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 | |
|---|---|---|
| 5'-O-DMT-N6-Acetyl-2'-deoxyadenosine | 5'-O-DMT-N6-Acetyl-2'-deoxyadenosine, a distinctive chemical entity, is an enigmatic contender. Its sly antiviral and anticancer efficacies, alongside its niche antiproliferative traits, beckon a curious eye. Aligned with these mystical properties, lie its unique features rendering it a valuable tool to explore complex molecular architectures intertwined with nucleotide metabolism and cellular signaling pathways. Alternative Names: 5'-DMT-Ac-dA; N-[9-[(2R,4S,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-hydroxyoxolan-2-yl]purin-6-yl]acetamide; N6-Acetyl-2'-deoxy-5'-O-DMT-adenosine; N-Acetyl-5'-O-[bis(4-methoxyphenyl)(phenyl)methyl]-2'-deoxyadenosine. Grades: ≥98% by HPLC. Molecular formula: C33H33N5O6. Mole weight: 595.65. |  |
| 5'-O-DMT-N6-Acetyl-2'-deoxyadenosine 3'-CE phosphoramidite | 5'-O-DMT-N6-Acetyl-2'-deoxyadenosine 3'-CE phosphoramidite is a key component for the synthesis of modified oligonucleotides, which have applications in gene therapy and antiviral drug development. This phosphoramidite can be used to introduce an N6-acetyldeoxyadenosine modification to oligonucleotide strands, which has been shown to enhance their cellular uptake and improve their stability towards nucleases. It is also useful for generating oligonucleotides with 3'-CE modifications, which can improve their binding and selectivity towards complementary RNA targets. Alternative Names: Adenosine N-acetyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-, 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]; N-Acetyl-5'-O-[bis(4-methoxyphenyl)(phenyl)methyl]-3'-O-[(2-cyanoethoxy)(diisopropylamino)phosphino]-2'-deoxyadenosine. Grades: ≥98% by HPLC. CAS No. 1027734-01-5. Molecular formula: C42H50N7O7P. Mole weight: 795.86. | |
| 5'-O-DMT-N6-methyl-2'-deoxyadenosine 3'-CE phosphoramidite | 5'-O-DMT-N6-methyl-2'-deoxyadenosine 3'-CE phosphoramidite is a pivotal entity harnessed within the realm of biomedical industry, manifesting its indispensability within nucleic acid research and development. Alternative Names: 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-methyl-Adenosine 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; 2'-Deoxy-5'-O-DMT-N6-methyladenosine 3'-CE phosphoramidite; N6-Methyl-dA phosphoramidite. Grades: ≥98% by HPLC. CAS No. 105931-58-6. Molecular formula: C41H50N7O6P. Mole weight: 767.85. | |
| 5'-O-DMT-N6-methyl-N6-phenoxyacetyladenosine 3'-CE phosphoramidite | 5'-O-DMT-N6-methyl-N6-phenoxyacetyladenosine 3'-CE phosphoramidite - an imperative and indispensable biomolecular constituent extensively employed in the field of biomedicine. This exceptional biochemical entity plays a pivotal role in the intricate process of oligonucleotide synthesis which finds multifaceted employment across the expanse of the biomedical industry. Molecular formula: C49H56N7O9P. Mole weight: 917.98. | |
| 5'-O-DMT-N6-Phenoxyacetyl-2'-deoxyadenosine 3'-CE phosphoramidite | 5'-O-DMT-N6-Phenoxyacetyl-2'-deoxyadenosine 3'-CE phosphoramidite is a crucial recompound in the dynamic biomedical field, exhibiting unparalleled versatility in application in synthesizing sophisticated modified oligonucleotides. Alternative Names: 2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine 3'-CE phosphoramidite; DMT-dA(tac) Phosphoramidite; N-(Phenoxyacetyl)-3'-O-[2-cyanoethoxy(diisopropylamino)phosphino]-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine; 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-(phenoxyacetyl)-adenosine 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]. Grades: 95%. CAS No. 110543-74-3. Molecular formula: C48H54N7O8P. Mole weight: 887.98. | |
| 5-O-DMTr-1-Deoxyribose-3-O-TBDMS-2-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite | 5-O-DMTr-1-Deoxyribose-3-O-TBDMS-2-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite is a specialized phosphoramidite used in the synthesis of oligonucleotides, offering a combination of protective groups and functional modifications. It features a 5'-O-dimethoxytrityl (DMTr) group, which protects the 5'-hydroxyl group during oligonucleotide synthesis, allowing for selective deprotection and chain elongation. The 3'-O-tert-butyldimethylsilyl (TBDMS) group is a protecting group for the 3'-hydroxyl, preventing premature reactions during synthesis. This phosphoramidite is commonly used in oligonucleotide synthesis for applications that require specific structural modifications, such as enhanced stability, resistance to degradation, or customization for therapeutic uses, including gene editing, RNA interference, or antisense therapies. Alternative Names: 5'-O-DMTr-1-Deoxyribose-3'-O-TBDMS-2'-CE-phosphoramidite; DMT-1-Deoxyribose-3'-O-TBDMS-2'-CE-phosphoramidite. Grades: ≥95%. Molecular formula: C41H59N2O7PSi. Mole weight: 750.99. | |
| 5'-O-DMTr-2',2'-difluoro-dC(Bz)-methylphosphonamidite | 5'-O-DMTr-2',2'-difluoro-dC(Bz)-methylphosphonamidite is an indispensable entity employed in the biomedical sector for the purpose of constructing nucleic acids. Its function revolves around acting as an adjusted constituent that brings about the introduction of the 2',2'-difluoro modification at the 2'-position of a deoxycytidine (dC) nucleoside. This particular alteration augments the propensity for nucleic acids to bind and endure, thereby bestowing remarkable utility in the realms of pharmaceutical exploration, genetic repression and the elucidation of pathologies on a molecular scale. Grades: ≥95%. Molecular formula: C44H49F2N4O7P. Mole weight: 814.85. | |
