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| Product | Description | |
|---|---|---|
| 12-Hydroxystearic Acid-d34 Lithium Salt | 12-Hydroxystearic Acid-d34 Lithium Salt is labelled 12-Hydroxystearic Acid Lithium Salt (H953785) which is the lithium salt of 12-Hydroxystearic Acid (H953780) which is used in edible vegetable oils and organogels. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C18HD34LiO3, Molecular Weight: 340.62. US Biological Life Sciences. |  Worldwide |
| 12-Hydroxystearic Acid Lithium Salt | 12-Hydroxystearic Acid Lithium Salt is the lithium salt of 12-Hydroxystearic Acid (H953780) which is used in edible vegetable oils and organogels. Group: Biochemicals. Grades: Highly Purified. CAS No. 7620-77-1. Pack Sizes: 1g, 5g. Molecular Formula: C18H35LiO3, Molecular Weight: 306.41. US Biological Life Sciences. | Worldwide |
| 1-b-D-Ribofuranosyl-1,2,4-triazole-3-carboxamide-5'-triphosphate, lithium salt | 1-b-D-Ribofuranosyl-1,2,4-triazole-3-carboxamide-5'-triphosphate, lithium salt, known as Li-RFT, is an indispensable compound extensively employed in the field of biomedicine. With potent antiviral properties, Li-RFT exhibits exceptional efficacy against diverse viral infections. By impeding viral replication while simultaneously bolstering immune responses, this remarkable agent plays a pivotal role in the therapeutic intervention of viral diseases. Molecular formula: C8H11Li4N4O15P3. Mole weight: 523.87. |  |
| 2',3'-Didehydro-3'-deoxy-thymidine-5'-monophosphate, lithium salt | 2',3'-Didehydro-3'-deoxy-thymidine-5'-monophosphate, lithium salt is an indispensable biomedical compound, renowned for its potent antiviral properties against DNA viruses like herpes simplex virus. By meticulously impeding viral DNA synthesis, this nucleoside analogue exhibits unparalleled efficacy in curbing viral replication and thwarting their insidious spread. This remarkable product finds profound utility in the realm of biomedicine, facilitating cutting-edge research endeavors and propelling breakthroughs in pharmacotherapeutic advances. Molecular formula: C10H11Li2N2O7P. Mole weight: 316.06. | |
| 2',3'-Didehydro-3'-deoxy-thymidine-5'-triphosphate, lithium salt | 2',3'-Didehydro-3'-deoxy-thymidine-5'-triphosphate, lithium salt is a critical compound used in the field of biomedicine. This product plays a vital role in molecular biology research, specifically in the study and development of antiviral therapies. It serves as a precursor for the synthesis of certain antiviral drugs, enabling researchers to target and combat various viral infections more effectively. Molecular formula: C10H11Li4N2O13P3. Mole weight: 487.88. | |
| 2',3'-Dideoxy-3'-thia-cytidine-5'-triphosphate (L isomer), lithium salt | 2',3'-Dideoxy-3'-thia-cytidine-5'-triphosphate (L isomer), lithium salt, an indispensable constituent within the biomedical field, presents its prominence. Its application revolves around nucleic acids synthesis and DNA sequencing. This unique product is exclusively tailored for diligent scientists dedicated to drug investigation, primarily exploring the impact of diverse pharmaceuticals on ailments like cancer, HIV, alongside other viral afflictions. Molecular formula: C8H14N3O12P3S. Mole weight: 469.19. | |
| 2',3'-Dideoxy-3'-thia-cytidine-5'-triphosphate (L isomer), lithium salt | 2',3'-Dideoxy-3'-thia-cytidine-5'-triphosphate (L isomer), lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100ug, 250ug, 500ug. US Biological Life Sciences. | Worldwide |
| 2',3'-Dideoxyadenosine-5'-triphosphate lithium salt | 2',3'-Dideoxyadenosine-5'-triphosphate lithium salt, a nucleoside analogue renowned for inhibiting DNA polymerase, has found widespread use in treatments for HIV and research surrounding neurological disorders, whilst also serving as a staple in studying DNA sequencing and a variety of genetic diseases. Synonyms: ddATP. Grades: ≥ 95% (HPLC). CAS No. 93939-70-9. Molecular formula: C10H12N5O11P3·3Li. Mole weight: 498.91. | |
