Imidazole – Uses, Dosage, Side Effects, Interactions
Imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole.
Imidazole (ImH) is an organic compound with the formula C3N2H4. It is a white or colorless solid that is soluble in water, producing a mildly alkaline solution. In chemistry, it is an aromatic heterocycle, classified as a diazole, and has non-adjacent nitrogen atoms in meta-substitution.
Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.
Mechanism:
Imidazole has a unique structure that allows it to function as a heterocyclic aromatic compound. It is involved in various biological and pharmacological processes due to its ability to coordinate with metal ions and participate in electron transfer reactions. Imidazole also acts as a buffer in biochemical and chemical reactions, maintaining a stable pH. It can form coordination complexes with metal ions, making it important in metalloenzymes and metalloproteins.
Indications:
- Antifungal Agent: Imidazole derivatives, such as ketoconazole and miconazole, are used to treat fungal infections.
- Vasodilator: Imidazole can be used in some formulations to dilate blood vessels, aiding in conditions like Raynaud’s disease.
- Buffer Agent: Imidazole acts as a buffer in biochemical and chemical reactions.
- Chelating Agent: It can be used to chelate metal ions in analytical chemistry.
- Antiparasitic Agent: Some imidazole compounds are used in the treatment of parasitic infections.
- Chemical Synthesis: Imidazole is used as a reagent in various chemical syntheses.
- Coordination Chemistry: In coordination chemistry, imidazole is employed in the synthesis of metal complexes.
- Stabilizer: Imidazole is used in the formulation of certain pharmaceuticals and cosmetics to stabilize the product.
- Antibacterial Agent: Some imidazole derivatives have antibacterial properties.
- Research: Imidazole is used in research laboratories for a variety of applications, including protein purification and enzyme assays.
Contraindications:
- Hypersensitivity to clotrimazole or any of its components
- Use in the eyes
- Concurrent use with certain other medications without physician’s advice
- History of allergic reaction to other imidazole derivatives
- Before any diagnostic procedures of the vaginal area
- Children under a certain age without physician’s advice
- Bacterial infections (it’s anti-fungal, not antibacterial)
- Viral infections (like herpes or chickenpox)
- For internal use unless prescribed
- Use on open wounds or burns
Dosages:
- Topical preparations: Generally applied once to three times daily depending on the formulation and severity of the infection.
- Vaginal preparations: Usually inserted once daily, often at bedtime, for a duration determined by the severity of the infection.
Side Effects
- Redness
- Irritation
- Burning sensation
- Stinging
- Swelling
- Peeling
- Rash
- Itching
- Urticaria
- Blisters
- Dryness
- Crusting
- Numbness
- Edema
- Vesicles
- Pustules
- Discomfort
- Tenderness
- Foul-smelling discharge (with vaginal use)
- Abdominal cramps (with vaginal use)
- Nausea
- Contact dermatitis
- Erythema
- Scaling
- Tingling
- Maceration
- Striae (stretch marks)
- Secondary infection
- Hyperpigmentation
- Hypersensitivity reaction
Drug Interactions
- Amphotericin B
- Nystatin
- Flucytosine
- Other antifungal agents
- Topical corticosteroids
- Topical retinoids
- Topical calcineurin inhibitors
- Warfarin
- Certain antihistamines
- Certain antiseizure medications
- Certain antibiotics
- Antacids
- Certain antiarrhythmic medications
- Certain antipsychotics
- Antidiabetics
- Certain antihypertensives
- Immunosuppressants
- Antiretrovirals
- Benzodiazepines
- Beta-blockers
- Calcium channel blockers
- Certain cholesterol-lowering drugs
- Oral contraceptives
- Digitalis glycosides
- Diuretics
- Certain gastrointestinal motility drugs
- Opioid analgesics
- Certain antimalarials
- NSAIDs
- Thyroid hormones
Pregnancy and Lactation:
- Pregnancy: Clotrimazole is classified as pregnancy category B, which means there’s no evidence of risk in humans based on studies. However, it’s still crucial to consult a physician before using clotrimazole during pregnancy.
- Lactation: While clotrimazole is considered safe during breastfeeding, it’s essential to ensure that the infant doesn’t come into direct contact with treated areas
- DrugBank
Imidazole
- CAS Common Chemistry
1H-Imidazole, homopolymer1H-Imidazole, dimer
- ChemIDplus
ChemIDplus Chemical Information Classification
- DTP/NCI
- EPA Chemicals under the TSCA
1H-Imidazole
- EPA DSSTox
CompTox Chemicals Dashboard Chemical Lists
- European Chemicals Agency (ECHA)
- FDA Global Substance Registration System (GSRS)
- Hazardous Substances Data Bank (HSDB)
- Human Metabolome Database (HMDB)
HMDB0001525_cms_28004
- ILO-WHO International Chemical Safety Cards (ICSCs)
- ChEBI
- LOTUS – the natural products occurrence database
ImidazoleLOTUS Tree
- ChEMBL
ChEMBL Protein Target Tree
- Crystallography Open Database (COD)
- EPA Chemical and Products Database (CPDat)
EPA CPDat Classification
https://www.epa.gov/chemical-research/chemical-and-products-database-cpdat
- Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
Imidazole
- EU REGULATION (EC) No 1272/2008
- Hazardous Chemical Information System (HCIS), Safe Work Australia
- NITE-CMC
Imidazole – FY2012Imidazole – FY2021
- MassBank of North America (MoNA)
- NIST Mass Spectrometry Data Center
LICENSEData covered by the Standard Reference Data Act of 1968 as amended.1H-Imidazole
- SpectraBase
1H-IMIDAZOLE1H-ImidazoleIMUTEX, TECHNICALGlyoxalineImidazole1,3-diazole glyoxaline1,3-diazole glyoxaline
- Wikipedia
imidazole
- Japan Chemical Substance Dictionary (Nikkaji)
- KEGG
LICENSEAcademic users may freely use the KEGG website. Non-academic use of KEGG generally requires a commercial license
- KNApSAcK Species-Metabolite Database
- Natural Product Activity and Species Source (NPASS)
- MassBank Europe
RAXXELZNTBOGNW-UHFFFAOYSA-N
https://massbank.eu/MassBank/Result.jsp?inchikey=RAXXELZNTBOGNW-UHFFFAOYSA-N
- Metabolomics Workbench
- Nature Chemistry
- NIPH Clinical Trials Search of Japan
- NMRShiftDB
- NORMAN Suspect List Exchange
NORMAN Suspect List Exchange Classification
- Rhea – Annotated Reactions Database
- Springer Nature
- SpringerMaterials
- The Cambridge Structural Database
- Thieme Chemistry
- Wikidata
Imidazole
- Wiley
- PubChem
- Medical Subject Headings (MeSH)
Enzyme Inhibitors
- UN Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS Classification Tree
http://www.unece.org/trans/danger/publi/ghs/ghs_welcome_e.html
- EPA Substance Registry Services
EPA SRS List Classification
https://sor.epa.gov/sor_internet/registry/substreg/LandingPage.do
- PATENTSCOPE (WIPO)
SID 403029594SID 461726208

Carbimazole
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