| 5'-O-DMTr-2',3'-dideoxy-3'-fluoro-D-altritol-5-methyluridine | 5'-O-DMTr-2',3'-dideoxy-3'-fluoro-D-altritol-5-methyluridine is a modified nucleoside featuring a 5-methyluridine base attached to a D-altritol sugar backbone, which lacks the 2' and 3' hydroxyl groups (dideoxy) and has a fluorine atom at the 3' position. The 5'-hydroxyl group is protected with a dimethoxytrityl (DMTr) group, enabling its use in solid-phase oligonucleotide synthesis. This compound combines the enhanced chemical stability and nuclease resistance of the altritol backbone with the methylation at the 5-position of uridine, which can improve duplex stability and modulate biological activity, making it suitable for therapeutic and diagnostic oligonucleotide development. Alternative Names: 1,5-Anhydro-6-O-[bis(4-methoxyphenyl)phenylmethyl]-2,3-dideoxy-2-(3,4-dihydro-5-methyl-2,4-dioxo-1(2H)-pyrimidinyl)-3-fluoro-D-altritol; 1-((3R,4S,5R,6R)-6-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-fluoro-5-hydroxytetrahydro-2H-pyran-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione. Grades: ≥95%. CAS No. 1117903-20-4. Molecular formula: C32H33FN2O7. Mole weight: 576.61. | |
| 5'-O-DMTr-2',3'-dideoxy-3'-fluoro-D-altritol uridine | 5'-O-DMTr-2',3'-dideoxy-3'-fluoro-D-altritol uridine is a modified nucleoside analog where the uridine base is attached to a D-altritol sugar backbone, lacking the 2' and 3' hydroxyl groups (dideoxy) and containing a fluorine substitution at the 3' position. The 5'-hydroxyl group is protected with a dimethoxytrityl (DMTr) group to facilitate its use in solid-phase oligonucleotide synthesis. This analog is valuable in designing chemically modified nucleic acids, offering enhanced stability against nuclease degradation and improved biophysical properties, making it useful for therapeutic, diagnostic, or biochemical applications. Alternative Names: 1,5-Anhydro-6-O-[bis(4-methoxyphenyl)phenylmethyl]-2,3-dideoxy-2-(3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-3-fluoro-D-altritol. Grades: ≥95%. CAS No. 1117903-09-9. Molecular formula: C31H31FN2O7. Mole weight: 562.59. | |
| 5'-O-DMTr-2'-FU-methylphosphonamidite | 5'-O-DMTr-2'-FU-methylphosphonamidite is a vital component in the development of modified nucleosides used in the development of antiviral drugs. It plays a crucial role in the research of viral infections such as hepatitis C and HIV. This compound enables the efficient incorporation of modified nucleotides during the research and development of oligonucleotides. Alternative Names: 5'-O-DMTr-2'-deoxy-2'-fluorouridine-3'-O-(P-methyl-N,N-diisopropylamino)phosphonamidite. Grades: ≥95%. Molecular formula: C37H45FN3O7P. Mole weight: 693.74. | |
| 5'-O-DMTr-3'-deoxyuridine | 5'-O-DMTr-3'-deoxyuridine, a highly versatile compound extensively utilized in the field of biomedicine, serves as an indispensable entity in DNA synthesis and pharmaceutical investigations. Remarkably, this compound exhibits its prowess by acting as a transformative moiety, facilitating the integration of an array of functional groups into therapeutic agents. Grades: ≥95%. Molecular formula: C30H30N2O7. Mole weight: 530.57. | |
| 5'-O-DMTr-L-thymidine-3'-CED phosphoramidite | 5'-O-DMTr-L-thymidine-3'-CED phosphoramidite is a modified phosphoramidite used in solid-phase oligonucleotide synthesis. This compound is used for the preparation of custom oligonucleotides, such as for DNA sequencing, gene synthesis, or other nucleic acid-based applications. The L-configuration of the sugar in the name may imply a chiral modification, which could influence the nucleic acid's properties in certain contexts. Alternative Names: 1-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-deoxy-β-L-erythro-pentofuranosyl]-5-methyl-2,4(1H,3H)-pyrimidinedione; (2S,3R,5S)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; L-DNA T amidite; beta-L-dT-CE Phosphoramidite; 5'-Dimethoxytrityl-beta-L-2'-deoxyThymidine, 3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite; 5'-O-DMTr-L-dT-3'-CED phosphoramidite. Grades: ≥95%. CAS No. 141846-55-1. Molecular formula: C40H49N4O8P. Mole weight: 744.83. | |
| 5'-O-DMTr-N2-iBu-2'-L-deoxyguanosine 3'-CE phosphoramidite | 5'-O-DMTr-N2-iBu-2'-L-deoxyguanosine 3'-CE phosphoramidite is a modified phosphoramidite used in oligonucleotide synthesis. The 5'-O-DMTr group is a protective group at the 5' position of the nucleoside, which prevents unwanted reactions during synthesis and can be removed afterward. The N2-iBu modification attaches an isobutyl group to the N2 position of the guanine base, which alters its physical properties, such as hydrophobicity or stability. The 2'-L-deoxy indicates that the sugar is a 2'-deoxyribonucleotide with an L-enantiomer configuration, often used to enhance the stability or biological activity of the oligonucleotide. The 3'-CE phosphoramidite refers to a cyanoethyl group protecting the 3' phosphoramidite group, which is essential for the chemical ligation of nucleotides during oligonucleotide synthesis. This phosphoramidite is useful for synthesizing stable, modified DNA oligonucleotides with specific properties for research or therapeutic applications. Alternative Names: N-[9-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-deoxy-β-L-erythro-pentofuranosyl]-6,9-dihydro-6-oxo-1H-purin-2-yl]-2-methylpropanamide; Phosphoramidous acid, bis(1-methylethyl)-, mono(2-cyanoethyl) ester, ester with N-[9-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-2-deoxy-β-L-erythro-pentofuranosyl]-6,9-dihydro-6-oxo-1H-purin-2-yl]-2-methy | |
| 5'-O-DMTr-N2-isobutyroyl-2',3'-dideoxy-3'-fluoro-D-allitol guanidine | 5'-O-DMTr-N²-isobutyroyl-2',3'-dideoxy-3'-fluoro-D-allitol guanidine is a modified nucleoside analog featuring a guanine-like base with an N²-isobutyroyl protecting group attached to a D-allitol sugar backbone. The sugar is modified with a 3'-fluoro substitution and lacks the 2' and 3' hydroxyl groups (dideoxy). The 5'-hydroxyl group is protected with a dimethoxytrityl (DMTr) group, enabling its application in solid-phase oligonucleotide synthesis. This structure is designed for improved nuclease resistance, enhanced thermal stability of oligonucleotide duplexes, and optimized interactions in therapeutic or diagnostic nucleic acid applications. Alternative Names: 1,5-Anhydro-6-O-[bis(4-methoxyphenyl)phenylmethyl]-2,3-dideoxy-2-[1,6-dihydro-2-[(2-methyl-1-oxopropyl)amino]-6-oxo-9H-purin-9-yl]-3-fluoro-D-allitol. Grades: ≥95%. CAS No. 1197033-32-1. Molecular formula: C36H38FN5O7. Mole weight: 671.72. | |
| 5'-O-DMTr-N2-isobutyroyl-2',3'-dideoxy-3'-fluoro-D-altritol guanidine | 5'-O-DMTr-N²-isobutyroyl-2',3'-dideoxy-3'-fluoro-D-altritol guanidine is a modified nucleoside analog where a guanine-like base is attached to a D-altritol sugar backbone. This structure features a 3'-fluoro substitution and lacks the 2' and 3' hydroxyl groups (dideoxy). The base's N²-position is protected with an isobutyroyl group, and the 5'-hydroxyl is protected with a dimethoxytrityl (DMTr) group for use in solid-phase synthesis. This compound is engineered for enhanced nuclease resistance and improved thermal stability of oligonucleotides, making it valuable in therapeutic, diagnostic, or biochemical research involving modified nucleic acids. Alternative Names: 1,5-Anhydro-6-O-[bis(4-methoxyphenyl)phenylmethyl]-2,3-dideoxy-2-[1,6-dihydro-2-[(2-methyl-1-oxopropyl)amino]-6-oxo-9H-purin-9-yl]-3-fluoro-D-altritol. Grades: ≥95%. CAS No. 1117903-82-8. Molecular formula: C36H38FN5O7. Mole weight: 671.72. | |
| 5'-O-DMTr-N6-ethyl-2'-deoxyadenosine | 5'-O-DMTr-N6-ethyl-2'-deoxyadenosine, an essential element in biomedicine, holds immense potential in combating multiple ailments. Its remarkable ability to target drug-resistant cancers, such as leukemia and solid tumors, has gained significant recognition. By impeding crucial enzymes responsible for cancer cell proliferation, it emerges as a promising contender for tailored therapeutic interventions. Grades: ≥95%. Molecular formula: C33H35N5O5. Mole weight: 581.66. | |
| 5-O-DMT-thymidine 3'-H phosphonate triethylammonium salt | 5-O-DMT-thymidine 3'-H phosphonate triethylammonium salt, a pivotal ingredient in the dynamic field of biomedical science, emerges as an invaluable asset. Its multifaceted significance unfurls in the exploration of maladies etiology and the medley of therapeutic interventions. Expertly harnessed within scholarly interrogations, this compound illuminates the enigmatic realm of nucleotide analogues, unraveling the intricate tapestry governing DNA replication and restorative mechanisms. Veritably transcending boundaries, it assumes a decisive role in the innovative arena of antiviral drug fabrication, facilitating an in-depth comprehension of viral replications. Molecular formula: C37H48N3O9P. Mole weight: 709.77. | |
| 5'-O-DMT-thymidine-3'-lcaa-CPG | 5'-O-DMT-thymidine-3'-lcaa-CPG, an essential modified nucleotide, has garnered tremendous interest in the realm of biomedical research. Its purpose lies in the synthesis of oligonucleotides, granting researchers an unparalleled advantage in their studies. These resulting oligonucleotide conjugates play a pivotal role in the development of groundbreaking drug delivery systems, exhibiting immense potential as therapeutic agents targeting a plethora of diseases, including the infamous cancer and insidious viral infections. Alternative Names: DMT-T-lcaa-CPG. | |
| 5'-O-DMT-thymidine 3'-Me phosphonamidite | 5'-O-DMT-thymidine 3'-Me phosphonamidite, a pivotal compound utilized in the synthesis of modified oligonucleotides, holds immense significance within the realm of biomedical research. Its frequent application in the pursuit of therapeutics directed towards drug-resistant viral infections, including hepatitis B and HIV, showcases its indispensability. Furthermore, this product serves as a fundamental asset in the progression of drug discovery and the extensive molecular biology investigations targeting these afflictions. Alternative Names: 5'-O-DMT-D-thymidine 3'-Me phosphonamidite; 5'-(4,4'-Dimethoxytrityl)-thymidine, 3'-[methyl-(N,N-diisopropyl)]-phosphonamidite. Molecular formula: C38H48N3O7P. Mole weight: 689.78. | |
| 5'-O-DMT-thymidine 3'-Me phosphoramidite | 5'-O-DMT-thymidine 3'-Me phosphoramidite is a vital component in biomedical research for synthesizing modified DNA and RNA molecules. It is used to introduce a methyl group at the 3'-end of thymidine during solid-phase synthesis. This modified phosphoramidite enables the creation of customized nucleic acids for targeted drug delivery, gene therapy, and studying DNA-protein interactions. With its high purity and compatibility with automated synthesizers, it serves as an essential tool for advancing therapeutic developments and understanding genetic mechanisms. Alternative Names: dT-Me Phosphoramidite; 5'-(4,4'-Dimethoxytrityl)-thymidine, 3'-[methyl-(N,N-diisopropyl)]-phosphoramidite. Molecular formula: C38H48N3O8P. Mole weight: 705.78. | |
| 5'-O-DMT-thymidine-3'-O-succinic acid | 5'-O-DMT-thymidine-3'-O-succinic acid, an indispensable compound extensively employed in the biomedical sector for versatile applications, exhibits its profound significance. Functioning as a pivotal precursor in antiviral drug synthesis, it selectively combats RNA and DNA viruses. Additionally, it remarkably contributes to the advancement of pharmaceuticals dedicated to the treatment of HIV, hepatitis, and cancer. Alternative Names: 5'-O-(4,4'-Dimethoxytrityl)-thymidine-3'-O-succinic acid; 5'-O-(p,p'-Dimethoxytrityl)thymidine 3'-(hydrogen succinate). Grades: ≥ 99% (HPLC). CAS No. 74405-40-6. Molecular formula: C35H36N2O10. Mole weight: 644.67. | |
| 5'-O-DMT-thymidine 3'-Q Linker CPG | 5'-O-DMT-thymidine 3'-Q Linker CPG is a versatile product extensively used in the biomedical industry. Acting as a crucial component for solid-phase synthesis, it enables the synthesis of customized oligonucleotides, helping to study and develop therapeutic interventions for various diseases. Additionally, this linker CPG plays a vital role in drug discovery by facilitating the attachment of targeted molecules to nucleic acids, allowing for targeted drug delivery and enhanced treatment efficacy. | |
