetyl-purine riboside is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. Its biological activity primarily involves the inhibition of DNA synthesis and the induction of apoptosis, making it valuable for research in cancer therapy. This compound is essential for studies focusing on the mechanisms of nucleoside analogs in targeted cancer treatments. -
Cytidine Analog
N-(1-Oxopropyl)cytidine is a cytidine analog that serves as an inhibitor of DNA methyltransferases. This compound exhibits potential anti-metabolic and anti-tumor activities, making it a valuable tool in cancer research. Its ability to alter epigenetic regulation provides insights into gene expression modulation and therapeutic strategies in oncology. -
Purine Nucleoside Analog
2’-O-Methyl-5-methyl-4-thiouridine is a purine nucleoside analogue that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its biological effects are attributed to mechanisms such as the inhibition of DNA synthesis and the induction of apoptosis. This compound is valuable in cancer research for exploring therapeutic strategies and understanding the cellular processes involved in tumorigenesis. -
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.
