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COMBRETASTATIN A-4

CAS NO.117048-59-6

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  • Min.Order: 100 Kilogram
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Product Details

Keywords

  • COMBRETASTATIN A-4
  • 117048-59-6
  • C18H20O5

Quick Details

  • ProName: COMBRETASTATIN A-4
  • CasNo: 117048-59-6
  • Molecular Formula: C18H20O5
  • Appearance: powder
  • Application: 117048-59-6
  • DeliveryTime: Within 3-7 days
  • PackAge: Depended
  • Port: China Main Port
  • ProductionCapacity: 300 Kilogram/Month
  • Purity: 99%
  • Storage: Store in dry, dark and ventilated plac...
  • Transportation: by air or by sea
  • LimitNum: 100 Kilogram
  • Application: Multipurpose intermediate
  • Application: ISO/9001 Certificate

Superiority

COMBRETASTATIN A-4 Basic information
Product Name: COMBRETASTATIN A-4
Synonyms: (Z)-2-Methoxy-5-(3,4,5-Trimethoxystyryl)Phenol;(Z)-2-Methoxy-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]phenol,3,4,5-Trimethoxy-3hydroxy-4methoxy-(Z)-stilbene,CS-A4;Combrestatin A4( 2-Methoxy-5-[2-(3,4,5-trimethoxy-phenyl)-vinyl]-phenol );(Z)-2-Methoxy-5-(3,4,5-trimethoxystyryl)phenol ,98%;2-Methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenol;3-[(Z)-2-(3,4,5-Trimethoxyphenyl)ethenyl]-6-methoxyphenol;5-[(Z)-2-(3,4,5-Trimethoxyphenyl)ethenyl]-2-methoxyphenol;Combretastatin A4
CAS: 117048-59-6
MF: C18H20O5
MW: 316.3484
EINECS:  
Product Categories: Inhibitors;Combretastatin;Anti-cancer & immunity;API
Mol File: 117048-59-6.mol
COMBRETASTATIN A-4 Structure
 
COMBRETASTATIN A-4 Chemical Properties
mp  84.5-85.5°C
storage temp.  Desiccate at -20°C
 
Safety Information
Hazard Codes  T
Risk Statements  23/24/25-41
Safety Statements  26-36/37-39-45
RIDADR  UN 2811
MSDS Information
 
 
COMBRETASTATIN A-4 Usage And Synthesis
Chemical Properties Crystalline Powder
Usage Combretastatin is a small organic molecule found in the bark of the African bush willow tree Combretum caffrum. Combretastatin-A4 Prodrug Induces Mitotic Catastrophe in Chronic Lymphocytic Leukemia Cell Line Independent of Caspase Activation and Poly(ADP-ribose) Polymerase Cleavage. A potent cytotoxic agent which strongly inhibits the polymerization of tubulin by binding to the colchicine site.
Biological Activity Antitumor, antiangiogenic and antimetastatic agent, in vitro and in vivo . Acts by inhibiting tubulin polymerization (IC 50 = 2-3 μ M).

 

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