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 | |
|---|---|---|
| 2'-O-Methyl-2-Amino-ATP | 2'-O-Methyl-2-Amino-ATP, a modified adenine nucleotide, is renowned for its widespread use while studying RNA-dependent RNA polymerases and reverse transcriptases in the field of biochemical research. This marvel molecule is also recognized for unravelling the intricacies of ATP-sensitive potassium channels in smooth muscle tissue. Synonyms: 2'-O-Methyl-2-aminoadenosine-5'-Triphosphate; 2'-O-Methyl-2,6-Diaminopurine-ribose-5'-Triphosphate; 2'-O-Methyl-DAP-rTP. Grades: ≥90% by AX-HPLC. Molecular formula: C11H19N6O13P3. Mole weight: 536.2. |  |
| 2'-O-Methyl-2-thiouridine | 2'-O-Methyl-2-thiouridine is a valuable compound widely used in biomedicine. It acts as an RNA modification tool, incorporating into RNA molecules during synthesis. This powerful molecule exhibits antiviral activity against various viral infections, making it a potential therapeutic option for treating RNA virus-associated diseases. Its unique properties and versatility make it an essential tool for studying RNA biology and developing antiviral therapies. Synonyms: 2-thio-2'-O-methyluridine; Uridine, 2'-O-methyl-2-thio-; 1-(2-O-Methyl-β-D-ribofuranosyl)-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone; 4(1H)-Pyrimidinone, 2,3-dihydro-1-(2-O-methyl-β-D-ribofuranosyl)-2-thioxo-; 1-((2R,3R,4R,5R)-4-Hydroxy-5-hydroxymethyl-3-methoxy-tetrahydro-furan-2-yl)-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one. Grades: ≥95%. CAS No. 113886-72-9. Molecular formula: C10H14N2O5S. Mole weight: 274.29. | |
| 2'-O-Methyl-5-methyluridine 5'-triphosphate | 2'-O-Methyl-5-methyluridine 5'-triphosphate is a pivotal element for studying the captivating realm of RNA modifications. Profoundly influencing diverse cellular processes, this exquisite modified nucleotide assuming a paramount role in unraveling the enigmatic function of methylated RNA. As a versatile substrate for RNA-modifying enzymes, it unleashes unprecedented opportunities to scrutinize mesmeric methyltransferase activities and decode the multifaceted impact of this modification on the intricate structure and myriad functions of RNA. Synonyms: (((2R,3R,4R,5R)-3-Hydroxy-4-methoxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl)triphosphoric acid. CAS No. 444789-41-7. Molecular formula: C11H19N2O15P3. Mole weight: 512.19. | |
| 2'-O-Methyl-5-methyluridine 5'-triphosphate triethylammonium salt | 2'-O-Methyl-5-methyluridine 5'-triphosphate triethylammonium salt is a crucial recompound used in biomedical research. It acting as a modified nucleotide analog which aids in the research and development of RNA molecules with enhanced stability and resistance to degradation. This compound finding applications in studying RNA structure and function, RNA enzymology, and RNA-based therapeutics targeting various diseases including viral infections and cancer. Synonyms: triethylammonium ((2R,3R,4R,5R)-3-hydroxy-4-methoxy-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl triphosphate. Molecular formula: C35H79N6O15P3. Mole weight: 916.97. | |
| 2'-O-Methyl-5-methyl-UTP | 2'-O-Methyl-5-methyl-UTP is a sugar-modified nucleoside triphosphate that increases target affinity and nuclease stability, while reducing immune response. Synonyms: 2'-O-Methyl-5-methyluridine-5'-Triphosphate. Grades: ≥90% by AX-HPLC. Molecular formula: C11H19N2O15P3. Mole weight: 512.19. | |
| 2'-O-Methyladenosine | 2'-O-Me-Ado is the potential metabolite of 2'-O-Me-cAMP with an antiviral activity. Synonyms: Adenosine, 2'-O-methyl-; (2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol; Cordysinin B; 2'-O-Methyl-D-adenosine; 2'-O-Me-Ado. Grades: ≥95%. CAS No. 2140-79-6. Molecular formula: C11H15N5O4. Mole weight: 281.27. | |
| 2'-O-Methyladenosine-5'-a-thiotriphosphate sodium salt | 2'-O-Methyladenosine-5'-a-thiotriphosphate sodium salt is a crucial compound in compound used for various research purposes. It plays a significant role in studies related to molecular biology, biochemistry, and enzymology. This sodium salt derivative is commonly utilized in the research and development of modified nucleotides for investigating adenosine methylation and its impact on RNA function. Molecular formula: C11H14N5Na4O12P3S. Mole weight: 625.20. | |
| 2'-O-Methyladenosine 5'-monophosphate | 2'-O-Methyladenosine 5'-monophosphate is a pivotal compound extensively utilized in the realm of modified RNA molecules' research and development. Delving deeper, its significance permeates research domains encompassing RNA modifications, RNA-protein interactions, as well as comprehension of post-transcriptional modifications' role in governing gene expression regulation. Synonyms: 2'-O-Methyl-AMP. CAS No. 28516-86-1. Molecular formula: C11H16N5O7P. Mole weight: 361.25. | |
| 2'-O-Methyladenosine 5'-monophosphate triethylammonium salt | 2'-O-Methyladenosine 5'-monophosphate triethylammonium salt, a pivotal compound employed in the realm of biomedicine, emerges as a formidable countermeasure against diverse ailments. Its antiviral prowess positions it as an effective combatant against viral afflictions. Moreover, its indispensable involvement in RNA adjustments and RNA-processing enzymes renders it an invaluable instrument for investigating gene expression and RNA-related mechanisms. Synonyms: 2'-O-Methyl-5'-adenylic acid; 2'-O-Methyl-AMP. Molecular formula: C11H16N5O7P·xC6H15N. Mole weight: 361.25 (free acid). | |
| 2'-O-Methyladenosine-5'-triphosphate | 2'-O-Methyladenosine-5'-triphosphate, a pivotal compound within the realm of biomedicine, engenders cautious attention. Its versatility spans vast biomedical applications, including but not limited to the treatment of cancer, viral infections, and neurological disorders. This chemical entity's distinct molecular makeup renders it an auspicious instrument for refined therapeutic interventions. Consequently, the resolute exploration and multifarious prospects surrounding 2'-O-Methyladenosine-5'-triphosphate confer it profound significance within the dynamic milieu of the biomedical sector. Synonyms: 2'-O-Me-ATP; [[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-methoxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] phosphono hydrogen phosphate; Adenosine 5'-(tetrahydrogen triphosphate), 2'-O-Methyl-; 2'-O-Methyladenosine 5'-(tetrahydrogen triphosphate). Grades: ≥97% by HPLC. CAS No. 30948-06-2. Molecular formula: C11H18N5O13P3. Mole weight: 521.21. | |
| 2'-O-Methyladenosine-5'-triphosphate sodium salt | 2'-O-Methyladenosine-5'-triphosphate sodium salt is a crucial recompound extensively used in biomedical research. It acting as a precursor for synthesizing RNA molecules containing methylated adenosine residues. With its ability to introduce specific modifications in RNA, this compound allows for investigation of epigenetic regulation, RNA processing, and RNA-protein interactions. Its applications include studying RNA modifications related to various diseases, such as cancer, neurodegenerative disorders, and viral infections. Synonyms: 2'OMe-ATP Na. CAS No. 100020-58-4. Molecular formula: C11H14N5Na4O13P3. Mole weight: 609.14. | |
| 2'-O-Methyladenosine-5'-triphosphate trilithium salt | 2'-O-Methyladenosine-5'-triphosphate trilithium salt, a prominent nucleotide analog in enzymatic assays detecting ATP-utilizing proteins, and in RNA structure/function studies, specific to RNA modification and translation analysis, showcases its multifarious and intriguing features. Its utilization in diverse experimental applications underlines its enormous potential and capacity to facilitate cutting-edge researches in biomedical and pharmaceutical sciences. Synonyms: lithium ((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl hydrogen triphosphate; 2'-O-Me-ATP trilithium salt; Trilithium 5'-O-[ ({[ (hydroxyphosphinato) oxy]phosphinato}oxy) phosphinato]-2'-O-methyladenosine; Adenosine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), lithium salt (1:3). Grades: ≥97% by HPLC. Molecular formula: C11H15Li3N5O13P3. Mole weight: 539.00. | |
| 2'-O-Methyl-ATP | 2'-O-Methyl-ATP, a modified nucleotide analog with immense potential in biomedicine, specifically, in elucidating the intricacies of signaling pathways involving ATP. Remarkably, it has dual functions as a substrate for certain kinases as well as an inhibitor of others. Synonyms: 2'-O-Methyladenosine-5'-Triphosphate. Grades: ≥95% by AX-HPLC. Molecular formula: C11H18N5O13P3. Mole weight: 521.2. | |
| 2'-O-Methylcytidine-5'-monophosphate triethylammonium salt | 2'-O-methylcytidine 5'-monophosphate is a pyrimidine ribonucleoside 5'-monophosphate that is CMP monomethylated at position O-2'. Synonyms: 2'-O-Methyl-5'-cytidylic acid; ((2R,3R,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl dihydrogen phosphate; Poly(2'-O-methylcytidylic acid); Poly(rcm). CAS No. 18422-43-0. Molecular formula: C10H16N3O8P. Mole weight: 337.22. | |
| 2'-O-Methylcytidine 5'-triphosphate lithium salt | 2'-O-Methylcytidine 5'-triphosphate lithium salt, a pivotal agent in biomedicine, presents itself as a critical compound facilitating RNA modification. Its profound implications in the management of RNA-associated ailments, including viral infections and malignancies, underscore its significance. Moreover, this compound offers an invaluable avenue for investigating the dynamic nature of RNA methylation and its influence on disease advancement. Synonyms: 2'-O-Me-CTP. Molecular formula: C10H18N3O14P3·xLi. Mole weight: 497.18 (free acid). | |
| 2'-O-Methylcytidine-5'-triphosphate sodium salt | 2'-O-Methylcytidine-5'-triphosphate sodium salt, an indispensable compound in the field of biomedicine, demonstrates an paramount significance when it comes to the investigation of RNA molecules. Thanks to its distinctive molecular structure, this sodium salt derivative assumes a pivotal position in the exploration of RNA alterations and the consequences they bear on a multitude of afflictions, including cancer and viral infections. The availability of this compound in the form of a salt not only amplifies its solubility but also simplifies its integration into biochemical experiments. Thus, it emerges as an invaluable instrument in the advancement of groundbreaking therapeutic strategies. Synonyms: 2'OMe-CTP Na. Molecular formula: C10H18N3O14P3·xNa. Mole weight: 497.18 (free acid). | |
| 2'-O-Methylcytidine-5'-triphosphate trilithium salt | 2'-O-Methylcytidine-5'-triphosphate trilithium salt, a nucleotide derivative employed frequently in RNA biosynthesis and modification investigations, holds immense promise in cancer therapies, especially as a competitive inhibitor of RNA polymerase II elongation. Compelling evidence also demonstrates its success as an inhibitor of viral replication, particularly in the context of hepatitis C. Synonyms: 2'-O-Me-CTP trilithium salt; Trilithium 5'-O-[ ({[ (hydroxyphosphinato) oxy]phosphinato}oxy) phosphinato]-2'-O-methylcytidine; Cytidine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), lithium salt (1:3); lithium ((2R,3R,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl hydrogen triphosphate. Grades: ≥97% by HPLC. Molecular formula: C10H15Li3N3O14P3. Mole weight: 514.98. | |
| 2'-O-Methyl-GTP | 2'-O-Methyl-GTP is an extensively employed modified nucleotide in the biomedical research field to scrutinize RNA processing and gene expression. This outstanding nucleotide has been observed to impede cap-dependent translation, as well as disturb RNA splicing, making it a significant instrument for investigating cancer and other RNA metabolism-related ailments. Furthermore, the substrate ability of 2'-O-Methyl-GTP enables the labeling of RNA with biotin or other tags for recognition and purification, thereby amplifying its significance and versatility as a research tool. Synonyms: 2'-O-Methylguanosine-5'-Triphosphate. Grades: ≥90% by AX-HPLC. Molecular formula: C11H18N5O14P3. Mole weight: 537.21. | |
