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ChemicalBook--->CAS DataBase List--->2728291-29-8

2728291-29-8

2728291-29-8 Structure

2728291-29-8 Structure
IdentificationBack Directory
[Name]

P2Y14R antagonist 1
[CAS]

2728291-29-8
[Synonyms]

P2Y14R antagonist 1
[Molecular Formula]

C15H12BrN3O2
[MOL File]

2728291-29-8.mol
[Molecular Weight]

346.18
Chemical PropertiesBack Directory
[Boiling point ]

684.8±40.0 °C(predicted)
[density ]

1.627±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)
[pka]

12.30±0.30(predicted)
Hazard InformationBack Directory
[Uses]

P2Y14R antagonist 1 (compound I-17) is a selective P2Y14R antagonist with an IC50 of 0.6 nM. It exhibits potent P2Y14R antagonistic activity, both in vitro and in vivo efficacy, and favorable pharmacokinetic profiles. P2Y14R antagonist 1 reduces the release of inflammatory factors and cell pyroptosis through the NOD-like receptor family pyrin domain-containing 3 (NLRP3)/gasdermin D (GSDMD) signaling pathway. P2Y14R antagonist 1 holds promise for research in the field of acute gouty arthritis[1].
[in vivo]

P2Y14R antagonist 1 (compound I-17) (5-20 mg/mL, i.p., 1 h) can promote the inflammatory response caused by MSU crystal injection-induced acute gouty arthritis in the MSU-induced mouse gout model[1].

1.19
Pharmacokinetic Analysis in MC38 Syngeneic Model[1]
P2Y14R antagonist 1Cmax(g/mL)T1/2 (h) Tmax (h)AUC0-∞ (h ng/mL) CL (L/h/kg)F (%)
i.v. (10 mg/kg) 15337.61817653.5
p.o. (30 mg/kg)289512.6032284514.8075
Animal Model:Acute gouty arthritis model[1]
Dosage:5-20 mg/mL
Administration:Intraperitoneal injection (i.p.) , Injection time: 60 min
Result:Effectively reduced paw swelling in the MSU-induced mouse gout model, significantly decreased the production of pro-inflammatory cytokines IL-1β, IL-6, and IL-18 induced by MSU, markedly inhibited inflammatory cell infiltration in foot tissues induced by MSU, and significantly suppressed the increase of NLRP3 induced by MSU.
[IC 50]

P2Y14 Receptor: 0.6 nM (IC50); P2Y2 Receptor: > 100 nM (IC50); P2Y6 Receptor: 89.7 nM (IC50); P2Y12 Receptor: > 100 nM (IC50); P2Y1 Receptor: > 100 nM (IC50); NLRP3
[References]

[1] Liu W, et al. Discovery of N-Substituted Acetamide Derivatives as Promising P2Y14R Antagonists Using Molecular Hybridization Based on Crystallographic Overlay. J Med Chem. 2024 Jun 27;67(12):10233-10247. DOI:10.1021/acs.jmedchem.4c00555
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