| 5'-O-DMT-thymidine 3'-succinyl | 5'-O-DMT-thymidine 3'-succinyl, an essential biomedicine, exhibits remarkable efficacy in alleviating a wide range of afflictions. Through its potent nucleoside analog properties, it flawlessly impedes viral replication, thereby assuming a pivotal role in the realm of antiviral therapies. Furthermore, this exceptional compound assumes utmost importance in DNA synthesis and repair, offering respite to those grappling with DNA-related maladies. | |
| 5'-O-DMT-thymidine-3'-succinyl CPG | 5'-O-DMT-thymidine-3'-succinyl CPG. | |
| 5'-O-DMT-uridine | It is used for nucleoside modification and RNA synthesis. Alternative Names: 5'-DMT Uridine; 5'-O-DMT uridine; 5'-O-(4,4'-Dimethyltrityl)uridine; 5'-O-DMT-D-uridine; 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]uridine; 1-((2R,3R,4S,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3,4-dihydroxytetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione. Grades: ≥98% by HPLC. CAS No. 81246-79-9. Molecular formula: C30H30N2O8. Mole weight: 546.57. | |
| 5'-O-DMT-uridine 3'-CE phosphoramidite | 5'-O-DMT-uridine 3'-CE phosphoramidite, a pivotal compound employed in the realm of biomedical research and pharmaceutical advancement, stands as a vital cog in the synthesis of nucleotide analogs. By serving as a foundational unit, it facilitates the treatment of divergent ailments such as viral infections, cancer, and genetic disorders. Treading upon the path of nucleic acid synthesis, this product assumes a paramount stance in the augmentation of innovative therapeutic approaches within the realm of biomedicine. Alternative Names: 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]-uridine 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]. CAS No. 951777-44-9. Molecular formula: C39H47N4O9P. Mole weight: 746.79. | |
| 5'-O-DMT-uridine 3'-succinyl CPG | 5'-O-DMT-uridine 3'-succinyl CPG, a profoundly significant reagent within the biomedical field, serves as a catalyst for the synthesis of intricate oligonucleotides. Demonstrating its versatility, this compound finds wide-ranging applications in academic research, primarily within nucleic acid chemistry. | |
| 5-OH-dU-CE Phosphoramidite | 5-OH-dU-CE Phosphoramidite is an indispensable recompound within the realm of compound assuming a pivotal function in the research and development of altered nucleosides, thereby facilitating DNA/RNA investigations. It holds particular significance in the formulation of oligonucleotides, intended for diagnostics and therapeutics relating to hereditary afflictions or viral infestations. Alternative Names: 5'-Dimethoxytrityl-5-O-Acetyl-2'-deoxyUridine, 3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite. Grades: 95%. CAS No. 197229-19-9. Molecular formula: C41H49N4O10P. Mole weight: 788.83. | |
| 5-O-Lauryl-α-D-xylofuranose | 5-O-Lauryl-α-D-xylofuranose is a remarkable compound brandishing antiviral properties, used for the research of quell select viral aggressors. Alternative Names: α-D-Xylofuranose, 5-dodecanoate; 5-O-Lauryl-D-xylofuranose. CAS No. 176793-21-8. Molecular formula: C17H32O6. Mole weight: 332.43. | |
| 5'-O-Levulinoylthymidine | 5'-O-Levulinoylthymidine is a derivative of thymidine, acting as a quintessential investigative instrument for scrutinizing the intricate mechanisms governing DNA research and rectification. Its utilization transcends these boundaries and extends towards facilitating developments in anti-cancer therapeutics and addressing maladies linked to DNA aberrations. Alternative Names: 5'-O-Levulinoyl-D-thymidine. Grades: ≥ 98% (HPLC). CAS No. 440327-46-8. Molecular formula: C15H20N2O7. Mole weight: 340.33. | |
| 5'-O-Levulinoylthymidine 3'-CE phosphoramidite | 5'-O-Levulinoylthymidine 3'-CE phosphoramidite, an indispensable asset harnessed within the ever-evolving realms of the biomedical sector, emanates a profound influence upon the synthesis of tailored oligonucleotides. Reverberating as a catalyst for innovation, its innate ability to bestow a 5'-O-levulinoyl modification, combined with its role as a safeguarding entity during solid-phase synthesis, elicits transformative outcomes. Unveiling an extensive repertoire, this wondrous creation orchestrates a symphony of advancements in targeted drug delivery, gene therapy, and the diagnostic landscape. Alternative Names: ((2R,3S,5R)-3-(((2-Cyanoethoxy)(diisopropylamino)phosphanyl)oxy)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl 4-oxopentanoate. CAS No. 581076-14-4. Molecular formula: C24H37N4O8P. Mole weight: 540.55. | |
| 5'-OMe-dT-CE Phosphoramidite | 5'-OMe-dT-CE Phosphoramidite is a pivotal component in the research and development of customized oligonucleotides. Renowned for its unparalleled resilience and remarkable integration efficiency, 5'-OMe-dT-CE Phosphoramidite finds extensive utilization in the development of antiviral medication and gene therapeutics. Alternative Names: 5'-O-methyl-2'-deoxyThymidine, 3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite; 5'-OMe-dT-CEP. Grades: 95%. CAS No. 149681-62-9. Molecular formula: C20H33N4O6P. Mole weight: 456.48. | |
| 5'-O-Methoxytrityluridine 3'-CE phosphoramidite | 5'-O-Methoxytrityluridine 3'-CE phosphoramidite is an exceedingly intricate chemical, often employed in the creation of synthetic DNA and RNA. It plays a critical role in oligonucleotide fusion techniques, protecting the sensitive nucleotide bonds during synthesis. The proficiency exhibited by this product extends to cancer diagnoses, particularly in cases of colorectal and lung cancer, via the employment of diagnostic assays. Alternative Names: 5'-O-Methoxytrityl-D-uridine 3'-CE phosphoramidite. Molecular formula: C39H47N4O8P. Mole weight: 730.81. | |
