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

Details

Stereochemistry ACHIRAL
Molecular Formula C24H30N4O.C4H4O4
Molecular Weight 506.5934
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of IPAZILIDE FUMARATE

SMILES

OC(=O)\C=C\C(O)=O.CCN(CC)CCCNC(=O)CN1N=CC(=C1C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=KKMOBFCMCCFTDX-WLHGVMLRSA-N
InChI=1S/C24H30N4O.C4H4O4/c1-3-27(4-2)17-11-16-25-23(29)19-28-24(21-14-9-6-10-15-21)22(18-26-28)20-12-7-5-8-13-20;5-3(6)1-2-4(7)8/h5-10,12-15,18H,3-4,11,16-17,19H2,1-2H3,(H,25,29);1-2H,(H,5,6)(H,7,8)/b;2-1+

HIDE SMILES / InChI

Molecular Formula C24H30N4O
Molecular Weight 390.5212
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H4O4
Molecular Weight 116.0722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Ipazilide is an antiarrhythmic agent that prolongs ventricular refractoriness and possesses antiectopic activity. In clinical trials ipazilide administrations leads to dose- and time-dependent in decrease cardiac index and arterial pressure. Left ventricular filling pressure, right atrial pressure, and heart rate were not altered by ipazilide. Plasma concentrations of ipazilide peaked 90 minutes after administration of 100 or 200 of the drug, but peak concentrations were noted 3 hours after administration of 400 mg. The hemodynamic response correlated with the plasma concentration of ipazilide determined contemporaneously.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Subchronic oral and intravenous (i.v.) safety evaluation and pharmacokinetics in rats and dogs of ipazilide fumarate (Win 54, 177-4), an antiarrhythmic agent.
1992 May
Patents

Patents

Sample Use Guides

400, 200, and 100 mg single-dose
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:59:06 GMT 2023
Edited
by admin
on Fri Dec 15 15:59:06 GMT 2023
Record UNII
2MI60P494I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IPAZILIDE FUMARATE
USAN  
USAN  
Official Name English
1H-PYRAZOLE-1-ACETAMIDE, N-(3-(DIETHYLAMINO)PROPYL)-4,5-DIPHENYL-, (E)-2-BUTENEDIOATE (1:1)
Systematic Name English
N-[3-(Diethylamino)propyl]-4,5-diphenylpyrazole-1-acetamide fumarate (1:1)
Systematic Name English
WIN 54,177-4
Code English
WIN-54177-4
Code English
IPAZILIDE FUMARATE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
Code System Code Type Description
MESH
C076683
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
FDA UNII
2MI60P494I
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
PUBCHEM
5284403
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111169
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
NCI_THESAURUS
C81425
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
CAS
115436-74-3
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
USAN
AA-112
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID9020744
Created by admin on Fri Dec 15 15:59:06 GMT 2023 , Edited by admin on Fri Dec 15 15:59:06 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY