On ECHEMI
Home > Drugs > Jiangsu Tasly DIYI Pharmaceutical Co., Ltd.

Jiangsu Tasly DIYI Pharmaceutical Co., Ltd.

  • Founded in:

    1999-03-24
  • Country:

    China China
  • Address:

    No. 168, Chaoyang West Road, Qingpu Industrial Park, Huai'an City
  • Tax NO.:

    91320800139432975C
  • Registered Funds:

    66.86 million yuan
  • Website:

  • Email:

Related Drugs
Cilostazol Tablets
The main ingredient of this product is cilostazol, and its chemical name is: 6-[4-(1-cyclohexyl-1H-tetrazol-5-yl)butoxy]-3,4-dihydro-2(1H)-quinolone
Name Description Content CAS NO. Registered Holders
Cilostazol

This product and its metabolites are cyclic adenosine monophosphate (cAMP) phosphodiesterase III inhibitors (PDEIII inhibitors), which can reduce the degradation of cAMP by inhibiting the activity of phosphodiesterase, thereby increasing the cAMP level in platelets and blood vessels, inhibiting platelet aggregation and vasodilation.

More

This product and its metabolites are cyclic adenosine monophosphate (cAMP) phosphodiesterase III inhibitors (PDEIII inhibitors), which can reduce the degradation of cAMP by inhibiting the activity of phosphodiesterase, thereby increasing the cAMP level in platelets and blood vessels, inhibiting platelet aggregation and vasodilation.

73963-72-1 30
Blood and urine capsules
Palm Seed Smilax Coix Seed
Name Description Content CAS NO. Registered Holders
Palm seeds

0
SMILAGENIN

126-18-1 0
COICIS SEMEN

0
Ephedrine Diphenhydramine Tablets
This product is a compound preparation, each tablet containing 25 mg of ephedrine hydrochloride and 25 mg of diphenhydramine hydrochloride.
Name Description Content CAS NO. Registered Holders
Ephedrine hydrochloride

It can directly stimulate adrenaline receptors, and can also indirectly stimulate adrenaline receptors by prompting adrenaline nerve endings to release norepinephrine. It has a stimulating effect on both alpha and beta receptors. It can dilate bronchi and constrict local blood vessels, and its action time is longer; it strengthens myocardial contractility, increases cardiac output, and makes venous return to the heart sufficient; it has a stronger central nervous system stimulating effect than adrenaline.

More

It can directly stimulate adrenaline receptors, and can also indirectly stimulate adrenaline receptors by prompting adrenaline nerve endings to release norepinephrine. It has a stimulating effect on both alpha and beta receptors. It can dilate bronchi and constrict local blood vessels, and its action time is longer; it strengthens myocardial contractility, increases cardiac output, and makes venous return to the heart sufficient; it has a stronger central nervous system stimulating effect than adrenaline.

25mg 0
Diphenhydramine Hydrochloride

It has ① antihistamine effect, which can compete with histamine released from tissues for H1 receptors on effector cells, thereby stopping allergic reactions; ② at the same time, it inhibits central nervous system activity and causes sedative and hypnotic effects; ③ it enhances the effect of antitussive drugs.

More

It has ① antihistamine effect, which can compete with histamine released from tissues for H1 receptors on effector cells, thereby stopping allergic reactions; ② at the same time, it inhibits central nervous system activity and causes sedative and hypnotic effects; ③ it enhances the effect of antitussive drugs.

25mg 147-24-0 31
Nitrofurantoin enteric-coated tablets
The main ingredient of this product is nitrofurantoin.
Name Description Content CAS NO. Registered Holders
Nitrofurantoin

This product is an antibacterial drug. Escherichia coli is mostly sensitive to this product, and some strains of Enterobacteriaceae such as Enterobacter aerogenes, Enterobacter cloacae, Proteus, and Klebsiella are sensitive to this product. Aeruginosa is usually resistant to this product. This product has antibacterial effects on Gram-positive bacteria such as Enterococcus. The antibacterial activity of this product is not affected by pus and tissue decomposition products. It is more active in acidic urine. The antibacterial mechanism is to interfere with the oxidoreductase system in the bacteria, thereby blocking its metabolic process.

