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Postion:Product Catalog >API>Synthetic Anti-infective Drugs>Antifungal Drugs>Itraconazole
Itraconazole
  • Itraconazole

Itraconazole NEW

Price $34 $48 $178
Package 50mg 100mg 500mg
Min. Order:
Supply Ability: 10g
Update Time: 2025-07-24

Product Details

Product Name: Itraconazole CAS No.: 84625-61-6
Purity: 99.90% Supply Ability: 10g
Release date: 2025/07/24

Product Introduction

Bioactivity

NameItraconazole
DescriptionItraconazole (R51211) is a triazole antifungal agent that inhibits cytochrome P-450-dependent enzymes necessary for ERGOSTEROL synthesis.
In vitroLike other Hedgehog (Hh) pathway antagonists, Itraconazole can inhibit the activity of the Hh pathway and the growth of medulloblastoma in a murine syngeneic transplant model.
In vivoItraconazole exhibits affinity for mammalian cytochrome P-450 enzymes and fungal P-450-dependent enzymes, thereby possessing potential for clinically significant interactions with azoles (e.g., simvastatin, terfenadine, rifampin, oral contraceptives, H2 receptor antagonists, warfarin, cyclosporine). Metabolized into hydroxy-itraconazole (OH-ITZ) and two novel metabolites, keto-itraconazole (keto-ITZ) and N-desalkyl itraconazole (ND-ITZ), its metabolites are inhibitors of CYP3A4 as potent, or more so, than itraconazole itself. Itraconazole acts on the hedgehog (Hh) signaling pathway component Smoothened with a mechanism distinct from cyclopamine and other known SMO antagonists, preventing SMO accumulation stimulated by Hh activation. It inhibits 60 clinical isolates of Aspergillus with MICs at 0.25 mg/mL, primarily by damaging ergosterol synthesis, leading to defective fungal cell membranes with altered permeability and function.
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility InformationDMSO : 7.06 mg/mL (10 mM), Sonication is recommended.
10% DMSO+40% PEG300+5% Tween 80+45% Saline : 0.71 mg/mL (1.01 mM), Suspension.
KeywordsTriazole | Smoothened | R-51211 | R 51211 | lanosterol | Itraconazole | Inhibitor | inhibit | Hedgehog | Fungal | ergosterol | Cytochrome P450 | CYPs | CYP-450 | CYP3A4 | Autophagy | antifungal | anticancer | Antibiotic | antiangiogenic | 14α-demethylase
Inhibitors RelatedNeomycin sulfate | Stavudine | Cysteamine hydrochloride | Kanamycin sulfate | Sulfamethoxazole sodium | Terbinafine hydrochloride | Hydroxychloroquine | Guanidine hydrochloride | Doxycycline | Paeonol | Naringin | Alginic acid
Related Compound LibrariesBioactive Compound Library | Anti-Fungal Compound Library | Drug Repurposing Compound Library | Natural Product Library for HTS | Anti-Cancer Approved Drug Library | FDA-Approved Drug Library | Immunology/Inflammation Compound Library | Cosmetic Ingredient Compound Library | Bitter Compound library | GPCR Compound Library | Anti-Cancer Drug Library | Anti-Cancer Active Compound Library

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, MA
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