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| Product | Description | |
|---|---|---|
| 2'-Deoxy-3'-O-DMT-N2-isobutyrylguanosine 5'-thiophosphoramidite | 2'-Deoxy-3'-O-DMT-N2-isobutyrylguanosine 5'-thiophosphoramidite. Group: Biochemicals. Alternative Names: 2'-Deoxy-5'-dimethoxytrityl-N-isobutyryl-guanosine-3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences. |  Worldwide |
| 2'-Deoxy-5'-O-DMT-N2-isobutyrylguanosine 3'-thiophosphoramidite | 2'-Deoxy-5'-O-DMT-N2-isobutyrylguanosine 3'-thiophosphoramidite, an extensively utilized compound within the biomedical sector, displays promise for investigating nucleotide modifications and their influence on gene expression. Additionally, its plausible therapeutic applications have garnered attention, although additional research is imperative. Notably, this academically significant product holds potential for exploring disease treatment and condition amelioration. Synonyms: 2'-Deoxy-5'-dimethoxytrityl-N-isobutyryl-guanosine-3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C48H53N6O8PS2. Mole weight: 937.08. |  |
| 2'-OMe-A-Thiophosphoramidite | 2'-OMe-A-Thiophosphoramidite - an essential intermediate reagent employed in synthesizing oligonucleotides for targeting particular messenger RNA molecules, is employed in the management of various therapeutic conditions, including cancer and viral infections. By providing superior RNAi efficacy and specificity, 2'-OMe-A-Thiophosphoramidite has emerged as a vital tool in biomedical research and drug discovery. Its application ranges from oligonucleotide synthesis to the management of various diseases associated with RNA molecules - thus portraying its versatility in the ever-evolving healthcare industry. Synonyms: 5'-Dimethoxytrityl-N-benzoyl-Adenosine, 2'-O-methyl, 3'-[(β-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C52H53N6O8PS2. Mole weight: 985.12. | |
| 2'-OMe-C-Thiophosphoramidite | 2'-OMe-C-Thiophosphoramidite, a chemical compound utilized in the synthesis of nucleic acids, is essential for the creation of modified RNA molecules that possess heightened stability and specificity. This modality of RNA modification, which employs the 2'-OMe-C-Thiophosphoramidite, showcases potential in the management of pathologic states such as cancer and viral infections. Renewed focus on the utilization of this compound may lead to significant advancements in the therapeutic landscape. Synonyms: 5'-Dimethoxytrityl-N-acetyl-Cytidine, 2'-O-methyl, 3'-[(β-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C46H51N4O9PS2. Mole weight: 899.02. | |
| 2'-OMe-G-Thiophosphoramidite | 2'-OMe-G-Thiophosphoramidite, a synthetic compound, plays a vital role in the fabrication of RNA modifications. Being a prominent building block, it ameliorates the process of RNA oligonucleotide synthesis. With its advent, RNA-based therapeutics have garnered significant attention, especially for malignant tumors and aggravated viral infections. This high purity chemical entity encourages the development of groundbreaking RNA-based drugs by providing a stable foundation and promoting drug efficacy. Synonyms: 5'-Dimethoxytrityl-N-isobutyryl-Guanosine, 2'-O-methyl, 3'-[(β-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C49H55N6O9PS2. Mole weight: 967.10. | |
| 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. | |
| 5'-O-DMT-thymidine 3'-thiophosphoramidite | 5'-O-DMT-thymidine 3'-thiophosphoramidite, a highly indispensable reagent employed in numerous biomedical applications, has the capability to confer augmented stability and safeguard the resultant sequences against degradation by nucleases. Its employment facilitates the precise introduction of 5'-O-DMT-thymidine into the oligonucleotide chain, thereby enabling focused therapeutic interventions for drug administration, gene suppression, and pathological condition detection. Synonyms: 5'-Dimethoxytrityl-2'-deoxythymidine 3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite; dT-Thiophosphoramidite. Grades: 90%. Molecular formula: C44H48N3O8PS2. Mole weight: 841.97. | |
| 5'-O-DMT-thymidine 3'-thiophosphoramidite | 5'-O-DMT-thymidine 3'-thiophosphoramidite. Group: Biochemicals. Alternative Names: 5'-Dimethoxytrityl-2'-deoxythymidine 3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| dA-Thiophosphoramidite | dA-Thiophosphoramidite, a widely utilized chemical compound in the biomedical sector, is an imperative tool employed to fabricate chemically modified oligonucleotides and investigate the complexities of nucleic acids structure and biology. Furthermore, it holds significant value in designing therapeutic medications that selectively target genes responsible for the onset of malignant neoplasms and viral infections. Synonyms: 5'-Dimethoxytrityl-N-benzoyl-2'-deoxyAdenosine, 3'-[(ß-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C51H51N6O7PS2. Mole weight: 955.09. | |
