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Details

Stereochemistry RACEMIC
Molecular Formula C29H30Cl2F2N4O2.2ClH.H2O
Molecular Weight 666.414
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MIOFLAZINE HYDROCHLORIDE

SMILES

O.Cl.Cl.NC(=O)C1CN(CC(=O)NC2=C(Cl)C=CC=C2Cl)CCN1CCCC(C3=CC=C(F)C=C3)C4=CC=C(F)C=C4

InChI

InChIKey=CAEGSEJNBXUDOD-UHFFFAOYSA-N
InChI=1S/C29H30Cl2F2N4O2.2ClH.H2O/c30-24-4-1-5-25(31)28(24)35-27(38)18-36-15-16-37(26(17-36)29(34)39)14-2-3-23(19-6-10-21(32)11-7-19)20-8-12-22(33)13-9-20;;;/h1,4-13,23,26H,2-3,14-18H2,(H2,34,39)(H,35,38);2*1H;1H2

HIDE SMILES / InChI

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C29H30Cl2F2N4O2
Molecular Weight 575.477
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Mioflazine, a calcium antagonist, was developed as a cardioprotector. It protected a human atrial muscle against the destructive effects of high concentrations of Ca2+. Information about the current study of this agent is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Protection of human, rat, and guinea-pig atrial muscle by mioflazine, lidoflazine, and verapamil against the destructive effects of high concentrations of Ca2+.
1992-02
A comparison of the cardioprotective effects of calcium antagonists from different classes upon ischaemic damage in the guinea-pig working heart.
1989-07
[Protective effects of lidoflazine and mioflazine in ischemic myocardium].
1988-04
[Preventive effect of mioflazine on myocardial calcium-overload during postischemic reperfusion in the rabbit heart].
1988-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:30:34 GMT 2025
Edited
by admin
on Mon Mar 31 19:30:34 GMT 2025
Record UNII
DU5M1YH1M1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
R-51,469
Preferred Name English
MIOFLAZINE HYDROCHLORIDE
USAN  
USAN  
Official Name English
1-PIPERAZINEACETAMIDE, 3-(AMINOCARBONYL)-4-(4,4-BIS(4-FLUOROPHENYL)BUTYL)-N-(2,6-DICHLOROPHENYL)-, HYDROCHLORIDE, HYDRATE (1:2:1)
Systematic Name English
4-(4,4-BIS(P-FLUOROPHENYL)BUTYL)-3-CARBAMOYL-2,6-DICHLORO-1-PIPERAZINEACETANILIDE DIHYDROCHLORIDE MONOHYDRATE
Common Name English
MIOFLAZINE HYDROCHLORIDE [USAN]
Common Name English
1-PIPERAZINEACETAMIDE, 3-(AMINOCARBONYL)-4-(4,4-BIS(4-FLUOROPHENYL)BUTYL)-N-(2,6-DICHLOROPHENYL)-, DIHYDROCHLORIDE, MONOHYDRATE
Common Name English
R-51469
Code English
Code System Code Type Description
ChEMBL
CHEMBL2110980
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID001000495
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
NCI_THESAURUS
C170179
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
CAS
79467-24-6
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
PUBCHEM
21896660
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
MESH
C041518
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
USAN
T-41
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
FDA UNII
DU5M1YH1M1
Created by admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
PRIMARY
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PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
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ACTIVE MOIETY