A4386

Adenosine 5′-diphosphate bis(cyclohexylammonium) salt

≥95% (HPLC), crystalline, bacterial

• Synonym(e): A2P5P, ADP
• Empirische Formel (Hill-System): C₁₀H₁₅N₅O₁₀P₂ · 2C₆H₁₃N
• CAS-Nummer: 102029-87-8
• Molekulargewicht: 625.55
• MDL-Nummer: MFCD00058338
• UNSPSC-Code: 41106305
• PubChem Substanz-ID: 329770855
• NACRES: NA.51

Eigenschaften

• Biologische Quelle: bacterial
• Qualitätsniveau: 200
• Assay: ≥95% (HPLC)
• Form: crystalline
• Löslichkeit: H₂O: soluble, clear to slightly hazy, colorless to faintly yellow
• Lagertemp.: −20°C
• SMILES String: NC1CCCCC1.NC2CCCCC2.Nc3ncnc4n(cnc34)[C@@H]5O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]5O
• InChI: 1S/C10H15N5O10P2.2C6H13N/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20;2*7-6-4-2-1-3-5-6/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20);2*6H,1-5,7H2/t4-,6-,7-,10-;;/m1../s1
• InChIKey: SCOUEIPNDLFPCX-IDIVVRGQSA-N

Beschreibung

Anwendung

Adenosine 5′-diphosphate (ADP) is an adenine nucleotide involved in energy storage and nucleic acid metabolism via its conversion into ATP by ATP synthases. ADP affects platelet activation through its interaction with ADP receptors P2Y1, P2Y12 and P2X1. Upon its conversion to adenosine by ecto-ADPases, platelet activation is inhibited via adenosine receptors.

Adenosine5′-diphosphate bis(cyclohexylammonium) salt has been used as a standard in luminometry. It has also been used in suramin inhibition assays.

Vorsicht

Stable, non-hygroscopic

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)