2231664-45-0

2231664-45-0 structure
2231664-45-0 structure
  • Name: BMT-090605 hydrochloride
  • Chemical Name: BMT-090605 hydrochloride
  • CAS Number: 2231664-45-0
  • Molecular Formula: C21H25ClN4O2
  • Molecular Weight: 400.90
  • Catalog: Research Areas Neurological Disease
  • Create Date: 2022-11-21 18:41:11
  • Modify Date: 2024-07-15 18:06:30
  • BMT-090605 hydrochloride is a potent, selective the adapter protein-2 associated kinase 1 (AAK1) inhibitor with an IC50 value of 0.6 nM. BMT-090605 hydrochloride shows antinociceptive activity. BMT-090605 hydrochloride inhibits BMP-2-inducible protein kinase (BIKE) and Cyclin G-associated kinase (GAK) with IC50 values of 45 nM and 60 nM, respectively. BMT-090605 hydrochloride can be used for the research of neuropathic pain[1].

Name BMT-090605 hydrochloride
Description BMT-090605 hydrochloride is a potent, selective the adapter protein-2 associated kinase 1 (AAK1) inhibitor with an IC50 value of 0.6 nM. BMT-090605 hydrochloride shows antinociceptive activity. BMT-090605 hydrochloride inhibits BMP-2-inducible protein kinase (BIKE) and Cyclin G-associated kinase (GAK) with IC50 values of 45 nM and 60 nM, respectively. BMT-090605 hydrochloride can be used for the research of neuropathic pain[1].
Related Catalog
Target

IC50: 0.6 nM (AAK1); 45 nM (BIKE); 60 nM (GAK)[1]

In Vitro BMT-090605 hydrochloride shows AAK1inhibitory activity with an IC50 of 0.63 nM[1]. BMT-090605 hydrochloride inhibits BMP-2-inducible protein kinase (BIKE) and Cyclin G-associated kinase (GAK) with IC50 values of 45 nM and 60 nM, respectively[1].
In Vivo BMT-090605 hydrochloride(intrathecal; 0.3-3 µg/rat) causes antinociception by inhibiting AAK1 in the spinal cord[1]. Animal Model: Male Sprague-Dawley rats (chronic constriction injury (CCI) model)[1] Dosage: 0.3-3 µg/rat Administration: Intrathecal Result: Caused a dose-dependent reduction in thermal hyperalgesia.
Molecular Formula C21H25ClN4O2
Molecular Weight 400.90
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