Catalog No.
Product Name
Application
Product Information
Citations
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Nucleoside Analog
3'-OMe-m7GMP is a nucleoside analog that serves as a vital monomeric building block in nucleic acid synthesis. Its modified structure enhances stability and incorporation into nucleic acid polymers, making it useful for studies in molecular biology and genetic engineering. This compound supports research in RNA synthesis and the development of therapeutic oligonucleotides. -
Nucleoside Analog
2'-OMe-CTP is a nucleoside analog that serves as a monomer for nucleic acid synthesis. This modified nucleotide exhibits enhanced nucleotide stability and improved binding affinity, making it useful in the development of ribonucleic acid (RNA) therapeutics and diagnostic applications. Its incorporation into oligonucleotides can enhance RNA's resistance to enzymatic degradation, facilitating studies in molecular biology and genetic engineering. -
Nucleoside Analog
5'-O-DMTr-2'-O-4'-C-Locked-rG(dmf) is a nucleoside analog designed for use in nucleic acid synthesis. This compound features a protective group that ensures stability and efficiency during oligonucleotide assembly. Its unique structure facilitates the incorporation of modified ribonucleotides, making it valuable for advancing research in molecular biology and genetic engineering. -
Nucleoside Analog
2'-F-CDP is a nucleoside analog that serves as a key building block in the synthesis of oligonucleotides. Its fluorinated structure enhances metabolic stability and may improve the pharmacokinetic properties of RNA-based therapeutics. This compound is valuable in research applications such as oligonucleotide design and development, enabling advancements in gene therapy and RNA interference studies. -
Nucleoside Analog
Im-3'-OMe-GMP is a nucleoside analog that serves as a key monomer for nucleic acid synthesis. It demonstrates stability and incorporation in RNA and DNA processes, making it suitable for investigating cellular functions and developing therapeutics. This compound is valuable in the study of gene expression, oligonucleotide design, and other applications in nucleic acid research. -
Guanosine Nucleoside
N-Acetyl-2',3'-acetyl-guanosine is a modified guanosine nucleoside that serves as a substrate for various enzymatic processes. This compound is utilized in biochemical research to study nucleoside metabolism and nucleotide synthesis. Its unique acetyl modifications enhance solubility and stability, making it suitable for exploring nucleoside interactions and applications in RNA biochemistry. -
Nucleoside Analog
3'-ONH2-dGTP is a nucleoside analog that serves as a crucial monomeric substrate for nucleic acid synthesis. Its unique chemical structure allows for incorporation into DNA and RNA, facilitating studies in molecular biology, genetic engineering, and pharmacology. This reagent is instrumental for researchers exploring nucleotide modifications and their implications in various biological processes. -
Nucleoside Analog
5'-O-DMTr-2'-O-(2-Aminoethyl)-5-Me-rU is a nucleoside analog that serves as a key monomer in nucleic acid synthesis. This compound can facilitate the incorporation of modified ribonucleotides into RNA, enhancing the stability and functionality of oligonucleotides. It is particularly valuable in research applications involving RNA therapeutics and the development of novel RNA-based biomolecules. -
Thymidine Analog
5-(3-Azidopropyl)uridine is a thymidine analog that displays insertional activity towards replicated DNA, making it valuable in studies of DNA synthesis and cellular labeling. This compound features an azide group, allowing it to function as a click chemistry reagent. It can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules, and also engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, facilitating diverse applications in chemical biology. -
Nucleoside Analog
Fluorescein-12-dUTP is a nucleoside analog that serves as a fluorescently labeled deoxyuridine triphosphate. Its primary mechanism involves incorporation into nucleic acids during DNA synthesis, facilitating the visualization of nucleic acids in various applications. This reagent is particularly valuable in molecular biology techniques such as DNA labeling, in situ hybridization, and studying gene expression. -
