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Founded in:
1997-05-24 -
Country:
China -
Address:
No. 89, Gongye West Road, Shaoguan City, Guangdong -
Tax NO.:
91440200618357941C -
Registered Funds:
61.56101 million yuan -
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| MIDECAMYCIN |
This product is a macrolide antibiotic produced by Streptomyces mycarofaciens. It works by acting on the 50S subunit of bacterial ribosomes, hindering the synthesis of bacterial proteins, and is a growth-stage antibacterial drug. Its antibacterial properties are similar to those of erythromycin, and it shows strong antibacterial effects on Gram-positive bacteria and mycoplasmas, and also has antibacterial effects on some Gram-negative bacteria such as Neisseria meningitidis and Neisseria gonorrhoeae.
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This product is a macrolide antibiotic produced by Streptomyces mycarofaciens. It works by acting on the 50S subunit of bacterial ribosomes, hindering the synthesis of bacterial proteins, and is a growth-stage antibacterial drug. Its antibacterial properties are similar to those of erythromycin, and it shows strong antibacterial effects on Gram-positive bacteria and mycoplasmas, and also has antibacterial effects on some Gram-negative bacteria such as Neisseria meningitidis and Neisseria gonorrhoeae. |
35457-80-8 | 2 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| 1-Benzhydryl-4-(3-phenyl-ethyl-propenyl)-piperazine |
This product is a piperazine calcium channel antagonist that can block calcium influx into vascular smooth muscle, causing vasodilation and improving cerebral and coronary circulation, especially having a certain selective effect on cerebral blood vessels. This product can inhibit phosphodiesterase, prevent cAMP from decomposing into inactive 5′-AMP, thereby increasing the intracellular cAMP concentration, inhibiting the release of various biologically active substances such as histamine, 5-hydroxytryptamine, bradykinin, and also inhibiting the activation of complement C4.
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This product is a piperazine calcium channel antagonist that can block calcium influx into vascular smooth muscle, causing vasodilation and improving cerebral and coronary circulation, especially having a certain selective effect on cerebral blood vessels. This product can inhibit phosphodiesterase, prevent cAMP from decomposing into inactive 5′-AMP, thereby increasing the intracellular cAMP concentration, inhibiting the release of various biologically active substances such as histamine, 5-hydroxytryptamine, bradykinin, and also inhibiting the activation of complement C4. |
0 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Sodium ferulic |
Non-peptide endothelin receptor antagonists can antagonize endothelin-induced vasoconstriction, blood pressure increase, and vascular smooth muscle cell proliferation; increase NO synthesis, relax vascular smooth muscle; inhibit platelet aggregation, anti-coagulation, and improve blood rheology characteristics. It can also inhibit cholesterol synthesis, lower blood lipids, scavenge free radicals, prevent and treat lipid peroxidation damage; affect complement, enhance immune function, and have certain analgesic and antispasmodic effects.
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Non-peptide endothelin receptor antagonists can antagonize endothelin-induced vasoconstriction, blood pressure increase, and vascular smooth muscle cell proliferation; increase NO synthesis, relax vascular smooth muscle; inhibit platelet aggregation, anti-coagulation, and improve blood rheology characteristics. It can also inhibit cholesterol synthesis, lower blood lipids, scavenge free radicals, prevent and treat lipid peroxidation damage; affect complement, enhance immune function, and have certain analgesic and antispasmodic effects. |
24276-84-4 | 8 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Stugeron |
This product is a piperazine calcium channel antagonist, which can prevent pathological calcium influx in smooth muscle cells of vascular walls and relieve vascular spasm. It has the effect of dilating cerebral and peripheral blood vessels, improving cerebral circulation and coronary circulation, especially for cerebral blood vessels. This product can also inhibit phosphodiesterase, prevent cAMP from decomposing into inactive 5prime;-AMP, thereby increasing the concentration of cAMP in cells, inhibiting the release of various biologically active substances such as histamine, 5-hydroxytryptamine, bradykinin, and also inhibiting the activation of complement C4.
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This product is a piperazine calcium channel antagonist, which can prevent pathological calcium influx in smooth muscle cells of vascular walls and relieve vascular spasm. It has the effect of dilating cerebral and peripheral blood vessels, improving cerebral circulation and coronary circulation, especially for cerebral blood vessels. This product can also inhibit phosphodiesterase, prevent cAMP from decomposing into inactive 5prime;-AMP, thereby increasing the concentration of cAMP in cells, inhibiting the release of various biologically active substances such as histamine, 5-hydroxytryptamine, bradykinin, and also inhibiting the activation of complement C4. |
93.0%～107.0%Label quantity | 298-57-7 | 15 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| CALCIUM GLUCONATE MONOHYDRATE |
Not yet clear
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Not yet clear |
150mg | 66905-23-5 | 35 |
| Thiamine chloride |
Not yet clear
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Not yet clear |
0.3mg | 59-43-8 | 9 |
| Vitamin D3 |
Not yet clear
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Not yet clear |
0.011mg | 67-97-0 | 23 |