ChemicalBook CAS DataBase List 1454555-29-3

1454555-29-3

Name	LP-935509
CAS	1454555-29-3
Molecular Formula	C20H24N6O3
MDL Number	MFCD31689756
Molecular Weight	396.44
MOL File	1454555-29-3.mol

Chemical Properties

density	1.34±0.1 g/cm3(Predicted)
solubility	DMSO: Soluble
form	Solid
pka	1.73±0.12(Predicted)
color	Light yellow to yellow

Hazard Information

Description

LP-935509 is a potent inhibitor of the Adapter protein-2 Associated Kinase 1 (AAK1).

Uses

LP-935509 is an orally active, potent, selective, ATP-competitive and brain-penetrant inhibitor of adaptor protein-2 associated kinase 1 (AAK1) with an IC50 of 3.3 nM and a Ki of 0.9 nM, respectively. LP-935509 is also a potent inhibitor of BIKE (IC50=14 nM) and a modest inhibitor of GAK (IC50=320 nM). LP-935509 shows antinociceptive activity. LP-935509 can be used for neuropathic pain and SARS-CoV-2 research[1].

in vivo

LP-935509 (0-60 mg/kg; PO, single) causes a robust reduction in pain behavior^[1].
? LP-935509 (0.1-30 mg/kg; PO, single dosage) causes a dose-dependent reversal of thermal hyperalgesia in CCI model^[1].
? LP-935509 (IV (1 mg/kg) or orally (10 mg/kg); once) has 100% oral bioavailability and a plasma half life of 3.6 hours^[1].

Animal Model:	Male C57BL/6J mice (with SNL(spinal nerve ligation) injury, n=8-10 male mice per group)^[1]
Dosage:	0, 10, 30 and 60 mg/kg (10 ml/kg)
Administration:	PO, single
Result:	Caused a dose-dependent reduction in phase II paw flinches that was significantly lower than the vehicle-treated animals; exhibited a dose-dependent reversal of the mechanical allodynia; Caused a robust reduction in pain behavior.

Animal Model:	Male Sprague-Dawley rats (CCI (chronic constriction injury)-operated rats)^[1]
Dosage:	0, 0.1, 0.3, 1, 3, 10, or 30 mg/kg
Administration:	PO, two daily, for 5 days
Result:	Caused a dose-dependent reversal of thermal hyperalgesia, cold allodynia, mechanical allodynia, and mechanical hyperalgesia in CCI animals. Reversed the behavioral deficits, with ED₅₀ values ranging from 2 mg/kg to 10 mg/kg.

Animal Model:	Male Sprague-Dawley rats^[1]
Dosage:	1 mg/kg (IV), 10 mg/kg (PO)
Administration:	IV, PO; once (Pharmacokinetic Analysis)
Result:	Had 100% oral bioavailability and a plasma half life of 3.6 hours; The Cmax for the 10 mg/kg oral dose was 5.2 μM at 0.5-hour postdose; had a plasma-free fraction of 2.6% in mice. Brain drug levels exceeded plasma drug levels with a brain/plasma drug ratio typically between 3 and 4, showing that LP-935509 was highly brain-penetrant.

References

[1] Kostich W, et al. Inhibition of AAK1 Kinase as a Novel Therapeutic Approach to Treat Neuropathic Pain. J Pharmacol Exp Ther. 2016 Sep;358(3):371-86. DOI:10.1124/jpet.116.235333
[2] Mushtaq, et al. Role Of Endocytic Machinery Regulators in EGFR Traffic and Viral Entry (2021). Theses & Dissertations. 532.

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