| 5-O-Methyl-myo-inositol | 5-O-Methyl-myo-inositol is a compound used in biomedicine to treat various diseases such as diabetes, hyperlipidemia, and obesity. It acts as an insulin sensitizer and increases glucose uptake in cells, leading to improved blood glucose control. It also has potential applications in cancer treatment due to its ability to regulate cell proliferation and differentiation. Alternative Names: Sequoyitol; Inositol, 5-O-methyl-, myo-; Sequoyit. CAS No. 523-92-2. Molecular formula: C7H14O6. Mole weight: 194.18. | |
| 5'-O-Methylthymidine | 5'-O-Methylthymidine is a vital component used in the biomedical industry for the research and development of antiviral drugs like Acyclovir and Ganciclovir. It plays a crucial role in studying viral infections caused by herpes simplex virus (HSV) and cytomegalovirus (CMV) as well as preventing their replication. Alternative Names: 5'-O-Methyl-D-thymidine; 1-[(2R,4S,5R)-4-hydroxy-5-(methoxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione; 5A'A inverted exclamation markA'A-O-Methyl-D-thymidine; Thymidine,5'-O-methyl. Grades: ≥ 95%. CAS No. 14504-60-0. Molecular formula: C11H16N2O5. Mole weight: 256.26. | |
| 5'-O-MMT-thymidine 3'-CE phosphoramidite | 5'-O-MMT-thymidine 3'-CE phosphoramidite is a highly prized biochemical recompound, profoundly impacting the realm of DNA and RNA molecule research and development within the biomedical landscape. Through its remarkable attributes, this recompound deftly enables the precise and efficacious integration of thymidine nucleotides during the solid-phase oligonucleotide research and development process. Alternative Names: 5'-O-MMT-D-thymidine 3'-CE phosphoramidite. Molecular formula: C39H47N4O7P. Mole weight: 714.81. | |
| 5'-O-p-Anisoyl-2,2'-anhydrouridine | 5'-O-p-Anisoyl-2,2'-anhydrouridine is an essential biomedical compound assuming an integral role in the development of antiviral and antineoplastic pharmaceuticas. Alternative Names: 5'-O-p-Anisoyl-2,2'-anhydro-D-uridine. Molecular formula: C17H16N2O7. Mole weight: 360.32. | |
| 5'-O-p-Anisoyl-2'-deoxyuridine | 5'-O-p-Anisoyl-2'-deoxyuridine is a vital compound widely used in the biomedical industry. It plays a significant role in the development of antiviral drugs due to its potent anti-HIV properties. Additionally, it shows promising effects in the treatment of cancer and autoimmune diseases. This product acts as a crucial building block in the synthesis of various pharmaceutical compounds. Molecular formula: C17H18N2O7. Mole weight: 362.33. | |
| 5'-O-p-Anisoyl-2'-deoxyuridine 3'-CE phosphoramidite | 5'-O-p-Anisoyl-2'-deoxyuridine 3'-CE phosphoramidite - a pivotal component in oligonucleotide synthesis, essential for developing treatments against viral infections and cancer. Through its potent ability to hinder RNA and DNA virus replication and selectively restrain tumor cells, this product has become a fundamental instrument in biomedical research, promoting the creation of novel therapeutic drugs against critical illnesses. Molecular formula: C26H35N4O8P. Mole weight: 562.55. | |
| 5'-O-p-Anisoyl-2'-O-tert-butyldimethylsilyl-5-methyluridine 3'-CE phosphoramidite | 5'-O-p-Anisoyl-2'-O-tert-butyldimethylsilyl-5-methyluridine 3'-CE phosphoramidite, an indispensable compound within the biomedical industry, plays a pivotal role in the synthesis of modified RNA oligonucleotides. The incorporation of 5'-O-p-Anisoyl-2'-O-tert-butyldimethylsilyl-5-methyluridine into oligonucleotide chains, facilitated by this phosphoramidite derivative, grants remarkable efficiency and precision. Consequently, it empowers the development of targeted therapies and drug delivery systems, lending itself to the realm of treating diverse ailments encompassing cancer, genetic disorders, and viral infections. Manifesting unrivaled purity and stability, this exceptional tool stands poised to revolutionize the landscape of disease management via academic and scientific means. Alternative Names: 5'-O-p-Anisoyl-2'-O-tert-butyldimethylsilyl-D-thymidine 3'-CE phosphoramidite. Molecular formula: C33H51N4O9PSi. Mole weight: 706.84. | |
| 5'-O-p-Anisoyl-2'-O-tert-butyldimethylsilyluridine 3'-CE phosphoramidite | 5'-O-p-Anisoyl-2'-O-tert-butyldimethylsilyluridine 3'-CE phosphoramidite is a phosphoramidite recompound used as an indispensable tool for DNA research and development. Its significance lies in facilitating the compoundion of oligonucleotides, thereby assuming a pivotal role in fostering the development of nucleic acid-based therapeutics and diagnostics. Molecular formula: C32H49N4O9PSi. Mole weight: 692.83. | |
| 5'-O-p-Anisoyl-3'-azido-2',3'-dideoxyuridine | 5'-O-p-Anisoyl-3'-azido-2',3'-dideoxyuridine, an exceptionally robust antiviral agent, has shown remarkable efficacy against a spectrum of viral infections such as herpes simplex virus and human immunodeficiency virus (HIV). With its unique mechanism of action, this compound acts as a nucleoside analog, exerting potent inhibition on viral DNA synthesis. Alternative Names: 5'-O-p-Anisoyl-3'-O-azido-2',3'-dideoxy-D-uridine. Molecular formula: C17H17N5O6. Mole weight: 387.35. | |
| 5'-O-p-Anisoyl-3'-azido-3'-deoxythymidine | 5'-O-p-Anisoyl-3'-azido-3'-deoxythymidine, an antiviral drug used for the treatment of HIV infection, operates by impeding the reverse transcriptase enzyme obligatory for viral replication. Intriguingly, this compound has also been probed for its budding usefulness in cancer treatment. It has come to light that this antiviral drug holds great potential in the treatment of cancer due to its distinctive attributes in mitigating the enzymes involved in the propagation of cancer cells. Alternative Names: 5'-O-p-Anisoyl-3'-azido-3'-deoxy-D-thymidine. Molecular formula: C18H19N5O6. Mole weight: 401.37. | |
| 5'-O-p-Anisoyl-3'-fluoro-2',3'-dideoxyuridine | 5'-O-p-Anisoyl-3'-fluoro-2',3'-dideoxyuridine, a formidable antiviral agent extensively employed in the biomedicine sphere, showcases remarkable efficacy in combating both herpes simplex virus (HSV) and varicella-zoster virus (VZV). This robust compound serves as an efficacious remedy for viral infections engendered by these malevolent pathogens by obstructing viral DNA synthesis, exerting its proficiency in hindering viral proliferation. Alternative Names: 5'-O-p-Anisoyl-3'-fluoro-2',3'-dideoxy-D-uridine. Molecular formula: C17H17FN2O6. Mole weight: 364.33. | |
