BAPTA
BAPTA | |
---|---|
File:BAPTA.svg | |
1,2-bis(o-aminophenoxy)ethane- N,N,N',N'-tetraacetic acid | |
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
CAS number | 85233-19-8 |
PubChem | 104751 |
style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
Molecular formula | C22H24N2O10 |
Molar mass | 476.433 |
Density | 1.494 g/cm3 |
Melting point |
177-179 °C |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Infobox references |
BAPTA (1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid) is a calcium-specific polyamino carboxylic acid. The presence of four carboxylic acid functional groups makes possible the binding of two magnesium ions. The extensive flexibility of the carboxylate ligands is critical to the coordination of magnesium, or other metal ions. Recent studies have demonstrated that the BAPTA moiety actually binds to zinc ions with a substantially higher affinity than calcium.[1] Interestingly, it appears that the assumption of the chelator's calcium preference may have contributed to evidence for the role of calcium ions as causal agents in ischemia (stroke), and brain trauma. Based on this evidence, pharmacological agents en masse have been designed and synthesized, yet have met with little success.[citation needed]
There are a range of reported values for the dissociation constant of BAPTA, though 0.2 µM appears consistently.[2] The rate constant for calcium binding is 500 µM−1 s−1.[2]
See also
References
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External links
- ↑ Hyrc KL, Bownik JM, and Goldberg MP (2005). "Ionic selectivity of low affinity ratiometric calcium indicators: mag-fura-2, fura-2FF and BTC". Cell Calcium. 27 (2): 75–86. doi:10.1054/ceca.1999.0092. PMID 10756974.
- ↑ 2.0 2.1 Ricci AJ, Wu YC, Fettiplace R (15 October 1998). "The endogenous calcium buffer and the time course of transducer adaptation in auditory hair cells". The Journal of Neuroscience. 18 (20): 8261–77. PMID 9763471.
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- Amines
- Aromatic compounds
- Carboxylic acids
- Chelating agents
- Phenol ethers
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