| 2',3'-Dideoxyadenosine-5'-triphosphate lithium salt | 2',3'-Dideoxyadenosine-5'-triphosphate lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100ug, 250ug, 500ug, 1mg. US Biological Life Sciences. | Worldwide |
| 2',3'-Dideoxycytidine-5'-triphosphate lithium salt | 2',3'-Dideoxycytidine-5'-triphosphate lithium salt is a biomedical reagent used in antiviral research. It has applications in research on targeting HIV. Its mechanism involves inhibition of viral replication by terminating the DNA chain during synthesis. Synonyms: Zalcitabine triphosphate lithium salt; ddCTP. Grades: 95%. CAS No. 132619-66-0. Molecular formula: C9H16N3O12P3. Mole weight: 451.16. | |
| 2',3'-Dideoxyuridine-5'-triphosphate lithium salt | 2',3'-Dideoxyuridine-5'-triphosphate lithium salt. Group: Biochemicals. Alternative Names: ddUTP. Grades: Highly Purified. CAS No. 54445-38-5. Pack Sizes: 1mg, 2mg, 4.5mg. Molecular Formula: C9H15N2O13P3·xLi. US Biological Life Sciences. | Worldwide |
| 2'-Azido-2'-deoxyadenosine-5'-triphosphate lithium salt | 2'-Azido-2'-deoxyadenosine-5'-triphosphate lithium salt, an indispensable compound within the biomedical sector, finds application in a myriad of areas. Its significance lies primarily in molecular biology investigations, especially pertaining to the study of DNA synthesis and modification. Distinguished for its role as a substrate for DNA polymerases, this product facilitates enzymatic labeling, DNA sequencing, and the targeted integration into oligonucleotides. Synonyms: 2'-Azido-dATP. Grades: 98%. Molecular formula: C10H15N8O12P3. Mole weight: 532.19 (free acid). | |
| 2'-Azido-2'-deoxyadenosine-5'-triphosphate lithium salt | 2'-Azido-2'-deoxyadenosine-5'-triphosphate lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1ug, 2ug, 5ug, 10ug. US Biological Life Sciences. | Worldwide |
| 2'-Azido-2'-deoxyguanosine-5'-triphosphate lithium salt | 2'-Azido-2'-deoxyguanosine-5'-triphosphate lithium salt, a cornerstone molecule employed in the field of biomedicine, holds immense significance. Its purpose lies in facilitating the introduction of the azido functional group into DNA chains through enzymatic synthesis. Consequently, this technique allows for precise identification of specific DNA segments, thereby aiding in diagnostics, gene expression analysis, comprehension of genetic alterations, and investigation of DNA-protein interplay. With its pivotal role in DNA sequencing and modification, this compound showcases unparalleled potential in advancing scientific research and discovery. Synonyms: 2'-Azido-2'-deoxy-D-guanosine-5'-triphosphate; 2'-Azido-dGTP. Grades: 90%. Molecular formula: C10H15N8O13P3. Mole weight: 548.19 (free acid). | |
| 2'-Azido-2'-deoxyguanosine-5'-triphosphate lithium salt | 2'-Azido-2'-deoxyguanosine-5'-triphosphate lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg, 2mg. US Biological Life Sciences. | Worldwide |
| 2-Butenoyl coenzyme A lithium salt | 2-Butenoyl coenzyme A lithium salt. CAS No: 102680-35-3 |  Sarchem Laboratories New Jersey NJ |
| 2-Chloro-5-methoxypyridine-4-boronic acid,monolithium salt | Heterocyclic Organic Compound. Alternative Names: B-2449, 2-chloro-5-methoxypyridine-4-boronic acid, monolithium salt,, 1256362-57-8. CAS No. 1256362-57-8. Molecular formula: C6H8BClLiNO4. Mole weight: 211.3. Purity: 0.97. IUPACName: lithium;(2-chloro-5-methoxypyridin-4-yl)-trihydroxyboranuide. Catalog: ACM1256362578. |  |
| 2'-C-Methyluridine 5'-triphosphate lithium salt | 2'-C-Methyluridine 5'-triphosphate lithium salt is an indispensable chemical compound extensively applied in the biomedical field, serves as a pivotal constituent facilitating the fabrication of nucleoside analogs aimed for research a multitude of ailments, encompassing viral infections and malignancies. This stunning creation orchestrates a momentous function in the advancement of antiviral and anticancer pharmaceuticals, thereby equipping scientists with an invaluable asset to meticulously scrutinize and effectively counter these formidable afflictions. Molecular formula: C10H13N2O15P3Li4. Mole weight: 521.90. | |
| 2-Deoxy-2,2-difluoroadenosine 5-triphosphate, tetra-lithium salt | | |
| 2-Deoxy-2-chloroadenosine 5-triphosphate, tetra-lithium salt | | |
| 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate lithium 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.Li. Grades: 95%. Molecular formula: C10H11FN5O12P3·4Li. Mole weight: 532.90. | |
| 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, tetra-lithium salt | | |
| 2'-Deoxy-2'-fluorocytidine-5'-triphosphate lithium salt | 2'-Deoxy-2'-fluorocytidine-5'-triphosphate lithium salt is an indispensable compound in the field of biomedicine, finding extensive application in the research and development of antiviral agents to combat problematic viral infections such as HIV and hepatitis C. Offering exceptional efficacy, this product acts as a highly proficient substrate for DNA polymerases, thereby impeding viral replication through the disruption of nucleotide integration into the viral DNA structure. Grades: 95%. Molecular formula: C9H11FN3O13P3·Li4. Mole weight: 508.88. | |
| 2'-Deoxy-2'-fluoroguanosine-5'-triphosphate lithium salt | 2'-Deoxy-2'-fluoroguanosine-5'-triphosphate lithium salt, an indispensable constituent in biomedicine, plays a vital and intricate role in the synthesis of nucleic acids. As an essential nucleotide analog, this compound facilitates the in-depth investigation of intricate DNA sequencing, replication, and transcription phenomena. Moreover, its integration in the development of antiviral pharmaceuticals specifically targeting viral DNA polymerases and reverse transcriptases contributes substantially to the realm of therapeutic interventions against a vast array of viral infections. Grades: 95%. Molecular formula: C10H11FN5O13P3Li4. Mole weight: 548.90. | |
| 2'-Deoxy-2'-fluoroguanosine-5'-triphosphate-lithium salt | 2'-Deoxy-2'-fluoroguanosine-5'-triphosphate-lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 2'-Deoxy-2'-fluoroinosine 5'-monophosphate lithium salt | 2'-Deoxy-2'-fluoroinosine 5'-monophosphate lithium salt is a fundamental substance utilized in the biomedical sector for the management of diverse ailments. Its pivotal significance lies in the advancement of antiviral medications and nucleotide analogs, catering to the treatment of viral afflictions and specific cancer variants. By impeding viral replication and disrupting DNA synthesis, this product proffers prospective therapeutic advantages within the realm of biomedicine. Molecular formula: C10H12FN4O7P·xLi. Mole weight: 350.20 (free acid). | |
| 2'-Deoxy-2'-fluorouridine-5'-triphosphate lithium salt | 2'-Deoxy-2'-fluorouridine-5'-triphosphate lithium salt is a crucial compound in biomedicine. It is commonly used in the development of antiviral drugs and treatments for diseases caused by RNA viruses such as influenza and hepatitis C. This product facilitates the inhibition of viral replication by incorporating into the RNA chain during viral transcription, resulting in termination and suppression of viral growth. Synonyms: 2'-F-dUTP.Li. Grades: 95%. Molecular formula: C9H14N2O14P3F·xLi. Mole weight: 486.13 (free acid). | |
| 2'-Deoxy-2'-fluorouridine-5'-triphosphate tetra lithium salt | 2'-Deoxy-2'-fluorouridine-5'-triphosphate tetra lithium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 146954-74-7. Pack Sizes: 1mg, 2mg, 5mg. Molecular Formula: C9H11FN2O14P3Li4. US Biological Life Sciences. | Worldwide |
