CAS 157141-16-7 | Cyclopropaneacetic acid, α-amino-2-carboxy-α-methyl-, (αS,1S,2S)- | CAS Number 157141-16-7

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157141-16-7 | Cyclopropaneacetic acid, α-amino-2-carboxy-α-methyl-, (αS,1S,2S)-

CAS No: 157141-16-7 Catalog No: AG001P8P MDL No:MFCD05865221

Product Description

Catalog Number:

AG001P8P

Chemical Name:

Cyclopropaneacetic acid, α-amino-2-carboxy-α-methyl-, (αS,1S,2S)-

CAS Number:

157141-16-7

Molecular Formula:

C7H11NO4

Molecular Weight:

173.1665

MDL Number:

MFCD05865221

IUPAC Name:

2-(1-amino-1-carboxyethyl)cyclopropane-1-carboxylic acid

InChI:

InChI=1S/C7H11NO4/c1-7(8,6(11)12)4-2-3(4)5(9)10/h3-4H,2,8H2,1H3,(H,9,10)(H,11,12)

InChI Key:

KFACHLANPCGTFI-UHFFFAOYSA-N

SMILES:

OC(=O)[C@H]1C[C@@H]1[C@@](C(=O)O)(N)C

Properties

Complexity:

240

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

173.069g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

173.168g/mol

Monoisotopic Mass:

173.069g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

101A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

-3.3

Literature

Title	Journal
D1 and D2 dopamine receptors contribute to the locomotor response induced by Group II mGluRs activation in the rat nucleus accumbens.	Pharmacology, biochemistry, and behavior 20020901
Synaptic transmission in nucleus tractus solitarius is depressed by Group II and III but not Group I presynaptic metabotropic glutamate receptors in rats.	The Journal of physiology 20020201
Synthesis of N(1)-substituted analogues of (2R,4R)-4-amino-pyrrolidine-2,4-dicarboxylic acid as agonists, partial agonists, and antagonists of group II metabotropic glutamate receptors.	Bioorganic & medicinal chemistry letters 20010723