| 5'-O-p-Anisoyl-3'-fluoro-3'-deoxythymidine | 5'-O-p-Anisoyl-3'-fluoro-3'-deoxythymidine, also known as AFT, is an exceptionally powerful antiviral agent employed in the management of HIV infection. Its remarkable capability lies in its ability to effectively impede the reverse transcriptase enzyme, thereby impeding the virus's replication. In addition to this impressive mechanism, AFT exhibits unparalleled selectivity and minimal cytotoxicity. Molecular formula: C18H19FN2O6. Mole weight: 378.4. | |
| 5'-O-p-Anisoyl-N4-benzoyl-2',3'-dideoxycytidine | 5'-O-p-Anisoyl-N4-benzoyl-2',3'-dideoxycytidine, a highly potent antiviral compound widely utilized in the biomedical field, is primarily indicated for the management of viral ailments, particularly those caused by retroviruses. By functioning as a nucleoside analogue and interfering with viral DNA synthesis, this medication exemplifies its inhibitory prowess against retroviruses such as HIV. Alternative Names: 5'-O-p-Anisoyl-N4-benzoyl-2',3'-dideoxy-D-cytidine. CAS No. 1241674-34-9. Molecular formula: C24H23N3O6. Mole weight: 449.46. | |
| 5'-O-p-Anisoyl-N4-benzoyl-2'-O-tert-butyldimethylsilylcytidine 3'-CE phosphoramidite | 5'-O-p-Anisoyl-N4-benzoyl-2'-O-tert-butyldimethylsilylcytidine 3'-CE phosphoramidite, a highly important compound, is extensively utilized in the synthesis of altered nucleic acids for advanced biomedical investigations. It occupies a pivotal position in the advancement of innovative therapeutics aiming at precise ailment targeting. Endowed with elevated stability and impeccable compatibility, this exemplary product exhibits utmost suitability for addressing a diverse range of drug-resistant pathologies and viral afflictions. Alternative Names: 5'-O-p-Anisoyl-N4-benzoyl-2'-O-tert-butyldimethylsilyl-D-cytidine 3'-CE phosphoramidite. Molecular formula: C39H54N5O9PSi. Mole weight: 795.95. | |
| 5'-O-p-Anisoyl-N4-benzoyl-3'-fluoro-2',3'-dideoxycytidine | 5'-O-p-Anisoyl-N4-benzoyl-3'-fluoro-2',3'-dideoxycytidine is a potent antiviral compound used in biomedicine. It exhibits activity against HIV-1 and is commonly employed in the development of novel antiretroviral therapies. Being structurally modified, this compound enhances its effectiveness against drug-resistant strains of the virus, making it a valuable tool in the fight against HIV / AIDS. Alternative Names: 5'-O-p-Anisoyl-N4-benzoyl-3'-fluoro-2',3'-dideoxy-D-cytidine. Molecular formula: C24H22FN3O6. Mole weight: 467.45. | |
| 5'-O-p-Anisoyl-N6-benzoyl-2'-deoxyadenosine | 5'-O-p-Anisoyl-N6-benzoyl-2'-deoxyadenosine, a potent antineoplastic agent, has emerged as a viable treatment option for various malignancies. Its robust tumor-suppressing mechanisms include disruption of cell proliferation and activation of programmed cell death pathways within malignant cells, illustrating promising prospects for future oncological therapies. Molecular formula: C25H23N5O6. Mole weight: 489.48. | |
| 5'-O-p-Anisoyl-N6-benzoyl-2'-O-tert-butyldimethylsilyladenosine 3'-CE phosphoramidite | 5'-O-p-Anisoyl-N6-benzoyl-2'-O-tert-butyldimethylsilyladenosine 3'-CE phosphoramidite, a versatile chemical reagent, finds wide application in the field of molecular biology. Its utility lies in the synthesis of oligonucleotides by enhancing the stability of modified DNA sequences and RNAs. Researchers rely on this reagent to unravel complex biological phenomena and their underlying mechanisms. Alternative Names: 5'-O-p-Anisoyl-N4-benzoyl-2'-O-tert-butyldimethylsilyl-D-adenosine 3'-CE phosphoramidite. Molecular formula: C40H54N7O8PSi. Mole weight: 819.98. | |
| 5'-O-p-Anisoylthymidine | 5'-O-p-Anisoylthymidine, a well-known biomedical compound, is extensively utilized for the therapeutic management of viral infections instigated by both RNA and DNA viruses. Exhibiting potent antiviral characteristics, it demonstrates remarkable efficacy specifically against the herpes simplex viruses, namely HSV-1 and HSV-2. By impeding the synthesis of viral DNA, this compound proficiently hinders viral replication, thus curbing the progression of the infection. Molecular formula: C18H20N2O7. Mole weight: 376.36. | |
| 5'-O-p-Anisoylthymidine 3'-CE phosphoramidite | 5'-O-p-Anisoylthymidine 3'-CE phosphoramidite is an indispensable reagent in the world of biomedicine, utilized extensively in the synthesis of DNA and RNA oligonucleotides. Its molecular makeup grants a myriad of research opportunities in the realm of disease research, from the minute intricacies of genetic disorders to the rampant growth of malignant cancers and treacherous viral infections. With its impeccable efficiency in integrating itself into nucleic acid chains, this reagent proves itself as a pivotal tool in drug development, guiding humanity towards a brighter, healthier future. Molecular formula: C27H37N4O8P. Mole weight: 576.58. | |
| 5'-O-Pixylthymidine | 5'-O-Pixylthymidine is a crucial component in biomedicine, commonly used in the development of antiviral drugs and treatments for viral infections such as HIV. This compound can inhibit viral replication and RNA synthesis, thereby reducing the viral load within the body. Additionally, it plays a vital role in molecular diagnostics, aiding in the detection and quantification of viral nucleic acids. Alternative Names: 5'-O-Pixyl-D-thymidine. Molecular formula: C29H26N2O6. Mole weight: 498.53. | |
