Ethylmethanethiosulfonate-2-carboxy[(5’-amino-1’-carboxypentyl)iminodiacetic Acid] Amide, Trifluoroacetic Acid Salt
Product Code
TRC-E925020
Product Format
Neat
Molecular Formula
C14 H24 N2 O9 S2 . C2 H F3 O2
Molecular Weight
542.502
Product Categories
GABA receptors, TRC, Neurotransmission, Nociception, Alzheimer's, Depression, Epilepsy, Memory, Learning and Cognition, Parkinson's, Schizophrenia, Sleep, Stress and Anxiety, Stroke, Addiction, Pain and Inflammation
Product Type
Stable Isotope LabelledProduct Information
Chemical Data
Analyte Name
Ethylmethanethiosulfonate-2-carboxy[(5’-amino-1’-carboxypentyl)iminodiacetic Acid] Amide, Trifluoroacetic Acid Salt
Molecular Formula
C14 H24 N2 O9 S2 . C2 H F3 O2
Molecular Weight
542.502
Accurate Mass
542.085
SMILES
CS(=O)(=O)SCCC(=O)NCCCCC(N(CC(=O)O)CC(=O)O)C(=O)O.OC(=O)C(F)(F)F
InChI
InChI=1S/C14H24N2O9S2.C2HF3O2/c1-27(24,25)26-7-5-11(17)15-6-3-2-4-10(14(22)23)16(8-12(18)19)9-13(20)21;3-2(4,5)1(6)7/h10H,2-9H2,1H3,(H,15,17)(H,18,19)(H,20,21)(H,22,23);(H,6,7)
IUPAC
2-[bis(carboxymethyl)amino]-6-(3-methylsulfonylsulfanylpropanoylamino)hexanoic acid;2,2,2-trifluoroacetic acid
Product Data
Shipping Temperature
Room Temperature
Country of Origin
CANADA
Product Format
Neat
Product Description
Reacts specifically and rapidly with thiols to form mixed disulfides. Used to probe the structures of the ACh receptor channel of the GABA receptor channel and of lactose permease.
References: Xu, M. & Akabus, M.H.: J. Biol. Chem., 268, 21505 (1993), Duhten, R.L., et al.: Biochemistry, 32, 3139 (1993), Yang, N. et al.: Neuron, 16, 113 (1996), Kuner, T. et al.: Neuron, 17, 343 (1996)
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