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| Product | Description | |
|---|---|---|
| γ-[(8-Aminooctyl)-imido]-2-Hydroxy-ATP | γ-[(8-Aminooctyl)-imido]-2-Hydroxy-ATP, a formidable and discriminating agonist for the P2Y11 receptor, a G protein-coupled receptor activated by ATP, exhibits potential for various immune-related conditions including chronic lymphocytic leukemia and rheumatoid arthritis. Its multifaceted properties as an immune modulator correspond to manifold roles, rendering it a promising therapeutic agent in the battle against immune-related maladies. Synonyms: γ-[(8-Aminooctyl)-imido]-2-hydroxy-adenosine-5'-triphosphate; γ-[(8-Aminooctyl)-imido]-iso-GTP. Grades: ≥ 95 % by HPLC. Molecular formula: C18H34N7O13P3(free acid). Mole weight: 649.42 (free acid). |  |
| γ-[(8-Aminooctyl)-imido]-8-Oxo-GTP | Gamma-[(8-Aminooctyl)-imido]-8-Oxo-GTP is an important compound utilized in the field of biomedical research to investigate the intricate interactions between G proteins and their signaling pathways. Moreover, it is also extensively employed in the study of diseases associated with G protein dysfunction, encompassing cancer, neurological disorders, and cardiovascular disorders. Synonyms: γ-[(8-Aminooctyl)-imido]-8-oxo-guanosine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C18H34N7O14P3(free acid). Mole weight: 665.42 (free acid). | |
| γ-[(8-Aminooctyl)-imido]-ATP | γ-[(8-Aminooctyl)-imido]-ATP is a compound product used in the research of various diseases. This compound acts as a potent inhibitor of enzymatic reactions involving ATP, particularly those related to cell signaling and energy metabolism. Its research applications include targeting cancer cells, as well as managing autoimmune disorders and metabolic diseases. Synonyms: γ-[(8-Aminooctyl)-imido]-adenosine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C18H34N7O12P3(free acid). Mole weight: 633.42 (free acid). | |
| γ-[(8-Aminooctyl)-imido]-CTP | γ-[(8-Aminooctyl)-imido]-CTP, a biochemical compound, functions as a substrate for enzymes essential for DNA synthesis and repair. Considerably employed in in vitro research for studying DNA replication and transcription and scrutinizing the aftermath of diverse drugs, γ-[(8-Aminooctyl)-imido]-CTP has an extensive range of potential therapeutic applications. Notably, it can be utilized for treating cancer and other ailments caused by glitches in DNA damage and repair mechanisms. Synonyms: γ-[(8-Aminooctyl)-imido]-cytidine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C17H34N5O13P3(free acid). Mole weight: 609.40 (free acid). | |
| γ-[(8-Aminooctyl)-imido]-dCTP | γ-[(8-Aminooctyl)-imido]-dCTP, an esteemed modified nucleotide, finds varied biomedical applications. As a substrate for DNA polymerases, it facilitates exploration of DNA replication and repair, laying foundations for diagnostic tool development for detection of cancer and infectious diseases. These medicinal breakthroughs often employ the potential of this modified nucleotide in gene therapy for treatment of diseases including cystic fibrosis. Synonyms: γ-[(8-Aminooctyl)-imido]-2'-deoxycytidine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C17H34N5O12P3(free acid). Mole weight: 593.40 (free acid). | |
| γ-[(8-Aminooctyl)-imido]-dUTP | γ-[(8-Aminooctyl)-imido]-dUTP, a modified nucleotide with an 8-carbon linker, exhibits great potential in molecular biology applications. Labeling DNA with fluorescent dyes or biotin had never been so easy! This versatile and dynamic molecule has been demonstrated to be highly effective in a wide spectrum of exercises including DNA sequencing and Nucleic Acid amplification. Its applications even extend to the study of DNA-protein interactions and imaging! Synonyms: γ-[(8-Aminooctyl)-imido]-2'-deoxyuridine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C17H33N4O13P3(free acid). Mole weight: 594.38 (free acid). | |
| γ-[(8-Aminooctyl)-imido]-GTP | γ-[(8-Aminooctyl)-imido]-GTP is an essential biomolecule employed, exhibiting its prowess as a formidable and discriminating inhibitor specifically targeting GTPases implicated in cancer and neurological afflictions. Synonyms: γ-[(8-Aminooctyl)-imido]-guanosine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C18H34N7O13P3(free acid). Mole weight: 649.42 (free acid). | |
| γ-[(8-Aminooctyl)-imido]-ITP | γ-[(8-Aminooctyl)-imido]-ITP, a biomedicine research compound, finds frequent use in investigations examining purinergic signaling and platelet biology, while simultaneously offering potential as a therapy for various platelet disorders. Synonyms: γ-[(8-Aminooctyl)-imido]-inosine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C18H33N6O13P3(free acid). Mole weight: 634.41 (free acid). | |
| γ-[(8-Aminooctyl)-imido]-XTP | γ-[(8-Aminooctyl)-imido]-XTP, a biochemical reagent utilized for studying enzymes involved in RNA synthesis and processing, mimics ATP's structure and has demonstrated compatibility as a substrate for RNA polymerases. This versatile compound enables research on ribonucleases and ATP-dependent RNA helicases. Moreover, its utility extends to the study of the HIV-1 reverse transcriptase enzyme. Synonyms: γ-[(8-Aminooctyl)-imido]-xanthosine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C18H33N6O14P3(free acid). Mole weight: 650.41 (free acid). | |
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