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thielavin A

Base Information
  • Chemical Name:thielavin A
  • CAS No.:71950-66-8
  • Molecular Formula:C29H30 O10
  • Molecular Weight:538.54
  • Hs Code.:
  • Mol file:71950-66-8.mol
thielavin A

Synonyms:Thielavin A

Suppliers and Price of thielavin A
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Thielavin A
  • 500ug
  • $ 582.00
  • TRC
  • ThielavinA
  • 1mg
  • $ 735.00
  • Cayman Chemical
  • Thielavin A ≥95%
  • 2.5mg
  • $ 1156.00
  • Cayman Chemical
  • Thielavin A ≥95%
  • 500μg
  • $ 289.00
  • AK Scientific
  • ThielavinA
  • 2.5mg
  • $ 1660.00
Total 7 raw suppliers
Chemical Property of thielavin A
Chemical Property:
  • Vapor Pressure:9.92E-31mmHg at 25°C 
  • Boiling Point:850°C at 760 mmHg 
  • Flash Point:281°C 
  • PSA:170.82000 
  • Density:1.371g/cm3 
  • LogP:5.11280 
Purity/Quality:

99% *data from raw suppliers

Thielavin A *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Description Thielavin A is a fungal metabolite originally isolated from T. terricola that is related to thielavin B . Thielavin A inhibits COX, blocking both the conversion of arachidonic acid to prostaglandin H2 (PGH2; ) and the conversion of PGH2 to PGE2 (; IC50s = 10 and 40 μM, respectively). Thielavin A also inhibits glucose-6-phosphatase in rat liver microsomes (IC50 = 4.6 μM). It is a non-competitive inhibitor of α-glucosidase from S. cerevisiae (IC50 = 23.8 μM; Ki = 27.8 μM).
  • Uses The fungal metabolite, thielavin A, and its relatives are glucose-6-phosphatase inhibitors. The three benzoic acid units are essential for inhibition. Thielavin A was originally isolated as a inhibitor of prostaglandin biosynthesis. The closely related thielavin B is a telomerase and cell wall transglycosylation inhibitor. Thielavin A acts as an inhibitor of prostagladins biosynthesis.
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