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Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
  • Founded in:

    1995-08-08
  • Country:

    China China
  • Address:

    No. 333, Jiangnan Road, Hengdian, Dongyang City, Zhejiang Province
  • Tax NO.:

    913307831475538495
  • Registered Funds:

    108.75 million yuan
  • Website:

  • Email:

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Indapamide Tablets
Indapamide, N-(2-methyl-2,3-dihydro-1H-indolyl)-3-sulfamoyl-4-chlorobenzamide. [Molecular formula] C16H16ClN3O3S [Molecular weight] 365.8 [Structural formula]
Name Description Content CAS NO. Registered Holders
Indapamide

It achieves a diuretic effect by inhibiting the reabsorption of sodium by the dilution segment of the renal cortex, increasing the excretion of urinary sodium and chloride, and to a lesser extent, potassium and magnesium, thereby increasing urine volume and exerting an antihypertensive effect. Its antihypertensive effect is related to its improvement of arterial compliance and reduction of arteriolar and entire peripheral circulation resistance. It can reverse left ventricular hypertrophy caused by hypertension. It does not affect lipid metabolism and carbohydrate metabolism.

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It achieves a diuretic effect by inhibiting the reabsorption of sodium by the dilution segment of the renal cortex, increasing the excretion of urinary sodium and chloride, and to a lesser extent, potassium and magnesium, thereby increasing urine volume and exerting an antihypertensive effect. Its antihypertensive effect is related to its improvement of arterial compliance and reduction of arteriolar and entire peripheral circulation resistance. It can reverse left ventricular hypertrophy caused by hypertension. It does not affect lipid metabolism and carbohydrate metabolism.

26807-65-8 28
Liver Cleansing Granules
Isatis root, Artemisia capillaris, Licorice root
Name Description Content CAS NO. Registered Holders
Isatidis Radix

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Artemisiae Scopariae Herba

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DGL

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Cucurbitacin Tablets
Cucurbitacin.
Name Description Content CAS NO. Registered Holders
CUCURBITACIN I

No specific pharmacological effects mentioned

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No specific pharmacological effects mentioned

2222-07-3 0
Ofloxacin Tablets
The chemical name of this product is (±)-9-fluoro-2,3-dihydro-trimethyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyridinium[1,2,3-de][1,4]benzoxazine-6-carboxylic acid, and its molecular weight is 361.37.
Name Description Content CAS NO. Registered Holders
(±)-9-Fluoro-2,3-dihydro-trimethyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyridinium[1,2,3-de][1,4]benzoxazine-6-carboxylic acid

This product has a broad-spectrum antibacterial effect, especially high antibacterial activity against aerobic Gram-negative bacilli, and has high antibacterial activity against penicillin-resistant Neisseria gonorrhoeae, enzyme-producing Haemophilus influenzae, and Moraxella. It has antibacterial activity against most strains of Pseudomonas, such as Pseudomonas aeruginosa. It has antibacterial activity against methicillin-sensitive Staphylococci, and only moderate antibacterial activity against Streptococcus pneumoniae, hemolytic Streptococcus, and Enterococcus faecalis. It has good antimicrobial effects against Chlamydia trachomatis, Mycoplasma, and Legionella, and also has antibacterial activity against Mycobacterium tuberculosis and atypical mycobacteria. It has poor antibacterial activity against anaerobic bacteria. Ofloxacin is a bactericide that acts on the A subunit of bacterial DNA helicase, inhibiting DNA synthesis and replication, leading to bacterial death.

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This product has a broad-spectrum antibacterial effect, especially high antibacterial activity against aerobic Gram-negative bacilli, and has high antibacterial activity against penicillin-resistant Neisseria gonorrhoeae, enzyme-producing Haemophilus influenzae, and Moraxella. It has antibacterial activity against most strains of Pseudomonas, such as Pseudomonas aeruginosa. It has antibacterial activity against methicillin-sensitive Staphylococci, and only moderate antibacterial activity against Streptococcus pneumoniae, hemolytic Streptococcus, and Enterococcus faecalis. It has good antimicrobial effects against Chlamydia trachomatis, Mycoplasma, and Legionella, and also has antibacterial activity against Mycobacterium tuberculosis and atypical mycobacteria. It has poor antibacterial activity against anaerobic bacteria. Ofloxacin is a bactericide that acts on the A subunit of bacterial DNA helicase, inhibiting DNA synthesis and replication, leading to bacterial death.

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Albendazole granules
Main ingredient: Albendazole Chemical name: [5-(propylthio)-1H-benzimidazol-2-yl] methyl carbamate. Molecular formula: C12H15N3O2S Molecular weight: 265.34
Name Description Content CAS NO. Registered Holders
Albendazole

This product is a benzimidazole derivative, which is rapidly metabolized into sulfoxide, sulfone alcohol and 2-amine sulfone alcohol in the body. It selectively and irreversibly inhibits the polymerization of the microtubule system of the parasite's intestinal wall cells, blocks its absorption of various nutrients and glucose, leads to the depletion of endogenous glycogen in the worm, and inhibits the fumarate reductase system, preventing the production of adenosine triphosphate, making it impossible for the worm to survive and reproduce. Similar to mebendazole, this product can also cause the degeneration of the cytoplasmic microtubules of the worm's intestinal cells, and bind to its microtubule protein, causing intracellular transport blockage, resulting in the accumulation of Golgi endocrine granules, the gradual dissolution of the cytoplasm, and the complete degeneration of the absorbing cells, causing the death of the worm. This product has the effect of completely killing hookworm eggs and whipworm eggs and partially killing ascarid eggs. In addition to killing and expelling various nematodes parasitic in animals, it also has a significant killing and expelling effect on tapeworms and cysticerci.

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This product is a benzimidazole derivative, which is rapidly metabolized into sulfoxide, sulfone alcohol and 2-amine sulfone alcohol in the body. It selectively and irreversibly inhibits the polymerization of the microtubule system of the parasite's intestinal wall cells, blocks its absorption of various nutrients and glucose, leads to the depletion of endogenous glycogen in the worm, and inhibits the fumarate reductase system, preventing the production of adenosine triphosphate, making it impossible for the worm to survive and reproduce. Similar to mebendazole, this product can also cause the degeneration of the cytoplasmic microtubules of the worm's intestinal cells, and bind to its microtubule protein, causing intracellular transport blockage, resulting in the accumulation of Golgi endocrine granules, the gradual dissolution of the cytoplasm, and the complete degeneration of the absorbing cells, causing the death of the worm. This product has the effect of completely killing hookworm eggs and whipworm eggs and partially killing ascarid eggs. In addition to killing and expelling various nematodes parasitic in animals, it also has a significant killing and expelling effect on tapeworms and cysticerci.

54965-21-8 27
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