Products Categories
    Product Certification&
    Enterprise Certification

  • Ms.Wendy Wang
    Tel: +86-0731-85910593

  • Mr.Jack Xiong
    Tel: 86-13967532999

  • Mobile:+86 15116362720
  • Tel:+86-0731-85910593
  • Fax:+86-0731-85910593
  • URL:http://www.hwcpharm.com
  • Province/state:Hunan Province
  • City:Changsha
  • Street:LuTian Road No.28
  • MaxCard:
Home > Products >  Entecavir trader 209216-23-9 wholesaler

Entecavir trader 209216-23-9 wholesaler CAS NO.209216-23-9

  • Min.Order: 0 Metric Ton
  • Payment Terms:
  • Product Details

Keywords

  • Entecavir trader
  • 209216-23-9 compective price
  • 209216-23-9 wholesaler

Quick Details

  • ProName: Entecavir trader 209216-23-9 wholesale...
  • CasNo: 209216-23-9
  • Molecular Formula: C12H15N5O3
  • Appearance: White powder
  • Application: API,pharmaceutical raw material
  • DeliveryTime: prompt
  • PackAge: 10g/bag or as customer's require
  • Port: according to details
  • ProductionCapacity: Metric Ton/Day
  • Purity: 99%
  • Storage: sealed and dry preservation
  • Transportation: by air/by sea/by courier
  • LimitNum: 0 Metric Ton

Superiority

Entecavir trader 209216-23-9 wholesaler

After taking the medicine in the mouth of a healthy population, the product is quickly absorbed and reaches peak concentration (Cmax) in 0.5 to 1.5 hours. Once a day, 6 to 10 days after the steady state, the cumulative amount is about twice. Effects of food on oral absorption: Eating a standard high-fat or low-fat meal while taking 0.5 mg of this product will result in a slight delay in drug absorption (from 0.75 hours to 1.0 to 1.5 hours), Cmax reduced by 44% to 46%, and the area under the drug-time curve (AUC) decreased by 18% to 20%. Therefore, this product should be taken on an empty stomach (at least 2 hours before or after meals).
Distribution: Pharmacokian dynamics data show that the apparent distribution volume exceeds the amount of liquid in the whole body, which indicates that the product is widely distributed in various organizations. In vitro experiments showed that the binding rate of this product to human plasma protein was 13%. Metabolism and removal: No oxidation or acetylation metabolites were observed after 14C-labeled Entikawe was taken in humans and rats, but a small amount of phase II metabolites glucodehyde glycoside bindings and sulphuric acid bindings were observed. Entikave is not the substrate, inhibitor or inducer of the cytomegline P450 (CYP450) enzyme system. After reaching the plasma peak concentration, the blood drug concentration decreased exponentially, and it took about 128 to 149 hours to reach the end of the half-life of the purge. The drug accumulation index is about twice the daily dose, indicating an effective cumulative half-life of about 24 hours. This product is mainly in its original form through kidney removal, the removal rate is 62% to 73% of the amount of administration. The kidney clearance rate was 360 to 471 mL/min and did not depend on the dose of the drug, which indicated that Ntekave was secreted through both renal globalls and mesh tubes.

Details

WHY CHOOSE US

1. Quality

Our products meet MSDS safe standard and we have ISO and other certificate so yan can get high quality products from our company.

2. Price

We are the company which is the joint of trade and industry so we cao provide the competitive price and high quality product.

3. Packing

We can do according to the customers' request.

4. Transport

The products can be transported by DHL, FEDEX, TNT, EMS, EUB, by air and by sea.

5. Service

We offer specialized logistic service including export declaration,customs clearance and every detail during shipment,this makes us able to offer you one-stop service from the order to the products transported to your hand.

Other products of this supplier

lookchemhot product CAS New CAS Cas Database Article Data Chemical Catalog