4-Hexynoic acid, 2-amino-

Details

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Internal ID 10376b08-f735-40e7-a492-2bd4af006e12
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-aminohex-4-ynoic acid
SMILES (Canonical) CC#CCC(C(=O)O)N
SMILES (Isomeric) CC#CCC(C(=O)O)N
InChI InChI=1S/C6H9NO2/c1-2-3-4-5(7)6(8)9/h5H,4,7H2,1H3,(H,8,9)
InChI Key VDWGCMRALYSYJV-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO2
Molecular Weight 127.14 g/mol
Exact Mass 127.063328530 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -2.30

Synonyms

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4-Hexynoic acid, 2-amino-
2-Amino-4-hexynoic acid
29834-75-1
52523-53-2
(2R)-2-Amino-4-hexynoic acid
346707-82-2
NSC134451
2-aminohex-4-ynoicacid
SCHEMBL455292
(2s)-2-amino-4-hexynoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Hexynoic acid, 2-amino-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.49% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 94.16% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 87.37% 83.82%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.17% 92.29%
CHEMBL2581 P07339 Cathepsin D 83.85% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.56% 91.11%
CHEMBL4822 P56817 Beta-secretase 1 81.77% 97.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.64% 94.45%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.72% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 187846
LOTUS LTS0061263
wikiData Q82007326