A selective β2 receptor agonist, it has a strong and lasting dilating effect on bronchial smooth muscle, and a weaker excitatory effect on the heart. Its effect in relaxing bronchial smooth muscle is 2-10 times that of clofarabine, and its excitatory effect on the heart is 1/1000 of that of isoproterenol, and its duration of action is more than 10 times longer than that of isoproterenol. Clinically, it has obvious antiasthmatic effect and certain antitussive effect, and takes effect within 5-10 minutes after oral administration, and the effect can last for 4-6 hours.

Extract from the above information

Fluconazole is a triazole broad-spectrum antifungal drug that inhibits the reproduction and growth of fungi by highly selectively inhibiting the C-14-alpha;-demethylation of fungal cytochrome P-450 sterols, causing the accumulation of 14-alpha;-methyl sterols in fungi. In vitro tests have shown that this product has antibacterial activity against Cryptococcus neoformans and Candida species. Oral and intravenous injection of fluconazole in animals is effective in the following animal fungal infection models: Candida infection (including systemic candidiasis in immunodeficient animals); Cryptococcus neoformans infection (including intracranial infection); Microsporum and Trichophyton infection, etc. Fluconazole is also effective against Blastomyces dermatitidis infection and Coccidioides immitis infection (including intracranial infection); and is also effective against infections caused by Histoplasma capsulatum in normal animals and immunosuppressed animals.