2-trimethylsilyl-ethyl-N-butylcarbamate

Inhibitor of ACHE but activator of BCHE

General

Type : Carbamate,Analogue of substrate,Sulfur Compound

Chemical_Nomenclature : 2-trimethylsilylethyl N-butylcarbamate

Canonical SMILES : CCCCNC(=O)OCC[Si](C)(C)C

InChI : InChI=1S\/C10H23NO2Si\/c1-5-6-7-11-10(12)13-8-9-14(2,3)4\/h5-9H2,1-4H3,(H,11,12)

InChIKey : FUDAOOVSPCANMW-UHFFFAOYSA-N

Other name(s) : 2-trimethylsilyl-ethyl-N-n-butylcarbamate,Butylcarbamic acid 2-(trimethylsilyl)ethyl ester


MW : 217.38

Formula : C10H23NO2Si

CAS_number :

PubChem : 102394632

UniChem : FUDAOOVSPCANMW-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : 2-trimethylsilyl-ethyl-N-butylcarbamate ligand of proteins in family: BCHE || ACHE

Stucture :

Protein :

References (2)

Title : Activation mechanisms of butyrylcholinesterase by 2,4,6-trinitrotoluene, 3,3-dimethylbutyl-N-n-butylcarbamate, and 2-trimethylsilyl-ethyl-N-n-butylcarbamate - Chiou_2008_Appl.Biochem.Biotechnol_150_337
Author(s) : Chiou SY , Wu YG , Lin G
Ref : Appl Biochem Biotechnol , 150 :337 , 2008
Abstract : Chiou_2008_Appl.Biochem.Biotechnol_150_337
ESTHER : Chiou_2008_Appl.Biochem.Biotechnol_150_337
PubMedSearch : Chiou_2008_Appl.Biochem.Biotechnol_150_337
PubMedID: 18563305

Title : Substrate activation of butyrylcholinesterase and substrate inhibition of acetylcholinesterase by 3,3-dimethylbutyl-N-n-butylcarbamate and 2-trimethylsilyl-ethyl-N-n-butylcarbamate - Chiou_2007_J.Biochem.Mol.Toxicol_21_24
Author(s) : Chiou SY , Wu YG , Lin YF , Lin LY , Lin G
Ref : J Biochem Mol Toxicol , 21 :24 , 2007
Abstract : Chiou_2007_J.Biochem.Mol.Toxicol_21_24
ESTHER : Chiou_2007_J.Biochem.Mol.Toxicol_21_24
PubMedSearch : Chiou_2007_J.Biochem.Mol.Toxicol_21_24
PubMedID: 17366539