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KIRENOL

Base Information Edit
  • Chemical Name:KIRENOL
  • CAS No.:52659-56-0
  • Molecular Formula:C20H34O4
  • Molecular Weight:338.48
  • Hs Code.:29399990
  • Mol file:52659-56-0.mol
KIRENOL

Synonyms:Kirel

Suppliers and Price of KIRENOL
Supply Marketing:Edit
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
  • Kirenol
  • 20mg
  • $ 390.00
  • TRC
  • Kirenol
  • 250mg
  • $ 375.00
  • TCI Chemical
  • Kirenol >98.0%(GC)
  • 25mg
  • $ 194.00
  • TCI Chemical
  • Kirenol >98.0%(GC)
  • 100mg
  • $ 580.00
  • Medical Isotopes, Inc.
  • Kirenol
  • 1 g
  • $ 2125.00
  • Medical Isotopes, Inc.
  • Kirenol
  • 250 mg
  • $ 875.00
  • JR MediChem
  • Kirenol 98%
  • 20mg
  • $ 600.00
  • DC Chemicals
  • kirenol >98%,StandardReferencesGrade
  • 20 mg
  • $ 280.00
  • Crysdot
  • Kirenol 95+%
  • 50mg
  • $ 119.00
  • Crysdot
  • Kirenol 95+%
  • 25mg
  • $ 74.00
Total 72 raw suppliers
Chemical Property of KIRENOL Edit
Chemical Property:
  • Melting Point:197.0 to 201.0 °C 
  • Refractive Index:1.57 
  • Boiling Point:516.902 °C at 760 mmHg 
  • PKA:14.06±0.20(Predicted) 
  • Flash Point:233.593 °C 
  • PSA:80.92000 
  • Density:1.177 g/cm3 
  • LogP:2.25190 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Ethanol (Slightly), Methanol (Slightly) 
Purity/Quality:

98%,99%, *data from raw suppliers

Kirenol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Description Kirenol is a diterpenoid that has been found in S. orientalis and has diverse biological activities, including anti-arthritic and anti-inflammatory properties. It inhibits Gram-positive and Gram-negative bacterial growth in disc diffusion assays with MICs ranging from 39 to 156 and 312.5 to 625 μg/ml, respectively. Kirenol also reduces K652 chronic myeloid leukemia cell viability with a 48 hour IC50 value of 18.19 μg/ml and induces apoptosis. In vivo, kirenol (2 mg/kg, p.o.) reduces motor deficit, delays disease onset by approximately five days, and downregulates inflammatory CD4+IFN-γ+ Th1 cells and CD4+IL-17A+ Th17 cells in a mouse model of experimental autoimmune encephalomyelitis (EAE). Intragastric administration of kirenol (1-4 mg/kg) reduces the arthritis index, NF-kB activity, and paw swelling and increases annexin-1 expression without affecting glucocorticoid receptor α (GRα) expression in the synovium in a rat model of collagen-induced arthritis. Topical administration of kirenol (0.3-0.5% w/w) reduces edema induced by carrageenan, complete Freund''s adjuvant (CFA), and formalin in rats up to 44, 67, and 65%, respectively.
  • Uses Kirenol is a pharmaceutical agent that induces apoptosis in human chronic myeloid leukemia cells.
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