Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H16Cl2N2O3.ClH |
| Molecular Weight | 403.687 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.ClC1=CC=C(C(Cl)=C1)[C@]3(CN2C=CN=C2)OC[C@@H](COCC#C)O3
InChI
InChIKey=ZDZOAQMHMJXDBU-SATBOSKTSA-N
InChI=1S/C17H16Cl2N2O3.ClH/c1-2-7-22-9-14-10-23-17(24-14,11-21-6-5-20-12-21)15-4-3-13(18)8-16(15)19;/h1,3-6,8,12,14H,7,9-11H2;1H/t14-,17-;/m1./s1
| 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 | C17H16Cl2N2O3 |
| Molecular Weight | 367.227 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Parconazole is used in veterinary as an oral fungicide with a broad-spectrum activity against dermatophytes, yeasts, and others fungi. This compound does not have any antibacterial effect. The mechanism of action involves inhibition of the fungal cytochrome P450 dependent 14alpha-dimethylation of lanosterol to ergosterol.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:27:23 GMT 2025
by
admin
on
Mon Mar 31 18:27:23 GMT 2025
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| Record UNII |
8IF7HES548
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C514
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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300000023786
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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263-777-7
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admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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CHEMBL2110654
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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DTXSID00212181
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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PRIMARY | |||
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C66317
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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PRIMARY | |||
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8IF7HES548
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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PRIMARY | |||
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3047813
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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PRIMARY | |||
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62973-77-7
Created by
admin on Mon Mar 31 18:27:23 GMT 2025 , Edited by admin on Mon Mar 31 18:27:23 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |