(+)-cis-2-Aminomethylcyclopropane carboxylic acid

(+)-*cis*-2-Aminomethylcyclopropane carboxylic acid
Names
	Systematic IUPAC name (1S,2R)-2-(Aminomethyl)cyclopropane-1-carboxylic acid
Identifiers
CAS Number	36489-13-1 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL230115 ;
ChemSpider	1236854 ;
PubChem CID	1502041;
	InChI InChI=1S/C5H9NO2/c6-2-3-1-4(3)5(7)8/h3-4H,1-2,6H2,(H,7,8)/t3-,4-/m0/s1 Key: QUFMERRXRMSAPZ-IMJSIDKUSA-N ;
	SMILES NC[C@@H]1C[C@@H]1C(O)=O;
Properties
Chemical formula	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	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 an 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.{{cite journal}}: CS1 maint: unflagged free DOI (link)

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