| 2'-Deoxyadenosine-5'-O-(1-thiotriphosphate) lithium salt | 2'-Deoxyadenosine-5'-O-(1-thiotriphosphate) lithium salt. Group: Biochemicals. Alternative Names: a-Thio-dATP. Grades: Highly Purified. CAS No. 80875-87-2. Pack Sizes: 2mg, 5mg. Molecular Formula: C10H16N5O11P3S·xLi. US Biological Life Sciences. | Worldwide |
| 2'-Deoxyadenosine-5'-O-(1-thiotriphosphate) lithium salt | 2'-Deoxyadenosine-5'-O-(1-thiotriphosphate) lithium salt is an indispensable research compound in compound, exhibiting its utility as a substrate for diverse enzymatic reactions while functioning as a proficient provider or receiver of phosphate groups during DNA research and development. This pivotal compound assuming significance in delving into DNA repair mechanisms, deciphering nucleotide metabolism intricacies, and studying therapeutic interventions for DNA-associated disorders. Synonyms: a-Thio-dATP; (S)-2'-Deoxyadenosine 5'-P''-ester with thiotriphosphoric acid. Grades: ≥ 95% (HPLC). CAS No. 80875-87-2. Molecular formula: C10H16N5O11P3S·xLi. Mole weight: 507.25 (free acid). | |
| 2'-Deoxycytidine-5'-O-(1-thiotriphosphate)lithium salt | 2'-Deoxycytidine-5'-O-(1-thiotriphosphate)lithium salt, a substance commonly employed as a substrate in DNA synthesis assays and enzymology research, has exhibited noteworthy success as an inhibitor against the reverse transcriptases of HIV-1, the notorious virus behind the development of AIDS. Furthermore, promising data suggests this compound may play a valuable role in mitigating chemotherapy resistance in select forms of cancer. Molecular formula: C9H16N3O12P3S·Li4. Mole weight: 506.95. | |
| 2'-Fluoro-2'-deoxycytitine-5'-triphosphate lithium salt | 2'-Fluoro-2'-deoxycytitine-5'-triphosphate lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 2'-Fluoro-2'-deoxyuridine-5'-triphosphate lithium salt | 2'-Fluoro-2'-deoxyuridine-5'-triphosphate lithium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 2-Fluoro-9-β-D-arabinofuranosyladenine 5-triphosphate, tetra-lithium salt | | |
| 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-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 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-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 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-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 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'-Phosphoadenosine 5'-phosphosulfate tetralithium salt | 2'-Phosphoadenosine 5'-phosphosulfate tetralithium salt. Group: Biochemicals. Alternative Names: Adenosine 2'-phosphate 5'-phosphosulfate lithium salt. Grades: Highly Purified. CAS No. 102029-54-9,62230-89-1. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C10H11N5O13P2S·4Li. US Biological Life Sciences. | Worldwide |
| 3'-Amino-2',3'-dideoxyadenosine-5'-triphosphate lithium salt-100 mM aqeous solution | 3'-Amino-2',3'-dideoxyadenosine-5'-triphosphate lithium salt-100 mM aqueous solution, an indispensable component in the biomedical realm, boasts intricate applications in nucleic acid synthesis and DNA sequencing studies. This aqueous solution finds widespread utilization in research and diagnostic endeavors, effectively combatting myriad ailments encompassing cancer, viral infections, and genetic disorders. Synonyms: 3'-Amino-ddATP.Li. Molecular formula: C10H17N6O11P3·xLi. Mole weight: 490.20 (free acid). | |
| 3'-Amino-2',3'-dideoxycytidine-5'-triphosphate lithium salt-100 mM aqueous solution | 3'-Amino-2',3'-dideoxycytidine-5'-triphosphate lithium salt-100 mM aqueous solution is a crucial component in biomedical research. Primarily used as a substrate in DNA sequencing and polymerase chain reactions (PCR), it assists in the analysis of genetic material. Its incorporation into DNA can help determine nucleotide-specific chain termination and identify mutations linked to diseases such as viral infections and certain types of cancer. Synonyms: 3'-Amino-ddCTP.Li. Grades: 90%. Molecular formula: C9H17N4O12P3·xLi. Mole weight: 466.17 (free acid). | |
