4-Chloro-N-[2-[[5-(trifluoromethyl)-2-pyridinyl]sulfonyl]ethyl]benzamide manufacturers and suppliers

4-Chloro-N-[2-[[5-(trifluoromethyl)-2-pyridinyl]sulfonyl]ethyl]benzamide suppliers

4-Chloro-N-[2-[[5-(trifluoromethyl)-2-pyridinyl]sulfonyl]ethyl]benzamide

CAS:: 188591-46-0

MF:: C15H12ClF3N2O3S

MW:: 392.78

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Properties

Boiling point:: 585.1±50.0 °C(Predicted)

Density: 1.448±0.06 g/cm3 (20 ºC 760 Torr)

storage temp.: 2-8°C

solubility: DMSO: ≥10mg/mL

form: White solid

pka: 12.92±0.46(Predicted)

color: white to off-white

Stability:: Stable for 1 year for up to year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.

InChI: InChI=1S/C15H12ClF3N2O3S/c16-12-4-1-10(2-5-12)14(22)20-7-8-25(23,24)13-6-3-11(9-21-13)15(17,18)19/h1-6,9H,7-8H2,(H,20,22)

InChIKey: JFUIMTGOQCQTPF-UHFFFAOYSA-N

SMILES: C(NCCS(C1=NC=C(C(F)(F)F)C=C1)(=O)=O)(=O)C1=CC=C(Cl)C=C1

CAS DataBase Reference: 188591-46-0

Safety Information

Symbol(GHS): GHS07

Signal word: Warning

Hazard statements: H319

Precautionary statements: P264-P280-P305+P351+P338-P337+P313P

Hazard Codes: Xi

Risk Statements: 36

Safety Statements: 26

WGK Germany: 3

Use

PPARβ/δ is thought to play a role in lipid homeostasis and glucose disposal by regulating genes involved in fatty acid oxidation, reverse cholesterol transport, and carbon substrate utilization in skeletal muscle. It has also been implicated in the progression of certain cancers. GSK3787 is an irreversible antagonist of PPARβ/δ (pIC50 = 6.6) with no measurable affinity for PPARα or PPARγ (pIC50 5). At 1μM, it inhibits the expression of PPARβ/δ-regulated target genes, pyruvate dehydrogenase kinase 4 and carnitine palmitoyl transferase 1a, which are important for energy homeostasis in human skeletal muscle cells. GSK3787 (at 1 μM) also antagonizes agonist-induced expression of angiopoietin-like protein 4 in mouse fibroblasts, mouse keratinocytes, and human MCF-7, Huh7, and HepG2 cancer cell lines.[Cayman Chemical]

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