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Nanjing Chia Tai-tianqing Pharmaceutical Co., Ltd.
  • Founded in:

    2001-08-31
  • Country:

    China China
  • Address:

    No. 9 Huiou Road, Nanjing Economic and Technological Development Zone
  • Tax NO.:

    91320100730586189T
  • Registered Funds:

    336.031726 yuan
  • Website:

  • Email:

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Irbesartan and Hydrochlorothiazide Tablets
This product is a compound preparation of irbesartan and hydrochlorothiazide. Its composition is: each tablet contains 150mg of irbesartan and 12.5mg of hydrochlorothiazide.
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Irbesartan

It offsets the compensatory mechanism induced by diuretics, enhances the antihypertensive effect of diuretics, selectively blocks AT1 subtype receptors to exert antihypertensive effects, and weakens the increase in serum uric acid and decrease in blood potassium induced by hydrochlorothiazide.

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It offsets the compensatory mechanism induced by diuretics, enhances the antihypertensive effect of diuretics, selectively blocks AT1 subtype receptors to exert antihypertensive effects, and weakens the increase in serum uric acid and decrease in blood potassium induced by hydrochlorothiazide.

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Hydrochlorothiazide

It causes activation of the sympathetic nervous system and the renin-angiotensin system, counteracts the antihypertensive effect, and reduces blood potassium levels. Combination with irbesartan can enhance the antihypertensive effect.

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It causes activation of the sympathetic nervous system and the renin-angiotensin system, counteracts the antihypertensive effect, and reduces blood potassium levels. Combination with irbesartan can enhance the antihypertensive effect.

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Azasetron Hydrochloride Injection
The main ingredient of this product is azasetron hydrochloride
Name Description Content CAS NO. Registered Holders
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Azasetron hydrochloride is a selective 5-HT3 receptor antagonist, which has a significant inhibitory effect on nausea and vomiting caused by anticancer drugs such as cisplatin. Animal studies have shown that the affinity of azasetron hydrochloride for the 5-HT3 receptor in the rat cerebral cortex is about 410 times stronger than that of metoclopramide, twice that of ondansetron, and basically the same as that of granisetron.

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Azasetron hydrochloride is a selective 5-HT3 receptor antagonist, which has a significant inhibitory effect on nausea and vomiting caused by anticancer drugs such as cisplatin. Animal studies have shown that the affinity of azasetron hydrochloride for the 5-HT3 receptor in the rat cerebral cortex is about 410 times stronger than that of metoclopramide, twice that of ondansetron, and basically the same as that of granisetron.

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Puerarin Glucose Injection
The main ingredient of this product is puerarin. The chemical name of puerarin is: 8-β-D-glucose pyranose-4',7-dihydroxyisoflavone. Molecular formula: C21H20O9 Molecular weight: 416.4 The auxiliary materials are glucose, EDTA-2Na and water for injection, and appropriate amount of NaOH or HCl is added to adjust the pH value.
Name Description Content CAS NO. Registered Holders
Puerarin

Animal experiments have shown that (1) Effects on smooth muscle: Various total flavonoid compounds in Pueraria root have the effect of relaxing smooth muscle; (2) Effects on body temperature: Oral administration of Pueraria root decoction or ethanol infusion can reduce the body temperature of febrile rabbits, and the effect of the infusion is particularly obvious; (3) Effects on the cardiovascular system: Pueraria root has a certain antihypertensive effect on normal and hypertensive animals. Pueraria root total flavonoids and puerarin have a significant effect of dilating coronary arteries, which can increase coronary blood flow, reduce vascular resistance, and inhibit thrombin-induced 5-HT release in platelets.

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Animal experiments have shown that (1) Effects on smooth muscle: Various total flavonoid compounds in Pueraria root have the effect of relaxing smooth muscle; (2) Effects on body temperature: Oral administration of Pueraria root decoction or ethanol infusion can reduce the body temperature of febrile rabbits, and the effect of the infusion is particularly obvious; (3) Effects on the cardiovascular system: Pueraria root has a certain antihypertensive effect on normal and hypertensive animals. Pueraria root total flavonoids and puerarin have a significant effect of dilating coronary arteries, which can increase coronary blood flow, reduce vascular resistance, and inhibit thrombin-induced 5-HT release in platelets.

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Puerarin Glucose Injection
The main ingredient of this product is puerarin. The chemical name of puerarin is: 8-β-D-glucose pyranose-4',7-dihydroxyisoflavone. Molecular formula: C21H20O9 Molecular weight: 416.4 The auxiliary materials are glucose, EDTA-2Na and water for injection, and appropriate amount of NaOH or HCl is added to adjust the pH value.
Name Description Content CAS NO. Registered Holders
Puerarin

Animal experiments have shown the following: (1) Effects on smooth muscle: various total flavonoid compounds in Pueraria root have the effect of relaxing smooth muscle; (2) Effects on body temperature: Pueraria root can reduce the body temperature of artificially fevered rabbits; (3) Effects on the cardiovascular system: Pueraria root has a certain antihypertensive effect on normal and hypertensive animals. Pueraria root total flavonoids and puerarin have a significant effect of dilating coronary arteries, increasing coronary blood flow and reducing vascular resistance, and can also inhibit thrombin-induced 5-HT release in platelets.

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Animal experiments have shown the following: (1) Effects on smooth muscle: various total flavonoid compounds in Pueraria root have the effect of relaxing smooth muscle; (2) Effects on body temperature: Pueraria root can reduce the body temperature of artificially fevered rabbits; (3) Effects on the cardiovascular system: Pueraria root has a certain antihypertensive effect on normal and hypertensive animals. Pueraria root total flavonoids and puerarin have a significant effect of dilating coronary arteries, increasing coronary blood flow and reducing vascular resistance, and can also inhibit thrombin-induced 5-HT release in platelets.

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