TMTFA

Transition state analogue TMTFA is an equilibrium mixture of the free ketone and ketone hydrate NAF in aqueous solution, with a hydration equilibrium constant of 60 000

General

Type : Trifluoro,Trimethylammonium,Quaternary compound,Transition state analogue,Halo ketone

Chemical_Nomenclature : m-(N,N,N-Trimethylammonio)trifluoroacetophenone

Canonical SMILES : C[N+](C)(C)C1=CC=CC(=C1)C(=O)C(F)(F)F

InChI : InChI=1S\/C11H13F3NO\/c1-15(2,3)9-6-4-5-8(7-9)10(16)11(12,13)14\/h4-7H,1-3H3\/q+1

InChIKey : JIBZSTPMDKSJOX-UHFFFAOYSA-N

Other name(s) : m-(N,N,N-trimethylammonio)-2,2,2-trifluro-1,1-dihydroxyethylbenzene,CHEMBANK2333,TFK


MW : 232.222

Formula : C11H13F3NO+

CAS_number :

PubChem : 5492

UniChem : JIBZSTPMDKSJOX-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : TMTFA ligand of proteins in family: ACHE

Stucture :

Protein : torca-ACHE || mouse-ACHE

References (10)

Title : Drug and pro-drug substrates and pseudo-substrates of human butyrylcholinesterase - Masson_2023_Biochem.Pharmacol_218_115910
Author(s) : Masson P , Shaihutdinova Z , Lockridge O
Ref : Biochemical Pharmacology , 218 :115910 , 2023
Abstract : Masson_2023_Biochem.Pharmacol_218_115910
ESTHER : Masson_2023_Biochem.Pharmacol_218_115910
PubMedSearch : Masson_2023_Biochem.Pharmacol_218_115910
PubMedID: 37972875

Title : 1-(3-Tert-Butylphenyl)-2,2,2-Trifluoroethanone as a Potent Transition-State Analogue Slow-Binding Inhibitor of Human Acetylcholinesterase: Kinetic, MD and QM\/MM Studies - Zueva_2020_Biomolecules_10_1608
Author(s) : Zueva IV , Lushchekina SV , Pottie IR , Darvesh S , Masson P
Ref : Biomolecules , 10 : , 2020
Abstract : Zueva_2020_Biomolecules_10_1608
ESTHER : Zueva_2020_Biomolecules_10_1608
PubMedSearch : Zueva_2020_Biomolecules_10_1608
PubMedID: 33260981

Title : Substrate and product trafficking through the active center gorge of acetylcholinesterase analyzed by crystallography and equilibrium binding - Bourne_2006_J.Biol.Chem_281_29256
Author(s) : Bourne Y , Radic Z , Sulzenbacher G , Kim E , Taylor P , Marchot P
Ref : Journal of Biological Chemistry , 281 :29256 , 2006
Abstract : Bourne_2006_J.Biol.Chem_281_29256
ESTHER : Bourne_2006_J.Biol.Chem_281_29256
PubMedSearch : Bourne_2006_J.Biol.Chem_281_29256
PubMedID: 16837465
Gene_locus related to this paper: mouse-ACHE

Title : Theoretical and experimental investigations of electrostatic effects on acetylcholinesterase catalysis and inhibition - Malany_1999_Chem.Biol.Interact_119-120_99
Author(s) : Malany S , Baker NA , Verweyst M , Medhekar R , Quinn DM , Velan B , Kronman C , Shafferman A
Ref : Chemico-Biological Interactions , 119-120 :99 , 1999
Abstract : Malany_1999_Chem.Biol.Interact_119-120_99
ESTHER : Malany_1999_Chem.Biol.Interact_119-120_99
PubMedSearch : Malany_1999_Chem.Biol.Interact_119-120_99
PubMedID: 10421443

Title : A preliminary comparison of structural models for catalytic intermediates of acetylcholinesterase - Silman_1999_Chem.Biol.Interact_119-120_43
Author(s) : Silman I , Millard CB , Ordentlich A , Greenblatt HM , Harel M , Barak D , Shafferman A , Sussman JL
Ref : Chemico-Biological Interactions , 119-120 :43 , 1999
Abstract : Silman_1999_Chem.Biol.Interact_119-120_43
ESTHER : Silman_1999_Chem.Biol.Interact_119-120_43
PubMedSearch : Silman_1999_Chem.Biol.Interact_119-120_43
PubMedID: 10421437
Gene_locus related to this paper: torca-ACHE

Title : Nonequilibrium analysis alters the mechanistic interpretation of inhibition of acetylcholinesterase by peripheral site ligands - Szegletes_1998_Biochemistry_37_4206
Author(s) : Szegletes T , Mallender WD , Rosenberry TL
Ref : Biochemistry , 37 :4206 , 1998
Abstract : Szegletes_1998_Biochemistry_37_4206
ESTHER : Szegletes_1998_Biochemistry_37_4206
PubMedSearch : Szegletes_1998_Biochemistry_37_4206
PubMedID: 9521743

Title : Electrostatic influence on the kinetics of ligand binding to acetylcholinesterase. Distinctions between active center ligands and fasciculin - Radic_1997_J.Biol.Chem_272_23265
Author(s) : Radic Z , Kirchhoff PD , Quinn DM , McCammon JA , Taylor P
Ref : Journal of Biological Chemistry , 272 :23265 , 1997
Abstract : Radic_1997_J.Biol.Chem_272_23265
ESTHER : Radic_1997_J.Biol.Chem_272_23265
PubMedSearch : Radic_1997_J.Biol.Chem_272_23265
PubMedID: 9287336

Title : The X-ray structure of a transition state analog complex reveals the molecular origins of the catalytic power and substrate specificity of acetylcholinesterase. -
Author(s) : Harel M , Quinn DM , Nair HK , Silman I , Sussman JL
Ref : Journal of the American Chemical Society , 118 :2340 , 1996
PubMedID:
Gene_locus related to this paper: torca-ACHE

Title : Allosteric control of acetylcholinesterase catalysis by fasciculin - Radic_1995_J.Biol.Chem_270_20391
Author(s) : Radic Z , Quinn DM , Vellom DC , Camp S , Taylor P
Ref : Journal of Biological Chemistry , 270 :20391 , 1995
Abstract : Radic_1995_J.Biol.Chem_270_20391
ESTHER : Radic_1995_J.Biol.Chem_270_20391
PubMedSearch : Radic_1995_J.Biol.Chem_270_20391
PubMedID: 7657613

Title : Molecular recognition in acetylcholinesterase catalysis: free-energy correlations for substrate turnover and inhibition by trifluoro ketone transition-state analogs - Nair_1994_Biochemistry_33_8566
Author(s) : Nair HK , Seravalli J , Arbuckle T , Quinn DM
Ref : Biochemistry , 33 :8566 , 1994
Abstract : Nair_1994_Biochemistry_33_8566
ESTHER : Nair_1994_Biochemistry_33_8566
PubMedSearch : Nair_1994_Biochemistry_33_8566
PubMedID: 8031791