BOC Sciences provides a wide range of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
| Product | Description | |
|---|---|---|
| Aminoallyl-UTP - ATTO-580Q | Aminoallyl-UTP - ATTO-580Q is a valuable tool in the biomedical industry used for labeling RNA molecules in various applications, including gene expression analysand mRNA sequencing. This fluorescent dye-conjugated nucleotide allows for specific detection and visualization of RNA aiding in the study and understanding of cellular functions and diseases. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 580Q, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 580Q (free acid). Mole weight: 1215.22 (free acid). |  |
| Aminoallyl-UTP - ATTO-590 | Aminoallyl-UTP - ATTO-590 is a fluorescent nucleotide analog used for labeling RNA through enzymatic incorporation during transcription. Aminoallyl-UTP - ATTO-590 is commonly used in fluorescent in situ hybridization (FISH) experiments to detect specific RNA molecules and in microarray gene expression studies. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 590, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H56N5O19P3 (free acid). Mole weight: 1111.92 (free acid). | |
| Aminoallyl-UTP - ATTO-594 | Aminoallyl-UTP-ATTO-594, a modified nucleotide used mainly in biochemistry, enables the labeling of RNA molecules to investigate gene expression. Toxicogenomics has been adopted to discover gene expression patterns where this product proves valuable. Incorporating Aminoallyl-UTP-ATTO-594 into RNA through in vitro transcription allows for easy detection through fluorescence microscopy. The scientific community benefits from this versatile product that aids in the study of various diseases and their associated gene expression patterns. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 594, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 594 (free acid). Mole weight: 1326.22 (free acid). | |
| Aminoallyl-UTP - ATTO-612Q | Aminoallyl-UTP - ATTO-612Q is a vital tool extensively used in the biomedical industry employed to label RNA for various applications including fluorescence in situ hybridization (FISH), real-time PCR and microarray analysis. This compound facilitates the detection and identification of RNA molecules involved in gene expression and contributes to the study of diseases such as cancer, neurodegenerative disorders and viral infections. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 612Q, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 612Q (free acid). Mole weight: 1211.22 (free acid). | |
| Aminoallyl-UTP - ATTO-620 | Aminoallyl-UTP, a derivate of uridine triphosphate, stands as a proficient option for RNA detection assays. When paired with ATTO-620, it presents itself as an invaluable aid in visualizing and quantifying RNA, facilitating a more thorough domain for biomedical research. But alas, its potential doesn't stop there. Its medicinal application in the treatment of severe ailments, such as cancer and viral infections, only magnifies its already impressive nature. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 620, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 620 (free acid). Mole weight: 1032.22 (free acid). | |
| Aminoallyl-UTP - ATTO-633 | Aminoallyl-UTP is an indispensable compound employed for the purpose of labeling and analysis, playing a crucial role in RNA research by serving as a precursor. Through its utilization, the inclusion of aminoallyl groups into RNA molecules is made possible. By virtue of its conjugation with ATTO-633 dye is aminoallyl-UTP contributes to the enhancement of fluorescence detection, thereby facilitating the tracking and examination of RNA molecules. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 633, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 633 (free acid). Mole weight: 1072.22 (free acid). | |
| Aminoallyl-UTP - ATTO-647N | Aminoallyl-UTP is a nucleotide analog commonly used in biochemical and molecular biology research. It is utilized as a precursor for the synthesis of labeled RNA, allowing for specific tracking and analysis of RNA gene expression. Additionally, it has been employed in studies investigating the mechanism of RNA splicing and alternative splicing patterns. ATTO-647N is a fluorescent dye that can be conjugated to the aminoallyl-UTP for visualization and detection purposes. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 647N, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 647N (free acid). Mole weight: 1166.22 (free acid). | |
| Aminoallyl-UTP - ATTO-655 | Aminoallyl-UTP is an essential reagent in molecular biology for RNA labeling. It is used to synthesize aminoallyl-modified RNA that can be labeled with fluorescent dyes like ATTO-655 for microarray analysis, RNA FISH, and other imaging applications. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 655, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 655 (free acid). Mole weight: 1048.22 (free acid). | |
| Aminoallyl-UTP - ATTO-665 | Aminoallyl-UTP - ATTO-665 is a compound of biomedical research, emerging as a fluorescently labeled nucleotide. Its enzymatic integration into RNA during transcription paves the path to unveil the clandestine RNA molecules. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 665, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 665 (free acid). Mole weight: 1143.22 (free acid). | |
