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Catalog Number:
37718
CAS Number:
117048-59-6
Combréstatine A4
Purity:
≥ 98 % (HPLC)
Synonym(s):
( Z )-2-méthoxy-5-(3,4,5-triméthoxystyryl)phénol, 3'-Hydroxy-3,4,4',5-tétraméthoxy- cis -stilbène
Temperature Sensitive
Documents
$312.27 /25 mg
Taille
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Product Information

Conserver sous gaz inerte

Synonyms
( Z )-2-méthoxy-5-(3,4,5-triméthoxystyryl)phénol, 3'-Hydroxy-3,4,4',5-tétraméthoxy- cis -stilbène
CAS Number
117048-59-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C18H20O5
Molecular Weight
316.35
MDL Number
MFCD03453309
PubChem ID
72686
Melting Point
81 - 85 °C
Appearance
Poudre blanc cassé
Conditions
Conserver à <0°C
General Information
Synonyms
( Z )-2-méthoxy-5-(3,4,5-triméthoxystyryl)phénol, 3'-Hydroxy-3,4,4',5-tétraméthoxy- cis -stilbène
CAS Number
117048-59-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C18H20O5
Molecular Weight
316.35
MDL Number
MFCD03453309
PubChem ID
72686
Melting Point
81 - 85 °C
Appearance
Poudre blanc cassé
Conditions
Conserver à <0°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Combretastatin A4 is widely utilized in research focused on:

  • Cancer Treatment: This compound is primarily studied for its potent anti-cancer properties, particularly in targeting and disrupting the blood supply to tumors, making it a promising candidate for cancer therapies.
  • Drug Development: Researchers are exploring its potential as a lead compound in the development of new anti-cancer drugs, particularly in combination therapies that enhance efficacy and reduce resistance.
  • Vascular Disruption: Its ability to inhibit angiogenesis (the formation of new blood vessels) is being investigated for applications in treating various solid tumors, providing a unique approach compared to traditional chemotherapy.
  • Pharmaceutical Research: Combretastatin A4 serves as a valuable tool in pharmacological studies, helping scientists understand the mechanisms of action for vascular-targeting agents and their effects on cancer progression.
  • Natural Product Chemistry: As a natural compound derived from the willow tree, it is of interest in the field of natural product synthesis, inspiring the design of synthetic analogs with improved therapeutic profiles.

Citations