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924-49-2 | 4-Amino-3-hydroxybutanoic acid
CAS No: 924-49-2 Catalog No: AG003645 MDL No:MFCD00008141
Product Description
Catalog Number:
AG003645
Chemical Name:
4-Amino-3-hydroxybutanoic acid
CAS Number:
924-49-2
Molecular Formula:
C4H9NO3
Molecular Weight:
119.1192
MDL Number:
MFCD00008141
IUPAC Name:
4-amino-3-hydroxybutanoic acid
InChI:
InChI=1S/C4H9NO3/c5-2-3(6)1-4(7)8/h3,6H,1-2,5H2,(H,7,8)
InChI Key:
YQGDEPYYFWUPGO-UHFFFAOYSA-N
SMILES:
NCC(CC(=O)O)O
Properties
Complexity:
83.4
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
119.058g/mol
Formal Charge:
0
Heavy Atom Count:
8
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
3
Isotope Atom Count:
0
Molecular Weight:
119.12g/mol
Monoisotopic Mass:
119.058g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
83.6A^2
Undefined Atom Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
XLogP3:
-4.1
Literature
| Title | Journal |
|---|---|
| Differentiating enantioselective actions of GABOB: a possible role for threonine 244 in the binding site of GABA(C) ρ(1) receptors. | ACS chemical neuroscience 20120919 |
| Natural products from the Lithistida: a review of the literature since 2000. | Marine drugs 20111201 |
| Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. | Bioorganic & medicinal chemistry letters 20101101 |
| Enantioselective actions of 4-amino-3-hydroxybutanoic acid and (3-amino-2-hydroxypropyl)methylphosphinic acid at recombinant GABA(C) receptors. | Bioorganic & medicinal chemistry letters 20080101 |
| Synthesis of phosphonic analogues of carnitine and gamma-amino-beta-hydroxybutyric acid. | Bioorganic chemistry 20041201 |
| Dirhodium-catalyzed enantioselective C-H insertion of N-(2-benzyloxyethyl)-N-(tert-butyl)diazoacetamide and its application for the synthesis of chiral GABOB. | Chirality 20041001 |
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