| Aminoallyl-UTP-ATTO-680 | Aminoallyl-UTP-ATTO-680 is recommended for direct enzymatic labeling of DNA / cDNA, such as PCR and Nick Translation. It was incorporated as an alternative to its natural counterpart, dTTP. The resulting dye-labeled DNA / cDNA probes are ideal for fluorescent hybridization applications such as FISH or microarray-based gene expression profiling. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 680, Triethylammonium salt. Grades: ≥95% by HPLC. Molecular formula: C39H49N6O20P3S (free acid). Mole weight: 1046.82 (free acid). | |
| Aminoallyl-UTP - ATTO-700 | Aminoallyl-UTP, a compound indispensably used in biomedical industries, is a notable reagent used for constructing aminoallyl-modified RNA for specific gene expression analysis. Its incomparable role in identifying RNA expression patterns and studying gene regulatory mechanisms makes it a critical tool in the scientific community. ATTO-700 labeled Aminoallyl-UTP, a variant of this compound, is a popular choice for real-time PCR and microarray analysis, especially in the area of cancer research and diagnosis. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 700, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 700 (free acid). Mole weight: 1086.22 (free acid). | |
| Aminoallyl-UTP - ATTO-740 | Aminoallyl-UTP - ATTO-740 is an indispensable compound serving as a fluorescent nucleotide analog. It facilitates the annotation of RNA while cDNA is synthesized. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 740, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 740 (free acid). Mole weight: 988.22 (free acid). | |
| Aminoallyl-UTP - ATTO-MB2 | Aminoallyl-UTP, a modified nucleotide employed in biomedical research for RNA transcript labeling, acts as a vital constituent of the "Amino Allyl MessageAmp II RNA Amplification Kit". Utilized in the amplification of RNA from minute samples, it facilitates distinct downstream applications which include gene expression profiling and disease biomarker identification. ATTO-MB2 - a variant of Aminoallyl-UTP suffused with a fluorescent tag - facilitates visualization of RNA labeling and detection. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO-MB2, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C31H39N6O16P3S (free acid). Mole weight: 876.66 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho101 | Aminoallyl-UTP is an essential recompound. It is utilized for the enzymatic labeling of RNA molecules with aminoallyl moieties. This labeled RNA can then be further conjugated with fluorescent dyes like ATTO-Rho101 for applications such as in vitro diagnostics, gene expression analysis and tracking RNA localization within cells. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho101, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H57N6O18P3 (free acid). Mole weight: 1110.29 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho11 | Aminoallyl-UTP, a highly-valued nucleotide analog in molecular biology, serves as a crucial tool for both RNA labeling and purification. By facilitating incorporation into RNA through in vitro transcription, it enables highly-sensitive fluorescent labeling with dyes such as ATTO-Rho11. Such versatility permits unexpected benefits for gene expression profiling, mRNA localization, and splicing site analysis. Its usage markedly opens new vistas in the exploration of RNA function. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho11, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C47H57N6O18P3 (free acid). Mole weight: 1086.29 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho12 | Aminoallyl-UTP, a modified nucleotide, serves as a substrate for in vitro transcription to enable RNA probe synthesis. Effective in its role as a label substrate, Aminoallyl-UTP effectively pairs and fluoresces with dyes like ATTO-Rho12 within the context of in situ hybridization and microscopy. For its varied applications, such as RNA labeling in quantitative PCR or microarray analysis, Aminoallyl-UTP remains adaptable and multifaceted in its role within biochemical research. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho12, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C53H69N6O18P3 (free acid). Mole weight: 1170.39 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho13 | Aminoallyl-UTP, a structurally modified nucleotide harboring the potential to be integrated into RNA for the ultimate objective of tagging and disclosure of the sequence data, stands out as an indispensable tool in the scientific arena specializing in the biomedical research domain. Its applications and implications in the field of mRNA labeling, microarray analysis and RNA sequencing exhibits its noteworthy significance in comprehending the genetics and epigenetics of an organism. Its proven utility in elucidating the mechanisms underlying several complex maladies such as cancer and neurological disorders stands as a powerful testament to its potential to unravel the intricate mysteries of cell differentiation and gene expression. Its synergistic binding with the fluorescent dye, ATTO-Rho13, empowers the scientific community to gain live imaging insights into the manifestation of RNA expression across healthy and stressed cells and tissues. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho13, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C53H65N6O18P3 (free acid). Mole weight: 1166.37 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho14 | Aminoallyl-UTP, the wondrous nucleotide analog indispensable in bioassays, faithfully marks RNA molecules when used in tandem with enzymes or fluorescent dyes - think ATTO-Rho14. Yet an even brighter future awaits: potential applications as an antiviral agent against respiratory syncytial virus (RSV). Be dazzled by its versatility! Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho14, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C53H61Cl4N6O18P3 (free acid). Mole weight: 1302.20 (free acid). | |
| Aminoallyl-UTP - ATTO-Rho6G | Aminoallyl-UTP - ATTO-Rho6G is an essential tool with remarkable significance within the realm of biomolecular investigation assuming a pivotal role in RNA labeling and crosslinking endeavors. The seamless combination with ATTO-Rho6G dye bestows upon it the power to effortlessly detect and monitor labeled RNA molecules. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Rho6G, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C43H53N6O18P3 (free acid). Mole weight: 1034.26 (free acid). | |
| Aminoallyl-UTP - ATTO-Thio12 | Aminoallyl-UTP - ATTO-Thio12 is emerging as a modified nucleotide of paramount importance when it comes to RNA labeling and research and development. Its unrivaled ability to functionalize RNA molecules paves the way for diverse applications, ranging from microarray analysis to fluorescence imaging. By successfully conjugating ATTO-Thio12 is a profoundly thiol-reactive fluorescent dye, with aminoallyl-UTP labeled RNA, groundbreaking advancements in gene expression profiling and molecular imaging can be achieved. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO Thio12, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C41H49N6O17P3S (free acid). Mole weight: 1022.84 (free acid). | |
| Aminoallyl-UTP - Cy3 | Aminoallyl-UTP - Cy3 is a valuable tool in the biomedical industry used for fluorescent labeling of RNA enabling efficient incorporation of the modified nucleotide into RNA during transcription. Coupled with the Cy3 dye, it allows for precise detection and visualization of RNA in various research applications, including gene expression analysis, RNA quantification and mRNA localization studies. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Cy3, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C43H56N5O22P3S2 (free acid). Mole weight: 1151.97 (free acid). | |
| Aminoallyl-UTP - DY-480XL | Aminoallyl-UTP - DY-480XL, a novel nucleotide, holds significance for the biomedicine industry as it serves as a crucial molecule for RNA labeling and detection. It plays a vital role in synthesizing fluorescently labeled RNA that not only assists in scrutinizing RNA expression levels but also sheds light on RNA localization. With its potential for investigating RNA-protein interactions and identifying RNA viruses and diseases, including cancer, Aminoallyl-UTP - DY-480XL is an invaluable asset for researchers and clinicians alike. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 480XL, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C38H48N5O21P3S (free acid). Mole weight: 1035.80 (free acid). | |
| Aminoallyl-UTP - DY-485XL | Aminoallyl-UTP is a modified form of uridine triphosphate that contains an amine and an allyl group. This product can be used as a substrate for RNA polymerase in an in vitro transcription reaction with incorporation into RNA. It is commonly used in the labeling of RNA for microarray analysis and RNA sequencing, as well as for site-specific RNA-protein crosslinking studies. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 485XL, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C37H48N5O21P3S (free acid). Mole weight: 1023.79 (free acid). | |
| Aminoallyl-UTP - DY-751 | Aminoallyl-UTP, a nucleotide that has undergone modification, is an instrumental component of RNA labeling and detection in biomedicine. It is capable of being integrated into RNA transcripts via in vitro transcription, leading to its labeling with fluorescent dye, which can then be utilized for imaging or detection through hybridization. Utilized in the detection of gene expression and the examination of mRNA localization, as well as the identification of RNA-protein interactions, Aminoallyl-UTP has been studied in various diseases, such as cancer and neurological disorders. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 751, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C54H70N5O23P3S2 (free acid). Mole weight: 1313.31 (free acid). | |
| Aminoallyl-UTP - DY-776 | Aminoallyl-UTP - DY-776 is an indispensable compound utilized in compound applications functioning as a modified ribonucleoside triphosphate. It assumes a critical role in labeling and detecting RNA molecules within diverse biological investigations. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DY 776, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C56H66N5O23P3S2 (free acid). Mole weight: 1334.20 (free acid). | |
| Aminoallyl-UTP - DYQ-660 | Aminoallyl-UTP, a modified nucleotide renowned for its efficiency, optimizes RNA labeling in biomedical contexts. Often utilized in microarray and fluorescence in situ hybridization (FISH), this operationalized compound enhances the yields of fluorescent dyes through its advantageous incorporation profile. With relatively reduced toxicity when compared to peer alternatives, Aminoallyl-UTP represents a highly sought after innovation in biochemical processing. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DYQ 660, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C51H62N5O20P3S (free acid). Mole weight: 1190.05 (free acid). | |
| Aminoallyl-UTP - DYQ-661 | Aminoallyl-UTP, a potent and versatile chemical reagent in the realm of biomedical research, is employed in the detection and labeling of RNA molecules. It plays a pivotal role in the analysis of microarrays and the synthesis of cDNA libraries. When used in tandem with reverse transcriptase, it is highly efficacious in labeling RNA for the purposes of Northern blotting and in situ hybridization assays. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with DYQ 661, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C51H61N5O23P3S2 (Anion). Mole weight: 1269.10 (Anion). | |
| Aminoallyl-UTP - MANT | Aminoallyl-UTP, a potent product having niche importance in the biomedical industry, is used for RNA molecules synthesis, particularly to introduce aminoallyl-uridine residues to facilitate expression analysis and labeling. The remarkable potential of this molecular tool lies in its ability to help researchers gain a deeper understanding of gene expression profiles, which hold the key to unraveling complex mechanisms of diseases like Alzheimers, Parkinsons, and cancer. This has led to its wide adoption in the pharmaceutical industry for drug discovery and development. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with MANT, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C20H27N4O16P3 (free acid). Mole weight: 672.37 (free acid). | |
| Aminoallyl-UTP - OYSTER-656 | Aminoallyl-UTP is a crucial recompound widely utilized for labeling RNA during enzymatic transcription reactions. This labeled RNA plays a vital role in various applications such as microarray analysis, RNA sequencing and in situ hybridization techniques. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with OYSTER 656, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- OYSTER 656 (free acid). Mole weight: 1255.19 (free acid). | |
| Aminoallyl-UTP - Texas Red | Aminoallyl-UTP - Texas Red is a chemical entity that has been purposefully engineered and altered to allow for highly refined and exacting labeling of RNA via intricate enzymatic processes, offering unique and novel solutions to pressing scientific challenges. This multifaceted and versatile compound has been at the forefront of evocative fluorescent labeling techniques, imbuing RNA microarray analysis and in situ hybridization with incredible depth and power. Moreover, the readily detectable Texas Red molecule appended to the amino group of Aminoallyl-UTP allows for stunningly clear imaging of labeled RNA in an unparalleled variety of biological test-beds, thereby opening up new avenues of investigation and discovery into the fundamental processes of gene expression and regulation. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Texas Red, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H59N6O22P3S2 (free acid). Mole weight: 1241.10 (free acid). | |
| Aminoallyl-UTP-X - Cy3 | Aminoallyl-UTP-X - Cy3 is a dazzlingly vibrant fluorescent dye, predominantly finding its purpose in the intricate art of RNA sequence labeling. Its presence pervades the abyss of scientific techniques, particularly microarray analysand the enigmatic fluorescence in situ hybridization (FISH). The magnificent capabilities of Aminoallyl-UTP-X - Cy3 are harnessed to exemplify the visual manifestation and meticulous quantification of remarkable RNA molecules. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Cy3, Triethylammonium salt; UTP-X-Cy3, UTP-17-Cy3, Cy3-17-UTP. Grades: ≥ 95% by HPLC. Molecular formula: C49H67N6O23P3S2 (free acid). Mole weight: 1165.13 (free acid). | |
| Aminoallyl-UTP-X - Cy5 | Aminoallyl-UTP-X - Cy5, a highly specialized reagent, has found wide-spread use in the domain of biomedicine as an efficient tool for detection and labeling procedures. With the ability to introduce several labels such as Alexa Fluor 647, Biotin, Cy3, Cy5.5, Cy7, Digoxigenin, and Rhodamine Red into RNA via in vitro transcription, Aminoallyl-UTP-X - Cy5 plays a pivotal role in DNA-microarrays, primed in-situ labeling (PRINS), and reverse transcription-polymerase chain reaction (RT-PCR). Its applicability is vast, ranging from research fields of cancer biology to neurobiology, and immunology. Alternative Names: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with Cy5, Triethylammonium salt; UTP-X-Cy5, UTP-17-Cy5, Cy5-17-UTP. Grades: ≥ 95% by HPLC. Molecular formula: C51H69N6O23P3S2 (free acid). Mole weight: 1291.17 (free acid). | |
| Amino-modifier-C2-dT CEP | Amino-modifier-C2-dT CEP is an indispensable compound harnessed within the biomedical domain, deftly altering nucleotides. Its applications, extensive in scope, encompass the research of DNA and RNA for diagnostic, therapeutic and investigatory objectives. Alternative Names: 5'-O-[Bis(4-Methoxyphenyl)Phenylmethyl]-2'-Deoxy-5-[3-Oxo-3-[[2-[(Trifluoroacetyl)Amino]Ethyl]Amino]-1-Propenyl]-Uridine 3'-[2-Cyanoethyl Bis(1-Methylethyl)Phosphoramidite]; Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[3-oxo-3-[[2-[(trifluoroacetyl)amino]ethyl]amino]-1-propenyl]-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite](9CI). Grades: >97% by HPLC. CAS No. 153512-22-2. Molecular formula: C46H54N6O10F3P. Mole weight: 938.94. | |
| Amino-Modifier C6 dA | Amino-Modifier C6 dA is designed for automatic synthesis. During oligonucleotide synthesis, the addition of the amino modifier dA can replace the dA residue to functionalize the target oligonucleotide. Alternative Names: 5'-Dimethoxytrityl-N6-benzoyl-N8-[6-(trifluoroacetylamino)-hex-1-yl]-8-amino-2'-deoxyadenosine-3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite; Adenosine, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-8-[[6-[(2,2,2-trifluoroacetyl)amino]hexyl]amino]-, 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]; 5'-DMTr-8-C6-linker-TFA-2'-deoxy-3'-O-CEP-adenosine; Amino Modifier C6-dA CE-Phosphoramidite. Grades: ≥95%. CAS No. 1301170-09-1. Molecular formula: C55H65F3N9O8P. Mole weight: 1068.14. | |
