221877-54-9 ZOTAR...

221877-54-9   ZOTAROLIMUS
221877-54-9   ZOTAROLIMUS
221877-54-9   ZOTAROLIMUS

221877-54-9 ZOTAROLIMUS

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100 Kilogram

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  • Min.Order :100 Kilogram
  • Purity: 99%
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Keywords

Rapamycin Tetrazolyl Deoxy

Quick Details

  • Appearance:Pale Yellow Solid
  • Application:221877-54-9
  • PackAge:As your request
  • ProductionCapacity:300|Kilogram|Month
  • Storage:Hygroscopic, -20°C Freezer, Under Inert Atmosphere
  • Transportation:by express or air or sea

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Tech Data Relevant

1.Certificate Of Analysis (COA)

2..Material Safety Data Sheet (MSDS)

3.Technical Data Sheet(TDS)

4.Route of synthesis (ROS)

5.Nuclear Magnetic Resonance(NMR)

6.Method of Analysis(MOA)

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Details:

Product Name: ZOTAROLIMUS
Synonyms: ZOTAROLIMUS;(42S)-42-Deoxy-42-(1H-tetrazol-1-yl)rapamycin;A 179578;ABT 578;Rapamycin, 42-deoxy-42-(1H-tetrazol-1-yl)-, (42S)-;Unii-H4gxr80ize;ZotaroliMus, >90%;42-(1-Tetrazolyl)rapamycin
CAS: 221877-54-9
MF: C52H79N5O12
MW: 966.219
EINECS:  
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Chiral Reagents;Heterocycles;Inhibitors
Mol File: 221877-54-9.mol
ZOTAROLIMUS Structure
 
ZOTAROLIMUS Chemical Properties
Melting point  100-105°C
density  1.25
storage temp.  Hygroscopic, -20°C Freezer, Under Inert Atmosphere
 
Safety Information
MSDS Information
 
 
ZOTAROLIMUS Usage And Synthesis
Chemical Properties Pale Yellow Solid
Usage Zotarolimus is a semi-synthetic macrocyclic lactone prepared from rapamycin by preparation of the 42-triflate ester, followed by displacement with tetrazole and purification of the two isomeric products. This structural change affords a less bioavailable product, a preferred profile for some applications. Like all tacrolimus analogues, zotarolimus binds to a receptor protein (FKBP12). The complex then binds to preventing it from interacting with target proteins. Zotarolimus is extensively cited in the literature with over 200 citations.
Usage Zotarolimus is a semi-synthetic macrocyclic lactone prepared from rapamycin by preparation of the 42-triflate ester, followed by displacement with tetrazole and purification of the two isomeric products. This structural change affords a less bioavailable product, a preferred profile for some applications. Like all tacrolimus analogues, zotarolimus binds to a receptor protein (FKBP12). The complex then binds to mTOR preventing it from interacting with target proteins. Zotarolimus is extensively cited in the literature with over 200 citations.
Usage A tetrazole-containing Rapamycin analog as immunomodulator and useful in the treatment of restenosis and immune and autoimmune diseases.
 
ZOTAROLIMUS Preparation Products And Raw materials

 

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