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Founded in:
1989-12-12 -
Country:
China -
Address:
Neptune Industrial City, Fifth Industrial Zone, Science and Technology Park, Nanshan District, Shenzhen -
Tax NO.:
914403006188508328 -
Registered Funds:
80 million yuan -
Website:
-
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Levodropropizine |
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99291-25-5 | 11 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Acyclovir |
Antiviral drug. It has an inhibitory effect on herpes simplex virus, varicella zoster virus, cytomegalovirus, etc. in vitro. After entering the cells infected by herpes virus, this product competes with deoxynucleoside for viral thymidine kinase or cell kinase, and the drug is phosphorylated into activated acyclovir triphosphate, and then inhibits viral replication in two ways: ① Interfering with viral DNA polymerase and inhibiting viral replication; ② Under the action of DNA polymerase, it binds to the growing DNA chain, causing the extension of the DNA chain to be interrupted. This product has a special affinity for viruses, but has low toxicity to mammalian host cells.
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Antiviral drug. It has an inhibitory effect on herpes simplex virus, varicella zoster virus, cytomegalovirus, etc. in vitro. After entering the cells infected by herpes virus, this product competes with deoxynucleoside for viral thymidine kinase or cell kinase, and the drug is phosphorylated into activated acyclovir triphosphate, and then inhibits viral replication in two ways: ① Interfering with viral DNA polymerase and inhibiting viral replication; ② Under the action of DNA polymerase, it binds to the growing DNA chain, causing the extension of the DNA chain to be interrupted. This product has a special affinity for viruses, but has low toxicity to mammalian host cells. |
59277-89-3 | 50 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Pioglitazone hydrochloride |
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112529-15-4 | 47 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Naftopidil dihydrochloride |
A selective α1 receptor antagonist that can inhibit the rise in blood pressure caused by α1 receptors, has a hypotensive effect on a variety of hypertensive animal models, has a long duration of hypotensive effect, does not cause reflex tachycardia during hypotensive treatment, and has no obvious first-dose effect or drug resistance after multiple oral administrations. It can reduce the total peripheral resistance of anesthetized open-chest dogs, dilate peripheral blood vessels, and has no significant effect on cardiac output. It can also relieve the sympathetic tension of the prostate and urethra caused by the excitement of the receptor through the α1 receptor blocking effect, reduce the intraurethral pressure, and improve symptoms such as urination disorders caused by benign prostatic hyperplasia.
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A selective α1 receptor antagonist that can inhibit the rise in blood pressure caused by α1 receptors, has a hypotensive effect on a variety of hypertensive animal models, has a long duration of hypotensive effect, does not cause reflex tachycardia during hypotensive treatment, and has no obvious first-dose effect or drug resistance after multiple oral administrations. It can reduce the total peripheral resistance of anesthetized open-chest dogs, dilate peripheral blood vessels, and has no significant effect on cardiac output. It can also relieve the sympathetic tension of the prostate and urethra caused by the excitement of the receptor through the α1 receptor blocking effect, reduce the intraurethral pressure, and improve symptoms such as urination disorders caused by benign prostatic hyperplasia. |
57149-07-2 | 13 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Flavoxate hydrochloride |
This product is a smooth muscle relaxant. It has the function of inhibiting adenylate cyclase and phosphodiesterase, antagonizing calcium ions, and has a weak anti-muscarinic effect. It has a selective spasmolytic effect on the smooth muscles of the urogenital system, and can directly relieve the spasm of the smooth muscles of the urogenital system, relax the muscles, and eliminate frequent urination, urgency, urinary incontinence, and lower abdominal pain caused by urethral bladder smooth muscle spasm.
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This product is a smooth muscle relaxant. It has the function of inhibiting adenylate cyclase and phosphodiesterase, antagonizing calcium ions, and has a weak anti-muscarinic effect. It has a selective spasmolytic effect on the smooth muscles of the urogenital system, and can directly relieve the spasm of the smooth muscles of the urogenital system, relax the muscles, and eliminate frequent urination, urgency, urinary incontinence, and lower abdominal pain caused by urethral bladder smooth muscle spasm. |
3717-88-2 | 12 |