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Founded in:
1980-11-26 -
Country:
China -
Address:
Building 18, No. 27 Chaoyang North Road, Chaoyang District, Beijing -
Tax NO.:
91110000101939631P -
Registered Funds:
660.6396 million yuan -
Website:
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Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Clotrimazole |
This product is a broad-spectrum antifungal drug with good antibacterial effect on many fungi, especially Candida albicans. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic process.
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This product is a broad-spectrum antifungal drug with good antibacterial effect on many fungi, especially Candida albicans. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic process. |
23593-75-1 | 46 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Primidone |
It is oxidized in the body to phenobarbital and phenethyl malonamide, which have anti-epileptic activity. Its anti-epileptic effect is similar to that of phenobarbital, but its intensity and toxicity are lower. It is rapidly and completely absorbed orally, reaching the peak plasma concentration in about 3 hours. The half-life is about 8 hours, and the plasma protein binding rate is 20%. It can easily pass through the blood-brain barrier, the placenta, and appear in breast milk. At therapeutic concentrations, it can reduce the excitatory effect of glutamate, enhance the inhibitory effect of gamma-aminobutyric acid, inhibit monosynaptic and polysynaptic transmission of the central nervous system, lead to a decrease in the excitability of the entire nerve cell, and increase the electrical stimulation threshold of the motor cortex. It can increase the threshold of seizures and inhibit the spread of discharges of epileptic foci.
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It is oxidized in the body to phenobarbital and phenethyl malonamide, which have anti-epileptic activity. Its anti-epileptic effect is similar to that of phenobarbital, but its intensity and toxicity are lower. It is rapidly and completely absorbed orally, reaching the peak plasma concentration in about 3 hours. The half-life is about 8 hours, and the plasma protein binding rate is 20%. It can easily pass through the blood-brain barrier, the placenta, and appear in breast milk. At therapeutic concentrations, it can reduce the excitatory effect of glutamate, enhance the inhibitory effect of gamma-aminobutyric acid, inhibit monosynaptic and polysynaptic transmission of the central nervous system, lead to a decrease in the excitability of the entire nerve cell, and increase the electrical stimulation threshold of the motor cortex. It can increase the threshold of seizures and inhibit the spread of discharges of epileptic foci. |
125-33-7 | 9 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| β-D-Glucopyranoside, [3-hydroxy-3-(methoxycarbonyl)-1,5-dioxo-1,5-pentanediyl]bis(oxymethylene-4,1-phenylene) bis- |
This product can inhibit platelet aggregation and prevent thrombosis. It can also counteract vascular damage caused by 5-hydroxytryptamine and bradykinin, increase capillary resistance, reduce capillary permeability, and prevent edema caused by increased vascular permeability.
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This product can inhibit platelet aggregation and prevent thrombosis. It can also counteract vascular damage caused by 5-hydroxytryptamine and bradykinin, increase capillary resistance, reduce capillary permeability, and prevent edema caused by increased vascular permeability. |
1971915-61-3 | 0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Fenbufen |
This product is a long-acting non-steroidal anti-inflammatory drug. After entering the body, it is metabolized into diphenyl ethyl ester, which inhibits the activity of cyclooxygenase and reduces the synthesis of prostaglandins. Animal experiments show that the anti-inflammatory and analgesic effects of this product are weaker than indomethacin, but stronger than aspirin.
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This product is a long-acting non-steroidal anti-inflammatory drug. After entering the body, it is metabolized into diphenyl ethyl ester, which inhibits the activity of cyclooxygenase and reduces the synthesis of prostaglandins. Animal experiments show that the anti-inflammatory and analgesic effects of this product are weaker than indomethacin, but stronger than aspirin. |
36330-85-5 | 8 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Domiphen bromide |
This product is a cationic surfactant with broad-spectrum bactericidal effect
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This product is a cationic surfactant with broad-spectrum bactericidal effect |
0.5mg | 0 | |
| Sucrose |
This product is a cationic surfactant with broad-spectrum bactericidal effect.
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This product is a cationic surfactant with broad-spectrum bactericidal effect. |
57-50-1 | 71 | |
| Dextrin |
This product is a cationic surfactant with broad-spectrum bactericidal effect.
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This product is a cationic surfactant with broad-spectrum bactericidal effect. |
9004-53-9 | 50 | |
| Sunset Yellow FCF |
This product is a cationic surfactant with broad-spectrum bactericidal effect.
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This product is a cationic surfactant with broad-spectrum bactericidal effect. |
2783-94-0 | 1 | |
| DL-Menthol |
This product is a cationic surfactant with broad-spectrum bactericidal effect.
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This product is a cationic surfactant with broad-spectrum bactericidal effect. |
89-78-1 | 8 | |
| Talc |
This product is a cationic surfactant with broad-spectrum bactericidal effect.
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This product is a cationic surfactant with broad-spectrum bactericidal effect. |
14807-96-6 | 26 |