Eprosartan mesylate dihydrateProduct ingredient for Eprosartan

Name
Eprosartan mesylate dihydrate
Drug Entry
Eprosartan

Eprosartan is an angiotensin II receptor antagonist used to treat hypertension. It performs 2 actions on the renin angiotensin system. By preventing the binding of angiotensin II to AT1, vascular smooth muscle relaxes and vasodilation occurs. By inhibiting norepinephrine production, blood pressure is further reduced.

Accession Number
DBSALT002994
Structure
Synonyms
Not Available
UNII
9G2HB74868
CAS Number
197855-71-3
Weight
Average: 556.65
Monoisotopic: 556.154922966
Chemical Formula
C24H32N2O9S2
InChI Key
HIUNDVRJXJGSGV-KMDBKMSFSA-N
InChI
InChI=1S/C23H24N2O4S.CH4O3S.2H2O/c1-2-3-6-21-24-14-19(12-18(23(28)29)13-20-5-4-11-30-20)25(21)15-16-7-9-17(10-8-16)22(26)27;1-5(2,3)4;;/h4-5,7-12,14H,2-3,6,13,15H2,1H3,(H,26,27)(H,28,29);1H3,(H,2,3,4);2*1H2/b18-12+;;;
IUPAC Name
4-({2-butyl-5-[(1E)-2-carboxy-2-[(thiophen-2-yl)methyl]eth-1-en-1-yl]-1H-imidazol-1-yl}methyl)benzoic acid methanesulfonic acid dihydrate
SMILES
O.O.CS(O)(=O)=O.[H]\C(=C(\CC1=CC=CS1)C(O)=O)C1=CN=C(CCCC)N1CC1=CC=C(C=C1)C(O)=O
ChemSpider
8048128
Predicted Properties
PropertyValueSource
Water Solubility0.00866 mg/mLALOGPS
logP3.57ALOGPS
logP3.75Chemaxon
logS-4.7ALOGPS
pKa (Strongest Acidic)3.47Chemaxon
pKa (Strongest Basic)6.67Chemaxon
Physiological Charge-2Chemaxon
Hydrogen Acceptor Count5Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area92.42 Å2Chemaxon
Rotatable Bond Count10Chemaxon
Refractivity117.02 m3·mol-1Chemaxon
Polarizability45.22 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveNoChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon