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
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
| 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 | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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
Edited
Mon Mar 31 19:30:34 GMT 2025
by
admin
on
Mon Mar 31 19:30:34 GMT 2025
|
| Record UNII |
DU5M1YH1M1
|
| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English | ||
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Common Name | English | ||
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Code | English |
| Code System | Code | Type | Description | ||
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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
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DTXSID001000495
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admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
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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
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79467-24-6
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admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
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21896660
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admin on Mon Mar 31 19:30:34 GMT 2025 , Edited by admin on Mon Mar 31 19:30:34 GMT 2025
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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
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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
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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
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> SALT/SOLVATE | |||
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ANHYDROUS->SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |