BCH
2-(BUTYRYLSULFANYL)-N,N,N-TRIMETHYLETHANAMINIUM
Find entries where: BCH
is present as a standalone ligand in 2 entries
Chemical Component Summary | |
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Name | 2-(BUTYRYLSULFANYL)-N,N,N-TRIMETHYLETHANAMINIUM |
Synonyms | BUTYRYLTHIOCHOLINE |
Identifiers | 2-butanoylsulfanylethyl-trimethyl-azanium |
Formula | C9 H20 N O S |
Molecular Weight | 190.326 |
Type | NON-POLYMER |
Isomeric SMILES | CCCC(=O)SCC[N+](C)(C)C |
InChI | InChI=1S/C9H20NOS/c1-5-6-9(11)12-8-7-10(2,3)4/h5-8H2,1-4H3/q+1 |
InChIKey | AWBGQVBMGBZGLS-UHFFFAOYSA-N |
Chemical Details | |
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Formal Charge | 1 |
Atom Count | 32 |
Chiral Atom Count | 0 |
Bond Count | 31 |
Aromatic Bond Count | 0 |
Drug Info: DrugBank
DrugBank ID | DB04250? |
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Name | Butyrylthiocholine |
Groups | experimental |
Description | A sulfur-containing analog of butyrylcholine which is hydrolyzed by butyrylcholinesterase to butyrate and thiocholine. It is used as a reagent in the determination of butyrylcholinesterase activity. [PubChem] |
Synonyms | Butyrylthiocholine |
Categories |
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Drug Targets
Name | Target Sequence | Pharmacological Action | Actions |
---|---|---|---|
Cholinesterase | MHSKVTIICIRFLFWFLLLCMLIGKSHTEDDIIIATKNGKVRGMNLTVFG... | unknown | substrate |
Cholinesterase | MHSKVTIICIRFLFWFLLLCMLIGKSHTEDDIIIATKNGKVRGMNLTVFG... | unknown | substrate |
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison
T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS.
Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682
Related Resource References
Resource Name | Reference |
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PubChem | 20689 |
ChEMBL | CHEMBL139908 |
ChEBI | CHEBI:41055 |
CCDC/CSD | YOGPUF |