Catalog No.
Product Name
Application
Product Information
Citations
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Purine Nucleoside Analog
6-(2-Furanyl)-9-β-D-ribofuranosyl-9H-purine is a purine nucleoside analog that exhibits significant antitumor activity, particularly 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 valuable for research applications focused on cancer therapeutics and the study of nucleoside metabolism. -
Purine Nucleoside Analog
5’-Deoxy-5’-(4-morpholinyl)thymidine is a purine nucleoside analog that demonstrates significant antitumor activity, particularly in indolent lymphoid malignancies. Its primary mechanism involves 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 uncover insights into the molecular mechanisms of tumor growth and response to treatment. -
Purine Nucleoside Analog
2-O-Benzoyl-3-O-t-butyldiphenylsilyl-L-threono lactone is a purine nucleoside analog that demonstrates significant antitumor activity by targeting indolent lymphoid malignancies. Its primary 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 in studies aimed at understanding its effects on cellular proliferation and tumorigenesis. -
Adenosine Analog
N6,N6-Dimethyl-xylo-adenosine is an adenosine analog with a primary mechanism of action involving modulation of adenosine receptors. This compound has demonstrated significant smooth muscle vasodilator activity and holds potential in inhibiting cancer progression. It is widely utilized in research applications focusing on vascular biology and oncology. -
Uridine Analog
N3-Methyl-2’-O-(2-methoxyethyl)uridine is a uridine analog that acts as a competitive inhibitor of uridine metabolism. This compound exhibits potential antiepileptic properties and is utilized in research to investigate anticonvulsant and anxiolytic activities. Additionally, it is a valuable tool for the development of novel antihypertensive agents. -
Purine Nucleoside Analog
3'-Deoxy-3'-fluoro-5-fluorouridine is a purine nucleoside analog known for its potent antitumor activity. This compound primarily functions by inhibiting DNA synthesis and inducing apoptosis, making it a valuable tool in the study of indolent lymphoid malignancies. Its application in cancer research aids in elucidating mechanisms of tumor cell proliferation and survival, contributing to the development of novel therapeutic strategies. -
Purine Nucleoside Analog
2-Amino-6-chloropurine-9-(2’-O-propargyl)riboside 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. Additionally, this compound serves as a click chemistry reagent due to the presence of an alkyne group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with azide-containing molecules, facilitating various bioconjugation applications in chemical biology. -
Purine Nucleoside Analog
2’,3’,5’-Tri-O-benzoyl-2’-β-C-methyl-5-methoxy uridine is a purine nucleoside analog known for its 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 compound for cancer research. This reagent is suitable for studies focused on nucleoside metabolism and anticancer therapeutics. -
Purine Nucleoside Analog
5’-O-DMTr-3’-deoxyuridine is a purine nucleoside analog that exhibits broad 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 and therapeutic studies. This compound can be utilized to investigate the pathways involved in tumor growth and resistance, providing insights into potential treatment strategies. -
Purine Nucleoside Analog
2-Amino-6-chloro-9-(3-deoxy-3-fluoro-beta-D-ribofuranosyl)-9H-purine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer effects are primarily mediated through the inhibition of DNA synthesis and the induction of apoptosis. This compound is valuable for research applications focused on cancer biology and the development of therapeutic strategies targeting nucleic acid metabolism. -
Purine Nucleoside Analog
2′,3′-O-Isopropylideneisocytidine is a purine nucleoside analog that exerts significant antitumor activity by targeting indolent lymphoid malignancies. This compound primarily functions through the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool in cancer research. Its unique mechanism highlights its potential in various therapeutic applications aimed at treating specific types of malignancies. -
Purine Nucleoside Analog
4’,5’-Didehydro-2’-O-(2-methoxyethyl)-5-methyluridine is a purine nucleoside analog that exerts its effects primarily through the inhibition of DNA synthesis. This compound demonstrates notable antitumor activity, particularly against indolent lymphoid malignancies, and induces apoptosis in cancer cells. Its applications in research provide valuable insights into the mechanisms of cancer treatment and therapeutic resistance. -
Purine Nucleoside Analog
2’-Amino-2’-deoxy-5-methyl uridine is a purine nucleoside analogue 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, making it a valuable tool in cancer research. This compound offers potential for exploring therapeutic strategies in oncology and advancing the understanding of nucleoside analog effects in tumor biology. -
Guanosine Analog
N1,N2-Dimethyl-2'-O-methylguanosine is a guanosine analog that primarily targets Toll-like receptor 7 (TLR7). It exhibits immunostimulatory activity and has been shown to induce type I interferons in various animal models, leading to significant antiviral effects. This compound is valuable in research applications focused on immune response modulation and the study of viral infections. -