Nucleotide Analogue
N-Acetyltryptamine α-D-Glucose-3-phosphate acts as a nucleotide analogue, facilitating the modification and stabilization of RNA through the covalent attachment of glucose nucleotides. This compound demonstrates significant potential in enhancing RNA stability, making it an invaluable tool in research applications related to cancer and infectious diseases. Its unique structure allows for exploration into novel therapeutic strategies and biomolecular interactions. -
Nucleoside Analog
Rp-dATPαS is a nucleoside analog that serves as a modified building block for nucleic acid synthesis. It is specifically designed to inhibit DNA polymerase activity, making it a valuable tool in studies of nucleic acid metabolism and replication processes. Rp-dATPαS can be employed in various research applications, including the development of novel therapeutics and the exploration of antiviral strategies. -
Nucleoside Analog
5'-O-DMTr-2'-O-(2-cyanoethoxymethyl)-rG(Pac) is a nucleoside analog designed for use in nucleic acid synthesis. This compound serves as a versatile building block for the formation of RNA sequences and other oligonucleotides. Its distinct chemical structure allows for specific modifications, enhancing the functionality and stability of synthesized nucleic acids for various research applications, including genetic studies and therapeutic development. -
Nucleoside Analog
3'-O-DMTr-2'-F-dA(Bz)-5'-CE-phosphoramidite is a nucleoside analog utilized for the synthesis of modified nucleic acids. This monomeric reagent incorporates a 2'-fluoro modification, which can enhance the stability and binding affinity of oligonucleotides. It is essential for researchers focusing on the development of therapeutic oligonucleotides and the study of nucleic acid interactions. -
Nucleoside Analog
2'-O-Propargyluridine is a nucleoside analog specifically designed for the synthesis of nucleic acids. Exhibiting properties that facilitate the formation of modified oligonucleotides, it serves as a versatile building block in research applications focusing on gene expression and RNA interference. Its unique structure provides potential advantages in enhancing the stability and binding affinity of nucleic acid strands. -
Nucleoside Analog
5-Aminoallyluridine-5'-triphosphate is a nucleoside analog that serves as a critical monomer for nucleic acid synthesis. Its unique structure facilitates incorporation into RNA and DNA, thereby enabling the study of nucleic acid dynamics and interactions. This reagent is valuable for applications in molecular biology, including the synthesis of modified nucleotides for investigations in gene expression and cellular assays. -
Nucleoside Analog
3′-O-Azidomethyl-dCTP is a nucleoside analog that serves as a building block for nucleic acid synthesis. This compound is particularly useful in the creation of modified nucleic acids and can facilitate the study of biological processes involving DNA. Its incorporation into oligonucleotides enables applications in nucleotide labeling, probing, and other molecular biology research. -
Nucleoside Analog
CAP m7G(5')ppp(5')(2'OMeG) is a nucleoside analog with a crucial role in nucleic acid synthesis. This compound acts as a building block for RNA modification, enhancing stability and resistance to degradation. It is widely used in the development of RNA-based therapeutics and molecular biology applications, including the study of messenger RNA (mRNA) capping and stability. -
Nucleoside Analog
DMTr-2'-O-Me-6-Deamino-6-(m-benzenepropanoic acid 2-cyanoethyl ester)-rA-3'-CE-phosphoramidite is a nucleoside analog that serves as a monomeric building block in nucleic acid synthesis. Its unique structural modifications enable enhanced incorporation into oligonucleotides, facilitating studies in gene expression and oligonucleotide therapeutics. This reagent is valuable for researchers focused on the development of custom RNA sequences and in exploring various applications in molecular biology. -
Nucleoside Analog
5-Hme-UTP is a nucleoside analog that serves as a key monomer for nucleic acid synthesis. It exhibits unique incorporation properties, allowing researchers to study RNA synthesis and function. This compound is widely utilized in applications such as the development of RNA-based therapeutics and the investigation of RNA structural dynamics. -
Nucleoside Analog
N,N-Dimethyl-ATP is a nucleoside analog primarily used as a monomer in nucleic acid synthesis. This compound serves as a building block in the preparation of modified nucleic acids, facilitating studies in molecular biology and biochemistry. Its structural modifications enhance stability and affinity in various applications, including enzyme assays and biological research involving nucleic acid manipulation. -
Nucleoside Analog
3',5'-TIPS-N-Ac-Cytidine is a nucleoside analog designed for use in nucleic acid synthesis applications. This compound acts as a protective reagent for nucleotides, aiding in the successful assembly of oligonucleotides. It is particularly valuable in the development of modified nucleic acids for research in molecular biology and related fields. -
Nucleoside Analog
(2'OMe-5'p-G)pG is a nucleoside analog that serves as a key monomer in nucleic acid synthesis. Its modified structure enhances stability and resistance to nuclease degradation, making it suitable for the development of oligonucleotides with improved pharmacological properties. This reagent is primarily utilized in various molecular biology applications, including antisense oligonucleotide design and RNA therapeutics research. -
Phosphonamide Acid
2'-OMe-4'-ODMT-5'-NO2 phenoxybutyric acid is a phosphonamide acid primarily utilized in nucleic acid synthesis. This compound serves as a key intermediate for the development of modified oligonucleotides, enhancing stability and binding affinity. It is valuable for applications in molecular biology, drug development, and genetic research. -
Nucleoside Analog
CTPαS (Sp isomer) is a nucleoside analog that serves as a crucial monomeric substrate for nucleic acid synthesis. This compound is particularly valuable in the study of molecular biology and genetic research, facilitating the development of oligonucleotides and other nucleic acid-based technologies. Researchers can utilize CTPαS (Sp isomer) to explore nucleotide incorporation mechanisms and investigate various biochemical pathways. -
Nucleoside Analog
2′-F-UDP is a nucleoside analog that serves as a building block in the synthesis of oligonucleotides. Its structural modifications provide enhanced stability and affinity for target sequences, making it valuable in various research applications, including genetic studies, RNA structure analysis, and the development of diagnostic tools. 2′-F-UDP is particularly useful in studies aimed at understanding nucleotide interactions and enhancing the efficacy of nucleic acid-based therapeutics. -
Nucleoside Analog
DMTr-S-5-C-Me-2'-O-Me-rC(Ac)-3'-CE-phosphoramidite is a nucleoside analog utilized in the synthesis of oligonucleotides. This phosphoramidite derivative features several modifications, enhancing stability and facilitating incorporation into nucleic acid sequences. It is suitable for applications in DNA and RNA synthesis, aiding in the development of therapeutics and diagnostics. -
Purine Nucleoside Analog
(2R,3S,4R)-2-(Hydroxymethyl)tetrahydrothiophene-3,4-diol is characterized as 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 useful in studies focused on understanding the cellular effects of purine metabolism and the development of targeted cancer therapies. -
Nucleoside Analog
3′-O-Azidomethyl-UTP is a nucleoside analog that serves as a versatile monomer for nucleic acid synthesis. Its unique azido group allows for specific modifications and incorporation into RNA strands, facilitating the study of RNA biology and the development of RNA-based therapeutics. This reagent is ideal for applications in molecular biology, including in vitro transcription and the creation of modified nucleic acid constructs. -
Nucleoside Analog
DMTr-2'-O-C6-rA(Bz)-3'-CE-Phosphoramidite is a nucleoside analog designed for use in solid-phase synthesis of oligonucleotides. It serves as a phosphoramidite monomer, allowing for the incorporation of modified nucleotide units into RNA and DNA sequences. This compound is essential for advancing research in areas such as gene expression studies, antisense oligonucleotide design, and therapeutic applications involving nucleic acids. -
Nucleoside Analog
