6 Results for "

LRRK2-IN-3

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "LRRK2-IN-3" in MCE Product Catalog:

Cat. No.: HY-145318
CAS No.: 2641054-60-4
Target:  

LRRK2

Research Areas:  

Neurological Disease

LRRK2-IN-3 (compoubd 24) is a potent, selective, orally active and brain-penetrant inhibitor LRRK2, with IC50 of 2.6 nM in human PBMCs. LRRK2-IN-3 can be used for the research of Parkinson's disease .
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Cat. No.: HY-112809
CAS No.: 1398695-47-0
Purity:  98.39%
Research Areas:  

Inflammation/Immunology

GSK2646264 (Compound 44) is a potent and selective spleen tyrosine kinase (SYK) inhibitor with a pIC50 of 7.1. GSK2646264 also inhibits other kinases with pIC50 values of 5.4, 5.4, 5.3, 5, 4.5, <4.6 and <4.3 against LCK, LRRK2, GSK3β, JAK2, VEGFR2, Aurora B and Aurora A, respectively. GSK2646264 is penetrable into the epidermis and dermis of the skin .
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Cat. No.: HY-178797
CAS No.: 3080678-98-1
Target:  

PROTACs LRRK2

PROTAC LRRK2 Degrader-3 (compound 6) is a PROTAC LRRK2 degrader with a DC50 of 0.17 nM. PROTAC LRRK2 Degrader-3 can be used for research in Parkinson’s disease and inflammation .
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Cat. No.: HY-178830
CAS No.: 2839672-81-8
Target:  

PROTAC Linkers

Research Areas:  

Neurological Disease

Azacyclohexane-O-cyclohexane-C-(OCH3)2 is a PROTAC linker that can be used to synthesize PROTAC LRRK2 Degrader-3 (HY-178797). PROTAC LRRK2 Degrader-3 is a potent LRRK2 PROTAC degrader with anti-neuroinflammatory activity .
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Cat. No.: HY-178828
CAS No.: 3040075-64-4
E3 ligase Ligand 29-azacyclohexane-O-cyclohexane-CO is a synthesized E3 ligase ligand-linker conjugate that can be used to synthesize PROTAC LRRK2 Degrader-3 (HY-178797). PROTAC LRRK2 Degrader-3 is a potent LRRK2 PROTAC degrader with anti-neuroinflammatory activity .
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Cat. No.: HY-184652
Target:  

LRRK2 JNK CaMK Casein Kinase

Research Areas:  

Neurological Disease

LRRK2/JNK3-IN-1 is a brain-penetrant multi-target inhibitor of LRRK2 (including G2019S mutant and wild-type) and JNK3, with enzymatic IC50 values of 3.90 nM against LRRK2 G2019S, 3.24 nM against wild-type LRRK2, and 22.1 nM against JNK3. LRRK2/JNK3-IN-1 displays favorable selectivity in a 97-kinase profiling screen, and also shows inhibitory activity against JNK1, JNK2, and MKNK2. LRRK2/JNK3-IN-1 can be used for the research of Parkinson's disease .
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