Nucleoside Metabolite
22-Oxodocosanoic acid is a nucleoside metabolite that plays a critical role in cellular metabolism. It is involved in the regulation of fatty acid metabolism and may influence various biological processes such as cell signaling and energy homeostasis. This compound is suitable for research applications focusing on metabolic pathways and the study of nucleoside-related biological activities. -
Purine Nucleoside Analog
3’-Azido-3’-deoxy-5-fluoro-beta-L-cytidine is a purine nucleoside analog known for its potent antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action involve the inhibition of DNA synthesis and the induction of apoptosis. Additionally, this compound features an azide group, making it suitable for click chemistry applications, including copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) with alkyne-containing molecules, as well as DBCO or BCN groups. -
Nucleoside Metabolite
5-Hydroxykynurenine is a nucleoside metabolite that primarily functions as a precursor in the kynurenine pathway, influencing the balance of neuroactive metabolites. This compound exhibits bioactivity related to neuroprotection and modulation of neurotransmitter systems. It is commonly utilized in research focused on neurodegenerative diseases, psychiatric disorders, and inflammation studies, making it valuable for understanding neurochemical mechanisms. -
Purine Nucleoside Analog
2-Bromoadenosine is a purine nucleoside analog that exhibits potential antimalarial and anticancer activities. It is known to target indolent lymphoid malignancies through mechanisms such as inhibition of DNA synthesis and induction of apoptosis. This compound is relevant for research applications focused on cancer therapy and elucidating the effects of purine analogs in cellular processes. -
Adenosine Analog
5'-O-DMTr-2'-O-methyl-N6-methyl adenosine 3'-CED phosphoramidite is an adenosine analog known for its role as a smooth muscle vasodilator. This compound has demonstrated potential in inhibiting cancer progression, making it valuable in various research applications related to cardiovascular health and oncology. Its structural properties allow for incorporation into oligonucleotides, facilitating studies on adenosine signaling pathways and therapeutic development. -
Antitumor Compound
LY207702 is a difluorinated purine nucleoside that exhibits antitumor activity primarily through cytotoxic effects on cancer cells. It demonstrates significant cytotoxicity against CEA-positive LS174T cells, with an IC50 value of 0.302 μg/mL. This compound is valuable for research applications in colon cancer studies, contributing to the understanding of therapeutic mechanisms and potential treatment strategies. -
Nucleoside Metabolite
(25S)-3Alpha,7alpha,12alpha-trihydroxy-5beta-cholestan-26-oyl-CoA is a nucleoside metabolite that plays a crucial role in lipid metabolism. This compound may participate in various biochemical pathways and can be utilized in research focused on cholesterol metabolism and related diseases. Its structural features suggest potential implications in studies of lipid biochemistry and cellular signaling. -
Purine Nucleoside Analog
2′,3′-Dideoxy-5-fluorouridine is a purine nucleoside analog that exerts its effects by inhibiting DNA synthesis. This compound demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies, by promoting apoptosis and disrupting cellular proliferation. It serves as a valuable tool in cancer research, aiding in the understanding of therapeutic mechanisms and the development of novel treatments. -
Nucleoside Antimetabolite/Analog
Thiamiprine is a nucleoside antimetabolite and analog related to azathioprine, primarily targeting DNA synthesis. This compound exhibits cytotoxic effects in vitro, demonstrating activity comparable to its parent compound, though its arabinoside variant is inactive and non-toxic. In vivo studies using the rat adjuvant arthritis model indicate that the riboside and 2'-deoxyriboside forms are less active than the parent compound, while maintaining a distinct safety profile. Thiamiprine is valuable for research applications focused on immunosuppression and cellular proliferation. -
Purine Nucleoside Analog
9-(2-β-C-Methyl-β-D-ribofuranosyl)purine is a purine nucleoside analog that exerts its effects by targeting cellular pathways involved in DNA synthesis. This compound demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies, by inducing apoptosis and inhibiting cellular proliferation. It serves as a valuable tool for research applications in cancer biology and therapeutics development. -
Purine Nucleoside Analog
7-n-Butyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl)guanine is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. Its biological activity includes inhibition of DNA synthesis and induction of apoptosis, making it a valuable tool for cancer research. This compound can be utilized to study mechanisms of cancer cell proliferation and therapeutic resistance, contributing to the development of targeted cancer therapies. -
Purine Nucleoside Analog
