2019
DOI: 10.1016/j.bmcl.2019.06.018
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The discovery of novel 3-aryl-indazole derivatives as peripherally restricted pan-Trk inhibitors for the treatment of pain

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Cited by 11 publications
(4 citation statements)
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“…15 ) of pan-Trk for the treatment of pain. 76 Among the synthesized compounds by varying the substitution in ring A, compound 39a with a methoxypyridine moiety was found to exhibit the highest potency but moderate metabolic stability. Replacement of the methoxy group with piperidine (39b) led to high cell permeability and significant potency (TRKA IC 50 = 1.6 nM).…”
Section: Mono-kinase Inhibitorsmentioning
confidence: 98%
“…15 ) of pan-Trk for the treatment of pain. 76 Among the synthesized compounds by varying the substitution in ring A, compound 39a with a methoxypyridine moiety was found to exhibit the highest potency but moderate metabolic stability. Replacement of the methoxy group with piperidine (39b) led to high cell permeability and significant potency (TRKA IC 50 = 1.6 nM).…”
Section: Mono-kinase Inhibitorsmentioning
confidence: 98%
“…The ratio of compound 88 in brain to plasma was found to be only 0.03 after an i.p. injection of 2.5 mg/kg in rats [ 98 ].…”
Section: Pyrazole-based Trk Inhibitorsmentioning
confidence: 99%
“…The availability of several structures of TrkA in the protein data bank enabled the use of chemoinformatic approaches for the development of new Trk inhibitors. For example, a structure-based drug design approach led to the discovery of 3-pyrazolyl-indazole 1 ( Figure 1 ) as a potent pan-Trk inhibitor with low brain penetration ability and in vivo activity in a thermal hypersensitivity inflammatory pain model induced by Complete Freund’s Adjuvant (CFA) [ 12 ].…”
Section: Tyrosine Kinase (Tk) Groupmentioning
confidence: 99%