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138-62-5

138-62-5 | Benzeneacetic acid, α-amino-3,4-dihydroxy-

CAS No: 138-62-5 Catalog No: AG0017SX MDL No:

Product Description

Catalog Number:
AG0017SX
Chemical Name:
Benzeneacetic acid, α-amino-3,4-dihydroxy-
CAS Number:
138-62-5
Molecular Formula:
C8H9NO4
Molecular Weight:
183.1614
IUPAC Name:
2-amino-2-(3,4-dihydroxyphenyl)acetic acid
InChI:
InChI=1S/C8H9NO4/c9-7(8(12)13)4-1-2-5(10)6(11)3-4/h1-3,7,10-11H,9H2,(H,12,13)
InChI Key:
ZBWTWPZGSGMRTG-UHFFFAOYSA-N
SMILES:
OC(=O)C(c1ccc(c(c1)O)O)N

Properties

Complexity:
197  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
183.053g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0
Molecular Weight:
183.163g/mol
Monoisotopic Mass:
183.053g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
104A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-3.1  

Literature

Title Journal
Group I mGluR activation enhances Ca(2+)-dependent nonselective cation currents and rhythmic bursting in main olfactory bulb external tufted cells. The Journal of neuroscience : the official journal of the Society for Neuroscience 20090923
Activation of mGluR5 induces spike afterdepolarization and enhanced excitability in medium spiny neurons of the nucleus accumbens by modulating persistent Na+ currents. The Journal of physiology 20090701
Activity-dependent induction and maintenance of epileptiform activity produced by group I metabotropic glutamate receptors in the rat hippocampal slice. Epilepsy research 20080901

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