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Founded in:
2006-09-27 -
Country:
China -
Address:
No. 52, Xiaogang Road, Xinshi Street, Baiyun District, Guangzhou -
Tax NO.:
914401017955021269 -
Registered Funds:
- -
Website:
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Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Halcinonide |
It is a highly effective fluorinated and chlorinated corticosteroid with anti-inflammatory, antipruritic and vasoconstrictive effects. Its anti-inflammatory and antipruritic mechanism is to increase the responsiveness of β receptors to catecholamine, increase the production of CAMP by activating adenylate cyclase, and reduce the destruction of CAMP by inhibiting phosphoethylesterase, resulting in an increase in the concentration of cAMP in cells and inhibiting the release of histamine.
More
It is a highly effective fluorinated and chlorinated corticosteroid with anti-inflammatory, antipruritic and vasoconstrictive effects. Its anti-inflammatory and antipruritic mechanism is to increase the responsiveness of β receptors to catecholamine, increase the production of CAMP by activating adenylate cyclase, and reduce the destruction of CAMP by inhibiting phosphoethylesterase, resulting in an increase in the concentration of cAMP in cells and inhibiting the release of histamine. |
3093-35-4 | 9 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Halcinonide |
A highly effective fluorinated and chlorinated corticosteroid with anti-inflammatory, antipruritic and vasoconstrictive effects. It increases the cAMP concentration in cells by increasing the responsiveness of β receptors to catecholamine, activating adenylate cyclase to increase CAMP production, and inhibiting phosphoethylesterase to reduce CAMP destruction, while inhibiting histamine release. Its anti-inflammatory and antipruritic mechanism is similar to that of dexamethasone.
More
A highly effective fluorinated and chlorinated corticosteroid with anti-inflammatory, antipruritic and vasoconstrictive effects. It increases the cAMP concentration in cells by increasing the responsiveness of β receptors to catecholamine, activating adenylate cyclase to increase CAMP production, and inhibiting phosphoethylesterase to reduce CAMP destruction, while inhibiting histamine release. Its anti-inflammatory and antipruritic mechanism is similar to that of dexamethasone. |
3093-35-4 | 9 |