| 2'-O-Methylguanosine 5'-monophosphate triethylammonium salt | 2'-O-Methylguanosine 5'-monophosphate triethylammonium salt is a critical compound extensively used in the biomedical industry. It plays a crucial role in the treatment and research of various diseases, including viral infections, cancer, and neurological disorders. This product contributes to the development of targeted therapies and is an essential component in nucleic acid-based drug formulations. Its high purity and quality make it a valuable tool for biomedical research and drug discovery. Synonyms: 2'-O-Methyl-5'-guanylic acid; 2'-O-Mgmp; 2'-O-Methylguanosine 5'-monophosphate; [(2R,3R,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxy-4-methoxyoxolan-2-yl]methyl dihydrogen phosphate. Grades: ≥ 95%. CAS No. 24121-01-5. Molecular formula: C11H16N5O8P. Mole weight: 377.25. | |
| 2'-O-Methylguanosine 5'-triphosphate | 2'-O-Methylguanosine 5'-triphosphate is a vital biomolecule extensively utilized in diverse biomedical applications, serving as an essential substrate for RNA research and development and modification. Notably, this compound finding extensive application in research endeavors aimed at unraveling the intricate mechanisms underlying RNA metabolism, RNA splicing, and RNA editing. Synonyms: 2'-O-Methyl-GTP; 2'-O-methylguanosine 5'-(tetrahydrogen triphosphate); [[(2R,3R,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxy-4-methoxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] phosphono hydrogen phosphate; 6H-Purin-6-one, 2-amino-1, 9-dihydro-9-[5-O-[hydroxy[[hydroxy (phosphonooxy) phosphinyl]oxy]phosphinyl]-2-O-methyl-b-D-ribofuranosyl]-; Guanosine 5'-(tetrahydrogen triphosphate), 2'-O-methyl-. Grades: ≥97% by HPLC. CAS No. 61556-44-3. Molecular formula: C11H18N5O14P3. Mole weight: 537.21. | |
| 2'-O-Methylguanosine 5'-triphosphate lithium salt | 2'-O-Methylguanosine 5'-triphosphate lithium salt, a fundamental biomedical agent utilized in the therapeutic management of diverse ailments, assumes a pivotal role as a reagent of paramount importance in scientific investigations, thereby expediting the fabrication of altered RNA species. Notably, this compound finds utility in the formulation of antiviral medicinal compounds, specifically aimed at RNA-based viruses encompassing HIV, influenza, and hepatitis C. Moreover, it exerts a profound impact on the exploration and comprehension of RNA's intricate architecture, functionality, and interplays within the biomedical domain. Synonyms: 2'-O-Me-GTP. Molecular formula: C10H18N3O14P3·xLi. Mole weight: 497.18 (free acid). | |
| 2'-O-Methylguanosine-5'-triphosphate sodium salt | 2'-O-Methylguanosine-5'-triphosphate sodium salt is a vital compound extensively utilized in the biomedical field. It is a modified nucleotide analogue that can be incorporated into RNA molecules during transcription. This compound plays a crucial role in RNA research, particularly in studies involving RNA modification and RNA structure determination. Additionally, it serves as a precursor in the synthesis of modified RNA probes used for detection and quantification of specific RNA sequences, providing accurate results in various molecular biology applications. Synonyms: 2'OMe-GTP Na. Molecular formula: C11H18N5O14P3·Na. Mole weight: 537.21 (free acid). | |
| 2'-O-Methylguanosine-5'-triphosphate trilithium salt | 2'-O-Methylguanosine-5'-triphosphate trilithium salt, a highly versatile compound, can be employed as an efficient probe for investigating RNA metabolism. It possesses the remarkable capability of obstructing RNA chain elongation, thus making it an invaluable research tool in the field. In addition to its chain terminating property, it also exhibits remarkable affinity with RNA-binding proteins and catalytic ribozymes, rendering it ideal for studying complex RNA-protein interactions and enzymatic activities. Synonyms: 2'-O-Me-GTP trilithium salt; Trilithium 5'-O-[ ({[ (hydroxyphosphinato) oxy]phosphinato}oxy) phosphinato]-2'-O-methylguanosine; Guanosine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), lithium salt (1:3); lithium ((2R,3R,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl hydrogen triphosphate. Grades: ≥97% by HPLC. Molecular formula: C11H15Li3N5O14P3. Mole weight: 555.00. | |
| 2'-O-Methylinosine-5'-Triphosphate | 2'-O-Methylinosine-5'-Triphosphate is a crucial tool in compound used for various applications acting as an important building block in the research and development of modified nucleic acids, such as mRNA and siRNA, used in gene therapy and RNA interference. This triphosphate analog has demonstrated potential in the reserch of various viral infections and cancers by inhibiting viral replication and inducing apoptosis in tumor cells. Synonyms: 2'-O-Methyl-ITP. Grades: ≥90% by AX-HPLC. Molecular formula: C11H13N4O13P3. Mole weight: 502.16. | |
| 2'-O-Methyl-N1-methyladenosine | N1,O2'-Dimethyladenosine is a naturally occurring modified ribonucleotide found in tRNA. Synonyms: N1,O2'-Dimethyladenosine; 1-Methyl-2'-O-methyladenosine; 2'-O-Methyl-1-methyladenosine; 1,2'-O-dimethyladenosine. Grades: ≥95%. CAS No. 91101-00-7. Molecular formula: C12H17N5O4. Mole weight: 295.29. | |
| 2'-O-Methyl-N1-methylinosine | It is an RNA modified nucleosides m1Im. Synonyms: 9-((2R,3R,4R,5R)-4-Hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-1-methyl-2,9-dihydro-1H-purin-6-ol; 2'-O-Methyl-N1-methyl inosine; Inosine, 1-methyl-2'-O-methyl-; 1,2'-O-dimethylinosine; 1-Methyl-9-(2-O-methylpentofuranosyl)-1,9-dihydro-6H-purin-6-one. Grades: ≥95%. CAS No. 65150-69-8. Molecular formula: C12H16N4O5. Mole weight: 296.28. | |
