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About This Item
Empirical Formula (Hill Notation):
C21H22ClN3O
CAS Number:
Molecular Weight:
367.87
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
SMILES string
Clc1c(ccc(c1)C#N)O[C@H]2[C@@H](Cc4c2cccc4)N3C[C@@H](CCC3)N
InChI key
RLKRLNQEXBPQGQ-OZOXKJRCSA-N
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
-10 to -25°C
Quality Level
Related Categories
Biochem/physiol Actions
TRPC6-selective transient receptor potential channel (TRPC) inhibitor.
SAR7334 is a TRPC6-selective transient receptor potential channel (TRPC) inhibitor (IC50 against OAG-induced Ca2+ influx in TRPC3/6/7-expressing cells = 9.5/226/282 nM, IC50 >10 μM in TRPC4/10 cells; IC50 = 7.9 nM by whole-cell patch-clamp using TRPC6-HEK-FITR cells).
SAR7334 is a TRPC6-selective transient receptor potential channel (TRPC) inhibitor (IC50 against OAG-induced Ca2+ influx in TRPC3/6/7-expressing cells = 9.5/226/282 nM, IC50 >10 μM in TRPC4/10 cells; IC50 = 7.9 nM by whole-cell patch-clamp using TRPC6-HEK-FITR cells).
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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The role of TRPC6 calcium channels and P2 purinergic receptors in podocyte mechanical and metabolic sensing
Physiology international (2021)
TRPC6 inhibits renal tubular epithelial cell pyroptosis through regulating zinc influx and alleviates renal ischemia-reperfusion injury
Faseb Journal, 36(10) (2022)
Discovery and pharmacological characterization of a novel potent inhibitor of diacylglycerol-sensitive TRPC cation channels
British Journal of Pharmacology, 172(14), 3650-3660 (2015)
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