EMBL-EBI | Chemical Biology | ChEBI

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

CHEBI:9729 - trimethaphan camsylate

ChEBI IDCHEBI:9729
ChEBI Nametrimethaphan camsylate
Stars
DefinitionThe (S)-camphorsulfonate salt of trimethaphan.
Last Modified25 September 2014
DownloadsMolfile
FormulaC10H15O4S.C22H25N2OS
Net Charge0
Average Mass596.815
Monoisotopic Mass596.23786
SMILESCC1(C)[C@@H]2CC[C@@]1(CS(=O)(=O)[O-])C(=O)C2.O=C1N(Cc2ccccc2)C2C[S+]3CCCC3C2N1Cc1ccccc1
InChIInChI=1S/C22H25N2OS.C10H16O4S/c25-22-23(14-17-8-3-1-4-9-17)19-16-26-13-7-12-20(26)21(19)24(22)15-18-10-5-2-6-11-18;1-9(2)7-3-4-10(9,8(11)5-7)6-15(12,13)14/h1-6,8-11,19-21H,7,12-16H2;7H,3-6H2,1-2H3,(H,12,13,14)/q+1;/p-1/t;7-,10-/m.1/s1
InChIKeyHALWUDBBYKMYPW-STOWLHSFSA-M
Roles Classification
Application:
antihypertensive agent  Any drug used in the treatment of acute or chronic vascular hypertension regardless of pharmacological mechanism.
ChEBI Ontology
Outgoing Relation(s)
trimethaphan camsylate (CHEBI:9729) has part (S)-camphorsulfonate (CHEBI:55408)
trimethaphan camsylate (CHEBI:9729) has part trimethaphan (CHEBI:9728)
trimethaphan camsylate (CHEBI:9729) has role antihypertensive agent (CHEBI:35674)
trimethaphan camsylate (CHEBI:9729) is a camphorsulfonate salt (CHEBI:55339)
IUPAC Name 
1,3-dibenzyl-2-oxodecahydrothieno[1',2':1,2]thieno[3,4-d]imidazol-5-ium [(1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonate
INNs  Source
camsilate de trimetaphanChemIDplus
cansilato de trimetafanoChemIDplus
trimetaphani camsilasChemIDplus
trimetaphan camsilateKEGG DRUG
Synonyms  Source
(+)-1,3-Dibenzyldecahydro-2-oxoimidazo(4,5-c)thieno(1,2-a)-thiolium 2-oxo-10-bornanesulfonate (1:1)ChemIDplus
1,3-Dibenzyldecahydro-2-oxo-imidazo(4,5-c)thieno(1,2-a)thiolium 2-oxo-10-boranesulfonateChemIDplus
1,3-Dibenzyldecahydro-2-oxoimidazo(4,5-c)thieno(1,2-a)thiolium 10-camphorsulfonateChemIDplus
Trimetaphan camphorsulfonateChemIDplus
Trimetaphan camsilateChemIDplus
Trimetaphan camsylateChemIDplus
Manual XrefsDatabases
D00612KEGG DRUG
Registry NumbersSources
Reaxys:4114455Reaxys
CAS:68-91-7ChemIDplus
Citations