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Founded in:
2002-01-10 -
Country:
China -
Address:
Zhuangdian Pharmaceutical Park, Chuxiong High-tech Zone, Yunnan Province -
Tax NO.:
915304027342981338 -
Registered Funds:
19.8 million yuan -
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Palmitoyl Hydrochloride |
1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori.
More
1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori. |
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Palmitoyl Hydrochloride |
1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori.
More
1. Outstanding antibacterial effect: It has obvious antibacterial effect on Staphylococcus, Candida (fungus), Asian B virus, acid-fast bacilli and various Gram-positive and negative bacteria; 2. It has obvious inhibitory effect on Gram-positive and negative bacteria; 3. Enhance immune function: strengthen the body's defense function (enhance the phagocytic ability of white blood cells); 4. It has obvious antibacterial effect on Helicobacter pylori. |
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Acetaminophen |
It is a peripheral analgesic. Its mechanism of action is to inhibit the synthesis and release of prostaglandins (PGE1) in the hypothalamic temperature regulation center, thereby causing peripheral vasodilation and sweating to achieve an antipyretic effect. At the same time, it can inhibit the effects of PGE1, bradykinin and histamine, increase the pain threshold and produce analgesic effect.
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It is a peripheral analgesic. Its mechanism of action is to inhibit the synthesis and release of prostaglandins (PGE1) in the hypothalamic temperature regulation center, thereby causing peripheral vasodilation and sweating to achieve an antipyretic effect. At the same time, it can inhibit the effects of PGE1, bradykinin and histamine, increase the pain threshold and produce analgesic effect. |
0.15g | 103-90-2 | 68 |
| Aminopyrine |
It can inhibit the synthesis and release of prostaglandins in the hypothalamus, restore the normal responsiveness of the receptor neurons in the body temperature regulation center and have an antipyretic effect; at the same time, it also has an analgesic effect by inhibiting the synthesis of prostaglandins, etc., and can inhibit the synthesis and release of prostaglandins in local inflammatory tissues, stabilize lysosomal enzymes, and affect the phagocytic function of macrophages to have an anti-inflammatory effect.
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It can inhibit the synthesis and release of prostaglandins in the hypothalamus, restore the normal responsiveness of the receptor neurons in the body temperature regulation center and have an antipyretic effect; at the same time, it also has an analgesic effect by inhibiting the synthesis of prostaglandins, etc., and can inhibit the synthesis and release of prostaglandins in local inflammatory tissues, stabilize lysosomal enzymes, and affect the phagocytic function of macrophages to have an anti-inflammatory effect. |
0.1g | 0 | |
| Caffeine |
It is a central nervous system stimulant that can excite the cerebral cortex, increase sensitivity to the outside world, constrict cerebral blood vessels, and enhance the effect of the first two drugs in relieving headaches.
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It is a central nervous system stimulant that can excite the cerebral cortex, increase sensitivity to the outside world, constrict cerebral blood vessels, and enhance the effect of the first two drugs in relieving headaches. |
30mg | 0 | |
| Chlorphenamine maleate |
It has a strong histamine H1 receptor blocking effect, can alleviate other respiratory symptoms caused by allergies, and also has a mild inhibitory effect on the central nervous system.
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It has a strong histamine H1 receptor blocking effect, can alleviate other respiratory symptoms caused by allergies, and also has a mild inhibitory effect on the central nervous system. |
2mg | 113-92-8 | 28 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Sulfamethoxazole |
After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.
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After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk. |
0.4g | 723-46-6 | 33 |
| Trimethoprim |
After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk.
More
After oral administration, it is completely absorbed from the gastrointestinal tract, and the peak blood concentration is reached 1 to 4 hours after taking the drug. It is mainly filtered through the glomeruli and secreted by the renal tubules. The urine concentration is significantly higher than the blood concentration. It can be widely distributed in tissues and body fluids throughout the body, and can penetrate the blood-cerebrospinal fluid barrier to reach therapeutic concentrations. It can also cross the blood-placental barrier, enter the fetal blood circulation, and can be secreted into breast milk. |
0.08g | 738-70-5 | 44 |