| Amino-Modifier C6 dC | Amino-Modifier C6 dC is designed for automatic synthesis. During oligonucleotide synthesis, the addition of the amino modifier dC can replace the dC residue to functionalize the target oligonucleotide. Alternative Names: Amino-modifier-C6-dC Phosphoramidite; 5'-O-[Bis(4-methoxyphenyl)(phenyl)methyl]-3'-O-[(2-cyanoethoxy)(diisopropylamino)phosphino]-2'-deoxy-N-[(dimethylamino)methylene]-5-[(1E)-3-oxo-3-({6-[(trifluoroacetyl)amino]hexyl}amino)-1-propen-1-yl]cytidine; 5'-Dimethoxytrityl-N-dimethylformamidine-5-[N-(trifluoroacetylaminohexyl)-3-acrylimido]-2'-deoxycytidine, 3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite; Amino-Modifier C6 dC CEP; Amino-modifier-C6-dC-CE-Phosphoramidite; Cytidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-[(dimethylamino)methylene]-5-[3-oxo-3-[[6-[(trifluoroacetyl)amino]hexyl]amino]-1-propenyl]-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]. Grades: ≥95%. CAS No. 853955-92-7. Molecular formula: C53H68F3N8O9P. Mole weight: 1049.12. | |
| Amino-Modifier C6 dC(N-Bz) CE Phosphoramidite | Amino-Modifier C6 dC(N-Bz) CE Phosphoramidite is a phosphoramidite reagent designed for solid-phase oligonucleotide synthesis, enabling site-specific incorporation of an amino group at the 5-position of deoxycytidine (dC). The amino group is protected by a trifluoroacetyl (TFA) group, which can be removed post-synthesis to facilitate conjugation with labels (e.g., fluorophores, biotin) via amide bond formation. A C6 spacer arm provides a six-carbon linker between the amino group and the nucleotide backbone, optimizing accessibility for subsequent reactions while minimizing steric hindrance. It is particularly useful for applications requiring internal or 5'-terminal amino modifications in oligonucleotides, such as molecular probes, diagnostic assays, or therapeutics. Alternative Names: Amino-Modifier C6 dC(N-Bz) Phosphoramidite; Amino-Modifier C6 dC(Bz) CE Phosphoramidite. Grades: ≥97%. Molecular formula: C57H67F3N7O10P. Mole weight: 1098.17. | |
| Amino-Modifier C6 dT | Amino-Modifier C6 dT is a pivotal aspect, serving as a prized instrument for conducting comprehensive nucleic acid investigations. This extraordinary compound has played a crucial role in augmenting the realm of pharmaceutical transport mechanisms and diagnostic apparatuses. Alternative Names: Amino-modifier C6 dT CE Phosphoramidite; Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[(1E)-3-oxo-3-[[6-[(2,2,2-trifluoroacetyl)amino]hexyl]amino]-1-propen-1-yl]-, 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]; 5'-O-[Bis(4-methoxyphenyl)(phenyl)methyl]-3'-O-[(2-cyanoethoxy)(diisopropylamino)phosphino]-2'-deoxy-5-[(1E)-3-oxo-3-({6-[(trifluoroacetyl)amino]hexyl}amino)-1-propen-1-yl]uridine; Amino-modifier C6 dT Phosphoramidite; Amino-Modifier C6 dT CEP. Grades: 95%. CAS No. 210534-16-0. Molecular formula: C50H62F3N6O10P. Mole weight: 995.03. | |
| Amino-Modifier C7 CE Phosphoramidite | Amino-Modifier C7 CE Phosphoramidite is a valuable recompound acting as a versatile building block in the chemical research and development of modified nucleic acids. This compound plays a crucial role in creating oligonucleotides for applications such as gene expression analysis, DNA sequencing and antisense therapeutics. Its introduction enhances the stability and specificity of these nucleic acid-based drugs. Grades: >95% by HPLC. Molecular formula: C52H62N3O7P. Mole weight: 872.06. | |
| Amino-Modifier Serinol Phosphoramidite | Amino-Modifier Serinol Phosphoramidite, a chemical reagent synonymous with biomedical synthesis, plays a key role in the modification of oligonucleotides - mercifully, chock-full of amino functionalities. As a potent building block, this product holds potential for therapeutic and diagnostic development, with applications pertaining to the likes of cancer, viral infections, and genetic disorders. Well-renowned for its high purity and stability, it remains a stand-out performer in the realm of gene therapy and all matters nucleic acid drug delivery. Alternative Names: 3-Dimethoxytrityloxy-2-(3-(fluorenylmethoxycarbonylamino)propanamido)propyl-1-O-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite; 9-Oxa-2,6,11-triaza-10-phosphatridecanoic acid, 7-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-10-(2-cyanoethoxy)-12-methyl-11-(1-methylethyl)-5-oxo-, 9H-fluoren-9-ylmethyl ester; 9,11-Dioxa-2,6-diaza-10-phosphatridecanoic acid, 7-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-10-[bis(1-methylethyl)amino]-13-cyano-5-oxo-, 9H-fluoren-9-ylmethyl ester; 9H-Fluoren-9-ylmethyl 7-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-10-(2-cyanoethoxy)-12-methyl-11-(1-methylethyl)-5-oxo-9-oxa-2,6,11-triaza-10-phosphatridecanoate. CAS No. 196297-83-3. Molecular formula: C51H59N4O8P. Mole weight: 887.01. | |
| Aminooxy N-acetyl-β-D-Glucosaminide | Aminooxy N-acetyl-β-D-Glucosaminide. Alternative Names: Aminooxy N-acetyl-b-D-Glucosaminide; Aminooxy N-acetyl-beta-D-Glucosaminide; amino 2-acetamido-2-deoxy-beta-D-gluco-hexopyranoside; GlcNAc(b)-O-NH2. Molecular formula: C8H16N2O6. Mole weight: 236.22. | |
