Record Information
Version1.0
Creation Date2016-05-22 05:14:33 UTC
Update Date2016-11-09 01:15:48 UTC
Accession NumberCHEM018423
Identification
Common NameGabexate mesilate
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
Gabexate mesylateKegg
ArodateKegg
Gabexic acid mesylic acidGenerator
Arodic acidGenerator
Ethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoate; methanesulfonateGenerator
Ethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoate; methanesulphonateGenerator
Ethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoic acid; methanesulfonic acidGenerator
Ethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoic acid; methanesulphonic acidGenerator
[N'-[6-(4-ethoxycarbonylphenoxy)-6-oxohexyl]carbamimidoyl]azanium;methanesulfonic acidGenerator
[N'-[6-(4-ethoxycarbonylphenoxy)-6-oxohexyl]carbamimidoyl]azanium;methanesulphonateGenerator
[N'-[6-(4-ethoxycarbonylphenoxy)-6-oxohexyl]carbamimidoyl]azanium;methanesulphonic acidGenerator
Ethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoate
methanesulfonate
methanesulphonate
Ethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoic acid
methanesulfonic acid
methanesulphonic acid
Chemical FormulaC17H27N3O7S
Average Molecular Mass417.480 g/mol
Monoisotopic Mass417.157 g/mol
CAS Registry Number56974-61-9
IUPAC Nameethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoate; methanesulfonic acid
Traditional Nameethyl 4-[(6-carbamimidamidohexanoyl)oxy]benzoate; methanesulfonic acid
SMILESCS(O)(=O)=O.CCOC(=O)C1=CC=C(OC(=O)CCCCCNC(N)=N)C=C1
InChI IdentifierInChI=1S/C16H23N3O4.CH4O3S/c1-2-22-15(21)12-7-9-13(10-8-12)23-14(20)6-4-3-5-11-19-16(17)18;1-5(2,3)4/h7-10H,2-6,11H2,1H3,(H4,17,18,19);1H3,(H,2,3,4)
InChI KeyDNTNDFLIKUKKOC-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassBenzoic acids and derivatives
Direct ParentBenzoic acid esters
Alternative Parents
Substituents
  • Benzoate ester
  • Phenol ester
  • Phenoxy compound
  • Benzoyl
  • Fatty acid ester
  • Dicarboxylic acid or derivatives
  • Fatty acyl
  • Organic sulfonic acid or derivatives
  • Organosulfonic acid or derivatives
  • Organosulfonic acid
  • Sulfonyl
  • Alkanesulfonic acid
  • Carboxylic acid ester
  • Guanidine
  • Organic 1,3-dipolar compound
  • Propargyl-type 1,3-dipolar organic compound
  • Carboxylic acid derivative
  • Carboximidamide
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxygen compound
  • Organic oxide
  • Organopnictogen compound
  • Carbonyl group
  • Organic salt
  • Organosulfur compound
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkNot Available
External DescriptorsNot Available
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility0.11 g/LALOGPS
logP1.83ALOGPS
logP2.1ChemAxon
logS-3.5ALOGPS
pKa (Strongest Basic)12.13ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area114.5 ŲChemAxon
Rotatable Bond Count11ChemAxon
Refractivity96.7 m³·mol⁻¹ChemAxon
Polarizability35.28 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
LC-MS/MSLC-MS/MS Spectrum - LC-ESI-qTof , Positivesplash10-00di-5922100000-17b17a7746dacf569151Spectrum
LC-MS/MSLC-MS/MS Spectrum - , positivesplash10-00di-5922100000-17b17a7746dacf569151Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-0000900000-05c56d1907ec2573ce22Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-0000900000-05c56d1907ec2573ce22Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-014i-0000900000-05c56d1907ec2573ce22Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014i-0000900000-957891dfe5e047876604Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014i-0000900000-957891dfe5e047876604Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-014i-0000900000-957891dfe5e047876604Spectrum
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)Not Available
Uses/SourcesNot Available
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDDBSALT002364
HMDB IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider IDNot Available
ChEBI IDNot Available
PubChem Compound ID42080
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available