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Cat. No. Product Name Information
PC-49823

LRRK2 inhibitor 25

LRRK2 inhibitor

LRRK2 inhibitor 25 is a potent, selective, CNS-penetrant and ATP competitive LRRK2 inhibitor with biochemical IC50 of 0.9 nM, cellular IC50 of 0.3 nM.
PC-49822

LRRK2 GTP binding inhibitor 68

LRRK2 inhibitor

LRRK2 GTP binding inhibitor 68 is a potent, GTP binding inhibitor of LRRK2 with IC90 of 10 nM, inhibits LRRK2 GTP binding and kinase activities.
PC-49821

FX2149

LRRK2 inhibitor

FX2149 (FX 2149) is a potent, BBB permeable inhibitor of LRRK2 GTP binding activity with IC90 of 10 nM, reduces PD-linked mutant LRRK2 variants (G2019S and R1441C) that bound with GTP.
PC-49820

BIIB122

LRRK2 inhibitor

BIIB122 (DNL151) is a potent, selective, CNS-penetrant LRRK2 inhibitor.
PC-72161

G2019S-LRRK2 inhibitor 38

G2019S-LRRK2 inhibitor

G2019S-LRRK2 inhibitor 38 is a potent, selective, brain penetrant G2019S-LRRK2 kinase inhibitor with IC50 of <1 nM, cellular EC50 of 40 nM, >2,000-fold selectivity over WT LRRK2 (cellular EC50>100 uM).
PC-72160

EB-42486

G2019S-LRRK2 inhibitor

EB-42486 (EB42486) is a potent, highly selective G2019S-LRRK2 kinase inhibitor with biochemical IC50 of <0.2 nM.
PC-43416

GSK2578215A

GSK2578215A is a highly potent, selective, BBB-permeable LRRK2 inhibitor with IC50 of 10.9 and 9.9 nM for wild-type LRRK2 and the G2019S mutant, respectively.
PC-42945

GNE-9605

GNE-9605 is a highly potent, selective, brain penetrant LRRK2 inhibitor with Ki of 2 nM, pLRRK2 IC50 of 19 nM.
PC-62508

PFE-360

PFE-360 is a novel potent, selective, brain-penetrating LRRK2 inhibitor with IC50 of 3 nM.
PC-62372

SR 9444

SR 9444 is a small molecule bidentate-binding dual inhibitor probe of the LRRK2 and JNK with IC50 of 12 nM and 99 nM respectively.
PC-42726

LRRK2-IN-1

A potent LRRK2 inhibitor with IC50s of 13 nM/6 nM for wild-type/G2019S mutant LRRK2 repectively (0.1 mM ATP in the assay).
PC-45094

JH-II-127

A potent and selective inhibitor of both wild-type and G2019S mutant LRRK2 with IC50 of 6.6 and 2.2 nM, respectively.

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