| 2'-O-Methyl-N2-isobutyroylguanosine | 2'-O-Methyl-N2-isobutyroylguanosine is a biomedicine used in the reserch of certain diseases, including cancer. It acting as an antineoplastic compound and exhibiting potent activity against specific tumor cells. Its mechanism of action involves inhibiting cell growth and inducing apoptosis. Synonyms: N2-Isobutyryl-2'-O-methylguanosine; N2-Isobutyryl-2'-O-methyl-D-guanosine; IBU-2'-OME-G; N2-isobutyryl-O2'-methyl-guanosine; N-(9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide; Guanosine, 2'-O-methyl-N-(2-methyl-1-oxopropyl)-. Grades: ≥95%. CAS No. 63264-29-9. Molecular formula: C15H21N5O6. Mole weight: 367.36. | |
| 2'-O-Methyl-N2,N2-dimethyl-guanosine | It is a modified nucleoside in tRNA of hyperthermophilic archaebacteria. Synonyms: N2,N2,2'-O-Trimethylguanosine; Guanosine, N,N-dimethyl-2'-O-methyl-; N,N,2'-O-Trimethylguanosine; N,N-Dimethyl-2'-O-methylguanosine. Grades: ≥95%. CAS No. 113886-73-0. Molecular formula: C13H19N5O5. Mole weight: 325.32. | |
| 2'-O-Methyl-N6-Methyl-ATP | 2'-O-Methyl-N6-Methyl-ATP, a powerful and exclusive agonist for the renowned P2Y1 receptor renowned for inspiring platelet aggregation and blood clot formation, has proven its potential in biomedical research to investigate the correlation between the P2Y1 receptor and thrombosis as well as related health concerns of great significance, such as stroke and heart attack. Synonyms: 2'-O-Methyl-N6-Methyladenosine-5'-Triphosphate; 2'-O-Me-N6-Me-ATP. Grades: ≥95% by AX-HPLC. Molecular formula: C12H20N5O13P3. Mole weight: 535.2. | |
| 2'-O-Methyl-N6-phenoxyacetyladenosine | 2'-O-Methyl-N6-phenoxyacetyladenosine, a compelling pharmaceutical compound extensively utilized in the field of biomedicine, showcases remarkable inhibitory properties against distinct enzymes implicated in the etiology of autoimmune disorders and cancer. Its distinctive characteristics render it an auspicious contender for precision therapy. Synonyms: 2'-O-Methyl-N6-phenoxyacetyl-adenosine. Grades: ≥ 98%. CAS No. 128219-80-7. Molecular formula: C19H21N5O6. Mole weight: 415.41. | |
| 2'-O-MethylpseudoUridine-5'-Triphosphate Lithium | 2'-O-MethylpseudoUridine-5'-Triphosphate Lithium is a nucleotide analog commonly used in molecular biology research to investigate RNA modification and translation. It has been shown to enhance ribosomal reading efficiency and suppress frameshifting during translation. It may also play a role in regulating immune function and has potential therapeutic applications in autoimmunity and inflammatory diseases. Synonyms: 2'-O-Methylpseudo-UTP tetralithium salt. Grades: ≥90% by AX-HPLC. Molecular formula: C10H13Li4N2O15P3. Mole weight: 521.89. | |
| 2'-O-Methyl-pyrrolo C CEP | 2'-O-Methyl-pyrrolo C CEP is a fluorescent analog of cytidine and a highly fluorescent proven to be useful for monitoring RNA secondary structure formation, where its fluorescence is reversibly quenched upon base-pairing. Synonyms: 3-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-methyl-β-D-ribofuranosyl]-1,3-dihydro-6-methyl-2H-pyrrolo[2,3-d]pyrimidin-2-one. CAS No. 644962-95-8. Molecular formula: C43H52N5O8P. Mole weight: 797.88. | |
| 2'-O-Methyluridine 3',5'-Bis(4-nitrophenyl)phosphate Diester | 2'-O-Methyluridine 3',5'-Bis(4-nitrophenyl)phosphate Diester can be obtained from 2'-O-Methyl Uridine which is uridine analog and is used for preparation of antiviral nucleoside derivatives as inhibitors of subgenomic hepatitis C virus RNA replication. Molecular formula: C22H22N4O16P2. Mole weight: 660.37. | |
| 2'-O-Methyluridine-5'-monophosphate triethylammonium salt | 2'-O-Methyluridine-5'-monophosphate triethylammonium salt is a compelling pharmaceutical compound employed in the research of combatting an array of ailments encompassing viral infections, genetic disorders, and cancer. Its indispensability encompasses the research and development of antiviral medications, pioneering investigations in gene therapy. Synonyms: 2'-O-Me-UMP. CAS No. 67624-43-5. Molecular formula: C10H15N2O9P. Mole weight: 338.21. | |
| 2'-O-Methyluridine-5'-triphosphate | 2'-O-Methyluridine-5'-triphosphate is a nucleotide analog commonly used in biochemistry research. It can be used as a substrate for RNA polymerases or as a terminoligical ATP analog for use in RNA synthesis reactions. Its effectiveness as an antiviral and antitumor agent is also being investigated. Synonyms: 2'-methoxy-UTP; 2'-O-Methyluridine 5'-triphosphoric acid; uridine 5'-(tetrahydrogen triphosphate), 2'-O-methyl-; 5'-(tetrahydrogen triphosphate), 2'-O-methyl-Uridine; 2'-O-Methyluridine 5'-(tetrahydrogen triphosphate); ({[ ({[ (2R, 3R, 4R, 5R)-5- (2, 4-dioxo-1, 2, 3, 4-tetrahydropyrimidin-1-yl)-3-hydroxy-4-methoxyoxolan-2-yl]methoxy} (hydroxy)phosphoryl)oxy] (hydroxy)phosphoryl}oxy)phosphonic acid. Grades: ≥97% by HPLC. CAS No. 143028-99-3. Molecular formula: C10H17N2O15P3. Mole weight: 498.17. | |
| 2'-O-Methyluridine-5'-triphosphate lithium salt | 2'-O-Methyluridine-5'-triphosphate lithium salt, an indispensable reagent within the realm of biomedicine, bears immense significance for the exploration of RNA and its alterations. Its utilization encompasses pivotal functional inquiries, particularly concerning the impact of RNA methylation on gene expression. Synonyms: 2'-O-Me-UTP. Molecular formula: C10H17N3O15P3·xLi. Mole weight: 512.17 (free acid). | |
| 2'-O-Methyluridine-5'-triphosphate sodium salt | 2'-O-Methyluridine-5'-triphosphate sodium salt is a crucial reagent widely used in the field of biomedicine. It plays a vital role as a substrate for various enzymes involved in cellular processes. This product is commonly utilized in research related to RNA synthesis, RNA modification, and RNA labeling. Additionally, it serves as a key component in studies involving antiviral drug development and understanding certain diseases at the molecular level. Synonyms: 2'OMe-UTP Na. Molecular formula: C10H17N2O15P3·xNa. Mole weight: 498.17 (free acid). | |
