-
Founded in:
1999-01-16 -
Country:
China -
Address:
No. 6, Xiyou Road, Yanhe Community, Changqing Street, Baohe District, Hefei City -
Tax NO.:
91340100711742115T -
Registered Funds:
53.5 million yuan -
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Nateglinide |
Nateglinide is an amino acid derivative and an oral antidiabetic drug used to treat patients with type 2 diabetes. The action of nateglinide depends on the function of pancreatic beta cells. Nateglinide binds to the ATP-sensitive K channel receptor on the beta cell membrane and closes it, causing cell depolarization, calcium channel opening, calcium influx, stimulating insulin secretion, and lowering blood sugar. The insulin secretion-promoting effect of nateglinide depends on the glucose level. When the glucose level is low, the insulin secretion is weakened. Nateglinide has a high degree of tissue selectivity and has a low affinity for cardiac muscle and skeletal muscle.
More
Nateglinide is an amino acid derivative and an oral antidiabetic drug used to treat patients with type 2 diabetes. The action of nateglinide depends on the function of pancreatic beta cells. Nateglinide binds to the ATP-sensitive K channel receptor on the beta cell membrane and closes it, causing cell depolarization, calcium channel opening, calcium influx, stimulating insulin secretion, and lowering blood sugar. The insulin secretion-promoting effect of nateglinide depends on the glucose level. When the glucose level is low, the insulin secretion is weakened. Nateglinide has a high degree of tissue selectivity and has a low affinity for cardiac muscle and skeletal muscle. |
105816-04-4 | 24 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Nateglinide |
Nateglinide is an amino acid derivative and an oral antidiabetic drug used to treat patients with type 2 diabetes. The action of nateglinide depends on the function of pancreatic beta cells. Nateglinide binds to the ATP-sensitive K channel receptor on the beta cell membrane and closes it, causing cell depolarization, calcium channel opening, calcium influx, stimulating insulin secretion, and lowering blood sugar. The insulin secretion-promoting effect of nateglinide depends on the glucose level. When the glucose level is low, the insulin secretion is weakened. Nateglinide has a high degree of tissue selectivity and has a low affinity for cardiac muscle and skeletal muscle.
More
Nateglinide is an amino acid derivative and an oral antidiabetic drug used to treat patients with type 2 diabetes. The action of nateglinide depends on the function of pancreatic beta cells. Nateglinide binds to the ATP-sensitive K channel receptor on the beta cell membrane and closes it, causing cell depolarization, calcium channel opening, calcium influx, stimulating insulin secretion, and lowering blood sugar. The insulin secretion-promoting effect of nateglinide depends on the glucose level. When the glucose level is low, the insulin secretion is weakened. Nateglinide has a high degree of tissue selectivity and has a low affinity for cardiac muscle and skeletal muscle. |
105816-04-4 | 24 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Nateglinide |
Nateglinide is an amino acid derivative and an oral antidiabetic drug used to treat patients with type 2 diabetes. The action of nateglinide depends on the function of pancreatic beta cells. Nateglinide binds to the ATP-sensitive K channel receptor on the beta cell membrane and closes it, causing cell depolarization, calcium channel opening, calcium influx, stimulating insulin secretion, and lowering blood sugar. The insulin secretion-promoting effect of nateglinide depends on the glucose level. When the glucose level is low, the insulin secretion is weakened. Nateglinide has a high degree of tissue selectivity and has a low affinity for cardiac muscle and skeletal muscle.
More
Nateglinide is an amino acid derivative and an oral antidiabetic drug used to treat patients with type 2 diabetes. The action of nateglinide depends on the function of pancreatic beta cells. Nateglinide binds to the ATP-sensitive K channel receptor on the beta cell membrane and closes it, causing cell depolarization, calcium channel opening, calcium influx, stimulating insulin secretion, and lowering blood sugar. The insulin secretion-promoting effect of nateglinide depends on the glucose level. When the glucose level is low, the insulin secretion is weakened. Nateglinide has a high degree of tissue selectivity and has a low affinity for cardiac muscle and skeletal muscle. |
105816-04-4 | 24 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Thiamine chloride |
Vitamin B1 is an important component of coenzymes required for sugar metabolism
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Vitamin B1 is an important component of coenzymes required for sugar metabolism |
3mg | 59-43-8 | 9 |
| Riboflavin |
Vitamin B2 is an important coenzyme component required for tissue respiration
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Vitamin B2 is an important coenzyme component required for tissue respiration |
1.5mg | 83-88-5 | 19 |
| Vitamin B6 |
Vitamin B6 is a cofactor for many enzymes and is involved in the metabolism of amino acids and fats.
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Vitamin B6 is a cofactor for many enzymes and is involved in the metabolism of amino acids and fats. |
0.2mg | 8059-24-3 | 13 |
| Nicotinamide |
Nicotinamide is a component of coenzymes I and II, essential for lipid metabolism and oxidation of tissue respiration
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Nicotinamide is a component of coenzymes I and II, essential for lipid metabolism and oxidation of tissue respiration |
10mg | 98-92-0 | 12 |
| Calcium D-Pantothenate |
Calcium pantothenate is a component of coenzyme A and is involved in the metabolism of sugar, fat, and protein.
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Calcium pantothenate is a component of coenzyme A and is involved in the metabolism of sugar, fat, and protein. |
1mg | 137-08-6 | 8 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Benproperine phosphate |
This product is a non-addictive antitussive drug that can inhibit the cough center, inhibit the pulmonary vagus nerve reflex caused by lung and pleural stretch receptors, and relax bronchial smooth muscles. That is, it has both central and peripheral antitussive mechanisms.
More
This product is a non-addictive antitussive drug that can inhibit the cough center, inhibit the pulmonary vagus nerve reflex caused by lung and pleural stretch receptors, and relax bronchial smooth muscles. That is, it has both central and peripheral antitussive mechanisms. |
19428-14-9 | 19 |