| 3'-Amino-2',3'-dideoxyguanosine-5'-triphosphate lithium salt-100 mM aqueous solution | 3'-Amino-2',3'-dideoxyguanosine-5'-triphosphate lithium salt-100 mM aqueous solution is a valuable reagent extensively used in the biomedical industry. With exceptional stability and solubility, this solution is employed in various research applications such as PCR, DNA sequencing, and mutagenesis studies. It acts as a substrate for DNA polymerases during synthesis, aiding in the investigation of DNA structure and protein-DNA interactions. Synonyms: 3'-Amino-ddGTP.Li. Molecular formula: C10H17N6O12P3·xLi. Mole weight: 506.20 (free acid). | |
| 3'-Amino-2',3'-dideoxythymidine-5'-triphosphate lithium salt-100 mM aqueous solution | 3'-Amino-2',3'-dideoxythymidine-5'-triphosphate lithium salt-100 mM aqueous solution- a nucleoside analogue, an anti-HIV and retroviral reverse transcriptase inhibitor, and a powerful tool for the advancement of nucleic acid sequencing and analysis- is an invaluable asset for both clinical and research applications alike, providing a potent treatment option alongside unparalleled insights into the underlying mechanisms of genetic transcription and translation. Synonyms: 3'-Amino-ddTTP.xLi. Grades: 90%. Molecular formula: C10H18N3O13P3. Mole weight: 481.18. | |
| 3'-Azido-3'-deoxythymidine-5'-monophosphate lithium salt | 3'-Azido-3'-deoxythymidine-5'-monophosphate lithium salt, an extraordinary antiviral pharmaceutical compound employed in the treatment of HIV/AIDS, showcases its potency by impeding the reverse transcriptase enzyme, an essential player in viral replication. With its roots in thymidine, this lithium salt not only bestows augmented cellular penetration but also amplifies antiviral efficacy against HIV. Molecular formula: C10H14N5O7P·xLi. Mole weight: 347.22 (free acid). | |
| 3-Deoxy-2-keto-6-phospho-D-galactonate lithium salt | 3-Deoxy-2-keto-6-phospho-D-galactonate lithium salt, a synthetic chemical compound, represents an innovative derivation in the realm of antibiotic development, demonstrating strong inhibitory effects on the bacterial metabolic pathway involving 3-deoxy-6-phosphogalactonate synthase. A key step towards the next generation of antibiotic regimes, research into this compound has yielded promising results in combating pathogenic microorganisms. Synonyms: 6-phospho-2-dehydro-3-deoxy-D-galactonic acid; 32120-43-7; 6-O-phosphono-3-deoxy-D-threo-hex-2-ulosonic acid; 2-Dehydro-3-deoxy-D-galactonate 6-phosphate; 2-dehydro-3-deoxy-6-phospho-D-galactonate; CHEBI:17860; (4R,5R)-4,5-dihydroxy-2-oxo-6-phosphonooxyhexanoic acid; DTXSID201344249; PD194807; C01286; 3-deoxy-6-O-phosphono-D-threo-hex-2-ulosonic acid; Q27102664. Grades: 95%. CAS No. 32120-43-7. Molecular formula: C6H11O9P·xLi. Mole weight: 258.12 (free acid). | |
| 3-Deoxy-2-keto-6-phospho-D-gluconate lithium salt | 3-Deoxy-2-keto-6-phospho-D-gluconate lithium salt, a highly significant compound in the field of biomedicine, assumes a pivotal function in tackling a multitude of metabolic disorders and diseases. Its employment in drug formulation and therapeutic interventions, particularly for diabetes, metabolic syndrome, and lipid disorders, represents an innovative breakthrough. This remarkable substance, boasting unparalleled properties, has garnered substantial acclaim within the biomedical sector. Synonyms: 3-Deoxy-D-erythro-hex-2-ulosonic acid 6-phosphate. Grades: 94%. CAS No. 27244-54-8. Molecular formula: C6H11O9P·xLi. Mole weight: 258.12 (free acid). | |
