(+)-cis-2-Aminomethylcyclopropane carboxylic acid
Not to be confused with Cyclic adenosine monophosphate.
Names | |
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Systematic IUPAC name
(1S,2R)-2-(Aminomethyl)cyclopropane-1-carboxylic acid[1] | |
Identifiers | |
36489-13-1 | |
3D model (Jmol) | Interactive image |
ChEMBL | ChEMBL230115 |
ChemSpider | 1236854 |
PubChem | 1502041 |
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Properties | |
C5H9NO2 | |
Molar mass | 115.13 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 |
ACPD |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
(+)-cis-2-Aminomethylcyclopropane carboxylic acid ((+)-CAMP) is a agonist for the GABAA-rho receptor.[2][3]
References
- ↑ "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.
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