U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C19H24N2O4S
Molecular Weight 376.47
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MESUDIPINE

SMILES

CCOC(=O)C1=C(C)NC(C)=C(C1C2=CC=CN=C2SC)C(=O)OCC

InChI

InChIKey=DYGIPCPWPHKLMC-UHFFFAOYSA-N
InChI=1S/C19H24N2O4S/c1-6-24-18(22)14-11(3)21-12(4)15(19(23)25-7-2)16(14)13-9-8-10-20-17(13)26-5/h8-10,16,21H,6-7H2,1-5H3

HIDE SMILES / InChI
Mesudipine, a dihydropyridine analog, is a calcium antagonistic drug (slow channel blocker). It blocks electrical activity in smooth muscle cells and Purkinje fibers.

Approval Year

PubMed

PubMed

TitleDatePubMed
Depression of contractions of rabbit aorta and guinea pig vena cava by mesudipine and other slow channel blockers.
1983
Comparison of the effects of several calcium antagonistic drugs on the electrical activity of guinea pig Purkinje fibers.
1983 Mar 25
Effects of calcium antagonistic drugs on the electrical activity of rabbit sino-atrial node.
1986 May
New dihydropyridine drug, nilvadipine, blocks the calcium slow action potential in rat-cultured aortic smooth muscle cells.
1986 May 13

Sample Use Guides

In Vitro Use Guide
Mesudipine at 10 nM and 40 nM depressed the Vmax, amplitude and duration of the slow action potentials of guinea pig Purkinje fibers and abolished excitability within 11 min at 100 nM. At 100 nM, mesudipine blocked the slow action potentials earlier (within 3 min) at higher stimulation frequency (from the usual drive rate of 0.5-1.5 Hz).
Name Type Language
MESUDIPINE
INN  
INN  
Official Name English
DIETHYL 1',4'-DIHYDRO-2',6'-DIMETHYL-2-(METHYLTHIO)(3,4'-BIPYRIDINE)-3',5'-DICARBOXYLATE
Systematic Name English
mesudipine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C333
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
Code System Code Type Description
MESH
C036653
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
PUBCHEM
68817
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
FDA UNII
DT27W93DFF
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
EVMPD
SUB08792MIG
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID00978230
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
NCI_THESAURUS
C66102
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
INN
4461
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
263-677-3
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106863
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
CAS
62658-88-2
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY
SMS_ID
100000081188
Created by admin on Fri Dec 15 15:46:12 GMT 2023 , Edited by admin on Fri Dec 15 15:46:12 GMT 2023
PRIMARY