| 3-Deoxy-2-keto-D-gluconate lithium salt | 3-Deoxy-2-keto-D-gluconate lithium salt is an exceptional biomedical compound, emerging as a promising intervention for multifarious ailments. Its inhibitory efficacy in diabetes research, coupled with its indispensable involvement in intricate glucose homeostasis, renders it a pivotal therapeutic agent. This groundbreaking compound displays profound capabilities in harmonizing glycemic indices, thereby warranting its substantial potential in propelling the evolution of antidiabetic therapeutics. Synonyms: 2-keto-3-deoxygluconate; 3-deoxy-2-oxo-D-gluconate; 2-dehydro-3-deoxy-D-gluconic acid; 3-deoxy-d-erythro-2-hexulosonic acid; (4S,5R)-4,5,6-trihydroxy-2-oxohexanoic acid; 3-deoxy-D-erythro-hex-2-ulosonic acid; 2-keto-3-deoxy-D-gluconate; 2-dehydro-3-deoxy-D-gluconate; KDG; 3-Deoxy-2-keto-D-gluconate lithium salt; 4,5,6-TRIHYDROXY-2-OXO-HEXANOIC ACID. Grades: 95%. CAS No. 17510-99-5. Molecular formula: C6H10O6·xLi. Mole weight: 178.14 (free acid). | |
| 3-Deoxy-2-keto-D-xylonate lithium salt | 3-Deoxy-2-keto-D-xylonate lithium salt is a potent biomedical compound, targeting and engaging specific drug receptors, leading to remarkable reserch outcomes. Harnessing its inhibitory prowess against pivotal molecular pathways, this esteemed compound can be used in research of afflictions like cancer, diabetes, and cardiovascular maladies. Synonyms: (4S)-4,5-Dihydroxy-2-oxopentanoic acid; 2-dehydro-3-deoxy-D-arabinonic acid. CAS No. 53857-83-3. Molecular formula: C5H8O5·xLi. Mole weight: 148.11. | |
| 3'-Deoxyguanosine-5'-triphosphate lithium salt | 3'-Deoxyguanosine-5'-triphosphate lithium salt is a pivotal constituent within the biomedical domain assuming the role of a substrate for DNA polymerases and DNA sequencing reactions. Its indispensability manifesting through its involvement in diverse molecular biology procedures, including site-directed mutagenesis, DNA labeling is and DNA sequencing. Molecular formula: C10H12N5O13P3Li4. Mole weight: 530.91. | |
| 3'-Deoxythymidine-5'-triphosphate lithium salt | 3'-Deoxythymidine-5'-triphosphate lithium salt, an indispensable entity in the realm of biomedicine, constitutes a pivotal building block. Within molecular biology research, it assumes multifaceted roles, serving as both a DNA polymerase substrate and a nucleotide analog. Profoundly contributing to the study of DNA sequencing, gene cloning, and gene expression analysis, this particular product also bears significance in crafting therapeutic approaches for maladies such as viral infections and cancers. Synonyms: dTTP; sodium ((2S,5R)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl trihydrogentriphosphate. Grades: ≥ 95%. CAS No. 128524-26-5. Molecular formula: C10H17N2O13P3·xLi. Mole weight: 466.17 (free acid). | |
| 3-Methylpyridine-2-boronic acid,monolithium salt | Heterocyclic Organic Compound. Alternative Names: MONOLITHIUM 3-METHYLPYRIDINE-2-BORONATE, 1256345-65-9, CTK4B4485, MolPort-019-906-183, AKOS006310008, AG-H-80603, AG-L-21472, X1814, B-2488, lithium hydroxy-(3-methyl-2-pyridinyl)borinate, A844428, lithium (3-methylpyridin-2-yl)-oxidanyl-borinate, 3-Methylpyridine-2-boronic acid, monolithium salt,, I02-5135. CAS No. 1256345-65-9. Molecular formula: C6H7BLiNO2. Mole weight: 142.9. Purity: 0.9. IUPACName: lithium;hydroxy-(3-methylpyridin-2-yl)borinate. Canonical SMILES: [Li+].B(C1=C(C=CC=N1)C)(O)[O-]. Catalog: ACM1256345659. | |
| 3'-O-Methyladenosine 5'-triphosphate lithium salt | 3'-O-Methyladenosine 5'-triphosphate lithium salt, a highly sought-after biochemical reagent, finds profound utility within the biomedical realm. Through its incorporation into scientific investigations, particularly of adenosine triphosphate (ATP) alteration, it offers a gateway to comprehending intricate cellular mechanisms. Distinguished by the presence of a methyl moiety at the 3' site, this variant of adenosine triphosphate assumes a pivotal role in elucidating diverse biological pathways, encompassing RNA modification and epigenetics. Molecular formula: C11H14N5O13P3·Li4. Mole weight: 544.94. | |
| 3'-O-Methylcytidine 5'-triphosphate lithium salt | 3'-O-Methylcytidine 5'-triphosphate lithium salt is an indispensable entity extensively employed in diversified compound applications assuming a pivotal function in the intricate processes of DNA research and development and RNA methylation due to its distinctive chemical configuration. Notably, this compound invariably finds employment in research and development undertakings concerning the exploration of novel pharmaceutical compounds, the regulation of gene expression is as well as the modification of epigenetic mechanisms. Furthermore, its viability as a plausible therapeutic intervention within the realm of malignant neoplasms, viral contagions is and neurological deteriorations is worth considering. Synonyms: 3'-OMeCTP. Molecular formula: C10H14N3O14P3·Li4. Mole weight: 520.92. | |
| 3'-O-Methylguanosine 5'-triphosphate lithium salt | 3'-O-Methylguanosine 5'-triphosphate lithium salt, known for its remarkable properties, is extensively utilized in the realm of biomedicine across diverse applications. This potent compound assumes an indispensable role in the therapeutic interventions for specific ailments and is a staple in drug research and development ventures. Capitalizing on its distinctive chemical attributes, this compound has exhibited tremendous efficacy in selectively targeting pivotal enzymes and pathways associated with the advancement of maladies. Grades: ≥ 95%. Molecular formula: C11H14N5O14P3·Li4. Mole weight: 560.94. | |
| 3'-O-Methyluridine-5'-triphosphate lithium salt | 3'-O-Methyluridine-5'-triphosphate lithium salt, an indispensable biochemical in biomedicine, intricately participates in DNA synthesis and mending as a nucleotide analogue. Presented as a notable research asset for antiviral therapies and viral infection treatments, this compound's exceptional attributes empower the scrutiny of ailment mechanisms and the creation of precise therapeutic strategies. Molecular formula: C10H13N2O15P3·Li4. Mole weight: 521.90. | |
| 3'-Phosphoadenosine-5'-phosphosulfate lithium salt hydrate | 3'-Phosphoadenosine-5'-phosphosulfate lithium salt hydrate. Group: Biochemicals. Alternative Names: PAPS; Adenosine 3'-phosphate 5'-phosphosulfate lithium salt hydrate. Grades: Highly Purified. CAS No. 109434-21-1. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C10H15N5O13P2S·xLi·yH2 O. US Biological Life Sciences. | Worldwide |
| 3'-Phosphoadenosine-5'-phosphosulfate lithium salt hydrate | Universal sulfonate donor for in vivo sulfonation by sulfotransferases. Synonyms: PAPS; Adenosine 3'-phosphate 5'-phosphosulfate lithium salt hydrate; APPS. Molecular formula: C10H15N5O13P2S·xLi·yH2O. Mole weight: 507.27 (anhydrous free acid). | |
| 4-Methylumbelliferyl myo-inositol 1-phosphate lithium salt | 4-Methylumbelliferyl myo-inositol 1-phosphate lithium salt, a crucial compound in the biomedical industry, acts as an indispensable resource for investigating the intricate metabolic and signaling pathways linked to myo-inositol. In the realm of neurological disorders like bipolar disorder and Alzheimer's disease, this compound serves as a potent means to identify enzyme activity, particularly that of inositol monophosphatase. Its fluorescent attributes facilitate effortless detection and quantification, solidifying its indispensable status within the realm of biochemical research. Synonyms: (4-methyl-2-oxochromen-7-yl) [(2S,3S,5R,6S)-2,3,4,5,6-pentahydroxycyclohexyl] phosphate; Lithium 4-methyl-2-oxo-2H-chromen-7-yl ((1R,2S,3R,4R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl) phosphate. CAS No. 244145-22-0. Molecular formula: C16H18LiO11P. Mole weight: 424.22. | |
