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Anhui Huarun Jinchan Pharmaceutical Co., Ltd.
  • Founded in:

    2000-07-18
  • Country:

    China China
  • Address:

    No. 39, Longfa Road, Huaibei City, Anhui Province
  • Tax NO.:

    913406007199864132
  • Registered Funds:

    165.9 million yuan
  • Website:

  • Email:

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Oryzanol Tablets
Oryzanol
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Gamma oryzanol

This product has the function of regulating autonomic nervous system dysfunction and endocrine balance disorders.

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This product has the function of regulating autonomic nervous system dysfunction and endocrine balance disorders.

11042-64-1 10
Lincomycin Hydrochloride Injection
The main ingredient is lincomycin hydrochloride, and its chemical name is 6-(1-methyl-trans-4-propyl-L-2-pyrrolidinecarboxamido)-1-thio-6,8-dideoxy-D-erythro-alpha;-D-galacto-octinopyranoside hydrochloride hydrate. Its structural formula is: Molecular formula: C18H34N2O6SHClH2O Molecular weight: 461.02
Name Description Content CAS NO. Registered Holders
Lincomycin hydrochloride

It has high antibacterial activity against common aerobic Gram-positive bacteria, such as Staphylococcus aureus (including those resistant to penicillin G), Staphylococcus epidermidis, β-hemolytic Streptococcus, viridans Streptococcus and Streptococcus pneumoniae. It has good antibacterial effect on anaerobic bacteria, including Clostridium diphtheriae, and Clostridium perfringens. It has no activity against Gram-negative bacteria such as Enterococcus, meningococci, Neisseria gonorrhoeae, and Haemophilus influenzae, as well as fungi. There is no cross-resistance with penicillin, chloramphenicol, cephalosporins and tetracyclines, and there is partial cross-resistance with macrolides. It acts on the 50S subunit of the ribosome of sensitive bacteria, preventing the extension of the peptide chain, thereby inhibiting the protein synthesis of bacterial cells. It is generally an antibacterial agent, but at high concentrations, it also has a bactericidal effect on certain bacteria.

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It has high antibacterial activity against common aerobic Gram-positive bacteria, such as Staphylococcus aureus (including those resistant to penicillin G), Staphylococcus epidermidis, β-hemolytic Streptococcus, viridans Streptococcus and Streptococcus pneumoniae. It has good antibacterial effect on anaerobic bacteria, including Clostridium diphtheriae, and Clostridium perfringens. It has no activity against Gram-negative bacteria such as Enterococcus, meningococci, Neisseria gonorrhoeae, and Haemophilus influenzae, as well as fungi. There is no cross-resistance with penicillin, chloramphenicol, cephalosporins and tetracyclines, and there is partial cross-resistance with macrolides. It acts on the 50S subunit of the ribosome of sensitive bacteria, preventing the extension of the peptide chain, thereby inhibiting the protein synthesis of bacterial cells. It is generally an antibacterial agent, but at high concentrations, it also has a bactericidal effect on certain bacteria.

859-18-7 30
Compound acetaminophen tablets
This product is a compound preparation. Each tablet contains the main ingredients of 126 mg of acetaminophen, 230 mg of aspirin, and 30 mg of caffeine.
Name Description Content CAS NO. Registered Holders
Acetaminophen

By inhibiting cyclooxygenase, it selectively inhibits the synthesis of prostaglandins in the hypothalamic temperature regulation center, leading to peripheral vasodilation and sweating to achieve an antipyretic effect; by inhibiting the synthesis and release of prostaglandins, it increases the pain threshold and has an analgesic effect. It is a peripheral analgesic, weaker than aspirin, and is only effective for mild and moderate pain. This product has no obvious anti-inflammatory effect.

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By inhibiting cyclooxygenase, it selectively inhibits the synthesis of prostaglandins in the hypothalamic temperature regulation center, leading to peripheral vasodilation and sweating to achieve an antipyretic effect; by inhibiting the synthesis and release of prostaglandins, it increases the pain threshold and has an analgesic effect. It is a peripheral analgesic, weaker than aspirin, and is only effective for mild and moderate pain. This product has no obvious anti-inflammatory effect.

126mg 103-90-2 68
Acetylsalicylic acid

By inhibiting cyclooxygenase, it selectively inhibits the synthesis of prostaglandins in the hypothalamic temperature regulation center, leading to peripheral vasodilation and sweating to achieve the effect of antipyretic; by inhibiting the synthesis and release of prostaglandins, it increases the pain threshold and plays an analgesic role. It is a peripheral analgesic, with a stronger effect than acetaminophen, and is only effective for mild and moderate pain. This product has no obvious anti-inflammatory effect.

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By inhibiting cyclooxygenase, it selectively inhibits the synthesis of prostaglandins in the hypothalamic temperature regulation center, leading to peripheral vasodilation and sweating to achieve the effect of antipyretic; by inhibiting the synthesis and release of prostaglandins, it increases the pain threshold and plays an analgesic role. It is a peripheral analgesic, with a stronger effect than acetaminophen, and is only effective for mild and moderate pain. This product has no obvious anti-inflammatory effect.

230mg 50-78-2 35
Caffeine

It can help enhance the antipyretic and analgesic effects, but its individual pharmacological mechanism is not specifically explained.

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It can help enhance the antipyretic and analgesic effects, but its individual pharmacological mechanism is not specifically explained.

30mg 0
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