More

This product is an antibacterial drug. Escherichia coli is mostly sensitive to this product, and some strains of Enterobacteriaceae such as Enterobacter aerogenes, Enterobacter cloacae, Proteus, and Klebsiella are sensitive to this product. Aeruginosa is usually resistant to this product. This product has antibacterial effects on Gram-positive bacteria such as Enterococcus. The antibacterial activity of this product is not affected by pus and tissue decomposition products. It is more active in acidic urine. The antibacterial mechanism is to interfere with the oxidoreductase system in the bacteria, thereby blocking its metabolic process.

67-20-9 26
Licorice Tablets
Glycyrrhizic acid monopotassium salt.
Name Description Content CAS NO. Registered Holders
Monopotassium glycyrrhizate

1. Anti-inflammatory effect: (1) Anti-allergic effect. Glycyrrhizin has anti-allergic effects such as inhibiting local allergic necrosis reaction in rabbits and inhibiting Schwartzman phenomenon. For corticosteroids, it can enhance the hormone's inhibitory effect on stress response and antagonize the hormone's anti-granulation and thymic atrophy effect. It has no effect on the exudation of hormones. (2) Inhibitory effect on arachidonic acid metabolic enzymes. Glycyrrhizin can directly bind to phospholipase A2 and lipoxygenase, selectively inhibiting the phosphorylation of these enzymes and inhibiting their activation. 2. Immunomodulatory effect: Glycyrrhizin has the following immunomodulatory effects in in vitro tests: (1) Regulatory effect on T cell activation; (2) Induction effect on interferon; (3) Activation of NK cells; (4) Promoting the differentiation of extrathymic T lymphocytes. 3. Inhibitory effect on experimental hepatocyte damage: In the primary cultured rat hepatocyte cell line in vitro, glycyrrhizin has the effect of inhibiting hepatocyte damage caused by carbon tetrachloride. 4. Inhibit virus proliferation and inactivate viruses: In the MHV infection experiment of mice, glycyrrhizin can prolong their survival days. In the vaccinia virus pox prevention experiment of rabbits, it has the effect of preventing pox; in the in vitro experiment system, it has also been observed to inhibit the proliferation of herpes viruses and the inactivation of viruses.

More

1. Anti-inflammatory effect: (1) Anti-allergic effect. Glycyrrhizin has anti-allergic effects such as inhibiting local allergic necrosis reaction in rabbits and inhibiting Schwartzman phenomenon. For corticosteroids, it can enhance the hormone's inhibitory effect on stress response and antagonize the hormone's anti-granulation and thymic atrophy effect. It has no effect on the exudation of hormones. (2) Inhibitory effect on arachidonic acid metabolic enzymes. Glycyrrhizin can directly bind to phospholipase A2 and lipoxygenase, selectively inhibiting the phosphorylation of these enzymes and inhibiting their activation. 2. Immunomodulatory effect: Glycyrrhizin has the following immunomodulatory effects in in vitro tests: (1) Regulatory effect on T cell activation; (2) Induction effect on interferon; (3) Activation of NK cells; (4) Promoting the differentiation of extrathymic T lymphocytes. 3. Inhibitory effect on experimental hepatocyte damage: In the primary cultured rat hepatocyte cell line in vitro, glycyrrhizin has the effect of inhibiting hepatocyte damage caused by carbon tetrachloride. 4. Inhibit virus proliferation and inactivate viruses: In the MHV infection experiment of mice, glycyrrhizin can prolong their survival days. In the vaccinia virus pox prevention experiment of rabbits, it has the effect of preventing pox; in the in vitro experiment system, it has also been observed to inhibit the proliferation of herpes viruses and the inactivation of viruses.

42294-03-1 2
Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.