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Founded in:
2002-06-24 -
Country:
China -
Address:
Southeast of Zhoubu Village, Huixian City -
Tax NO.:
91410700173249269M -
Registered Funds:
48 million yuan -
Website:
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Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Inosine |
Participate in cell energy metabolism and protein synthesis in the body, increase the activity of related metabolic enzymes, improve liver function, and promote the recovery of damaged liver
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Participate in cell energy metabolism and protein synthesis in the body, increase the activity of related metabolic enzymes, improve liver function, and promote the recovery of damaged liver |
0.2g | 58-63-9 | 8 |
| Starch |
Inosine participates in cellular energy metabolism and protein synthesis in the body, increases the activity of related metabolic enzymes, improves liver function, and promotes the recovery of damaged liver.
More
Inosine participates in cellular energy metabolism and protein synthesis in the body, increases the activity of related metabolic enzymes, improves liver function, and promotes the recovery of damaged liver. |
9005-25-8 | 77 | |
| Dextrin |
Inosine participates in cellular energy metabolism and protein synthesis in the body, increases the activity of related metabolic enzymes, improves liver function, and promotes the recovery of damaged liver.
More
Inosine participates in cellular energy metabolism and protein synthesis in the body, increases the activity of related metabolic enzymes, improves liver function, and promotes the recovery of damaged liver. |
9004-53-9 | 50 | |
| sugar |
Inosine participates in cellular energy metabolism and protein synthesis in the body, increases the activity of related metabolic enzymes, improves liver function, and promotes the recovery of damaged liver.
More
Inosine participates in cellular energy metabolism and protein synthesis in the body, increases the activity of related metabolic enzymes, improves liver function, and promotes the recovery of damaged liver. |
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Chlorphenamine maleate |
As a histamine H1 receptor antagonist, this product can counteract the capillary dilation caused by allergic reactions (histamine), reduce the permeability of capillaries, and relieve wheezing caused by bronchial smooth muscle contraction. This product has a long-lasting antihistamine effect and also has a significant central inhibitory effect, which can increase the effects of anesthetics, analgesics, hypnotics and local anesthetics. This product is mainly metabolized in the liver.
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As a histamine H1 receptor antagonist, this product can counteract the capillary dilation caused by allergic reactions (histamine), reduce the permeability of capillaries, and relieve wheezing caused by bronchial smooth muscle contraction. This product has a long-lasting antihistamine effect and also has a significant central inhibitory effect, which can increase the effects of anesthetics, analgesics, hypnotics and local anesthetics. This product is mainly metabolized in the liver. |
113-92-8 | 28 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| 4-(8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylic acid ethyl ester |
This product is a long-acting tricyclic antihistamine that competitively inhibits histamine H1 receptors and inhibits allergic symptoms caused by histamine. This product has no obvious anticholinergic and central nervous system inhibitory effects.
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This product is a long-acting tricyclic antihistamine that competitively inhibits histamine H1 receptors and inhibits allergic symptoms caused by histamine. This product has no obvious anticholinergic and central nervous system inhibitory effects. |
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| (+/-)-Verapamil hydrochloride |
Calcium ion antagonists exert their pharmacological effects by regulating the influx of calcium ions on the cell membranes of myocardial conduction cells, myocardial contractile cells, and arterial smooth muscle cells, but do not change the serum calcium concentration; they dilate the main coronary arteries and arterioles in normal and ischemic parts of the heart, antagonize spontaneous or ergonovine-induced coronary artery spasm, increase myocardial oxygen delivery in patients with coronary artery spasm, relieve and prevent coronary artery spasm; reduce total peripheral resistance and myocardial oxygen consumption; reduce calcium ion influx, prolong the effective refractory period of the atrioventricular node, and slow down conduction.
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Calcium ion antagonists exert their pharmacological effects by regulating the influx of calcium ions on the cell membranes of myocardial conduction cells, myocardial contractile cells, and arterial smooth muscle cells, but do not change the serum calcium concentration; they dilate the main coronary arteries and arterioles in normal and ischemic parts of the heart, antagonize spontaneous or ergonovine-induced coronary artery spasm, increase myocardial oxygen delivery in patients with coronary artery spasm, relieve and prevent coronary artery spasm; reduce total peripheral resistance and myocardial oxygen consumption; reduce calcium ion influx, prolong the effective refractory period of the atrioventricular node, and slow down conduction. |
152-11-4 | 13 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| FLUPHENAZINE HYDROCHLORIDE |
This product belongs to the piperazine phenothiazine. Its antipsychotic effect is mainly related to its blocking of dopamine receptors (DA11) in the brain, inhibiting the ascending activation system of the reticular formation and having a sedative effect. Its antiemetic and blood pressure lowering effects are weaker.
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This product belongs to the piperazine phenothiazine. Its antipsychotic effect is mainly related to its blocking of dopamine receptors (DA11) in the brain, inhibiting the ascending activation system of the reticular formation and having a sedative effect. Its antiemetic and blood pressure lowering effects are weaker. |
146-56-5 | 16 |