(-)-2-Aminobutyric acid
PubChem CID: 80283
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| Compound Synonyms | 1492-24-6, L-2-Aminobutyric acid, (S)-2-Aminobutanoic acid, (2S)-2-aminobutanoic acid, h-abu-oh, Butanoic acid, 2-amino-, (2S)-, L-alpha-Aminobutyric acid, L-Butyrine, (S)-(+)-2-Aminobutyric Acid, L-(+)-2-aminobutyric acid, l-aminobutyric acid, (-)-2-Aminobutyric acid, (S)-2-Amino-butyric acid, L-alpha-Amino-n-butyric acid, (S)-2-Aminobutyric acid, L-alpha-Aminobutyrate, 2S-amino-butanoic acid, l(+)-2-aminobutyric acid, L-Ethylglycine, S-Butyrine, 2-Aminobutyric acid, L-, L-2-Aminobuttersaeure, Butanoic acid, 2-amino-, (S)-, MFCD00064415, 0QAJ5KN9IM, l-2-amino-n-butyric acid, (S)-2-Aminobutanoate, CHEMBL1230782, CHEBI:35619, Butyric acid, 2-amino-, L-, l-2-aminobutanoic acid, L-2-aminobutyrate, Homoalanine, (2S)-2-aminobutanoate, L-a-aminobutyric acid, UNII-0QAJ5KN9IM, (2S)-2-Aminobutyric acid, L-homoalanine, NSC-97060, 2S-amino-butanoate, EINECS 216-083-3, NSC 97060, h-abu(2)-oh, (+)-2-Aminobutanoate, 2(s)-aminobutyric acid, (S)-amino butyric acid, (S)-2-amino-Butanoate, (+)-2-Aminobutyric acid, (+)-2-Aminobutanoic acid, (S)-2-amino-Butanoic acid, alpha-Aminobutyric acid, L-, SCHEMBL78599, (+)-alpha-Aminobutyric acid, (2S)-2-amino butanoic acid, DTXSID10883684, (S)-(+)-alpha-Aminobutyric acid, Butanoic acid, 2-amino-, (R)-, STR03331, BDBM50357210, LMFA01100034, s6203, AKOS015923108, .ALPHA.-AMINOBUTYRIC ACID, L-, AC-1817, CS-W011305, FA09856, HY-W010589, BP-12164, (S)-(+)-2-Aminobutyric acid L-Abu-OH, A0826, L-2-Aminobutyric acid, >=99% (titration), EN300-86145, C02356, Q27104317, Z1741965569, L-2-Aminobutyric acid, BioReagent, suitable for cell culture, (S)-2-Amino-butanoic acid, (S)-2-Aminobutyric acid, L-Homoalanine, 02A4013E-092F-4F03-9966-02E7F6164833 |
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| Topological Polar Surface Area | 63.3 |
| Hydrogen Bond Donor Count | 2.0 |
| Inchi Key | QWCKQJZIFLGMSD-VKHMYHEASA-N |
| Rotatable Bond Count | 2.0 |
| State | Solid |
| Substituent Name | L-alpha-amino acid, Amino fatty acid, Fatty acyl, Fatty acid, Monocarboxylic acid or derivatives, Carboxylic acid, Hydrocarbon derivative, Primary amine, Organooxygen compound, Organonitrogen compound, Primary aliphatic amine, Carbonyl group, Amine, Aliphatic acyclic compound |
| Synonyms | (-)-2-Aminobutyrate, (-)-2-Aminobutyric acid, (+)-2-Aminobutanoate, (+)-2-Aminobutanoic acid, (+)-2-Aminobutyric acid, (+)-alpha-Aminobutyric acid, (2S)-2-Aminobutanoate, (2S)-2-Aminobutanoic acid, (2S)-2-Aminobutyrate, (2S)-2-Aminobutyric acid, (S)-(+)-alpha-Aminobutyric acid, (S)-2-amino-Butanoate, (S)-2-amino-Butanoic acid, (S)-2-Aminobutanoate, (S)-2-Aminobutanoic acid, (S)-2-Aminobutyrate, (S)-2-Aminobutyric acid, 2-Aminobutanoate, 2-Aminobutanoic acid, 2-Aminobutanoic acid, 9CI, L-form, 2-Aminobutyrate, 2-Aminobutyric acid, L-, 2S-amino-Butanoate, 2S-amino-Butanoic acid, AABA, Alpha-Aminobutyric acid, Butanoic acid, 2-amino-, (2S)-, Butanoic acid, 2-amino-, (S)- (9CI), Butyric acid, 2-amino-, L- (8CI), L-(+)-2-Aminobutyrate, L-(+)-2-Aminobutyric acid, L-&alpha, -Amino-n-butyric acid, L-&alpha, -Aminobutyrate, L-&alpha, -Aminobutyric acid, L-2-Amino-n-butyric acid, L-2-Aminobuttersaeure, L-2-Aminobutyrate, L-2-Aminobutyric acid, L-a-amino-N-Butyrate, L-a-amino-N-Butyric acid, L-a-Aminobutyrate, L-a-Aminobutyric acid, L-AABA, L-alpha-amino-N-Butyrate, L-alpha-Amino-n-butyric acid, L-alpha-Aminobutyrate, L-alpha-Aminobutyric acid, L-butyrine, L-Ethylglycine, L-α-amino-N-butyrate, L-α-amino-N-butyric acid, L-α-aminobutyrate, L-α-aminobutyric acid, S-Butyrine, L-alpha-Amino-N-butyric acid, L-Butyrine, L-a-Amino-N-butyrate, L-a-Amino-N-butyric acid, L-alpha-Amino-N-butyrate, L-Α-amino-N-butyrate, L-Α-amino-N-butyric acid, L-Α-aminobutyrate, L-Α-aminobutyric acid, alpha-Aminobutyric acid, L-2-amino-N-Butyric acid, Butyrine, (R)-isomer, 2-Aminobutyric acid, alpha-Aminobutyric acid, (+-)-isomer, Butyrine, Butyrine, (S)-isomer, L-Homoalanine, alpha-Aminobutyric acid, (S)-isomer, Homoalanine, alpha-Aminobutyric acid, (R)-isomer, Butyrine, (+-)-isomer, L-2-Aminobutanoate |
| Heavy Atom Count | 7.0 |
| Compound Name | (-)-2-Aminobutyric acid |
| Kingdom | Organic compounds |
| Description | alpha-Aminobutyric acid (AABA) is an isomer of the amino acid aminobutyric acid. It is a key intermediate in the biosynthesis of ophthalmic acid or ophthalmate. L-2-Aminobutanoic acid is found in common pea. |
| Exact Mass | 103.063 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 103.063 |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 72.1 |
| Hydrogen Bond Acceptor Count | 3.0 |
| Molecular Weight | 103.12 |
| Database Name | fooddb_chem_all;hmdb_chem_all;pubchem |
| Covalent Unit Count | 1.0 |
| Enzyme Uniprot Id | P50440 |
| Uniprot Id | P50440, P01133 |
| Defined Atom Stereocenter Count | 1.0 |
| Iupac Name | (2S)-2-aminobutanoic acid |
| Total Atom Stereocenter Count | 1.0 |
| Molecular Framework | Aliphatic acyclic compounds |
| Total Bond Stereocenter Count | 0.0 |
| Class | Carboxylic acids and derivatives |
| Inchi | InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1 |
| Smiles | CC[C@@H](C(=O)O)N |
| Xlogp | -2.5 |
| Superclass | Organic acids and derivatives |
| Defined Bond Stereocenter Count | 0.0 |
| Subclass | Amino acids, peptides, and analogues |
| Taxonomy Direct Parent | L-alpha-amino acids |
| Molecular Formula | C4H9NO2 |
- 1. Outgoing r'ship
FOUND_INto/from Pisum Sativum (Plant) Rel Props:Source_db:fooddb_chem_all