Itraconazole, Cytochrome P450 inhibitor

  • Catalog number
    SIH-543-50MG
  • Price
    Please ask
  • Size
    50 mg
  • Stock availabilitIn Stock
    In Stock
  • CAS number
    84625-61-6
  • Description
    Cytochrome P450 inhibitor
  • Molecular weight
    705,6 g/mol
  • Primary research fields
    Cancer, Autophagy, Cardiovascular System, Angiogenesis, Growth Factors
  • Other name
    none
  • Product category
    Small Molecules
  • Product type
    Inhibitor
  • Chemical formula
    C35H38Cl2N8O4
  • Origin
    Synthetic
  • Purity pourcentage
    >98%
  • Soluble in
    Soluble in chloroform (50 mg/ml)
  • Physical appearance
    Contact our support service
  • Storage recommendations
    -20ºC
  • Shipping recommendations
    Shipped Ambient
  • Safety information
    Classification: D1B Toxic Material Causing Immediate and Serious Toxic Effects - Toxic by ingestion D2A Very Toxic Material Causing Other Toxic Effects - Teratogen D2B Toxic Material Causing Other Toxic Effects - Moderate skin irritant, Moderate respiratory irritant, Moderate eye irritant Hazard statement(s): H302 Harmful if swallowed. H315 Causes skin irritation. H319 Causes serious eye irritation. H335 May cause respiratory irritation. Precautionary statement(s): P261 Avoid breathing dust/ fume/ gas/ mist/ vapours/ spray. P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
  • PubChem number
    3793
  • Scientific context
    Itraconazole is an triazol antifungal agent. It inhibits P-450 dependent enzymes, which results in the inhibition of ergosterol synthesis.
  • Release date
    30/Aug/2016
  • PubMed number
    Refer to PubMed
  • Tested applications
    To be tested
  • Tested reactivity
    To be tested
  • Representative figure legend
    Chemical structure of Itraconazole (SIH-543), a Cytochrome P450 inhibitor. CAS #: 84625-61-6. Molecular Formula: C35H38Cl2N8O4. Molecular Weight: 705.6 g/mol. Chemical structure of Itraconazole, a Cytochrome P450 inhibitor (SIH-543). CAS # 84625-61-6. Molecular Formula: C35H38Cl2N8O4.
  • Warning information
    Non-hazardous
  • Country of production
    Canada
  • Total weight kg
    0.25
  • Net weight g
    0.05
  • Additional description
    Tissue, pathway, proteinase, peptidase, protease ,acrosin, lipoprotein, activator, caspase, trypsin, papain, esterase inhibitors are proteins or receptor ligands or receptor antagonists that bind to an enzyme receptor and decreases its activity. Since blocking an enzyme's activity can kill a pathogen or correct a metabolic imbalance, many drugs are enzyme inhibitors. Not all receptor antagonist that bind to enzymes are inhibitors; enzyme activator ligands or agonists bind to enzymes and increase their enzymatic activity, while enzyme substrates bind and are converted to products in the normal catalytic cycle of the enzyme.
  • Gene target
  • Gene symbol
    CYP3A7, CYP24A1, CYP1A1, CYP51A1, CYP2D6
  • Short name
    Itraconazole, Cytochrome P450 inhibitor
  • Alternative name
    Itraconazole, Cytochrome P450 suppressor
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    cytochrome P450 family 24 subfamily A member 1
  • Synonyms gene
  • Synonyms gene name
    • cytochrome P450, subfamily XXIV (vitamin D 24-hydroxylase)
    • cytochrome P450, family 24, subfamily A, polypeptide 1
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1992-09-09
  • Entrez gene record
  • Classification
    • Cytochrome P450 family 24
  • VEGA ID
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    cytochrome P450 family 51 subfamily A member 1
  • Synonyms gene
  • Synonyms gene name
    • cytochrome P450, 51 (lanosterol 14-alpha-demethylase)
    • cytochrome P450, family 51, subfamily A, polypeptide 1
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1996-10-26
  • Entrez gene record
  • Pubmed identfication
  • Classification
    • Cytochrome P450 family 51
  • VEGA ID
Gene info
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