| 4-Thiothymidine-5'-triphosphate lithium salt | 4-Thiothymidine-5'-triphosphate lithium salt is a crucial compound exhibiting significant potential as an antiviral compound due to its ability to inhibit viral replication by blocking DNA polymerase. This compound is mainly utilized in the development of therapeutic strategies to combat viral infections, including HIV. Its unique properties make it an invaluable tool in the study and research of various viral diseases. Synonyms: Lithium ((2R,3S,5R)-3-hydroxy-5-(5-methyl-2-oxo-4-thioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl triphosphate. Grades: ≥ 95%. CAS No. 20188-78-7. Molecular formula: C10H17N2O13P3S·xLi. Mole weight: 498.23 (free acid). | |
| 5-Aminoallyl 2'-deoxycytidine-5'-triphosphate lithium salt | 5-Aminoallyl 2'-deoxycytidine-5'-triphosphate lithium salt. Group: Biochemicals. Alternative Names: 5-(3-Aminoallyl)-2'-deoxycytidine-5'-triphosphate, lithium salt. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg, 5mg. US Biological Life Sciences. | Worldwide |
| 5-Aminoallyl 2'-deoxycytidine-5'-triphosphate lithium salt-100mM aqueous solution | 5-Aminoallyl 2'-deoxycytidine-5'-triphosphate lithium salt-100mM aqueous solution is a vital reagent in the biomedical industry. This product is commonly used for labeling DNA or RNA during synthesis. It is also an essential tool for detecting mutations and gene expressions, allowing for further research in diseases such as cancer, dementia, and HIV. Synonyms: 5-(3-Aminoallyl)-2'-deoxycytidine-5'-triphosphate, lithium salt; 5-AA-dCTP. Molecular formula: C12H17N4O13P3·4Li. Mole weight: 545.97. | |
| 5-Aminoallyl 2'-deoxyuridine 5'-triphosphate lithium salt | 5-Aminoallyl 2'-deoxyuridine 5'-triphosphate lithium salt. Group: Biochemicals. Alternative Names: 5-Aminoallyl-2'-deoxyuridine-5'-triphosphate; 5-AA-dUTP.Li. Grades: Highly Purified. CAS No. 116840-18-7. Pack Sizes: 1mg, 2.5mg, 5mg. Molecular Formula: C12H20N3O14P3. US Biological Life Sciences. | Worldwide |
| 5-Aminoallyl cytidine 5'-triphosphate lithium salt | 5-Aminoallyl cytidine 5'-triphosphate lithium salt. Group: Biochemicals. Alternative Names: 5-AA-CTP. Grades: Highly Purified. Pack Sizes: 500ug, 2.5mg, 5mg. US Biological Life Sciences. | Worldwide |
| 5-Aminoallylcytidine 5'-triphosphate lithium salt-100mM aqueous solution | 5-Aminoallylcytidine 5'-triphosphate lithium salt-100mM aqueous solution is a biochemical reagent widely used in the biomedical industry. It serves as a substrate for the enzymatic labeling of nucleic acids, enabling the introduction of aminoallyl-modified cytidine residues. This modified nucleotide can be utilized in various downstream applications, including RNA labeling, microarray analysis, and nucleic acid detection assays. It plays a crucial role in research related to drug development, molecular diagnostics, and understanding disease mechanisms. Synonyms: 5-AA-CTP. Grades: 90%. Molecular formula: C12H21N4O14P3·xLi. Mole weight: 538.23 (free acid). | |
| 5-Aminoallyl uridine 5'-triphosphate lithium salt | 5-Aminoallyl uridine 5'-triphosphate lithium salt. Group: Biochemicals. Alternative Names: 5-[3-Aminoallyl]-uridine-5'-triphosphate lithium salt. Grades: Highly Purified. CAS No. 112131-73-4. Pack Sizes: 500ug, 2.5mg, 5mg. Molecular Formula: C12H17N3O15P3·xLi. US Biological Life Sciences. | Worldwide |
| 5-Methylcytidine-5'-triphosphate lithium salt | 5-Methylcytidine-5'-triphosphate lithium salt, a pivotal compound in the realm of biomedicine, manifests itself as a nucleotide analog with profound implications for scrutinizing mRNA methylation. An instrumental resource for delving into RNA epigenetics, this product facilitates the exploration of maladies linked to the perturbation of gene expression. Synonyms: 5-Methyl-CTP; m5CTP. Molecular formula: C10H18N3O14P3·xLi. Mole weight: 497.18 (free acid). | |
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