Metabolite Card
Formula: C18H14Cl4N2O (413.986)
SMILES: ClC1=CC(Cl)=C(COC(CN2C=CN=C2)C2=C(Cl)C=C(Cl)C=C2)C=C1
Synonyms [en]
miconazole; Miconazole Nitrate; imidazole, 1-(2-(2,4-dichlorophenyl)-2-((2,4-dichlorophenyl) methoxy)ethyl)- (9CI); 1-[2-(2,4-Dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]-1H-imidazole; Miconazole (Monistat); Miconasil Nitrate
Last reviewed on 2024-06-28.
Cite this Page
Miconazole. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000026285). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Miconazole is only found in individuals that have used or taken this drug. It is an imidazole antifungal agent that is used topically and by intravenous infusion. [PubChem]Miconazole interacts with 14-α demethylase, a cytochrome P-450 enzyme necessary to convert lanosterol to ergosterol. As ergosterol is an essential component of the fungal cell membrane, inhibition of its synthesis results in increased cellular permeability causing leakage of cellular contents. Miconazole may also inhibit endogenous respiration, interact with membrane phospholipids, inhibit the transformation of yeasts to mycelial forms, inhibit purine uptake, and impair triglyceride and/or phospholipid biosynthesis.
DBLinks
- CAS Registry Number: 22916-47-8
- PubChem CID: 4189
- ChEBI: 82892
- HMDB: HMDB0015242
- LipidMaps:
- KEGG: C08070
- BioCyc: CPD-4501
- NCBI MeSH: Miconazole
- Wikipedia: Miconazole
Other DBLinks
- CAS Registry Number: 22916-47-8
- CAS Registry Number: 47447-52-9
- CAS Registry Number: 47447-53-0
- CAS Registry Number: 75319-47-0
- PubChem: 4189
- ChEBI: ChEBI:6923
- ChEBI: ChEBI:82892
- HMDB: HMDB0015242
- KEGG: C07223
- KEGG: C08070
- KEGG: D00416
- BioCyc: CPD-4501
- NCBI MeSH: Miconazole
- Wikipedia: Miconazole
- DrugBank: DB01110
- RefMet: RM0200855
- MoNA: Alkaloids000042
- MoNA: AU270602
- MoNA: AU270603
- MoNA: AU270604
- MoNA: AU270605
- MoNA: AU270606
- MoNA: CCMSLIB00000078506
- MoNA: SM860201
- MoNA: TOF_alkaloids_pos000037
- Metlin: METLIN_1283
- Coconut NaturalProduct: CNP0194606.1
- Coconut NaturalProduct: CNP0194606.2
Class / Ontology
- WishartLab ClassyFire: [Benzylethers] Benzylethers
- RefMet: [Benzylethers] Benzylethers
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| BioCyc:META_PWY-5469 | sesamin biosynthesis |
| BioCyc:META_PWY-5660 | taxol biosynthesis |
| BioCyc:META_PWY-6074 | zymosterol biosynthesis |
| BioCyc:HUMAN_PWY66-5 | superpathway of cholesterol biosynthesis |
| BioCyc:HUMAN_PWY66-341 | cholesterol biosynthesis I |
| BioCyc:META_PWY-5048 | rosmarinic acid biosynthesis I |
| BioCyc:META_PWY-5071 | superpathway of rosmarinic acid biosynthesis |
| BioCyc:HUMAN_PWY66-4 | cholesterol biosynthesis III (via desmosterol) |
| PlantCyc:PLANT_PWY-5469 | sesamin biosynthesis |
| PlantCyc:PLANT_PWY-5048 | rosmarinic acid biosynthesis I |
| PlantCyc:PLANT_PWY-5071 | superpathway of rosmarinic acid biosynthesis |