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| Product | Description | |
|---|---|---|
| 2'-Deoxy-2'-fluoroadenosine | 2'-Deoxy-2'-fluoroadenosine. Group: Biochemicals. Alternative Names: 2'-Fluoro-2'-deoxy-D-adenosine; 9-(2-Fluoro-2-deoxy-b-D-ribofuranosyI)-adenine. Grades: Highly Purified. CAS No. 64183-27-3. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C10H12FN5O3. US Biological Life Sciences. |  Worldwide |
| 2'-Deoxy-2'-fluoroadenosine | 2'-Deoxy-2'-fluoroadenosine is a modified nucleoside where a fluorine atom is substituted at the 2' position of the ribose sugar in adenosine. This modification enhances the stability and alters the biochemical properties of the nucleoside. It is used in studying nucleotide metabolism, enzymatic reactions involving nucleosides, and exploring nucleic acid-protein interactions. Synonyms: 2'-Fluoro Adenosine; 2'-Fluoro-2'-deoxyadenosine; (2R,3R,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-fluoro-2-(hydroxymethyl)tetrahydrofuran-3-ol; 9-(2-Fluoro-2-deoxy-beta-D-ribofuranosyl)-purin-6-amine; 9-(2-Deoxy-2-fluoro-beta-D-ribofuranosyl)adenine; 6-Amino-9-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)-9H-purine; 2'-F-dA. Grade: ≥95%. CAS No. 64183-27-3. Molecular formula: C10H12FN5O3. Mole weight: 269.23. |  |
| 2'-Deoxy-2'-fluoroadenosine-3'-CE-phosphoramidite | 2'-Deoxy-2'-fluoroadenosine-3'-CE-phosphoramidite is an indispensable tool in biomedical research, finding extensive applications in synthesizing modified nucleic acids to combat a vast array of diseases. By harnessing its unparalleled attributes, this phosphoramidite contributes to drug research and development. Grade: ≥ 95%. | |
| 2'-Deoxy-2'-fluoroadenosine-5'-diphosphate | 2'-Deoxy-2'-fluoroadenosine-5'-diphosphate, an indispensable tool in the biomedical industry, exhibits versatile applications in the synthesis of RNA-targeting antiviral drugs. This vital compound serves as a significant precursor, thwarting viral replication and manifesting its potential to combat RNA virus-induced ailments such as respiratory viral infections and viral hepatitis. Synonyms: 2'-deoxy-2'-fluoroadenosine 5'-(trihydrogen diphosphate); 2'-DE-2'-Fladdp; ((2R,3R,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl trihydrogen diphosphate; 2'-Deoxy-2'-fluoroadenosine 5'-diphosphate; SCHEMBL9394807; DTXSID80987906; Adenosine 5'-(trihydrogen diphosphate), 2'-deoxy-2'-fluoro-; 9-{2-Deoxy-2-fluoro-5-O-[hydroxy(phosphonooxy)phosphoryl]pentofuranosyl}-9H-purin-6-amine. CAS No. 68357-16-4. Molecular formula: C10H14FN5O9P2. Mole weight: 429.19. | |
| 2'-Deoxy-2'-fluoroadenosine-5'-monophosphate | 2'-Deoxy-2'-fluoroadenosine-5'-monophosphate is an immensely powerful pharmaceutical compound, finding its application in biomedicine to study an array of maladies such as viral infections and specific cancerous forms. By impeding pivotal nucleic acid synthesis enzymes, this compound exerts control over viral replication. Synonyms: 2'-Deoxy-2'-fluoro-5'-adenylic acid. CAS No. 68245-91-0. Molecular formula: C10H13FN5O6P. Mole weight: 349.21. | |
| 2'-Deoxy-2'-fluoroadenosine 5'-monophosphate triethylammonium | 2'-Deoxy-2'-fluoroadenosine 5'-monophosphate triethylammonium is a complex nucleotide analog, frequently employed in advanced biomedical research. The compound has been observed to interact with several essential enzymes, specifically those catalyzing the removal of RNA molecule's 3'-end. Promisingly, 2'-Deoxy-2'-fluoroadenosine 5'-monophosphate triethylammonium has not only displayed inhibitory properties against viruses such as hepatitis C and HIV but has also shown potential as a therapeutic agent for these viral diseases. Synonyms: [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-fluoro-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate di(triethylammonium). Grade: ≥95%. Molecular formula: C22H43FN7O6P. Mole weight: 551.59. | |