| 2'-O-Methyluridine-5'-triphosphate trilithium salt | 2'-O-Methyluridine-5'-triphosphate trilithium salt, a biochemical reagent widely applied in biomedicine to investigate RNA transcription and modification, is a valuable research tool with incomparable properties that afford an accurate insight of cellular processes related to RNA function and modification. Scientists favor its use as a substrate for RNA polymerase, that enables them to scrutinize RNA synthesis and modification of transcripts. Furthermore, this trilithium salt is constructive in analyzing RNA-protein interactions and probing ribozymes. Synonyms: lithium ((2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxy-4-methoxytetrahydrofuran-2-yl)methyl hydrogen triphosphate; 2'-OMe-UTP trilithium salt; Trilithium 5'-O-[ ({[ (hydroxyphosphinato) oxy]phosphinato}oxy) phosphinato]-2'-O-methyluridine; Uridine, 2'-O-methyl-, 5'-(tetrahydrogen triphosphate), lithium salt (1:3); 2'-methoxy-UTP trilithium salt. Grades: ≥97% by HPLC. Molecular formula: C10H14Li3N2O15P3. Mole weight: 515.96. | |
| 2'-O-Methyl-UTP | 2'-O-Methyl-UTP, a chemical compound utilized in RNA transcription and regulation research, is imperative for RNA synthesis and modification. Through experimentation, it has been demonstrated to augment the stability and translation efficiency of mRNA. This product has amplified interest in studying RNA viruses, cancer, and neurological disorders due to its instrumental role in these fields. Synonyms: 2'-O-Methyluridine-5'-Triphosphate; 2'OMe-UTP. Grades: ≥90% by AX-HPLC. Molecular formula: C10H17N2O15P3. Mole weight: 498.2. | |
| 2'-OMe-U-PACE Phosphoramidite | 2'-OMe-U-PACE Phosphoramidite is a paramount ingredient indispensable in the synthesis of oligonucleotides, a crucial component in the mRNA therapeutics, gene silencing and diagnostic assays arena. The remarkable specificity that it confers on the oligonucleotides' binding capabilities with RNA targets unquestionably renders it the undisputed champion in the fight against cancer and viral infections. Synonyms: 5'-Dimethoxytrityl-2'-OMe-Uridine, 3'-O-(N,N-diisopropylamino)-phosphinyl-1,1-dimethyl-2-cyanoethyl acetate. Molecular formula: C44H55N4O10P. Mole weight: 830.92. | |
| 2'-OMe-U-Thiophosphoramidite | 2'-OMe-U-Thiophosphoramidite, a chemical compound extensively employed in the production of oligonucleotides for biomedical inquiries, embarks on the critical task of modifying RNA and DNA oligomers' backbone, eliciting their augmented bonding proficiency and stability. Its indispensability, especially in cancer therapy and gene research studies, renders it a boon to molecular biology's advancement and exploration. Synonyms: 5'-Dimethoxytrityl-Uridine, 2'-O-methyl, 3'-[(β-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C44H48N3O9PS2. Mole weight: 857.97. | |
| 2'-O-MS-cAMP | 2'-O-MS-cAMP is a cAMP analogue used for coupling of ligands including proteins for ELISA. Synonyms: 2'- O- Monosuccinyladenosine- 3', 5'- monophosphate, free acid. Grades: ≥ 98% by HPLC. CAS No. 36940-87-1. Molecular formula: C14H16N5O9P. Mole weight: 429.3. | |
| 2'-O-MS-cGMP | 2'-O-MS-cGMP is a cGMP analogue, which is used for coupling of ligands including proteins for ELISA. Synonyms: 2'- O- Monosuccinylguanosine- 3', 5'- cyclic monophosphate, free acid. Grades: ≥ 98% by HPLC. CAS No. 39118-26-8. Molecular formula: C14H16N5O10P. Mole weight: 445.3. | |
| 2'-O-MS-TME-cAMP | 2'-O-MS-TME-cAMP is an analogue of cAMP for radio-iodination used in cAMP immunoassays. Synonyms: 2'- O- Monosuccinyladenosine- 3', 5'- cyclic monophosphate, tyrosylmethyl ester, sodium salt. Grades: ≥ 95% by HPLC. CAS No. 60448-20-6. Molecular formula: C24H26N6O11P · Na. Mole weight: 628.5. | |
| 2'-O-MS-TME-cGMP | 2'-O-MS-TME-cGMP is an analogue of cGMP, which is used for radio-iodination in cGMP immunoassays. Synonyms: 2'- O- Monosuccinylguanosine- 3', 5'- cyclic monophosphate, tyrosylmethyl ester, sodium salt. Grades: ≥ 95% by HPLC. CAS No. 104872-93-7. Molecular formula: C24H26N6O12P · Na. Mole weight: 644.5. | |
| 2'-O-(N-Methylanthraniloyl)-3'-deoxy-adenosine-5'-triphosphate triethylammonium salt | 2'-O-(N-Methylanthraniloyl)-3'-deoxy-adenosine-5'-triphosphate triethylammonium salt, a highly significant compound in biomedical studies, serves as the triethylammonium salt version of 2'-O-(N-Methylanthraniloyl)-3'-deoxy-adenosine-5'-triphosphate. This invaluable substance finds noteworthy applications in the exploration of ATP-dependent cellular mechanisms and signaling cascades within the realm of biomedical research. Notably, it assumes a pivotal role in the examination of ATP-binding proteins, including receptors, kinases, and nucleotide hydrolases, thereby contributing to the emergence of innovative therapeutic strategies for diverse pathological conditions and ailments. Synonyms: 2'-Mant-3'-dATP. Molecular formula: C18H23N6O13P3·xC6H15N. Mole weight: 624.33 (free acid). | |
| 2'-O-Propargylcytidine | 2'-O-Propargylcytidine, a compound of utmost importance in the biomedical sector, serves as an indispensable agent in combatting a myriad of afflictions. Garnering wide-ranging acclaim, it displays promising potential in thwarting the proliferation of menacing viruses like SARS-CoV and MERS-CoV. Furthermore, its notable efficacy in addressing diverse manifestations of neoplasms, notably pulmonary and mammary carcinoma, instills hope and marks it as a prime contender for the synthesis of revolutionary antiviral and anticarcinogenic therapeutics. Synonyms: 2'-O-Propargyl-D-cytidine; 4-amino-1-[(2-O-propargyl)-β-D-ribofuranosyl]-2H-pyrimidin-2-one. Grades: ≥ 95%. CAS No. 206552-85-4. Molecular formula: C12H15N3O5. Mole weight: 281.26. | |
