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Pyr6

Pyr6
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Purity:99.18%
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Pyr6

Catalog No. T16688Cas No. 245747-08-4
Pyr6 (N-[4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-3-fluoro-4-pyridinecarboxamide) is a selective TRPC3 inhibitor with IC50 of 0.49 uM(Ca2+ influx inhibition in thapsigargin depleted native RBL-2H3 cells).Pyr6 is an inhibitor of Ca2+ entry, which displays higher potency to inhibit Ca2+ entry mediated by CRAC channel than by TRPC3.
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Pack SizePriceAvailabilityQuantity
2 mg$33In Stock
5 mg$52In Stock
10 mg$87In Stock
25 mg$143In Stock
50 mg$213In Stock
100 mg$319In Stock
1 mL x 10 mM (in DMSO)$58In Stock
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Product Introduction

Bioactivity
Description
Pyr6 (N-[4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-3-fluoro-4-pyridinecarboxamide) is a selective TRPC3 inhibitor with IC50 of 0.49 uM(Ca2+ influx inhibition in thapsigargin depleted native RBL-2H3 cells).Pyr6 is an inhibitor of Ca2+ entry, which displays higher potency to inhibit Ca2+ entry mediated by CRAC channel than by TRPC3.
In vitro
Pyr3 is selective inhibitor of TRPC3, inhibited Orai1- and TRPC3-mediated Ca(2+) entry and currents as well as mast cell activation with similar potency.?By contrast, Pyr6 exhibited a 37-fold higher potency to inhibit Orai1-mediated Ca(2+) entry as compared with TRPC3-mediated Ca(2+) entry and potently suppressed mast cell activation.
AliasN-[4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-3-fluoro-4-pyridinecarboxamide
Chemical Properties
Molecular Weight418.27
FormulaC17H9F7N4O
Cas No.245747-08-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 95 mg/mL (227.12 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3908 mL11.9540 mL23.9080 mL119.5400 mL
5 mM0.4782 mL2.3908 mL4.7816 mL23.9080 mL
10 mM0.2391 mL1.1954 mL2.3908 mL11.9540 mL
20 mM0.1195 mL0.5977 mL1.1954 mL5.9770 mL
50 mM0.0478 mL0.2391 mL0.4782 mL2.3908 mL
100 mM0.0239 mL0.1195 mL0.2391 mL1.1954 mL

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