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Daiichi Sankyo Pharmaceutical (SHANGHAI) Co., Ltd.
  • Founded in:

    1999-11-18
  • Country:

    China China
  • Address:

    No. 500, Juli Road, China (Shanghai) Pilot Free Trade Zone
  • Tax NO.:

    91310000607410671R
  • Registered Funds:

    $53 million
  • Website:

  • Email:

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Pravastatin Sodium Tablets
Pravastatin sodium (pregnancy classification: X) has a molecular formula of C23H35NaO7 and a molecular weight of 446.52
Name Description Content CAS NO. Registered Holders
Pravastatin sodium

This product is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated catabolism of LDL-C and the clearance of LDL-C in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the production of low-density lipoprotein (LDL-C).

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This product is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated catabolism of LDL-C and the clearance of LDL-C in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the production of low-density lipoprotein (LDL-C).

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Pravastatin Sodium Tablets
Pravastatin sodium (pregnancy classification: X) has a molecular formula of C23H35NaO7 and a molecular weight of 446.52
Name Description Content CAS NO. Registered Holders
Pravastatin sodium

This product is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated catabolism of LDL-C and the clearance of LDL-C in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the generation of LDL-C.

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This product is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated catabolism of LDL-C and the clearance of LDL-C in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the generation of LDL-C.

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Pravastatin Sodium Tablets
Pravastatin sodium. The molecular formula is C23H35NaO7 and the molecular weight is 446.52.
Name Description Content CAS NO. Registered Holders
Pravastatin sodium

It is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated degradation of LDL and the clearance of LDL in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the production of low-density lipoprotein cholesterol (LDL-C).

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It is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated degradation of LDL and the clearance of LDL in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the production of low-density lipoprotein cholesterol (LDL-C).

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Pravastatin Sodium Tablets
Pravastatin sodium.
Name Description Content CAS NO. Registered Holders
Pravastatin sodium

This product is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated catabolism of LDL-C and the clearance of LDL-C in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the production of low-density lipoprotein (LDL-C).

More

This product is a competitive inhibitor of 3-hydroxy 3-methylglutaryl coenzyme A reductase (HMG-CoA reductase). It reduces the amount of intracellular cholesterol to a certain extent by reversibly inhibiting the activity of HMG-CoA reductase, leading to an increase in the number of low-density lipoprotein (LDL) receptors on the cell surface, thereby enhancing the receptor-mediated catabolism of LDL-C and the clearance of LDL-C in the blood; at the same time, it inhibits the synthesis of very low-density lipoprotein (VLDL-C) in the liver, thereby inhibiting the production of low-density lipoprotein (LDL-C).

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Compound Methoxyphenamine Capsules
It mainly contains four ingredients: methoxyphenamine hydrochloride, aminophylline, narcotine, and chlorpheniramine maleate.
Name Description Content CAS NO. Registered Holders
Methoxyphenamine hydrochloride

Beta-adrenergic receptor agonists, which relax bronchial smooth muscle

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Beta-adrenergic receptor agonists, which relax bronchial smooth muscle

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Aminophylline

It can relax bronchial smooth muscles and reduce bronchial mucosal congestion and edema

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It can relax bronchial smooth muscles and reduce bronchial mucosal congestion and edema

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NOSCAPINE HYDROCHLORIDE

Peripheral cough suppressants

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Peripheral cough suppressants

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Chlorphenamine maleate

H1 receptor blockers, which can counteract the H1-type effects of histamine

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H1 receptor blockers, which can counteract the H1-type effects of histamine

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