Basic information Safety Supplier Related

BAY 59-3074

Basic information Safety Supplier Related

BAY 59-3074 Basic information

Product Name:
BAY 59-3074
Synonyms:
  • BAY 59-3074
  • 3-[2-Cyano-3-(trifluoromethyl)phenoxy]phenyl4,4,4-trifluoro-1-butanesulfonicacidester
  • CS-2278
  • BAY-59-3074; BAY 59-3074; BAY59-3074
  • BAY 59-3074;BAY-59-3074
  • 1-Butanesulfonic acid, 4,4,4-trifluoro-, 3-[2-cyano-3-(trifluoromethyl)phenoxy]phenyl ester
  • inhibit,Cannabinoid Receptor,Bay 59-3074,Inhibitor,Bay 593074,Bay 59 3074
  • Bay 59-3074, 10 mM in DMSO
CAS:
406205-74-1
MF:
C18H13F6NO4S
MW:
453.36
Product Categories:
  • Pharmaceutical intermediate
Mol File:
406205-74-1.mol
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BAY 59-3074 Chemical Properties

Boiling point:
490.6±45.0 °C(Predicted)
Density 
1.49±0.1 g/cm3(Predicted)
storage temp. 
Store at +4°C
solubility 
DMSO:56.78(Max Conc. mg/mL);135.05(Max Conc. mM)
Ethanol:68.17(Max Conc. mg/mL);162.14(Max Conc. mM)
form 
A crystalline solid
color 
White to off-white
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BAY 59-3074 Usage And Synthesis

Uses

Bay 59-3074, is a novel cannabinoid CB1/CB2 receptor partial agonist with antihyperalgesic and antiallodynic effects.

Definition

ChEBI: 4,4,4-trifluoro-1-butanesulfonic acid is an aromatic ether.

Biological Activity

Novel CB 1 /CB 2 receptor partial agonist (K i values are 48.3 and 45.5 nM at human CB 1 and CB 2 receptors respectively). Orally active CB 1 agonist in vivo . Displays anti-hyperalgesic and antiallodynic properties in rat models of chronic neuropathic and inflammatory pain.

in vivo

BAY 59-3074 (0.3-3 mg/kg; oral administration; daily; for 2 weeks; male Wistar rats) treatment improves antihyperalgesic and antiallodynic effects against thermal or mechanical stimuli in rat models of chronic neuropathic and inflammatory pain.

Animal Model:Male Wistar rats (160-250 g)[1]
Dosage:0.3 mg/kg, 1 mg/kg, and 3 mg/kg
Administration:Oral administration; daily; for 2 weeks.
Result:Antiallodynic efficacy in the spared nerve injury model was maintained after 2 weeks of daily administration. Tolerance developed rapidly (within 5 days) for cannabinoid-related side effects. Antihyperalgesic and antiallodynic efficacy was maintained/increased.

IC 50

CB1: 48.3 nM (Ki); CB2: 45.5 nM (Ki)

BAY 59-3074Supplier

Shanghai Boyle Chemical Co., Ltd.
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Shanghai Boyle Chemical Co., Ltd.
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021-50182298 021-50180596
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3B Pharmachem (Wuhan) International Co.,Ltd.
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821-50328103-801 18930552037
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3bsc@sina.com
BOC Sciences
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1-631-485-4226; 16314854226
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Haoyuan Chemexpress Co., Ltd.
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021-58950125
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info@chemexpress.com