| 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate | 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate. Group: Biochemicals. Grades: Highly Purified. CAS No. 73449-07-7. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C10H15FNO12P3. US Biological Life Sciences. | Worldwide |
| 2'-Deoxy-2'-fluoroadenosine 5'-Triphosphate | 2'-Deoxy-2'-fluoroadenosine 5'-Triphosphate: A highly significant and invaluable modified nucleotide employed extensively in the fields of biochemistry and molecular biology for groundbreaking research purposes. Renowned for its pivotal role in the exploration of DNA replication, transcription, and translation mechanisms, this extraordinary compound serves as an indispensable tool. Its application spans across multifaceted investigations pertaining to drug resistance mechanisms, mutagenesis, and groundbreaking advancements in cancer research. Synonyms: (((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl)triphosphoric acid; Adenosine 5'-(tetrahydrogen triphosphate), 2'-deoxy-2'-fluoro-; 2'-Fluoro-2'-deoxyadenosine-5'-triphosphate; 2'-Deoxy-2'-fluoroadenosine 5'-(tetrahydrogen triphosphate); 2'-FdATP; 2'-Fluoro ATP; 2'-Fluoro-2'-deoxy-ATP; 2'-F-dATP2'-F-dATP. Grade: ≥95% by HPLC. CAS No. 73449-07-7. Molecular formula: C10H15FN5O12P3. Mole weight: 509.17. | |
| 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate lithium salt | 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate sodium salt | 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate sodium salt, a pivotal compound in the biomedical sector, exhibits extensive utility as a substrate for diverse enzymes implicated in DNA synthesis and repair. Acclaimed for its distinct characteristics, this product finds prominence in the realm of scientific investigation and inquiry pertaining to antiviral therapeutics and disease management. Synonyms: 2'-FdATP.Na. Grade: 95%. Molecular formula: C10H15FNO12P3·xNa. Mole weight: 453.15 (free acid). | |
| 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate tetralithium salt | 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate tetralithium salt, a pivotal compound within the realm of nucleic acid biology research and pharmaceutical advancement, warrants particular attention. Renowned for its exceptional fluorine substitution, this compound assumes a vital role in the exploration of nucleotide synthesis and finds extensive application in enzymatic assays. Synonyms: 2'-Fluoro-2'-deoxy-ATP.4Li. Grade: 95%. Molecular formula: C10H11FN5O12P3·4Li. Mole weight: 532.90. | |
| 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate trilithium salt | 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate lithium salt, a vital component employed in the field of biomedicine, exhibits remarkable attributes that contribute to its significance in academic and scientific pursuits. Particularly, it serves as a valuable resource for the advancement of antiviral therapeutics, focusing on the targeted treatment of widespread viral ailments including HIV and hepatitis. Operating as an adenosine triphosphate (ATP) analog, this compound showcases unparalleled capabilities in impeding viral replication and enhancing immune response. Synonyms: 2'-F-dATP lithium salt; 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate lithium salt; 2'-F-dATP.3Li; 2'-Deoxy-2'-fluoroadenosine 5'-(tetrahydrogen triphosphate) lithium salt (1:3); 2'-Fluoro ATP lithium salt; 2'-Fluoro-2'-deoxy-ATP lithium salt; 2'-Fluoro-2'-deoxyadenosine-5'-triphosphate lithium salt; Lithium ((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate. Grade: 95%. Molecular formula: C10H12FLi3N5O12P3. Mole weight: 526.97. | |
