Zhejiang Kinglyuan Pharmaceutical Co., Ltd.
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Founded in:
2002-12-18 -
Country:
China -
Address:
No. 3, Weijiu Road, Shangyu Economic and Technological Development Zone, Hangzhou Bay, Shangyu District, Shaoxing City, Zhejiang Province -
Tax NO.:
91330604746318437J -
Registered Funds:
68.2 million yuan -
Website:
-
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Irbesartan |
Extract from the above information
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Extract from the above information |
138402-11-6 | 65 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| PEARL POWDER |
|
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| ASIAN GINSENG |
|
0 | ||
| Royal Jelly |
|
8031-67-2 | 0 | |
| Ginseng Royal Jelly Capsules |
|
0 | ||
| GLUCOSE |
|
58367-01-4 | 15 | |
| Starch |
|
9005-25-8 | 79 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Telmisartan |
Telmisartan is a specific angiotensin II receptor (ATⅠ type) antagonist, which binds to the ATⅠ receptor subtype with high affinity, has no agonist effect, and has a selective and lasting binding. It does not inhibit plasma renin, ion channels, and angiotensin converting enzyme II, and does not cause adverse reactions such as enhanced bradykinin action. 80 mg can almost completely inhibit the increase in blood pressure caused by angiotensin II, and the effect lasts for more than 24 hours. The antihypertensive effect gradually becomes obvious within 3 hours after the first dose, and the maximum antihypertensive effect can be achieved and maintained in 4 weeks. Sudden interruption of treatment will not lead to rebound hypertension. Compared with ACE inhibitors, the incidence of dry cough is significantly lower.
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Telmisartan is a specific angiotensin II receptor (ATⅠ type) antagonist, which binds to the ATⅠ receptor subtype with high affinity, has no agonist effect, and has a selective and lasting binding. It does not inhibit plasma renin, ion channels, and angiotensin converting enzyme II, and does not cause adverse reactions such as enhanced bradykinin action. 80 mg can almost completely inhibit the increase in blood pressure caused by angiotensin II, and the effect lasts for more than 24 hours. The antihypertensive effect gradually becomes obvious within 3 hours after the first dose, and the maximum antihypertensive effect can be achieved and maintained in 4 weeks. Sudden interruption of treatment will not lead to rebound hypertension. Compared with ACE inhibitors, the incidence of dry cough is significantly lower. |
144701-48-4 | 108 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Telmisartan |
Telmisartan is a specific angiotensin II receptor (ATⅠ type) antagonist. Telmisartan replaces angiotensin II receptors and binds to ATⅠ receptor subtypes (known angiotensin II action sites) with high affinity. Telmisartan has no agonist effect at any site on the ATⅠ receptor site. Telmisartan selectively binds to ATⅠ receptors and the binding effect is long-lasting. Telmisartan has no affinity for other receptors (including AT2 and other AT receptors with fewer characteristics). The functions of the above other receptors are not yet known, and the excessive receptor stimulation effect that may be caused by the increase in angiotensin II levels caused by telmisartan is also unknown. Telmisartan does not inhibit human plasma renin or block ion channels. Telmisartan does not inhibit angiotensin converting enzyme II, which can also degrade bradykinin and cause adverse reactions. In humans, administration of 80 mg of telmisartan can almost completely inhibit the increase in blood pressure caused by angiotensin II. The inhibitory effect lasts for 24 hours and can still be measured after 48 hours. The antihypertensive effect gradually becomes apparent within 3 hours after the first dose of telmisartan. The maximum antihypertensive effect can be achieved 4 weeks after the start of treatment and can be maintained in long-term treatment. If telmisartan treatment is suddenly interrupted, blood pressure gradually returns to pre-treatment levels after a few days without rebound hypertension. In a clinical trial directly comparing two antihypertensive drugs, the incidence of dry cough in the telmisartan treatment group was significantly lower than that in the angiotensin-converting enzyme inhibitor treatment group.
More
Telmisartan is a specific angiotensin II receptor (ATⅠ type) antagonist. Telmisartan replaces angiotensin II receptors and binds to ATⅠ receptor subtypes (known angiotensin II action sites) with high affinity. Telmisartan has no agonist effect at any site on the ATⅠ receptor site. Telmisartan selectively binds to ATⅠ receptors and the binding effect is long-lasting. Telmisartan has no affinity for other receptors (including AT2 and other AT receptors with fewer characteristics). The functions of the above other receptors are not yet known, and the excessive receptor stimulation effect that may be caused by the increase in angiotensin II levels caused by telmisartan is also unknown. Telmisartan does not inhibit human plasma renin or block ion channels. Telmisartan does not inhibit angiotensin converting enzyme II, which can also degrade bradykinin and cause adverse reactions. In humans, administration of 80 mg of telmisartan can almost completely inhibit the increase in blood pressure caused by angiotensin II. The inhibitory effect lasts for 24 hours and can still be measured after 48 hours. The antihypertensive effect gradually becomes apparent within 3 hours after the first dose of telmisartan. The maximum antihypertensive effect can be achieved 4 weeks after the start of treatment and can be maintained in long-term treatment. If telmisartan treatment is suddenly interrupted, blood pressure gradually returns to pre-treatment levels after a few days without rebound hypertension. In a clinical trial directly comparing two antihypertensive drugs, the incidence of dry cough in the telmisartan treatment group was significantly lower than that in the angiotensin-converting enzyme inhibitor treatment group. |
144701-48-4 | 108 |