| Amiprilose | Amiprilose is a novel synthetic carbohydrate with anti-inflammatory and immunomodulatory properties. It is used primarily in the treatment of rheumatoid arthritis and has been shown to reduce the number of painful and swollen joints, as well as improve joint pain and swelling indices. The compound is also known for its ability to stimulate the proliferation of certain cell types, such as mouse thymocytes, and enhance the proliferation response of human synovial fibroblasts under IL-1 stimulation. Alternative Names: 3-O-[3-(Dimethylamino)propyl]-1,2-O-(1-methylethylidene)-α-D-glucofuranose; SM 1213; Therafectin; 1,2-O-Isopropylidene-3-O-[3-(N,N-dimethylamino)propyl]-α-D-glucofuranose. Grades: ≥95%. CAS No. 56824-20-5. Molecular formula: C14H27NO6. Mole weight: 305.37. | |
| Amiprilose hydrochloride | Amiprilose hydrochloride is a novel synthetic carbohydrate with anti-inflammatory and immunomodulatory properties. It is used primarily in the treatment of rheumatoid arthritis and has been shown to reduce the number of painful and swollen joints, as well as improve joint pain and swelling indices. The compound is also known for its ability to stimulate the proliferation of certain cell types, such as mouse thymocytes, and enhance the proliferation response of human synovial fibroblasts under IL-1 stimulation. Alternative Names: α-D-Glucofuranose, 3-O-[3-(dimethylamino)propyl]-1,2-O-(1-methylethylidene)-, hydrochloride (1:1); 1,2-O-Isopropylidene-3-O-3'-(N',N'-dimethylamino-n-propyl)-D-glucofuranose hydrochloride; Amiprilose monohydrochloride; 3-O-[3-(Dimethylamino)propyl]-1,2-O-isopropylidene-α-D-glucofuranose hydrochloride; Therafectin hydrochloride. Grades: ≥95%. CAS No. 60414-06-4. Molecular formula: C14H27NO6.HCl. Mole weight: 341.83. | |
| Ammonium 8-azido-3,8-dideoxy-D-manno-octulosonate | Ammonium 8-azido-3,8-dideoxy-D-manno-octulosonate is a profound compound extensively employed in the biomedical sector, facilitating the research and development of antibiotics targeting diverse ailments attributed to gram-negative bacteria. | |
| AMP-α-F | AMP-α-F, a catalytic ingredient interwoven within biochemical assays, constructs an exceptional mechanism for measuring AMP-activated protein kinase (AMPK), a cardinal energy receptor within cells. Moreover, AMPK has undeviating corollaries in a myriad of pathologies including type 2 diabetes, obesity, and cancer. Resounding implications result from AMP-α-F; foremost, it induces the examination of the impulse and restraint of AMPK and, secondly, for the screening of prospective therapeutics targeting this protein. Alternative Names: (ApF); Adenosine-5'-(α-fluoro)-monophosphate, Sodium salt; Adenosine-5'-(1-fluoro)-monophosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 19375-33-8. Molecular formula: C10H13FN5O6P (free acid). Mole weight: 349.21 (free acid). | |
| AMPαS | AMPαS, a research compound utilized in the pharmaceutical industry, exhibits potential in activating AMP-activated protein kinase (AMPK) pathways for treatment of metabolic disorders like cancer, diabetes, and obesity. Research has reported increases in glucose uptake and fatty acid oxidation while suppressing hepatic gluconeogenesis with AMPK activation. As a tool compound, AMPαS is beneficial in investigating the therapeutic benefits and roles of AMPK. Alternative Names: Adenosine-5'-(α-thio)-monophosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H14N5O6PS (free acid). Mole weight: 363.28 (free acid). | |
| Amrubicinol (Mixture of Diastereomers) | A metabolite of Amrubicin, which is active and possesses a cytotoxicity 10 to 100 times that of the parent drug. Uses: A metabolite of amrubicin, which is active and possesses a cytotoxicity 10 to 100 times that of the parent drug. Alternative Names: (7S,9S)-9-Amino-7-[(2-deoxy-β-D-erythro-pentopyranosyl)oxy]-7,8,9,10-tetrahydro-6,11-dihydroxy-9-(1-hydroxyethyl)-5,12-naphthacenedione; 13-Hydroxy SM 5887. CAS No. 186353-53-7. Molecular formula: C25H27NO9. Mole weight: 485.48. | |
| Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside | Amyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a versatile biomedical compound, finding applications in the research of an array of ailments. Identified as N-acetylmuramic acid, this compound showcases notable antibacterial attributes, rendering it invaluable in the enzymatic assessment of bacterial muramidases. Crucially, it assumes an indispensable role in peptidoglycan research and development, a pivotal constituent of bacterial cell walls. Alternative Names: N-((2R,3R,4R,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-2-(pentyloxy)tetrahydro-2H-pyran-3-yl)acetamide. CAS No. 94483-64-4. Molecular formula: C13H25NO6. Mole weight: 291.34. | |
| Amyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside | Amyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is an extensively employed compound in the realm of biomedicine, manifesting as an invaluable asset for the scrutiny of glycosylation mechanisms and the pioneering of groundbreaking pharmaceuticals. Alternative Names: beta-D-Glucopyranoside, pentyl 2-(acetylamino)-2-deoxy-, 3,4,6-triacetate. CAS No. 146288-30-4. Molecular formula: C19H31NO9. Mole weight: 417.45. | |
| Amylopectin - from maize | Amylopectin - from maize boasts its status as a paramount and environmentally sustainable byproduct obtained from maize starch. This versatile substance has been pervasively employed within the field of biomedical research due to its inherent biocompatibility and degradability. Serving as a formidable carrier for drug delivery systems and tissue engineering, its intricate composition exudes proficiency in encapsulating an array of pharmaceuticals, thus promoting precise release and optimized therapeutic effects. Alternative Names: Amaizo 839; Amioca; Amioca Powder T; Amioca TF; Amioca WCS; Amylopectins; Farinex WM 55; Honen Alpha Waxy Starch; Kosol; Matsunorin A; Matsunorin N; Novation 5600; Pectin, amylo; Starch, waxy; Ultraamylopectin N; Ultrasperse A; Versasheen; Waxilys; Waxy Alpha Y; Waxy corn starch; Waxy Corn Starch Y; Waxy maize starch; Waxy potato starch; Waxy starch; Waxy Starch Y; WCS. CAS No. 9037-22-3. Molecular formula: (C6H10O5)n. | |
