A4386

Adenosine 5′-diphosphate bis(cyclohexylammonium) salt

≥95% (HPLC), crystalline, bacterial

• Synonyme(s) : A2P5P, ADP
• Formule empirique (notation de Hill) : C₁₀H₁₅N₅O₁₀P₂ · 2C₆H₁₃N
• Numéro CAS: 102029-87-8
• Poids moléculaire : 625.55
• NACRES: NA.51
• PubChem Substance ID: 329770855
• UNSPSC Code: 41106305
• MDL number: MFCD00058338
• Assay: ≥95% (HPLC)
• Biological source: bacterial
• Form: crystalline
• Solubility: H₂O: soluble, clear to slightly hazy, colorless to faintly yellow
• Storage temp.: −20°C

Propriétés

• biological source: bacterial
• Quality Segment: 200
• assay: ≥95% (HPLC)
• form: crystalline
• solubility: H₂O: soluble, clear to slightly hazy, colorless to faintly yellow
• storage temp.: −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
• InChI key: SCOUEIPNDLFPCX-IDIVVRGQSA-N

Description

Application

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.

Disclaimer

Stable, non-hygroscopic

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)