3'-O-Methyl-2'-O-acetyl-5'-O-benzoyluridine is a purine nucleoside analog known for its broad antitumor activity against indolent lymphoid malignancies. Its primary mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis. This compound serves as a valuable tool in cancer research, particularly in studying cell proliferation and the apoptotic pathways in lymphoid malignancies. -
CARM1/HDAC2 inhibitor
CARM1/HDAC2-IN-1 is a dual inhibitor targeting both CARM1 and HDAC2, exhibiting IC50 values of 3.71 nM and 4.07 nM, respectively. This compound demonstrates significant antitumor activity, making it a valuable tool for cancer research. CARM1/HDAC2-IN-1 is suitable for studies investigating the role of these epigenetic regulators in tumor biology and therapeutic strategies. -
Nucleoside Analog
3'-O-Azidomethyl-CTP is a nucleoside analog that serves as a crucial building block for nucleic acid synthesis. It exhibits versatility in the synthesis of modified RNA and DNA, making it valuable for applications in molecular biology and genetic engineering. This compound enables researchers to incorporate azidomethyl groups into nucleic acid structures, facilitating studies in genetic function, drug development, and bioconjugation techniques. -
Nucleoside Analog
DMTr-2'-O-propyl-rC(Bz)-3'-CE-phosphoramidite is a nucleoside analog designed for use in oligonucleotide synthesis. This monomer plays a critical role in the formation of modified RNA molecules, facilitating studies in molecular biology and gene therapy applications. Its unique structure enhances stability and incorporation efficiency, making it an invaluable tool for researchers exploring nucleic acid functionality and behavior. -
Nucleoside Analog
DMTr-S-5-C-Me-2'-O-Me-rA(Bz)-3'-CE-phosphoramidite is a nucleoside analog used primarily in the synthesis of modified oligonucleotides. This phosphoramidite allows for the incorporation of modified ribonucleotides, enhancing stability and binding affinity in nucleic acid constructs. It is valuable for applications in therapeutic research, molecular biology, and gene delivery systems. -
Nucleoside Analog
m7ITP is a nucleoside analog that serves as a key monomer for nucleic acid synthesis. This compound exhibits essential properties for the development of RNA and DNA constructs, enabling detailed studies in molecular biology and genetic engineering. Its utility includes applications in the design of synthetic oligonucleotides and investigation of nucleic acid interactions. -
Nucleoside Analog
DMTr-2'-O-Me-rA(Bz)-3'-(D)-PSM-phosphoramidite is a nucleoside analog designed for efficient nucleic acid synthesis. This compound serves as a key monomer for the incorporation of modified ribonucleotides into oligonucleotides, enhancing stability and bioactivity. It is particularly useful in the development of RNA therapeutics, probes, and various molecular biology applications, facilitating precise manipulation of RNA structures. -
Nucleoside Analog
5'-OH-(2'OMe-U)pU is a nucleoside analog designed for use in nucleic acid synthesis. This compound serves as a monomeric building block, facilitating the incorporation of modified RNA structures. Its specific properties make it suitable for applications in RNA research, including the development of oligonucleotides and experimental RNA technologies. -
Nucleoside Analog
DMTr-2'-O-propyl-rA(Bz)-3'-CE-phosphoramidite is a specialized nucleoside analog designed for RNA synthesis. This phosphoramidite derivative facilitates the incorporation of modified nucleotides into RNA strands, enhancing the stability and functionality of nucleic acids. Its applications include the development of RNA-based therapeutics, probes, and biosensors, making it a valuable tool in nucleic acid research and biotechnological studies. -
Nucleoside Analog
5'-O-DMTr-2'-O-4'-C-Locked-rG(iBu) is a nucleoside analog specifically designed for use in nucleic acid synthesis. This compound functions as a protected monomer, facilitating the incorporation of modified guanosine units into oligonucleotide sequences. Its unique structural features enhance stability and enzymatic properties, making it an essential reagent for researchers focused on developing therapeutics and diagnostic tools involving RNA and DNA. -
Nucleoside Analog
2'-O-MOE-GTP is a nucleoside analog that serves as a substrate in the synthesis of oligonucleotides. Its unique substitution at the 2' position enhances the stability and binding affinity of RNA molecules. This compound is widely utilized in RNA research, including studies on RNA interference and the development of therapeutics targeting RNA-based diseases. -
Nucleoside Analog
Spacer C12 phosphoramidite is a nucleoside analog that serves as a building block for nucleic acid synthesis. This monomeric reagent enables the incorporation of spacer elements into oligonucleotide sequences, facilitating studies in molecular biology and genetics. Its unique structure allows for enhanced structural flexibility and potential applications in functionalized nucleic acids for research purposes. -
Nucleoside Analog
2',3'-Di-O-Methyladenosine is a nucleoside analog primarily utilized in nucleic acid synthesis. This compound serves as a valuable monomeric building block, facilitating the production of modified RNA and DNA. Its unique structural properties enhance the stability and functionality of nucleic acid constructs, making it an essential tool for researchers in molecular biology and genetic engineering applications. -
