(S)-2-Amino-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-1-(isoindolin-2-yl)butane-1,4-dione Struktur

(S)-2-Amino-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-1-(isoindolin-2-yl)butane-1,4-dione

Bezeichnung:(S)-2-Amino-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-1-(isoindolin-2-yl)butane-1,4-dione

Englisch Name:(S)-2-Amino-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-1-(isoindolin-2-yl)butane-1,4-dione

CBNumberCB23367548

SummenformelC29H30F2N4O2

Molgewicht504.57

(S)-2-Amino-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-1-(isoindolin-2-yl)butane-1,4-dione physikalisch-chemischer Eigenschaften

Siedepunkt	674.3±55.0 °C(Predicted)
Dichte	1.304±0.06 g/cm3(Predicted)
storage temp.	2-8°C(protect from light)
Löslichkeit	Soluble in DMSO (>20 mg/ml)
pka	7.25±0.33(Predicted)
Aggregatzustand	solid
Farbe	Off-white
Stabilität	Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.

(S)-2-Amino-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-1-(isoindolin-2-yl)butane-1,4-dione Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
1G244 (847928-32-9) is a potent and selective inhibitor of the prolyl dipeptidases DPP8 (IC50 = 14 nM) and DPP9 (IC50 = 53 nM).1,2? It does not inhibit DPP2, DPP4 or fibroblast activation protein (FAP) at 100 μM.1,2 1G244 is a slow binding competitive inhibitor of DPP8 but a competitive and reversible inhibitor of DPP9.2? Inhibition of DPP8/9 by 1G244 has been shown to cause pro-caspase-1-dependent pyroptosis in macrophages and monocytes.3 1G244 also induced cell death in DPP8/9 knockout cells at higher concentration indicating there may be some off-target effects.3 1G244 blocks adipogenesis in preadipocyte 3T3-L1 and 3T3-F422A cells.4? DPP8/9 inhibition attenuates PPARg2 induction during preadipocyte differentiation.4 Because of its inhibitory effects on pro-inflammatory macrophages, 1G244 inhibition of DPP8/9 has been examined as a potential therapy for reducing atherosclerosis and/or in the prevention of plaque rupture.5,6 Cell permeable.
Einzelnachweise
Jiaang et al. (2005), Novel isoindoline compounds for potent and selective inhibition of prolyl dipeptidase DPP8; Bioorg.Med.Chem.Lett.15 687 Wu et al. (2009), Biochemistry, pharmacokinetics, and toxicology of a potent and selective DPP8/9 inhibitor; Biochem.Pharmacol. 78 203 Okondo et al. (2017), DPP8/9 inhibition induces pro-caspase-1-dependent monocyte and macrophage pyroptosis; Nat.Chem.Biol. 13 46 Han et al. (2015), Inhibition of dipeptidyl peptidase 8/9 impairs preadipocyte differentiation; Sci.Rep. 5 12348 Matheeussen et al. (2013), Dipeptidyl peptidases in atherosclerosis: expression and role in macrophage differentiation, activation and apoptosis; Basic Res.Cardiol. 108 350 Waumans et al. (2016), The Dipeptidyl Peptidases 4,8, and 9 in Mouse Monocytes and Macrophages: DPP8/9 Inhibition Attenuates M1 Macrophage Activation in Mice; Inflammation 39 413

(S)-2-Amino-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-1-(isoindolin-2-yl)butane-1,4-dione Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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