CAS NO: | 1123231-07-1 |
规格: | ≥98% |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
250mg | 电议 |
500mg | 电议 |
Molecular Weight (MW) | 318.42 |
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Formula | C20H22N4 |
CAS No. | 1123231-07-1 |
Storage | -20℃ for 3 years in powder form |
-80℃ for 2 years in solvent | |
Solubility (In vitro) | DMSO: ≥ 42 mg/mL |
Water: <1 mg/mL | |
Ethanol: <1 mg/mL | |
Solubility (In vivo) | NCC1CCN(C2=NC=CC(C3=CC=C4C=CC=CC4=C3)=N2)CC1 |
Synonyms | WAY 262611; WAY-262611; WAY262611; WAY-262611 HCl |
In Vitro | In vitro activity: WAY-262611 is a novel agonist of the wingless β-Catenin pathway that increases bone formation rate with EC50 of 0.63 uM in TCF-Luciferase assay. WAY-262611 has excellent pharmacokinetic properties and showed a dose dependent increase in the trabecular bone formation rate in ovariectomized rats following oral administration. WAY-262611 acts via the Wnt β-catenin pathway and most likely through inhibition of Dkk-1. WAY-262611 has excellent pharmacokinetic properties and showed a dose dependent increase in the trabecular bone formation rate in ovariectomized rats following oral administration. WAY-262611 was discovered from a high-throughput screening (HTS) campaign to discover small molecule leads for the treatment of bone disorders concluded with the discovery of a compound with a 2-aminopyrimidine template that targeted the Wnt beta-catenin cellular messaging system. Hit-to-lead in vitro optimization for target activity and molecular properties led to the discovery of (1-(4-(naphthalen-2-yl)pyrimidin-2-yl)piperidin-4-yl)methanamine (5, WAY-262611). Kinase Assay: WAY-262611 is a novel agonist of the wingless β-Catenin pathway that increases bone formation rate with EC50 of 0.63 uM in TCF-Luciferase assay. WAY-262611 has the most potent activity in the primary assay, low kinase inhibition potential, and high solubility. |
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In Vivo | WAY-262611 has excellent pharmacokinetic properties and shows a dose dependent increase in the trabecular bone formation rate in ovariectomized rats following oral administration. Calvariae from wt mice treated with WAY-262611 shows statistically increased BFR, while similarly treated KO animals are no different from control. This indicates that WAY-262611 is acting via the Wnt β-catenin pathway and most likely through inhibition of Dkk-1. |
Animal model | Ovariectomized rats and mice |
Formulation & Dosage | Rats: WAY-262611 is dissolved in DMSO and diluted with saline for iv (Rats). WAY-262611 is prepared in 0.5% methylcellulose/2% Tween-80 for po OVX rats14 are treated orally with 5 (po, vehicle=0.5% methylcellulose/2% Tween-80, qd, 28 days) at four doses. Trabecular bone formation rate (BFR) in the tibia is established in all dose groups at the end of the in-life portion of the study. A clear dose response and activity as low as 0.3 mg/kg/day are observed; Mice: To confirm activity via the Wnt pathway, the calvariae of wild type (wt) and Dkk-1 knockout (KO) mice are treated with 5 once a day for 7 days (DMSO solution, sc injection). The KO animals are not expected to respond because of the inherent inability to inhibit a missing target protein, while wild type animals with fully expressed Dkk-1 are expected to show a pharmacological response. |
References | J Med Chem. 2009 Nov 26;52(22):6962-5. |