| 5'-O-(p-Toluenesulfonyl)-2'-deoxyuridine | 5'-O-(p-Toluenesulfonyl)-2'-deoxyuridine, can be used as antimalarials using QSAR, pharmacophore mapping and multiple docking studies in biological study of exploring structural requirements for class of nucleoside inhibitors. Alternative Names: 1-(5-O-Tosyl-2-deoxy-β-D-erythro-pentofuranosyl)uracil; 2'-Deoxy-5'-O-p-toluenesulfonyluridine; 5'-O-Tosyl-2'-deoxyuridine; 5'-O-p-Tolylsulfonyl-2'-deoxyuridine. Grades: 95%. CAS No. 27999-47-9. Molecular formula: C16H18N2O7S. Mole weight: 382.39. | |
| 5'-O-(p-Toluoyl)-2'-O-acetyl-3'-deoxy-3'-fluorouridine | 5'-O-(p-Toluoyl)-2'-O-acetyl-3'-deoxy-3'-fluorouridine, a remarkably potent antiviral compound, finds extensive application in the field of biomedicine for the treatment of viral infections. With its profound and exceptional inhibitory activity against the hepatitis C virus, this compound emerges as a pivotal player in preventing the relentless progression of this debilitating disease. Alternative Names: ((2R,3R,4S,5R)-4-acetoxy-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-fluorotetrahydrofuran-2-yl)methyl 4-methylbenzoate. Molecular formula: C19H19FN2O7. Mole weight: 406.37. | |
| 5'-O-TBDMS-2'-deoxyadenosine | 5'-O-TBDMS-2'-deoxyadenosine, a synthetic nucleoside derivative, utilized in the manufacturing of anti-cancer agents and antiviral drugs. It also plays a crucial role in gene therapy research and gene expression analyses as an oligonucleotide synthesizing agent. Moreover, this exceptional compound boasts of its remarkable metabolic stability, and is renowned for its potent DNA polymerase and reverse transcriptase inhibitory effects. Alternative Names: 5'-O-TBDMS-dA; Adenosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-; 5'-O-(tert-Butyldimethylsilyl)-2'-deoxyadenosine; (2R,3S,5R)-5-(6-Amino-9H-purin-9-yl)-2-(((tert-butyldimethylsilyl)oxy)methyl)tetrahydrofuran-3-ol; 2'-Deoxy-5'-O-[dimethyl(2-methyl-2-propanyl)silyl]adenosine. Grades: ≥97% by HPLC. CAS No. 51549-30-5. Molecular formula: C16H27N5O3Si. Mole weight: 365.51. | |
| 5'-O-TBDMS-2'-deoxyuridine | 5'-O-TBDMS-2'-deoxyuridine, a nucleoside analog, greatly perturbs the tedium of drug synthesis, serving as a galvanizing building block for the creation of antiviral and anticancer drugs. Unquestionably, its most notable uses include the synthesis of nucleoside derivatives with a potent antiviral effect against the herpes simplex virus and the human immunodeficiency virus (HIV). Alternative Names: Uridine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-; 5'-O-TBDMS-dU; 1-[(2R,4S,5R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-4-hydroxyoxolan-2-yl]pyrimidine-2,4-dione; 5'-O-(tert-butyldimethylsilyl)-2'-deoxyuridine; 2'-Deoxy-5'-O-[dimethyl(2-methyl-2-propanyl)silyl]uridine. Grades: ≥97% by HPLC. CAS No. 76223-04-6. Molecular formula: C15H26N2O5Si. Mole weight: 342.47. | |
| 5'-O-TBDMS-5-Fluoro-2'-deoxyuridine | 5'-O-TBDMS-5-Fluoro-2'-deoxyuridine, a nucleoside analogue employed as antiviral therapy for herpes simplex virus, varicella zoster virus, and cytomegalovirus infections in immunocompromised subjects, functions by halting elongation of DNA chains via cellular DNA synthesis to impede viral DNA replication. Its effectiveness in this role, derived through rigorous scientific study, makes it a key player in the fight against viral infections. Alternative Names: 5'-O-TBDMS-5-F-dU; 5'-O-(tert-Butyldimethylsilyl)-5-fluoro-2'-deoxyuridine; Uridine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-5-fluoro-; 5'-O-(tert-Butyldimethylsilyl)-2'-deoxy-5-fluorouridine. Grades: ≥97% by HPLC. CAS No. 129816-30-4. Molecular formula: C15H25FN2O5Si. Mole weight: 360.46. | |
| 5'-O-TBDMS-N2-isobutyryl-2'-deoxyguanosine | 5'-O-TBDMS-N2-isobutyryl-2'-deoxyguanosine, a nucleoside analog, is an intricate and multifaceted tool, crucial in the synthesis of antisense oligonucleotides, employed for the treatment of a variety of devastating ailments like viral infections and cancer. Alongside this, it is a significant addition to the biomedical arsenal as it helps researchers study gene expression. Its myriad of uses and intricate nature is indispensable in contemporary scientific research. Alternative Names: 5'-O-TBDMS-N2-ibu-dG; N2-isobutyryl-5'-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine; N-(9-((2R,4S,5R)-5-(((tert-Butyldimethylsilyl)oxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide; N-Isobutyryl-5'-O-tert-butyldiMethylsilyl-2'-deoxyguanosine; N2-iBu-5'-O-TBS-dG; Guanosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-N-(2-methyl-1-oxopropyl)-; 2'-Deoxy-5'-O-[dimethyl(2-methyl-2-propanyl)silyl]-N-isobutyrylguanosine. Grades: ≥97% by HPLC. CAS No. 85326-10-9. Molecular formula: C20H33N5O5Si. Mole weight: 451.60. | |
| 5'-O-TBDMS-N4-Acetyl-2'-deoxycytidine | 5'-O-TBDMS-N4-Acetyl-2'-deoxycytidine is a valuable compound widely used in compound with antineoplastic properties. It targets specific pathways involved in the growth and proliferation of cancer cells. Alternative Names: 5'-O-TBDMS-N4-AC-dC. Grades: ≥97% by HPLC. Molecular formula: C17H29N3O5Si. Mole weight: 383.52. | |
| 5'-O-TBDMS-N4-Acetyl-5-iodo-2'-deoxycytidine | 5'-O-TBDMS-N4-Acetyl-5-iodo-2'-deoxycytidine is an exceedingly powerful nucleoside analogue that finding usage in the research of a myriad of viruses, notably hepatitis B and HIV. Its mechanism of action entails impeding viral replication while simultaneously disrupting the formation of viral DNA. Alternative Names: 5'-O-TBDMS-N4-Ac-5-I-dC. Grades: ≥97% by HPLC. Molecular formula: C17H28IN3O5Si. Mole weight: 509.42. | |
| 5-O-TBDPS-2,3-Isopropuidene-D-ribono-1,4-lactone | 5-O-TBDPS-2,3-Isopropuidene-D-ribono-1,4-lactone is an intriguing and highly intricate compound, embodying an exceptional antiviral and antifungal prowess. Its extraordinary affinities allow it to combat and conquer targeted viral infiltrations and fungal scourges. Alternative Names: (3AR,6R,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one; 2-O,3-O-Isopropylidene-5-O-(tert-butyldiphenylsilyl)-D-ribonic acid 1,4-lactone; D-Ribonic acid, 5-O-[(1,1-dimethylethyl)diphenylsilyl]-2,3-O-(1-methylethylidene)-, γ-lactone; 5-O-t-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribono-1,4-lactone; (3aR,6R,6aR)-2,2-Dimethyl-6-({[(2-methyl-2-propanyl)(diphenyl)silyl]oxy}methyl)dihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one. Grades: ≥95% by HPLC. CAS No. 130222-84-3. Molecular formula: C24H30O5Si. Mole weight: 426.58. | |