| 2'-O-Propargyl G(iBu)-3'-phosphoramidite | 2'-O-Propargyl G(iBu)-3'-phosphoramidite is a vital compound extensively used in the field of biomedicine. This compound acting as a versatile building block for the synthesis of modified nucleosides and oligonucleotides. It finding applications in the development of therapeutic compounds, particularly for the reserch of viral infections and genetic diseases. Synonyms: N2-iBu-5'-O-DMTr-2'-O-propargylguanosine-3'-CED-phosphoramidite; N2-iso-Butyroyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-propargyl guanosine-3'-O-[(2-cyanoethyl)-(N,N-diisopropyl)]phosphoramidite; 5'-O-DMT-N2-isobutyryl-2'-O-propynylguanosine 3'-CE phosphoramidite; 5'-O-[bis(4-methoxyphenyl)?phenylmethyl]?-N-(2-methyl-1-oxopropyl)?-2'-O-2-propynyl-guanosine 3'-[2-cyanoethyl bis(1-methylethyl)?phosphoramidite]; 5'-O-[Bis (4-methoxyphenyl) (phenyl)methyl]-3'-O-[ (2-cyanoethoxy) (diisopropylamino)phosphino]-N-isobutyryl-2'-O-2-propyn-1-ylguanosine. Grades: ≥95%. CAS No. 171486-61-6. Molecular formula: C47H56N7O9P. Mole weight: 893.96. | |
| 2'-O-Propargyluridine | This cutting-edge product, 2'-O-Propargyluridine, plays a pivotal role in the realm of biomedicine. It serves as a crucial component in the treatment and comprehension of diverse diseases. Specifically, this modified nucleoside exhibits the exceptional ability to integrate into RNA molecules, thereby facilitating the exploration of RNA's intricate structure and functionality. Furthermore, this remarkable compound finds application in the development of antiviral medications, functioning as an invaluable research instrument for unraveling the complexities of RNA biology and viral replication mechanisms. Synonyms: 2'-O-2-Propyn-1-yluridine; 2'-O-Propargyl-D-uridine; 1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-prop-2-ynoxyoxolan-2-yl]pyrimidine-2,4-dione. Grades: 97%. CAS No. 129778-58-1. Molecular formula: C12H14N2O6. Mole weight: 282.25. | |
| 2'-O-Propygylguanosine | 2'-O-Propygylguanosine is a crucial compound extensively used in the biomedicine industry. This product acts as an antiviral agent, primarily targeting viral infections caused by RNA viruses. It demonstrates promising therapeutic potential in treating diseases like HIV, Ebola, and hepatitis C. Its unique structure and mechanism of action make it an invaluable tool in the fight against these life-threatening viral infections. Synonyms: 2'-O-(2-Propyn-1-yl)guanosine; 2'-O-Propargyl-guanosine; 2-Amino-9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-(prop-2-yn-1-yloxy)tetrahydrofuran-2-yl)-1H-purin-6(9H)-one; 2'-O-2-Propyn-1-ylguanosine. Grades: ≥95%. CAS No. 206552-86-5. Molecular formula: C13H15N5O5. Mole weight: 321.29. | |
| 2'-O-ribosyladenosine (phosphate) | 2'-O-ribosyladenosine (phosphate), a significant enzyme in RNA production, modifies nucleotides in RNA formation for mRNA molecule production used in protein synthesis. In addition, the product is crucial for biosynthesis of purine, a crucial molecular base in DNA and RNA. With targeted inhibition of certain cancer cells, this potent tool finds wide application in cancer treatment research. Synonyms: Adenosine, 2'-O-(5-O-phosphono-b-D-ribofuranosyl)-; O-beta-ribosyl(1''--2')adenosine-5''-phosphate; 2'-O-(5-O-Phosphono-beta-D-ribofuranosyl)adenosine. CAS No. 28050-13-7. Molecular formula: C15H22N5O11P. Mole weight: 479.34. | |
| 2'-O-TBS-Pyrrolo-C CEP | 2'-O-TBS-Pyrrolo-C CEP, a compound highly regarded in the biomedical sector, is widely employed for the purpose of synthesizing altered RNA. Its application facilitates the seamless integration of 2'-O-TBS-Pyrrolo-C modifications into RNA molecules, enabling comprehensive exploration of their structural and functional implications. Consequently, this remarkable product serves as an invaluable tool for scrutinizing the involvement of modified RNA in various aspects including gene expression, RNA interference, and therapeutic approaches targeting afflictions like cancer and viral infections. Molecular formula: C48H64N5O8PSi. Mole weight: 898.11. | |
| 2'-O-tert-Butyldimethylsilyl-3'-deoxy-5-methyluridine | 2'-O-tert-Butyldimethylsilyl-3'-deoxy-5-methyluridine is a crucial compound used in the biomedical industry. It plays a vital role in the synthesis of novel antiviral drugs specifically designed to target viral infections caused by diseases such as influenza and HIV. This compound's unique structure and properties contribute to the development of effective therapeutics against these viral pathogens. CAS No. 1622941-62-1. Molecular formula: C16H28N2O5Si. Mole weight: 356.49. | |
| 2'-O-tert-Butyldimethylsilyl-5-methyluridine | 2'-O-tert-Butyldimethylsilyl-5-methyluridine standing as an essential entity wielded within the biomedical realm to orchestrate the research and development of nucleoside analogs. Rendering itself instrumental in crafting antiviral medications and providing a foundational cornerstone for tackling an assortment of viral afflictions, this compound exhibiting indomitably consequential characteristics that have propelled it towards the forefront of pharmaceutical research and development. Synonyms: 2'-TBDMS-5-Me-rU; 2'-O-[(1,1-Dimethylethyl)dimethylsilyl]-5-methyluridine; 2'-O-[Dimethyl(2-methyl-2-propanyl)silyl]-5-methyluridine. Grades: ≥97% by HPLC. CAS No. 922508-26-7. Molecular formula: C16H28N2O6Si. Mole weight: 372.49. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-1-methylguanosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-1-methylguanosine 3'-CE phosphoramidite is a vital constituent in the sphere of compound, serving as an indispensable tool for the research and development of tailored oligonucleotides. Its extensive utilization prevails in the progressive exploration of drug conveyance systems and nucleic acid-oriented reserchs. CAS No. 1356084-46-2. Molecular formula: C47H64N7O8PSi. Mole weight: 914.11. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-5-iodouridine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-5-iodouridine 3'-CE phosphoramidite is a vital compound widely used in the biomedical industry. This phosphoramidite acts as a building block in nucleic acid synthesis and modifications. It is particularly valuable for introducing 5-iodouridine modifications, enabling targeted investigations and drug development towards diseases like cancer and viral infections. Its high purity and efficiency guarantee accurate and reliable results in molecular biology research. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-5-iodo-D-uridine 3'-CE phosphoramidite. Molecular formula: C45H60IN4O9PSi. Mole weight: 986.97. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-C2-methyladenosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-C2-methyladenosine 3'-CE phosphoramidite: This phosphoramidite derivative is essential in the biomedical industry for synthesizing modified RNA molecules. It acts as a building block during solid-phase RNA synthesis, enabling the introduction of 2'-O-tert-butyldimethylsilyl, 5'-O-DMT, and C2-methyladenosine modifications. This phosphoramidite facilitates research on RNA structure-function relationships, post-transcriptional modifications, and drug discovery targeting diseases like cancer and viral infections. Synonyms: (2R, 3R, 4R, 5R) -5- (6-Amino-2-methyl-9H-purin-9-yl) -2- ( (bis (4-methoxyphenyl) (phenyl) methoxy) methyl) -4- ( (tert-butyldimethylsilyl) oxy) tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite. CAS No. 1028723-99-0. Molecular formula: C47H64N7O7Si. Mole weight: 867.14. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)guanosine 3'-CE phosphoramidite is a critical recompound used in biomedical research for the research and development of modified oligonucleotides. It enables the introduction of a 3'-cyanoethyl (CE) phosphoramidite group, facilitating the research and development of chemically stable and biologically active nucleic acids. These modified oligonucleotides have application in the research of molecular diagnostics, gene therapy, and drug discovery targeting various diseases such as cancer and viral infections. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N2-(4-isopropylphenoxyacetyl)-D-guanosine 3'-CE phosphoramidite; iPr-Pac-G-CE Phosphoramidite. Molecular formula: C57H74N7O10PSi. Mole weight: 1076.33. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N2-methylguanosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N2-methylguanosine 3'-CE phosphoramidite is an invaluable compound in the field of compound, playing a pivotal role as a foundation for constructing modified nucleotides. By incorporating the N2-methylguanosine modification into oligonucleotides, this phosphoramidite enhances both stability and targeting functionalities, thereby facilitating the application of disease-specific reserchs. Synonyms: 2'-TBDMS-5'-Dimethoxytrityl-N2-methyl-guanosine 3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite. Molecular formula: C47H64N7O8PSi. Mole weight: 914.11. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N6-methyladenosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N6-methyladenosine 3'-CE phosphoramidite, a pivotal asset in the realm of biomedical study, finds application in the construction of altered RNA molecules. Its proficiency as a robust constituent facilitates the inclusion of the N^6-methyladenosine (m^6A) modification, a crucial factor governing mRNA metabolism and gene expression regulation. This phosphoramidite empowers the scrutiny of m^6A's influence on diverse ailments and therapeutic advancements, holding promise in revolutionizing targeted therapeutics. Synonyms: N6-Me-rAphosphoramidite. Grades: 96%. Molecular formula: C47H64N7O7PSi. Mole weight: 898.11. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N6-phenoxyacetyladenosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N6-phenoxyacetyladenosine 3'-CE phosphoramidite, a prominent compound in the realm of biomedicine, epitomizes paramount importance. Owing to its inherent potency, this phosphoramidite assumes a pivotal role in nucleic acid synthesis, with profound implications in DNA and RNA investigations. Its utilization facilitates precise modifications and labeling of nucleotides, thereby facilitating targeted examinations in genomics, transcriptomics, and molecular biology. Moreover, it exerts a remarkable influence in the domain of drug discovery and pharmaceutical research, furthering the advancement of therapeutic interventions for a wide spectrum of maladies. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-N6-phenoxyacetyl-D-adenosine 3'-CE phosphoramidite; Pac-A-CE Phosphoramidite. Grades: 90%. Molecular formula: C54H68N7O9PSi. Mole weight: 1018.25. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-MMT-uridine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-MMT-uridine 3'-CE phosphoramidite, an indispensable compound in the field of biomedicine, showcases its remarkable potential in safeguarding and altering nucleotides. This compound finds extensive utilization in the synthesis of oligonucleotides, serving as a catalyst for research inquiries. The pivotal significance of this product lies in its contribution towards the precise arrangement and alteration of DNA and RNA sequences, thus paving the way for groundbreaking advancements in drug development and therapeutic approaches. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-MMT-D-uridine 3'-CE phosphoramidite. Molecular formula: C44H59N4O8PSi. Mole weight: 831.04. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-toluoyluridine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-toluoyluridine 3'-CE phosphoramidite stands as a pivotal implement in the realm of biomedical sciences. Operating as a derivative of phosphoramidite, this product holds tremendous significance in the synthesis of oligonucleotides, catering to diverse applications. It plays a vital role in the alteration and creation of nucleic acids for the purpose of scientific exploration and advancement, encompassing the investigation of gene expression, nucleic acid diagnostics, as well as therapeutic interventions for pathologies like cancer and genetic disorders. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-toluoyl-D-uridine 3'-CE phosphoramidite. Molecular formula: C32H49N4O8PSi. Mole weight: 676.83. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-tritylthymidine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-tritylthymidine 3'-CE phosphoramidite, a crucial compound in the realm of biomedicine, finds extensive application in oligonucleotide synthesis, with a specific focus on drug and disease targeting. Its facilitation of nucleic acid assembly and modification plays a pivotal role in the advancement of therapeutic approaches to diverse medical ailments, endowing it with an indispensable stature within the biomedical industry. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-trityl-D-thymidine 3'-CE phosphoramidite. Molecular formula: C44H59N4O7PSi. Mole weight: 815.04. | |
| 2'-O-tert-Butyldimethylsilyl-5'-O-trityluridine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-trityluridine 3'-CE phosphoramidite, a crucial compound in the biomedicine industry, contributes significantly to the synthesis of nucleoside analogs. Its paramount role lies in the development of antiviral drugs, specifically targeting RNA viruses. This prolific phosphoramidite derivative extensively participates in antiviral research and drug discovery programs, combatting various viral diseases, encompassing HIV, hepatitis B, and respiratory infections. Simultaneously, it takes center stage as a fundamental building block, facilitating the synthesis of modified nucleic acids, thereby enabling the production of innovative therapeutic compounds. Synonyms: 2'-O-tert-Butyldimethylsilyl-5'-O-trityl-D-uridine 3'-CE phosphoramidite. Molecular formula: C43H57N4O7PSi. Mole weight: 801.02. | |
| 2'-O-tert-Butyldimethylsilyladenosine | 2'-O-tert-Butyldimethylsilyladenosine, a remarkable pharmaceutical compound found in the field of biomedicine, stands as an extraordinary weapon in the relentless fight against viral invasions. Unleashing its unparalleled antiviral prowess, it meticulously sabotages viral replication processes, emerging triumphant against an array of treacherous viruses. This unparalleled marvel strategically disrupts viral RNA synthesis, casting a long shadow over notorious viral diseases, including the persistent influenza and the formidable hepatitis C. Synonyms: Adenosine, 2'-O-[(1,1-dimethylethyl)dimethylsilyl]-; (2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)tetrahydrofuran-3-ol; (2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-[tert-butyl(dimethyl)silyl]oxy-2-(hydroxymethyl)oxolan-3-ol; 2'-o-tert-butyldimethylsilyladenosine;2'-O-[tert-Butyl(dimethyl)silyl]adenosine. CAS No. 69504-13-8. Molecular formula: C16H27N5O4Si. Mole weight: 381.5. | |
| 2-O-tert-Butyldimethylsilylemtricitabine Tenofovir Disoproxil Dimer | 2-O-tert-Butyldimethylsilylemtricitabine Tenofovir Disoproxil Dimer is an intermediate in the synthesis of Emtricitabine Tenofovir Monosoproxil Dimer, a derivative of Emtricitabine. Emtricitabine is a reverse transcriptase inhibitor. It is an effective antiviral agent against HIV, HBV, and other viruses replicating in a similar manner. Molecular formula: C34H54FN8O13PSSi. Mole weight: 892.96. | |
| 2-O-tert-Butyldimethylsilylemtricitabine Tenofovir Monosoproxil Dimer | 2-O-tert-Butyldimethylsilylemtricitabine Tenofovir Monosoproxil Dimer is an intermediate in the synthesis of Emtricitabine Tenofovir Monosoproxil Dimer, a derivative of Emtricitabine. Emtricitabine is a reverse transcriptase inhibitor. It is an effective antiviral agent against HIV, HBV, and other viruses replicating in a similar manner. Molecular formula: C29H46FN8O10PSSi. Mole weight: 776.85. | |
| 2'-O-tert-Butyldimethylsilyl-N2-DMF-5'-O-tritylguanosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-N2-DMF-5'-O-tritylguanosine 3'-CE phosphoramidite, known for its indispensable utility in the biomedicine sector, serves as a significant catalyst for DNA synthesis and alteration. Employed extensively in the creation of customized oligonucleotides and nucleic acid mimics, this essential substance assumes a critical part in the progression of novel pharmaceuticals, diagnostics, and therapeutics aimed at combatting diverse ailments and hereditary anomalies. Synonyms: 2'-O-tert-Butyldimethylsilyl-N2-DMF-5'-O-trityl-D-guanosine 3'-CE phosphoramidite. Molecular formula: C47H63N8O6PSi. Mole weight: 895.11. | |
| 2'-O-tert-Butyldimethylsilyl-N2-isobutyryl-5'-O-MMT-guanosine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-N2-isobutyryl-5'-O-MMT-guanosine 3'-CE phosphoramidite is a valuable recompound primarily utilized for the research and development of oligonucleotides, which find application in various fields including genetic research, drug development, and diagnostics. This phosphoramidite derivative assists in the efficient incorporation of guanosine into oligonucleotide sequences, enabling the study of specific diseases and conditions at the molecular level. Molecular formula: C49H66N7O8PSi. Mole weight: 940.17. | |
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