u48800

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Product
u48800
Posting date : Sep 13, 2017
Membership
Free Member Scince Sep 12, 2017
FOB Price
$100
Min. Order Quantity
10
Supply Abillity
200kg/Month
Port
Qingdao
Payment Terms
PayPal , T/T
Package
foil bag/ fiber can
Keyword :
Category
Contact
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Product Detail
Company Info
 
Quick Detail
Place of Origin
China [CN]
Brand Name
Huanmei Biological Technology Co.,Ltd
Model Number
powder and crystal
HS-CODE
2937-50
Package & Delivery Lead Time
Package
foil bag/ fiber can
Delivery Lead Time
2days
Detailed Description

The introduction of the U48800:

  U-48800 is an opioid analgesic drug developed by a team at Upjohn in the 1970s that acts as a selectiveagonist of the µ-opioid receptor with a Kd value of 5.3 nM compared to 910 nM for the κ-opioid receptor and has around 7.5 x the potency of morphine in animal models.

 

  U-48800 is a structural isomer of the earlier opioid AH-7921 and the result of a great deal of work elucidating the quantitative structure–activity relationship of the scaffold. Upjohn looked for the keymoieties which gave the greatest activity and posted over a dozen patents on related compounds, each optimizing one moiety until they discovered that U-47700 was the most active.

 

  U-48800 became the lead compound of selective kappa-opioid receptor ligands such as U-50488, U-51754 (containing a single methylene spacer difference) and U-69,593, which share very similar structures.Although not used medically, the selective kappa ligands are used in research

 

  • name: u-48800 

  • purity: 99.9% 

  • colour: many colour 

  • appearance: powder and crystal 

  • chemical: Pharmaceutical Intermediates 

  • delievery time: 2-3working days 

  • payment way: TT moneygram western union paypal bitcoin 

  • shipping way: ems,dhl,fedex,eub 

  • Model No.: researchh chemical 

  • Place of Origin: Shanghai  

  • Min.Order: 10 Gram

  • Means of Transport: Ocean, Air

The introduction of the U48800: U-48800 is an opioid analgesic drug developed by a team at Upjohn in the 1970s that acts as a selectiveagonist of the µ-opioid receptor with a Kd value of 5.3 nM compared to 910 nM for the κ-opioid receptor and has around 7.5 x the potency of morphine in animal models.

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