Nucleoside Analog
Cy3-CTP is a nucleoside analog that functions as a fluorescently labeled cytidine triphosphate. It is utilized in nucleic acid synthesis, allowing for the incorporation of Cy3 dye into RNA and DNA molecules. This compound is particularly beneficial for applications in molecular biology, including real-time PCR, in situ hybridization, and RNA imaging techniques, facilitating enhanced tracking and visualization of nucleic acids. -
Nucleoside Analog
2'-O-Propargyl-rC(Bz) is a nucleoside analog with a propargylic functionality that serves as a versatile monomer for nucleic acid synthesis. Its structure enables incorporation into RNA strands, facilitating the study of nucleic acid interactions and modifications. This compound is particularly useful in research applications involving RNA synthesis, bioconjugation, and the development of nucleic acid-based therapeutics. -
Nucleoside Analog
Pseudouridine 5'-phosphate is a nucleoside analog that serves as a key building block in nucleic acid synthesis. It is known to enhance the stability and biological activity of RNA molecules, making it a valuable reagent for studies involving RNA structure and function. This compound is frequently utilized in the development of RNA-based therapeutics and novel gene editing technologies. -
Nucleoside Analog
5-Formyl-Dctp is a nucleoside analog exhibiting structural properties that enable its incorporation into DNA during synthesis. This compound serves as a vital intermediate in the preparation of modified nucleotides, facilitating studies in nucleic acid research and synthetic biology. Its unique aldehyde functional group allows for further chemical modifications, making it useful in various applications, including the development of labeled oligonucleotides and probes for genomic studies. -
Nucleoside Analog
3'-O-NH2-2'-dA is a nucleoside analog that serves as a crucial building block for nucleic acid synthesis. It displays unique biochemical properties that facilitate the incorporation of amino groups into nucleic acid sequences, enhancing the versatility of synthetic oligonucleotides. This compound is essential for research applications involving genetic engineering, molecular diagnostics, and the development of novel therapeutic agents. -
Nucleoside Analog
(2'OMe-5'p-U)pU is a nucleoside analog that serves as a monomeric building block for nucleic acid synthesis. Its unique structural modifications enhance stability and binding affinity, making it a valuable tool for researchers in the fields of molecular biology and genetic engineering. This compound can be utilized in the development of oligonucleotides and other nucleic acid-based applications, providing insights into RNA structure and function. -
Nucleoside Analog
5'-O-DMTr-2'-O-4'-C-locked-5-Me-rC(Bz) is a nucleoside analog designed for use in nucleic acid synthesis. This compound features modifications that enhance stability and potential for incorporation into oligonucleotides. Its unique structural properties make it valuable for research applications involving RNA chemistry and the development of novel therapeutics. -
Nucleoside Analog
N1-Me-pUMP is a nucleoside analog that serves as a monomeric building block for nucleic acid synthesis. This reagent is essential for the preparation of modified oligonucleotides and plays a pivotal role in studies involving RNA and DNA characterization. Its incorporation into nucleic acid sequences can facilitate research in areas such as gene expression, molecular diagnostics, and therapeutic development. -
Nucleoside Analog
N6-Benzoyl-2'-O,4'-C-methyleneadenosine is a nucleoside analog that serves as a key building block in nucleic acid synthesis. Its unique structural modifications enhance incorporation into RNA and DNA sequences, facilitating the study of nucleic acid functioning and interactions. This compound is valuable for research in molecular biology, enabling investigations into gene expression, replication mechanisms, and therapeutic applications. -
Nucleoside Analog
(2'OMe-5'p-A)pU is a nucleoside analog designed for use in nucleic acid synthesis. This modified nucleotide contains a 2'-O-methyl group, enhancing its stability and affinity for complementary bases. It serves as a useful building block in the development of oligonucleotides for research applications including gene expression studies, antisense oligonucleotide design, and therapeutic development. -
Nucleoside Analog
CTPαS is a nucleoside analog that serves as a phosphonate monomer for nucleic acid synthesis. Its structural properties enable incorporation into RNA and DNA, facilitating the study of nucleic acid function and dynamics. This reagent is highly valuable in biochemical research, particularly in the development of oligonucleotide therapeutics and molecular biology applications. -
Nucleoside Analog
DMTr-2'-O-Bn-rG(iBu)-3'-CE-phosphoramidite is a nucleoside analog designed for use in nucleic acid synthesis. This compound serves as a monomeric raw material, facilitating the incorporation of modified ribonucleotides into oligonucleotides. It is particularly valuable for applications involving the synthesis of RNA molecules, enabling research in fields such as molecular biology, genetics, and therapeutic development.
