ChemicalBook--->CAS DataBase List--->1315323-00-2

1315323-00-2

1315323-00-2 Structure

1315323-00-2 Structure
IdentificationBack Directory
[Name]

Pyr10
[CAS]

1315323-00-2
[Synonyms]

Pyr10
PYR-10;PYR 10
Pyr10 >=98% (HPLC)
N-{4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}-4-methylbenzenesulfonamide
Benzenesulfonamide, N-[4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-4-methyl-
[Molecular Formula]

C18H13F6N3O2S
[MDL Number]

MFCD28411625
[MOL File]

1315323-00-2.mol
[Molecular Weight]

449.37
Chemical PropertiesBack Directory
[Melting point ]

105-107 °C
[Boiling point ]

470.1±55.0 °C(Predicted)
[density ]

1.47±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 100 mg/mL (222.53 mM);Water : < 0.1 mg/mL (insoluble)
[form ]

Solid
[pka]

6.98±0.10(Predicted)
[color ]

White to light yellow
[InChI]

1S/C18H13F6N3O2S/c1-11-2-8-14(9-3-11)30(28,29)26-12-4-6-13(7-5-12)27-16(18(22,23)24)10-15(25-27)17(19,20)21/h2-10,26H,1H3
[InChIKey]

CVALMMCIOLXHDM-UHFFFAOYSA-N
[SMILES]

FC(F)(F)c1[n](nc(c1)C(F)(F)F)c2ccc(cc2)N[S](=O)(=O)c3ccc(cc3)C
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319
[Precautionary statements ]

P301+P312+P330-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Pyr10 is a pyrazole derivative and a selective TRP cation 3 (TRPC3) inhibitor. Pyr10 inhibits Ca2+ influx in carbachol-stimulated TRPC3-transfected HEK293 cells with an IC50 of 0.72 μM (IC50 of 13.08 μM for store operated Ca2+ entry in BRL-2H3 cells). Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels[1].
[Biological Activity]

Pyr10 is a novelselective inhibitor of the transient receptor potential channel TRPC3. Pyr10 blocks carbachol-induced calcium entry into TRPC3-transfected HEK293 cells (IC50 = 0.72 μM)with significantly lower activity against STIM1/Orai1 mediated release of calcium from endoplasmic reticulum (store operated calcium entry) in BRL-2H3 cells (IC50 = 13.08 μM).
[in vivo]

Genetic deletion (TRPC3-/-) and pharmacological channel blockade with Pyr10 blunts ventricular cardiac fibroblast activation and myocardial fibrosis in N(ω)-nitro-l-arginine methyl ester (l-NAME) hypertensive mice[2].

[IC 50]

TRPC3: 0.72 μM (IC50)
[storage]

Store at -20°C
[References]

[1] Schleifer H, et al. Novel pyrazole compounds for pharmacological discrimination between receptor-operated and store-operated Ca(2+) entry pathways. Br J Pharmacol. 2012 Dec;167(8):1712-1722. DOI:10.1111/j.1476-5381.2012.02126.x
[2] Saliba Y, et al. Transient Receptor Potential Canonical 3 and Nuclear Factor of Activated T Cells C3 Signaling Pathway Critically Regulates Myocardial Fibrosis. Antioxid Redox Signal. 2019 Jun 1;30(16):1851-1879. DOI:10.1089/ars.2018.7545
Spectrum DetailBack Directory
[Spectrum Detail]

Pyr10(1315323-00-2)1HNMR
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