Di'ao Group Chengdu Pharmaceutical Co., Ltd.

It is a broad-spectrum anthelmintic that can inhibit the intestinal parasites' glucose uptake, leading to the depletion of glycogen in the worms and reducing the formation of adenosine triphosphate in the worms. However, it does not affect the host's blood glucose level. Ultrastructural observation showed that mebendazole caused the degeneration of microtubules in the cytoplasm of the worm's membrane cells and intestinal cells, resulting in the accumulation of Golgi endocrine granules. Transport blockage, cytoplasmic dissolution, and complete degeneration of absorptive cells caused the death of the worms. Mebendazole has the effect of completely killing hookworm eggs and whipworm eggs and partially killing ascarid eggs. In vitro tests have shown that 5 mg/L can inhibit the development of hookworm larvae.

It can selectively inhibit succinate dehydrogenase in the muscles of the worm, so that fumaric acid cannot be reduced to succinic acid, thereby affecting the anaerobic metabolism of the muscles of the worm and reducing energy production. In addition, the drug may have an inhibitory effect on the microtubule structure of the worm. Levamisole also has immune regulation and immune stimulation functions.

Benoryl ester is a neutral compound formed by ester bonding of aspirin and acetaminophen. It has antipyretic and analgesic effects, with fewer adverse reactions than aspirin and is easier to tolerate. After oral administration, it is not hydrolyzed in the gastrointestinal tract, is absorbed in the intestine and quickly reaches an effective concentration in the blood. It is characterized by rarely causing gastrointestinal bleeding.

Participate in the formation of coenzymes in the body and prevent vitamin B1 deficiency

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Extract from the above information

This product is an antifungal drug, which is effective against Candida albicans, Coccidioides, Cryptococcus neoformans, Histoplasma capsulatum, Blastomyces dermatitidis, and dermatophytes. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic process.

This product is an antifungal drug, which is effective against Candida albicans, Coccidioides, Cryptococcus neoformans, Histoplasma capsulatum, Blastomyces dermatitidis, and dermatophytes. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic process.

This product is an antifungal drug, which is effective against Candida albicans, Coccidioides, Cryptococcus neoformans, Histoplasma capsulatum, Blastomyces dermatitidis, and dermatophytes. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic process.

This product is an antifungal drug, which is effective against Candida albicans, Coccidioides, Cryptococcus neoformans, Histoplasma capsulatum, Blastomyces dermatitidis, and dermatophytes. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic process.