5'-DMTr-LNA-N6-Bz-A is a nucleoside analog designed for incorporation into nucleic acid sequences. This monomer exhibits enhanced stability and binding affinity, making it suitable for applications in oligonucleotide synthesis and development of therapeutics. Its modified structure offers potential advantages in gene regulation and antisense therapy research. -
Nucleoside Analog
3-Deoxy-1,2-O-isopropylidene-α-D-ribofuranose is a nucleoside analog that serves as a valuable building block for nucleic acid synthesis. Its structure enables the incorporation of modified sugar units into oligonucleotides, facilitating studies in molecular biology and biochemistry. This compound is essential for exploring the role of nucleoside modifications in nucleic acid stability, hybridization properties, and therapeutic applications. -
Nucleotide
Cytidine, 5′-(P,P′,P′′,P′′-tetrahydrogen imidotriphosphate) is a non-hydrolyzable nucleotide that serves as a stable analog of ATP. Its primary mechanism involves the inhibition of nucleotide hydrolysis, making it suitable for studying nucleotide interactions and enzymatic activities. This reagent is valuable for research applications such as exploring nucleotide metabolism, signaling pathways, and investigating the roles of nucleotides in cellular processes. -
Nucleoside Analog
DMTr-R-5'-C-Me-2'-O-Me-rA(Bz)-3'-CE-phosphoramidite is a nucleoside analog that serves as a building block for nucleic acid synthesis. This compound enhances the stability and flexibility of oligonucleotides, making it valuable for various applications in molecular biology, including the development of antisense oligonucleotides and siRNA. Its unique modifications allow for improved cellular uptake and therapeutic efficacy in gene modulation studies. -
Nucleoside Analog
GTPαS is a stable analog of guanosine triphosphate (GTP) that acts as a substrate for nucleic acid synthesis. It is predominantly utilized in cellular signaling studies and can inhibit GTPase activities, serving as a valuable tool in examining the functions of GTP-binding proteins. Its applications extend to investigations in molecular biology, particularly in the study of gene expression and regulatory mechanisms. -
Thymidine Phosphorylase Inhibitor
5-Phenyluracil is a potent inhibitor of thymidine phosphorylase, an enzyme involved in nucleoside metabolism. This compound exhibits significant anti-tumor activity by disrupting the salvage pathway of nucleotides, making it relevant for cancer research. Its selective inhibition of thymidine phosphorylase highlights its potential utility in exploring cancer therapeutics and related biological pathways. -
Nucleoside Analog
dTTPαS is a nucleoside analog that serves as a substrate for DNA polymerases during nucleic acid synthesis. It is utilized in research applications involving DNA replication and transcription studies. Its incorporation into DNA can aid in the design of experiments focusing on nucleotide incorporation fidelity and the exploration of DNA repair mechanisms. -
Nucleoside Analog
DMTr-2'-O-Propargyl-rU-3'-CE-phosphoramidite is a nucleoside analog designed for incorporation into RNA sequences during nucleic acid synthesis. This phosphoramidite derivative enables the introduction of propargyl groups, facilitating subsequent click chemistry applications and modifications. It is suitable for research in fields such as oligonucleotide development, RNA engineering, and therapeutic applications. -
Nucleoside Analog
DMTr-2'-O-C6-rC(Bz)-3'-CE-phosphoramidite is a nucleoside analog designed for the synthesis of oligonucleotides. This monomer is specifically utilized in automated DNA and RNA synthesis, contributing to the development of modified nucleic acids with enhanced stability and functionality. Applications include the production of therapeutically relevant RNA molecules and other nucleic acid constructs for research purposes. -
Antitumor Agent
DL-Alanosine is an amino acid analogue that acts primarily as an antitumor agent. It exhibits potent antitumor activities, making it a valuable reagent for cancer research. This compound can be utilized in studies focused on tumor cell metabolism and therapeutic resistance mechanisms. -
Nucleotide Derivative
DMT-dT is a nucleotide derivative that functions as a high-performance building block for DNA synthesis. It is commonly utilized in oligonucleotide synthesis and other molecular biology applications that require precision in nucleotide incorporation. With its unique chemical modifications, DMT-dT enhances the efficiency and fidelity of DNA strand assembly. -
