ATP
Catalog No.
C6931
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Adenosine triphosphate (ATP, CAS 56-65-5) is a nucleoside triphosphate comprising adenine linked to ribose, with three phosphate groups esterified sequentially. ATP primarily functions as a universal energy carrier in cellular metabolism, transferring phosphate groups to facilitate enzymatic reactions and drive biological activities. Additionally, ATP acts extracellularly as a neurotransmitter and signaling molecule, binding purinergic receptors to modulate physiological responses such as neurotransmission, vascular tone, inflammation, and immune cell function. Due to its versatile biological roles, ATP is extensively employed in biomedical research investigating metabolic pathways, receptor signaling dynamics, and cellular energetics.
- 1. Yingying Ma, Wenlu Fan, et al. "Pestivirus bovine viral diarrhea virus infection triggers lipophagy through the AMPK-PNPLA2/ATGL signaling pathway to promote viral replication." Autophagy, 1–20.
- 2. Wang Jiahui, Yu Xiang, et al. "The mitochondrial DNAJC co-chaperone TCAIM reduces α-ketoglutarate dehydrogenase protein levels to regulate metabolism." Molecular Cell Volume 85, Issue 3P638-651.E9, February 06, 2025 PMID: 39889707
- 3. Li Xu, Han Wang, et al. "The monomer derivative of paeoniflorin inhibits macrophage pyroptosis via regulating TLR4/NLRP3/GSDMD signaling pathway in adjuvant arthritis rats." Int Immunopharmacol. 2021 Dec;101(Pt A):108169. PMID: 34607227
- 4. Jeeyoung Lee, Ly Thi Huong Luu Le, et al. "Formation of Non-Nucleoplasmic Proteasome Foci during the Late Stage of Hyperosmotic Stress." Cells. 2021 Sep 21;10(9):2493. PMID: 34572142
| Storage | Store at -20°C |
| M.Wt | 507.18 |
| Cas No. | 56-65-5 |
| Formula | C10H16N5O13P3 |
| Synonyms | Adenosine 5'-triphosphate |
| Solubility | Insoluble in DMSO; insoluble in EtOH; ≥38 mg/mL in H2O |
| Chemical Name | ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate |
| SDF | Download SDF |
| Canonical SMILES | O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP(O)(OP(OP(O)(O)=O)(O)=O)=O)N2C=NC3=C2N=CN=C3N |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Quality Control & MSDS
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Chemical structure