| 2'-Deoxy-2'-fluoroadenosine-triphosphate tetralithium salt | 2'-Deoxy-2'-fluoroadenosine-triphosphate tetralithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. US Biological Life Sciences. | Worldwide |
| 2-Amino-2-deoxy-2-fluoroadenosine | 2-Amino-2-deoxy-2-fluoroadenosine is an invaluable compound extensively employed in the realm of biomedicine, assuming a pivotal function in the research of select malignancies and autoimmune maladies. Due to its distinctly idiosyncratic chemical attributes, this compound has demonstrated remarkable promise as an antineoplastic entity, efficaciously hindering the proliferation of malignant cells. Grade: ≥ 99%. | |
| 2-Amino-2'-deoxy-2'-fluoroadenosine | 2-Amino-2'-deoxy-2'-fluoroadenosine. Group: Biochemicals. Alternative Names: 9-(2-Fluoro-2-deoxy-b-D-ribofuranosyl)-2,6-diaminopurine; 2'-Deoxy-2'-fluoro-diaminopurine riboside; 2,6-Diamino-9-(2'-deoxy-2'-fluoro-b-D-ribopyranosyl)purine; 2-Amino-2'-deoxy-2'-fluoro-D-adenosine; 2-Amino-2'-fluoro-2'-deoxyadenosine. Grades: Highly Purified. CAS No. 134444-47-6. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C10H13FN6O3. US Biological Life Sciences. | Worldwide |
| 2-Amino-2'-deoxy-2'-fluoroadenosine | 2-Amino-2'-deoxy-2'-fluoroadenosine is a compound in the field of biomedicine, specifically engineered to combat debilitating Hepatitis C infections. By impeding the replication of the hepatitis C virus, this phenomenal product significantly diminishes the viral load. Synonyms: 9-(2-Fluoro-2-deoxy-b-D-ribofuranosyl)-2,6-diaminopurine; 2'-Deoxy-2'-fluoro-diaminopurine riboside; 2,6-Diamino-9-(2'-deoxy-2'-fluoro-b-D-ribopyranosyl)purine; 2-Amino-2'-deoxy-2'-fluoro-D-adenosine; 2-Amino-2'-fluoro-2'-deoxyadenosine. Grade: 97%. CAS No. 134444-47-6. Molecular formula: C10H13FN6O3. Mole weight: 284.25. | |
| 2-Chloro-2'-deoxy-2'-fluoroadenosine | 2-Chloro-2'-deoxy-2'-fluoroadenosine, renowned for its exceptional properties, stands as a paramount nucleoside analogue hailed within the biomedicine realm. Exhibiting formidable efficacy as an antiviral warrior, it garners prominence in combatting viral infections. Pertinently, its profound interaction with viral polymerases effectively hampers viral replication, rendering it a beacon of hope in the face of relentless viral diseases. CAS No. 156357-18-5. Molecular formula: C10H11ClFN5O3. Mole weight: 303.68. | |
| 2'-Deoxy-2'-fluoro-2-fluoroadenosine | 2'-Deoxy-2'-fluoro-2-fluoroadenosine is a remarkably potent antiviral compound employed extensively in biomedical investigations, manifesting its efficacy against an array of viruses encompassing the pernicious HIV and hepatitis C strains. By selectively antagonizing viral enzymes, this compound evinces auspicious prospects for impeding viral proliferation. Grade: ≥ 99%. | |
| 2'-Deoxy-2-fluoroadenosine | 2'-Deoxy-2-fluoroadenosine. Group: Biochemicals. Alternative Names: (9-(2-Deoxy-b-D-ribofuranosyl)-2-fluoroadenine. Grades: Highly Purified. CAS No. 21679-12-9. Pack Sizes: 250mg, 500g, 1g, 2g, 5g. Molecular Formula: C10H12FN5O3. US Biological Life Sciences. | Worldwide |
