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| Names | |
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| Preferred IUPAC name
(1S,2R)-2-(Aminomethyl)cyclopropane-1-carboxylic acid[1] | |
| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
PubChem CID
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| Properties | |
| C5H9NO2 | |
| Molar mass | 115.132 g·mol−1 |
| Density | 1.275 g/mL |
| Boiling point | 256.9 °C (494.4 °F; 530.0 K) |
| log P | −0.721 |
| Acidity (pKa) | 4.157 |
| Basicity (pKb) | 9.840 |
| Isoelectric point | 7.01 |
| Related compounds | |
Related cycloalkanes
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ACPD |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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(+)-cis-2-Aminomethylcyclopropane carboxylic acid ((+)-CAMP) is an agonist for the GABAA-rho receptor.[2][3]
References[edit]
- ^ "AC1LT400 - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 11 July 2005. Identification and Related Records. Retrieved 7 October 2011.
- ^ Duke, RK; Chebib, M; Balcar, VJ; Allan, RD; Mewett, KN; Johnston, GA (2000). "(+)- and (−)-cis-2-aminomethylcyclopropanecarboxylic acids show opposite pharmacology at recombinant rho(1) and rho(2) GABA(C) receptors". Journal of Neurochemistry. 75 (6): 2602–10. doi:10.1046/j.1471-4159.2000.0752602.x. PMID 11080214.
- ^ Carland, JE; Moorhouse, AJ; Barry, PH; Johnston, GA; Chebib, M (2004). "Charged residues at the 2' position of human GABAC rho 1 receptors invert ion selectivity and influence open state probability". The Journal of Biological Chemistry. 279 (52): 54153–60. doi:10.1074/jbc.M410625200. PMID 15485818.