| Amylose azure | Amylose azure is a derivative of amylose, a polysaccharide composed of glucose units. It is often used in biochemical assays to study enzyme activity, particularly for amylases, which break down starch. It is used as a substrate to detect and measure the activity of amylase enzymes. Alternative Names: Remazol brilliant blue carboxymethyl amylose; Alphachrome. CAS No. 71501-06-9. | |
| Amylostatin XG 1-Thiophenyl Nonaacetate | Amylostatin XG 1-Thiophenyl Nonaacetate is a protected intermediate of Amylostatin XG, an analogue of an α-glucosidase inhibitor, Acarbose. Molecular formula: C43H55NO21S. Mole weight: 953.96. | |
| Amylostatin XG Octamethoxybenzyl Ether | Amylostatin XG Octamethoxybenzyl Ether is a protected intermediate of Amylostatin XG, an analogue of an α-glucosidase inhibitor, Acarbose. Molecular formula: C97H109NO21S. Mole weight: 1656.96. | |
| Androstane-3a,17b-diol 3-O-b-D-glucuronide | Androstane-3a,17b-diol 3-O-b-D-glucuronide is a pivotal compound in the biomedical field assuming a fundamental function in the exploration of the metabolic processes, pharmacokinetics and therapeutic impacting of androstenediol as well as comparable steroids. Alternative Names: androstanediol-17g; 5alpha-androstane-3alpha,17beta-diol 17-glucuronide; 5alpha-androstane-3alpha,17beta-diol 17-glucuronoside; 5alpha-androstane-3alpha,17beta-diol 17-glucosiduronic acid; 3alpha-hydroxy-5alpha-androstan-17beta-yl beta-D-glucopyranosiduronic acid; (3alpha,5alpha,17beta)-3-hydroxyandrostan-17-yl beta-D-glucopyranosiduronic acid; androstane-3,17-diol 17-glucuronide ; Androstane- 3alpha,17beta-diol glucuronide. CAS No. 148616-25-5. Molecular formula: C25H40O8. Mole weight: 468.6. | |
| A-Neu5Ac-PEG3-azide | A-Neu5Ac-PEG3-azide is a PEGylated glycoside that can be used as a ligand for click chemistry. Alternative Names: α-Neu5Ac-PEG3-azide; alpha-Neu5Ac-PEG3-azide; α-NeuAc-PEG3-Azide; α-L-Neu5Ac-PEG3-N3; α-L-NeuAc-PEG3-N3; α-NeuAc-PEG3-N3; N-acetylneuraminyl-PEG3-Azide; Sialyl-PEG3-Azide; NANA-PEG3-N3; 2-{2-[2-azidoethoxy]ethoxy}ethyl 5-(acetylamino)-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosonic acid; (8-Azido-3,6-dioxaoctyl) 5-(acetylamino)-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosonic acid. Molecular formula: C17H30N4O11. Mole weight: 466.44. | |
| Anhydro-4-azido-5,6,8-tri-O-benzyl-1,2,4-trideoxy-D-glycero-D-gulo-oct-1-ynitol | Anhydro-4-azido-5,6,8-tri-O-benzyl-1,2,4-trideoxy-D-glycero-D-gulo-oct-1-ynitol is a fascinating biomedical compound boasting immense potential in studying diverse diseases such as viral infections and cancers. Alternative Names: 2-Azido-3,4,6-tri-O-benzyl-1,2-dideoxy-1-ethynyl-b-D-glucopyranose. CAS No. 443916-29-8. Molecular formula: C29H29N3O4. Mole weight: 483.56. | |
| Anhydrohexitol G | Anhydrohexitol G is an Intriguing biomedical compound assuming a remarkable standing in research of cancerous cells, with a keen focus on breast and prostate malignancies. Its exceptional attributes grant it the power to impede tumor proliferation while fostering apoptosis. Alternative Names: Anhydrohexitol guanine; 1,5-Anhydro-2-(guanin-9-yl)-2,3-dideoxy-D-arabinohexitol. CAS No. 149312-06-1. Molecular formula: C11H15N5O4. Mole weight: 281.27. | |
| a-Nicotinamide adenine dinucleotide phosphate | a-Nicotinamide adenine dinucleotide phosphate, commonly known as NADP+, stands as an indispensable coenzyme within the biomedical industry. Primarily responsible for driving cellular energy production and overseeing redox reactions, it assumes a vital role in numerous disease treatment modalities. Alternative Names: a-NADP; a-Triphosphopyridine nucleotide; a-TPN; a-Nicotinamide adenine dinucleotide phosphate; sodium [[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-oxidophosphoryl][(2R,3S,4R,5S)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate. Grades: 95%. CAS No. 108392-03-6. Molecular formula: C21H27N7NaO17P3. Mole weight: 765.39. | |
| Aniline β-D-Glucuronide | A metabolite of Aniline. Arylamines are predominantly conjugated by constitutive enzyme forms in the liver. Uses: A metabolite of aniline. arylamines are predominantly conjugated by constitutive enzyme forms in the liver. Alternative Names: 1-Deoxy-1-(phenylamino)-β-D-glucopyranuronic Acid. CAS No. 92117-30-1. Molecular formula: C12H15NO6. Mole weight: 269.25. | |
| Ant-ATP | Ant-ATP is a key reagent in the biomedicine industry used for the detection and measurement of ATP levels. It is particularly effective in studying the mechanisms of diseases associated with mitochondrial dysfunction, such as Parkinson's disease. Ant-ATP can also be used to screen potential drugs that target ATP production, making it a valuable tool in drug discovery and development. Alternative Names: 2'/3'-O-Anthraniloyl-adenosine-5'-triphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. CAS No. 289633-56-3. Molecular formula: C17H21N6O14P3 (free acid). Mole weight: 626.30 (free acid). | |
| Ant-GTP | Ant-GTP is a crucial recompound for studying GTP-binding protein playing a significant role in elucidating the functions of GTPases such as cell signaling, protein research and development and vesicle transport. By providing a stable source of GTP, ant-GTP facilitates the investigation of various diseases associated with GTPase dysregulation, including cancer, neurodegenerative disorders and cardiovascular diseases. Alternative Names: 2'/3'-O-Anthraniloyl-guanosine-5'-triphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C17H21N6O15P3 (free acid). Mole weight: 642.30 (free acid). | |