| 5'-O-TBDPS-5-methyl-2,2'-anhydrouridine | 5'-O-TBDPS-5-methyl-2,2'-anhydrouridine is a profoundly influential entity in the realm of compound, manifesting its exceptional antiviral potential, specifically against the scourge of RNA viruses like SARS-CoV-2 and influenza. Alternative Names: (2R,4R,5R,6S)-4-[[tert-butyl(diphenyl)silyl]oxymethyl]-5-hydroxy-11-methyl-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-10-one. Grades: ≥95%. CAS No. 171763-19-2. Molecular formula: C26H30N2O5Si. Mole weight: 478.61. | |
| 5'-O-(t-Butyldimethylsilyl)thymidine | 5'-O-(t-Butyldimethylsilyl)thymidine is a modified form of thymidine used in the biomedical industry. It is commonly employed in the synthesis of nucleic acid analogs and oligonucleotides for research purposes. Its t-butyldimethylsilyl group protects the thymidine molecule during the chemical reactions. It finding application in drug discovery, especially for developing antiviral and anticancer drugs. Alternative Names: 5'-tert-butyldimethylsilyloxy-2'-deoxythymidine; 5'-O-TBDMS-thymidine; 5'-O-(t-Butyldimethylsilyl)thymidine; 1-((2R,4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione; 5-Methyl-5'-O-(tert-butyldimethylsilyl)-2'-deoxyuridine. Grades: ≥97% by HPLC. CAS No. 40733-28-6. Molecular formula: C16H28N2O5Si. Mole weight: 356.49. | |
| 5-O-(t-Butyldiphenylsilyl)-1,2-O-isopropylidene-a-D-xylofuranose | 5-O-(t-Butyldiphenylsilyl)-1,2-O-isopropylidene-a-D-xylofuranose is an indispensable molecular entity extensively employed within the biomedical sector, exhibiting profound potency in the regulation of pivotal biological pathways. This compound can be used for the research of viral infections, metabolic anomalies and neurodegeneration. Alternative Names: alpha-D-Xylofuranose, 5-O-[(1,1-dimethylethyl)diphenylsilyl]-1,2-O-(1-methylethylidene)-; (3aR,5R,6S,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol; (3aR,5R,6S,6aR)-5-(((t-Butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol; (3aR,5R,6S,6aR)-5-{[(tert-butyldiphenylsilyl)oxy]methyl}-2,2-dimethyl-tetrahydro-2H-furo[2,3-d][1,3]dioxol-6-ol. CAS No. 114861-14-2. Molecular formula: C24H32O5Si. Mole weight: 428.59. | |
| 5'-O-tert-Butyldimethsilyl-2'-Deoxy-N2-isobutyrylguanosine 3'-CE phosphoramidite | 5'-O-tert-Butyldimethsilyl-2'-Deoxy-N2-isobutyrylguanosine 3'-CE phosphoramidite, a pivotal augmentation in the biomedical sector, furnishes an imperious apparatus for the assembly of tailored DNA sequences. By entwining the guanosine derivative into solid-phase DNA synthesis, it elucidates the intricate enigma surrounding DNA's configuration and operation. Synchronously, its multi-faceted employment engulfs drug innovation and malady identification, permeating versatile scientific domains. Molecular formula: C29H50N7O6PSi. Mole weight: 651.82. | |
| 5-O-tert-Butyldimethylsilyl-1,4-dideoxy-1,4-imino-2,3-O-isopropylidene-D-ribitol | 5-O-tert-Butyldimethylsilyl-1,4-dideoxy-1,4-imino-2,3-O-isopropylidene-D-ribitol is a compound frequently employed in the biomedical sector, exhibiting remarkable potency in research of a multitude of diseases and conditions, predominantly bacterial infections. Alternative Names: (3aR,4R,6aS)-4-{[(tert-butyldimethylsilyl)oxy]methyl}-2,2-dimethyl-hexahydro-[1,3]dioxolo[4,5-c]pyrrole; (3aR,4R,6aS)-4-(((tert-Butyldimethylsilyl)oxy)methyl)-2,2-dimethyltetrahydro-3aH-[1,3]dioxolo[4,5-c]pyrrole; (3aR,4R,6aS)-4-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyltetrahydro-4H-[1,3]dioxolo[4,5-c]pyrrole; (3aR,4R,6aS)-4-(tert-butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-C]pyrrole; (3aR,4R,6aS)-4-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]tetrahydro-2,2-dimethyl-4H-1,3-dioxolo[4,5-c]pyrrole. CAS No. 153172-31-7. Molecular formula: C14H29NO3Si. Mole weight: 287.47. | |
| 5-O-tert-Butyldimethylsilyl-1-chloro-2,3-O-isopropylidene-b-D-ribofuranose | 5-O-tert-Butyldimethylsilyl-1-chloro-2,3-O-isopropylidene-b-D-ribofuranose is an intermediary compound, serving as a pivotal constituent for the research and development of a diverse range of pharmaceuticals, encompassing potent antiviral and antitumor compounds. Alternative Names: 5-O-tert-Butyldimethylsilyl-2,3-O-isopropylidene-b-D-ribofuranosyl chloride. CAS No. 102690-94-4. Molecular formula: C14H27ClO5Si. Mole weight: 338.90. | |
| 5-O-tert-Butyldimethylsilyl-1,N-dehydro-1,4-dideoxy-1,4-imino-2,3-O-isopropylidene-D-ribitol | 5-O-tert-Butyldimethylsilyl-1,N-dehydro-1,4-dideoxy-1,4-imino-2,3-O-isopropylidene-D-ribitol is a multifaceted compound widely employed in the biomedical domain, serving as a crucial recompound for synthesizing nucleoside analogs. Alternative Names: [(3aR,4R,6aS)-2,2-dimethyl-4,6a-dihydro-3aH-[1,3]dioxolo[4,5-c]pyrrol-4-yl]methoxy-tert-butyl-dimethylsilane; (3aR,4R,6aS)-4-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-4,6a-dihydro-3aH-[1,3]dioxolo[4,5-c]pyrrole. CAS No. 153172-33-9. Molecular formula: C14H27NO3Si. Mole weight: 285.45. | |
| 5'-O-tert-Butyldimethylsilyl-2,2'-anhydrouridine | 5'-O-tert-Butyldimethylsilyl-2,2'-anhydrouridine is a crucial compound in biomedicine used for the synthesis of nucleoside analogs. It is commonly utilized in the development of antiviral drugs, particularly targeting diseases caused by RNA viruses. This product plays a pivotal role in the research and treatment of viral infections, helping advance scientific understanding and potentially leading to the development of novel therapeutics. Alternative Names: 5'-O-tert-Butyldimethylsilyl-2,2'-anhydro-D-uridine. Molecular formula: C15H24N2O5Si. Mole weight: 340.45. | |
Our database is helping our users find suppliers everyday.
