Nafamostat mesylateProduct ingredient for Nafamostat

Name
Nafamostat mesylate
Drug Entry
Nafamostat

Nafamostat is a synthetic serine protease inhibitor that is commonly formulated with hydrochloric acid due to its basic properties. It has been used in trials studying the prevention of Liver Transplantation and Postreperfusion Syndrome. The use of nafamostat in Asian countries is approved as an anticoagulant therapy for patients undergoing continuous renal replacement therapy due to acute kidney injury.

Accession Number
DBSALT002384
Structure
Synonyms
Nafamostat dimethanesulfonate / Nafamostat mesilate / Nafamostat mesylate
External IDs
FUT 175 / FUT-175
UNII
1D2T74921W
CAS Number
82956-11-4
Weight
Average: 539.58
Monoisotopic: 539.114455133
Chemical Formula
C21H25N5O8S2
InChI Key
SRXKIZXIRHMPFW-UHFFFAOYSA-N
InChI
InChI=1S/C19H17N5O2.2CH4O3S/c20-17(21)14-2-1-13-10-16(8-5-12(13)9-14)26-18(25)11-3-6-15(7-4-11)24-19(22)23;2*1-5(2,3)4/h1-10H,(H3,20,21)(H4,22,23,24);2*1H3,(H,2,3,4)
IUPAC Name
6-carbamimidoylnaphthalen-2-yl 4-carbamimidamidobenzoate; bis(methanesulfonic acid)
SMILES
CS(O)(=O)=O.CS(O)(=O)=O.NC(=N)NC1=CC=C(C=C1)C(=O)OC1=CC2=C(C=C1)C=C(C=C2)C(N)=N
KEGG Drug
D01670
ChemSpider
49623
ChEBI
31890
ChEMBL
CHEMBL3989553
Predicted Properties
PropertyValueSource
Water Solubility0.0341 mg/mLALOGPS
logP1.91ALOGPS
logP2.52Chemaxon
logS-4ALOGPS
pKa (Strongest Basic)11.32Chemaxon
Physiological Charge2Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count5Chemaxon
Polar Surface Area138.07 Å2Chemaxon
Rotatable Bond Count5Chemaxon
Refractivity122.12 m3·mol-1Chemaxon
Polarizability36.46 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveNoChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon