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Founded in:
2001-12-30 -
Country:
China -
Address:
No. 2, Jinyinhu South Third Street, Jinyinhu Office, Dongxihu District, Wuhan -
Tax NO.:
91420000177568347U -
Registered Funds:
30 million yuan -
Website:
-
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Amiodarone hydrochloride |
This product belongs to Class III antiarrhythmic drugs. The main electrophysiological effect is to prolong the action potential and effective refractory period of various myocardial tissues, which is conducive to eliminating reentrant excitement. At the same time, it has mild non-competitive α and β adrenergic receptor blocking and mild Class I and IV antiarrhythmic properties. Reduce the automaticity of the sinus node. It has no effect on the resting membrane potential and action potential height. The inhibition of forward conduction of the atrioventricular bypass pathway is greater than the reverse. Due to excessive prolongation of repolarization, the electrocardiogram after oral administration has a prolonged QT interval and T wave changes, which can slow down the heart rate by 15~20% and prolong the PR and Q-T intervals by about 10%. It has a direct dilation effect on the coronary arteries and peripheral blood vessels. It can affect thyroid hormone metabolism.
More
This product belongs to Class III antiarrhythmic drugs. The main electrophysiological effect is to prolong the action potential and effective refractory period of various myocardial tissues, which is conducive to eliminating reentrant excitement. At the same time, it has mild non-competitive α and β adrenergic receptor blocking and mild Class I and IV antiarrhythmic properties. Reduce the automaticity of the sinus node. It has no effect on the resting membrane potential and action potential height. The inhibition of forward conduction of the atrioventricular bypass pathway is greater than the reverse. Due to excessive prolongation of repolarization, the electrocardiogram after oral administration has a prolonged QT interval and T wave changes, which can slow down the heart rate by 15~20% and prolong the PR and Q-T intervals by about 10%. It has a direct dilation effect on the coronary arteries and peripheral blood vessels. It can affect thyroid hormone metabolism. |
19774-82-4 | 29 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| 5-Chloro-Benzisoxazolinone-2 |
Central muscle relaxants mainly act on the spinal cord and subcortical areas of the brain to produce muscle relaxation effects. They take effect within 1 hour after oral administration and last for 3-4 hours.
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Central muscle relaxants mainly act on the spinal cord and subcortical areas of the brain to produce muscle relaxation effects. They take effect within 1 hour after oral administration and last for 3-4 hours. |
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| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| D-CAMPHOR |
A cool feeling
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A cool feeling |
0.15g | 464-49-3 | 1 |
| Chloral hydrate |
Has a certain central sedative effect
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Has a certain central sedative effect |
0.1g | 302-17-0 | 6 |
| Clove oil |
Camphor has a cooling effect, and chloral hydrate has a certain central sedative effect. This product has a mild analgesic effect on neuralgia when used externally.
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Camphor has a cooling effect, and chloral hydrate has a certain central sedative effect. This product has a mild analgesic effect on neuralgia when used externally. |
0.015ml | 8000-34-8 | 4 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Tiapride hydrochloride |
This product belongs to the benzamide antipsychotic drug, which has an inhibitory effect on the hyperfunction of dopaminergic nerves in the midbrain limbic system and an antagonistic effect on dopaminergic nerve movement disorders in the striatum, thereby producing a calming and sedative effect. It is characterized by its good effect on sensory and motor neurological diseases and psychomotor behavioral disorders. Animal experiments have confirmed that this product can block the conduction of pain impulses through the spinal thalamic tract to the reticular formation. The analgesic effect of this drug may be related to the integration of pain impulses by the thalamus. In addition, it has an antiemetic effect.
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This product belongs to the benzamide antipsychotic drug, which has an inhibitory effect on the hyperfunction of dopaminergic nerves in the midbrain limbic system and an antagonistic effect on dopaminergic nerve movement disorders in the striatum, thereby producing a calming and sedative effect. It is characterized by its good effect on sensory and motor neurological diseases and psychomotor behavioral disorders. Animal experiments have confirmed that this product can block the conduction of pain impulses through the spinal thalamic tract to the reticular formation. The analgesic effect of this drug may be related to the integration of pain impulses by the thalamus. In addition, it has an antiemetic effect. |
51012-33-0 | 12 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Indometacin |
For external use, apply an appropriate amount of this product to the affected area and rub gently, 2 to 3 times a day.
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For external use, apply an appropriate amount of this product to the affected area and rub gently, 2 to 3 times a day. |
53-86-1 | 23 |