Pharmaceutical Grade API Vardenafil Hydrochloride CAS 224785-91-5

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Product
Pharmaceutical Grade API Vardenafil Hydrochloride CAS 224785-91-5
Posting date : May 18, 2023
Membership
Free Member Scince May 09, 2023
FOB Price
$1000/kg
Min. Order Quantity
1kg
Supply Abillity
500kg
Port
Qingdao
Payment Terms
TT,LC
Package
5kg/drum
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Contact
Melissa wang
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Product Detail
Company Info
 
Quick Detail
Place of Origin
China [CN]
Brand Name
Loncom
HS-CODE
-
Package & Delivery Lead Time
Package
5kg/drum
Detailed Description

Vardenafil hydrochloride is an benzenesulfonamide derivative acts as vasoconstrictor agent. It is indicated for the treatment of erectile dysfunction (ED) in adult men.
It is formulated as film-coated tablet for oral administration.

Mechanism of action:

Vardenafil hydrochloride is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5). During sexual stimulation, nitric oxide is released from nerve endings and endothelial cells in the corpus cavernosum. Nitric oxide activates the enzyme guanylate cyclase resulting in increased synthesis of cyclic guanosine monophosphate (cGMP) in the smooth muscle cells of the corpus cavernosum. The cGMP in turn triggers smooth muscle relaxation, allowing increased blood flow into the penis, resulting in erection. The tissue concentration of cGMP is regulated by both the rates of synthesis and degradation via phosphodiesterases (PDEs). The most abundant PDE in the human corpus cavernosum is the cGMP-specific phosphodiesterase type 5 (PDE5); therefore, the inhibition of PDE5 enhances erectile function by increasing the amount of cGMP. Because sexual stimulation is required to initiate the local release of nitric oxide, the inhibition of PDE5 has no effect in the absence of sexual stimulation.

Disclaimer
Products protected by valid patents are not offered for commercial sale in countries where the sale of such products constitutes patent infringement but are offered solely for uses reasonably related to the development and submission of information under a law regulating the manufacture, use or sale of drugs. It is within the buyer’s responsibility and liability to check the patent situation of the product in the imported market(s). 


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