Nucleoside Analog
DNA 5-Ethynyl(TIPS)-U amidite is a nucleoside analog used as a monomeric building block in oligonucleotide synthesis. Its ethynyl group enables bioconjugation applications and facilitates the study of nucleic acid interactions. This reagent is essential for researchers focusing on advanced nucleic acid chemistry and the development of novel therapeutic agents. -
Nucleoside Analog
DMTr-2'-O-Me-rU-3'-(L)-PSM-phosphoramidite is a nucleoside analog primarily utilized in nucleic acid synthesis. This unique monomeric reagent enables the incorporation of modified nucleotides, facilitating the generation of RNA and DNA sequences with enhanced stability and functionality. Its specific structure allows for optimized binding and recognition in various molecular biology applications, including gene expression studies and oligonucleotide design. -
Nucleoside Analog
5'-O-DMTr-2'-O-TOM-rA(Ac) is a nucleoside analog utilized in nucleic acid synthesis. This compound serves as a versatile building block for the assembly of oligonucleotides, facilitating the research of RNA structure and function. Its protective groups are designed for efficient incorporation during solid-phase synthesis, enabling the creation of modified nucleotides for various molecular biology applications. -
Nucleoside Analog
DMTr-2'-F-dU-3'-(D)-DPSE-phosphoramidite is a nucleoside analog designed for incorporation into oligonucleotides during automated solid-phase synthesis. It serves as a valuable building block for the creation of modified nucleic acids, enabling researchers to study nucleic acid function and stability. This reagent is particularly useful in applications such as genomics and antisense oligonucleotide development. -
dG Nucleoside
Dmf-dg (2'-Deoxy-N2-dimethylaminomethylene-guanosine) is a modified deoxyguanosine (dG) nucleoside featuring dimethylaminomethylamidine (DMF) protection. This compound serves as a critical building block in oligonucleotide synthesis, allowing for the incorporation of modified nucleotides into nucleic acid sequences. Its unique structural properties facilitate research applications in genetic engineering, molecular biology, and therapeutic development. -
Nucleoside Analog
Spacer Phosphoramidite 9 is a nucleoside analog that serves as a crucial monomeric building block for nucleic acid synthesis. Its structure facilitates the incorporation of spacer arms into oligonucleotides, allowing for precise control over spatial arrangements in nucleic acid assemblies. This reagent is valuable in various research applications, including DNA/RNA synthesis, molecular biology studies, and the development of therapeutic oligonucleotides. -
Nucleoside Analog
3'-O-TBDMS-2'-F-dA(Bz) is a nucleoside analog with a primary mechanism of incorporation into nucleic acid sequences. This compound serves as a crucial building block for the synthesis of modified nucleotides, enabling researchers to investigate nucleic acid function and stability. Its fluorinated structure enhances the stability and binding affinity of nucleic acid constructs, making it useful in various applications, including antisense oligonucleotide design and gene expression studies. -
Nucleoside Analog
DMTr-2'-F-dA(Bz)-3'-(D)-DPSE-phosphoramidite is a nucleoside analog that serves as a versatile monomer for nucleic acid synthesis. This compound plays a crucial role in the incorporation of modified nucleotides into oligonucleotides, enhancing stability and offering unique biochemical properties. Its applications include the development of RNA and DNA probes, as well as in the synthesis of oligonucleotides with tailored functionalities for various research purposes. -
Building block of Nucleic Acid
7-Methylguanosine 5′-monophosphate is a key building block of nucleic acids, functioning primarily as a nucleotide necessary for RNA synthesis. This compound plays a crucial role in the preservation of RNA stability and regulation of gene expression. It is widely used in molecular biology studies and applications involving RNA-based research, including the synthesis of modified RNA molecules and the investigation of RNA-protein interactions.