| 2-Deoxy-2-fluoroadenosine 5'-triphosphate, tetra-lithium salt | 2-Deoxy-2-fluoroadenosine 5'-triphosphate, tetra-lithium salt, a non-hydrolyzable ATP analog, plays an essential role in enzymatic studies, probing nucleic acid structure, and catalyzing drug design for cancer and related diseases. As a powerful tool in the hands of modern scientists, this chemical curiosity never ceases to amaze. Its unique properties continue to unlock some of the most perplexing mysteries of biochemical reactions. Grade: ≥ 95%. | |
| N6-Benzoyl-2'-deoxy-2'-fluoroadenosine | N6-Benzoyl-2'-deoxy-2'-fluoroadenosine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 2-Amino-3'-deoxy-3'-fluoroadenosine | 2-Amino-3'-deoxy-3'-fluoroadenosine is a potent nucleoside analog, boasting a distinctive structure and mechanism of action. Extensive research has highlighted the considerable potential of this compound for combating a spectrum of ailments, notably viral infections such as hepatitis B and C. Synonyms: Adenosine, 2-amino-3'-deoxy-3'-fluoro-; 3'F-2-NH2-3'dA; 3'-Fluoro-3'-deoxy-2-aminoadenosine; (2R,3S,4S,5R)-2-(2,6-Diamino-9H-purin-9-yl)-4-fluoro-5-(hydroxymethyl)tetrahydrofuran-3-ol. Grade: ≥95%. CAS No. 125391-75-5. Molecular formula: C10H13FN6O3. Mole weight: 284.25. | |
| 2'-Fluoro-2'-deoxyadenosine-5'-triphosphate trisodium salt | 2'-Fluoro-2'-deoxyadenosine-5'-triphosphate trisodium salt is a highly valuable compound in biomedicine, notably in the exploration, recognition, and mending of DNA. It is a versatile tool, integral in DNA synthesis and labeling, suitable for PCR, sequencing, and hybridization applications. Its potential in treating chronic lymphocytic leukemia is noteworthy in its antileukemic qualities; it has been reported to activate apoptosis in leukemia cells, thus emphasizing its capacity in potentially developing therapeutic regimens for this ailment. Synonyms: 2'-F-2'-dATP.Na3; 2'-F-dATP trisodium salt; 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate trisodium salt; 2'-Deoxy-2'-fluoroadenosine 5'-(tetrahydrogen triphosphate) sodium salt (1:3); 2'-Fluoro ATP trisodium salt; 2'-Fluoro-2'-deoxy-ATP trisodium salt; 2'-Fluoro-2'-deoxyadenosine-5'-triphosphate trisodium salt; trisodium ((2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate. Grade: ≥97% by HPLC. Molecular formula: C10H12FN5Na3O12P3. Mole weight: 575.12. | |
| 9-(2'-Deoxy-2'-fluoro-b-D-ribofuranosyl)-2-fluoroadenine | 9-(2'-Deoxy-2'-fluoro-b-D-ribofuranosyl)-2-fluoroadenine, an extraordinary antiviral compound, exhibits immense potential in the biomedical field for combating viral infections induced by DNA viruses. Its exceptional efficacy stems from its ability to disrupt viral DNA synthesis, thereby impeding viral replication. This nucleoside analogue has demonstrated remarkable effectiveness against a multitude of viruses, including herpes simplex virus type 1 (HSV-1) and 2 (HSV-2), varicella-zoster virus (VZV), and Epstein-Barr virus (EBV). Synonyms: 2'-Deoxy-2'-fluoro-2-fluoroadenosine. Grade: 95%. CAS No. 147048-53-1. Molecular formula: C10H11F2N5O3. Mole weight: 287.23. | |
| 9-(2'-Deoxy-2'-fluoro-b-D-ribofuranosyl)-2-fluoroadenine | 9-(2'-Deoxy-2'-fluoro-b-D-ribofuranosyl)-2-fluoroadenine. Group: Biochemicals. Alternative Names: 2'-Deoxy-2'-fluoro-2-fluoroadenosine. Grades: Highly Purified. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
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