Vamifeport hydrochlorideProduct ingredient for Vamifeport

Name
Vamifeport hydrochloride
Drug Entry
Vamifeport

Vamifeport is being investigated for the treatment of beta-thalassemia.

Accession Number
DBSALT003352
Structure
Synonyms
2-(2-((2-(1H-benzimidazol-2-yl)ethyl]amino}ethyl)-N-((3-fluoropyridin-2-yl)methyl)-1,3-oxazole-4-carboxamide trihydrochloride / 2-(2-{[2-(1H-benzimidazol-2-yl)ethyl]amino}ethyl)-N-[(3-fluoropyridin-2-yl)methyl]-1,3-oxazole-4-carboxamide trihydrochloride
UNII
9DV8VO33JX
CAS Number
2095668-11-2
Weight
Average: 517.81
Monoisotopic: 516.1010353
Chemical Formula
C21H24Cl3FN6O2
InChI Key
ZBVCLZMNYXJVMV-UHFFFAOYSA-N
InChI
InChI=1S/C21H21FN6O2.3ClH/c22-14-4-3-9-24-17(14)12-25-21(29)18-13-30-20(28-18)8-11-23-10-7-19-26-15-5-1-2-6-16(15)27-19;;;/h1-6,9,13,23H,7-8,10-12H2,(H,25,29)(H,26,27);3*1H
IUPAC Name
2-(2-{[2-(1H-1,3-benzodiazol-2-yl)ethyl]amino}ethyl)-N-[(3-fluoropyridin-2-yl)methyl]-1,3-oxazole-4-carboxamide trihydrochloride
SMILES
Cl.Cl.Cl.FC1=C(CNC(=O)C2=COC(CCNCCC3=NC4=CC=CC=C4N3)=N2)N=CC=C1
ChemSpider
128718076
ChEMBL
CHEMBL4475199
Predicted Properties
PropertyValueSource
logP1.3Chemaxon
Physiological Charge1Chemaxon
Hydrogen Acceptor Count5Chemaxon
Hydrogen Donor Count3Chemaxon
Polar Surface Area108.73 Å2Chemaxon
Rotatable Bond Count9Chemaxon
Refractivity107.34 m3·mol-1Chemaxon
Polarizability43.19 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveNoChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon