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About This Item
Empirical Formula (Hill Notation):
C10H14KN5O10P2 · 2H2O
CAS Number:
Molecular Weight:
501.32
UNSPSC Code:
12352208
NACRES:
NA.51
MDL number:
Assay:
≥98% dry basis (enzymatic)
Form:
solid
Storage condition:
OK to freeze, desiccated (hygroscopic)
Quality Segment
description
Merck USA index - 14, 154
assay
≥98% dry basis (enzymatic)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, desiccated (hygroscopic)
impurities
≤0.2% ATP (enzymatic), ≤1% AMP
color
white
solubility
water: 50 mg/mL
shipped in
ambient
storage temp.
2-8°C
SMILES string
[O-]P(OP(OC[C@H]([C@@H](O)[C@H]1O)O[C@H]1N2C3=C(N=C2)C(N)=NC=N3)(O)=O)(O)=O.[K+]
InChI
1S/C10H15N5O10P2.K/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;/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20);/q;+1/p-1/t4-,6-,7-,10-;/m1./s1
InChI key
ZNCWUOPIJTUALR-MCDZGGTQSA-M
Application
- Elevated plasma levels of factor VIII enhance arterial thrombus formation on erosive smooth muscle cell-rich neointima but not normal intima in rabbits.: This study explores the effects of elevated plasma levels of factor VIII on arterial thrombus formation, a crucial aspect in understanding vascular diseases and developing therapeutic interventions, where Adenosine 5 prime-diphosphate (ADP) is used for the analysis of platelet aggregation and plays a pivotal role in thrombosis and hemostasis (Sugita et al., 2024).
- An energy-conserving reaction in amino acid metabolism catalyzed by arginine synthetase.: This research highlights the biochemical role of ADP in facilitating energy-conserving reactions in amino acid metabolism, particularly through the catalytic action of arginine synthetase, underscoring its potential in metabolic engineering and therapeutic applications (Michimori et al., 2024).
- Transcriptome analysis of cultured human vascular endothelial cells after gamma-ray irradiation and correlation analysis with ATP, ADP, and adenosine as secondary soluble factors.: ADP is used as a cell culture component to study its impact alongside other nucleotides in modulating cellular responses to radiation, providing insights into cellular defense mechanisms and the potential for developing radioprotective strategies (Fujie et al., 2024).
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Standard Handling (A)
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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