| Anthrose | Anthrose, an imperative carbohydrate compound highly prevalent in the biomedicine industry, assumes a significant role in the advancement of pharmaceutical drugs targeting a myriad of ailments. Ranging from specific cancer types to inflammatory conditions, its diversified applicability emphasizes its intrinsic value and prominent contribution to the sphere of drug formulation and research. Alternative Names: 4,6-Dideoxy-4-(3-hydroxy-3-methylbutanamido)-2-O-methyl-D-glucopyranose. CAS No. 769959-88-8. Molecular formula: C12H23NO6. Mole weight: 277.31. | |
| Anthrose - ethylene diamine-N6-hydroxylhexanoic acid - biotin linker | Anthrose - ethylene diamine-N6-hydroxylhexanoic acid - biotin linker. | |
| Anthrose - ethylene diamine-N6-hydroxylhexanoic acid linker | Anthrose - ethylene diamine-N6-hydroxylhexanoic acid linker. | |
| Antiviral agent 24 | N6-(3-Trifluoromethylbenzyl)adenosine is a biomedical compound in the research of diverse ailments, exhibiting remarkable potential as an adenosine receptor agonist. Its profound influence on neurotransmitter regulation renders it highly efficacious in studying neurological disorders, cardiovascular afflictions and inflammation-related conditions. Alternative Names: Antiviral agent 24;23661-03-2;N6-(3-Trifluoromethylbenzyl)adenosine;1-(|A-D-Xylofuranosyl)-N6-(m-trifluoromethylbenzyl)adenine;SCHEMBL641041;CHEMBL225766;SDQKDCSBWUSBDO-LSCFUAHRSA-N;MS-27485;(2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[[3-(trifluoromethyl)phenyl]methylamino]purin-9-yl]oxolane-3,4-diol. Grades: ≥95%. CAS No. 23661-03-2. Molecular formula: C21H20O9. Mole weight: 416.4. | |
| Ant-m7GDP | Ant-m7GDP is an exceptional pharmacological compound characterized by its profound capacity to combat viral infections. This awe-inspiring compound exhibits an unparalleled proclivity for selectively targeting and disrupting the intricate guanosine triphosphate cap structures, thereby impeding the vital process of viral mRNA capping. Alternative Names: 2'/3'-O-Anthraniloyl-7-methylguanosine-5'-diphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C18H22N6O12P2 (free acid). Mole weight: 576.35 (free acid). | |
| Ant-m7GMP | Ant-m7GMP is a biomedical compound used for the research of RNA-related diseases specifically targeting RNA molecules with the modified nucleotide 7-methylguanosine. By inhibiting the function of these modified RNA molecules, ant-m7GMP offers potential in studying conditions such as cancer, viral infections and neurological disorders. Alternative Names: 2'/3'-O-Anthraniloyl-7-methylguanosine-5'-monophosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C18H21N6O9P (free acid). Mole weight: 496.37 (free acid). | |
| Ant-m7GTP | Ant-m7GTP is a crucial tool used to study mRNA splicing and translation. It assists in investigating cellular processes and protein research. By targeting modified nucleotides in the mRNA cap structure is ant-m7GTP aids in understanding diseases like cancer and viral infections, enhancing drug discovery and development efforts. Alternative Names: 2'/3'-O-Anthraniloyl-7-methylguanosine-5'-triphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C18H24N6O15P3 (free acid). Mole weight: 656.33 (free acid). | |
| AP2A | AP2A, a prized medication within the biomedical industry, has transcended the boundaries of healing, showcasing its versatility in treating numerous afflictions, including but not limited to, managing pain, alleviating inflammatory disorders, and thwarting cancer. Prized for its utmost efficacy, AP2A efficaciously binds and regulates the activity of specific enzymatic and protein molecules that initiate the cascade of these aforementioned conditions. With its potential for therapeutic use being exhaustively studied and researched, it stands as an invaluable asset in the biomedicine realm. Alternative Names: P1-(5'-Adenosyl) P3-(5'-adenosyl) triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 85065-24-3. Molecular formula: C20H26N10O13P2 (free acid). Mole weight: 676.43 (free acid). | |
| AP2Ribavirin | AP2Ribavirin, an antiviral drug, exerts its efficacy against the Hepatitis C virus (HCV) by curbing the replication of viral RNA through interference with RNA-dependent RNA polymerase. Coupled with other HCV drugs, AP2Ribavirin enhances therapeutic outcomes - serving as a frontline defense against this viral infection. Alternative Names: 1,2,4-Triazole-3-carboxamide adenine dinucleotide, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C18H25N9O14P2 (free acid). Mole weight: 653.39 (free acid). | |
| AP3A - solution | AP3A solution, a biochemical product entrenched in biomedical industry, commands center stage in studying purinergic signaling pathways, amongst others. This efficacious prodigy, a mainstay in academic research labs, abets multifarious research endeavors including, but not limited to, curing autoimmune disorders, neurodegenerative diseases, and cancer. AP3A solution, sourced from different research chemical providers, beckons an important armamentarium for scientists and researchers aiming to unearth the intricacies of cellular signaling pathways. Alternative Names: (ApppA); P1-(5'-Adenosyl) P3-(5'-adenosyl) triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C20H27N10O16P3 (free acid). Mole weight: 756.41 (free acid). | |
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