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Details

Stereochemistry RACEMIC
Molecular Formula C20H31NO2S.C6H8O7.H2O
Molecular Weight 559.669
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CETIEDIL CITRATE MONOHYDRATE

SMILES

O.OC(=O)CC(O)(CC(O)=O)C(O)=O.O=C(OCCN1CCCCCC1)C(C2CCCCC2)C3=CSC=C3

InChI

InChIKey=YIIFJFQCZWTTCW-UHFFFAOYSA-N
InChI=1S/C20H31NO2S.C6H8O7.H2O/c22-20(23-14-13-21-11-6-1-2-7-12-21)19(18-10-15-24-16-18)17-8-4-3-5-9-17;7-3(8)1-6(13,5(11)12)2-4(9)10;/h10,15-17,19H,1-9,11-14H2;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);1H2

HIDE SMILES / InChI
Cetiedil is effective potassium channel blocker used as a peripheral vasodilator to treat patients with painful crises in sickle cell anemia and pain in the extremities caused by an arterial disease. Known pharmacological properties of the drug include vascular smooth muscle relaxation, inhibition of phosphodiesterase with the consequent increase in circulating cyclic AMP concentration, blockade of the effect of bradykinin and serotonin, analgesia, inhibition of platelet aggregation and the decrease of plasma and blood viscosity and plasma fibrinogen level. The antisickling effect of cetiedil is explained mainly in the light of the changes it induces in the activities of membrane-bound ATPases and the permeability properties of the erythrocyte membrane to cations and anions.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacology of the human red cell voltage-dependent cation channel; Part I. Activation by clotrimazole and analogues.
2004-01-22
Inhibition of the antigen-induced activation of RBL-2H3 cells by cetiedil and some of its analogues.
2004-01-12
Inhibition of the antigen-induced activation of RBL-2H3 cells by charybdotoxin and cetiedil.
2004-01-12
An analysis of the mechanism by which cetiedil inhibits sickling.
2002-01-18
Synthesis and structure-activity relationships of cetiedil analogues as blockers of the Ca(2+)-activated K+ permeability of erythrocytes.
2001-09-27
Name Type Language
3-THIOPHENEACETIC ACID, .ALPHA.-CYCLOHEXYL-, 2-(HEXAHYDRO-1H-AZEPIN-1-YL)ETHYL ESTER, 2-HYDROXY-1,2,3-PROPANETRICARBOXYLATE HYDRATE(1:1:1)
Preferred Name English
CETIEDIL CITRATE MONOHYDRATE
Common Name English
Code System Code Type Description
PUBCHEM
165411860
Created by admin on Mon Mar 31 21:26:49 GMT 2025 , Edited by admin on Mon Mar 31 21:26:49 GMT 2025
PRIMARY
FDA UNII
8VF7HHY5PF
Created by admin on Mon Mar 31 21:26:49 GMT 2025 , Edited by admin on Mon Mar 31 21:26:49 GMT 2025
PRIMARY