Description: GABAA agonist. Also GABA-T substrate and GABA uptake inhibitor
Chemical Name:trans-4-Aminocrotonic acid
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
The trans-isomer of CACA. Potent GABAA agonist, GABA uptake inhibitor and substrate for GABA-T. Also GABAA-ρ agonist.
Technical Data
M. Wt
101.1
Formula
C4H7NO2
Storage
Store at RT
CAS Number
38090-53-8
PubChem ID
5310987
InChI Key
FMKJUUQOYOHLTF-OWOJBTEDSA-N
Smiles
NC/C=C/C(O)=O
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solubility
Soluble to 100 mM in water
Preparing Stock Solutions
The following data is based on the product molecular weight 101.1. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
9.89 mL
49.46 mL
98.91 mL
5 mM
1.98 mL
9.89 mL
19.78 mL
10 mM
0.99 mL
4.95 mL
9.89 mL
50 mM
0.2 mL
0.99 mL
1.98 mL
Molarity Calculator
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Reconstitution Calculator
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Dilution Calculator
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Chebibet al (1997) Analogues of γ-aminobutyric acid (GABA) and trans-4-aminocrotonic acid (TACA) substituted in the 2 position as GABAC receptor antagonists. Br.J.Pharmacol. 122 1551 PMID: 9422798
Johnstonet al (1975) cis and trans-4-Aminocrotonic acid as GABA analogues of restricted conformation. J.Neurochem. 24 157 PMID: 234147
Johnstonet al (1996) GABAC receptors: relatively simple transmitter-gated ion channels. TiPS 17 319 PMID: 8885697