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About This Item
Empirical Formula (Hill Notation):
C16H16F3NO2S
CAS Number:
Molecular Weight:
343.36
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
41106300
MDL number:
Quality Level
assay
>97% (HPLC)
form
powder
color
white
mp
114-114.8 °C (lit.)
solubility
DMSO: >20 mg/mL
SMILES string
Cc1cc(C)c(c(C)c1)S(=O)(=O)Nc2cccc(c2)C(F)(F)F
InChI
1S/C16H16F3NO2S/c1-10-7-11(2)15(12(3)8-10)23(21,22)20-14-6-4-5-13(9-14)16(17,18)19/h4-9,20H,1-3H3
InChI key
ZIIUUSVHCHPIQD-UHFFFAOYSA-N
Application
m-3M3FBS has been used for MAP kinase assay in 293T cells. It has also been used for intracellular calcium analysis1. Furthermore, it has been used (at a conc. of 1 μM) as a PLC activator for sensitizing TRPA1 in HEK293t cells2.
Biochem/physiol Actions
First known direct activator of phospholipase C (activates β2, β3, γ1, γ2, δ1 isoforms).
Preparation Note
m-3M3FBS is soluble in DMSO at a concentration that is greater than 20 mg/ml.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ondrej Cerny et al.
Journal of immunology (Baltimore, Md. : 1950), 198(3), 1285-1296 (2017-01-01)
The adenylate cyclase toxin-hemolysin (CyaA) plays a key role in immune evasion and virulence of the whooping cough agent Bordetella pertussis. CyaA penetrates the complement receptor 3-expressing phagocytes and ablates their bactericidal capacities by catalyzing unregulated conversion of cytosolic ATP
Kathryn P Trogden et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 32(5), 2841-2854 (2018-02-07)
Vimentin is a cytoskeletal intermediate filament protein that is expressed in mesenchymal cells and cancer cells during the epithelial-mesenchymal transition. The goal of this study was to identify vimentin-targeting small molecules by using the Tocriscreen library of 1120 biochemically active
Jieny Gröper et al.
Cells, 9(4) (2020-04-29)
Ligand-based selectivity in signal transduction (biased signaling) is an emerging field of G protein-coupled receptor (GPCR) research and might allow the development of drugs with targeted activation profiles. Human formyl peptide receptor 1 (FPR1) is a GPCR that detects potentially