| dC-Thiophosphoramidite | dC-Thiophosphoramidite is a reagent used in the synthesis of oligonucleotides for research purposes. It is a modified form of the nucleoside cytidine and contains a thiophosphate group, which allows for the creation of phosphorothioate linkages. These modified oligonucleotides have been shown to have increased stability and efficacy for use in gene therapy and antisense technology targeting diseases such as cancer and viral infections. Synonyms: 5'-Dimethoxytrityl-N-benzoyl-2'-deoxyCytidine, 3'-[(ß-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C50H51N4O8PS2. Mole weight: 931.07. | |
| dG-Thiophosphoramidite | dG-Thiophosphoramidite, a premium reagent, is widely utilized in biomedical research. Its application lies in the synthesis of DNA oligonucleotides equipped with thiophosphate links, rendering them incredibly potent agents for combating diseases such as cancer and viral infections, courtesy of enhanced nuclease resistance. Researchers entrust this reagent for its dependable performance as it is easily accessible and has a sound reputation. Synonyms: 5'-Dimethoxytrityl-N-isobutyryl-2'-deoxyGuanosine, 3'-[(ß-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C48H53N6O8PS2. Mole weight: 937.07. | |
| dT-Thiophosphoramidite | dT-Thiophosphoramidite, a chemical compound utilized in the synthetic process of oligonucleotides, characterized as a class of biomolecules with vast implications in the biomedical arena, specifically for diagnostics, gene therapy, and drug development, adds to the the structural and functional modification of oligonucleotides as an indispensable building block. Synonyms: 5'-Dimethoxytrityl-2'-deoxyThymidine, 3'-[(ß-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite; 5'-O- (4, 4'-Dimethoxytrityl) -3'-O-[pyrrolizino[[2- (benzoylthio) ethyl]thio]phosphino]thymidine. Molecular formula: C44H48N3O8PS2. Mole weight: 841.97. | |
| N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 3'-thiophosphoramidite | N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 3'-thiophosphoramidite, an indispensable reagent utilized in the synthesis of nucleotide analogs for cutting-edge biomedical investigations. This compound serves as an instrumental component in the creation of therapeutic medications and probes intended to combat an array of afflictions, encompassing viral infections and cancer. Its distinctive chemical attributes facilitate the alteration and amplification of nucleic acids, thus paving a groundbreaking path towards innovative therapeutics and diagnostic instruments. Synonyms: N-Benzoyl-2'-deoxy-5'-dimethoxytrityl-cytidine-3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C50H51N4O8PS2. Mole weight: 931.07. | |
| N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 5'-thiophosphoramidite | N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 5'-thiophosphoramidite. Group: Biochemicals. Alternative Names: N-Benzoyl-2'-deoxy-5'-dimethoxytrityl-cytidine-3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| N6-Benzoyl-2'-deoxy-5'-O-DMT-adenosine 3'-thiophosphoramidite | N6-Benzoyl-2'-deoxy-5'-O-DMT-adenosine 3'-thiophosphoramidite. Group: Biochemicals. Alternative Names: N-Benzoyl-2'-deoxy-5'-dimethoxytrityl-adenosine-3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| N6-Benzoyl-2'-deoxy-5'-O-DMT-adenosine 3'-thiophosphoramidite | N6-Benzoyl-2'-deoxy-5'-O-DMT-adenosine 3'-thiophosphoramidite is a vital tool used in biomedicine for synthesizing therapeutic drugs. With its unique structure, it serves as a key intermediate in the development of antiviral medications, specifically targeting viral DNA replication to treat infections caused by various viruses. Its precise chemical composition and reliable quality make it an essential component in drug discovery and development processes within the biomedical industry. Synonyms: N-Benzoyl-2'-deoxy-5'-dimethoxytrityl-adenosine-3'-[(B-thiobenzoylethyl)-(1-pyrrolidinyl)]-thiophosphoramidite. Molecular formula: C51H51N6O7PS2. Mole weight: 955.09. | |
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