
LRRK2
Os inibidores de LRRK2 são compostos que têm como alvo e inibem a atividade da Leucine-Rich Repeat Kinase 2 (LRRK2), uma enzima envolvida em vários processos celulares, incluindo autofagia, tráfego vesicular e inflamação. As mutações no gene LRRK2 estão associadas a um aumento do risco de desenvolver a doença de Parkinson, tornando o LRRK2 um alvo significativo para a pesquisa em doenças neurodegenerativas. Os inibidores de LRRK2 são cruciais para explorar o papel do LRRK2 na doença de Parkinson e para desenvolver potenciais estratégias terapêuticas. Na CymitQuimica, oferecemos uma seleção de inibidores de LRRK2 para apoiar sua pesquisa em neurodegeneração, sinalização de quinase e desenvolvimento terapêutico.
Foram encontrados 33 produtos de "LRRK2"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
GNE-9605
CAS:<p>GNE-9605 is a highly effective, specifical, and brain-penetrant LRRK2 inhibitor (IC50: 19 nM).</p>Fórmula:C17H20ClF4N7OPureza:98.55% - 98.75%Cor e Forma:SolidPeso molecular:449.83GNE-7915
CAS:<p>GNE-7915 is a highly potent, selective and brain-penetrable leucine-rich repeat kinase 2 (LRRK2) inhibitor.</p>Fórmula:C19H21F4N5O3Pureza:98% - ≥95%Cor e Forma:SolidPeso molecular:443.4CZC-54252
CAS:<p>CZC-54252 is a potent inhibitor of LRRK2.</p>Fórmula:C22H25ClN6O4SPureza:99.39%Cor e Forma:SolidPeso molecular:504.99PF-06455943
CAS:<p>PF-06455943: LRRK2 inhibitor, IC50=3nM, PET radioligand, used for ADME/neuro PK & Parkinson's research.</p>Fórmula:C17H14FN5OCor e Forma:SolidPeso molecular:323.32PF-06371900
CAS:<p>PF-06371900 is a potent and highly selective inhibitor of leucine-rich repeat kinase 2 (LRRK2).</p>Fórmula:C17H16N6O2SCor e Forma:SolidPeso molecular:368.41LRRK2-IN-10
CAS:<p>LRRK2-IN-10 (compound 34) is a potent, mutation-selective, brain-penetrant inhibitor targeting G2019S-LRRK2 kinase with IC50 values of 11 nM for G2019S-LRRK2</p>Fórmula:C20H15N5OPureza:98%Cor e Forma:SolidPeso molecular:341.37LRRK2-IN-7
CAS:<p>LRRK2-IN-7: potent, selective CNS-active LRRK2 inhibitor, IC50 0.9 nM, >1000x selectivity vs kinases/channels/CYPs.</p>Fórmula:C24H26N6OPureza:99.26%Cor e Forma:SolidPeso molecular:414.5LRRK2-IN-16
CAS:<p>LRRK2-IN-16 (compound 25) is an inhibitor of the LRRK2 kinase with an IC50 value of less than 5 μM. It is applicable for research in neurodegenerative and autoimmune diseases.</p>Fórmula:C18H19N5OSCor e Forma:SolidPeso molecular:353.441LRRK2-IN-4
CAS:<p>LRRK2-IN-4: Potent, selective LRRK2 inhibitor, oral, BBB-penetrating, IC50=2.6 nM, potential for Parkinson's.</p>Fórmula:C25H29ClF2N6O2Cor e Forma:SolidPeso molecular:518.99LRRK2-IN-5
<p>LRRK2-IN-5 is an oral, BBB-penetrating selective inhibitor for LRRK2 with IC50s: 1.2μM (GS) and 16μM (WT); halts LRRK2 autophosphorylation.</p>Fórmula:C24H26F2N4O2SCor e Forma:SolidPeso molecular:472.55LRRK2-IN-2
CAS:<p>LRRK2-IN-2: selective, potent LRRK2 inhibitor, IC50 of 0.6 nM, oral, crosses blood-brain barrier, for Parkinson's research.</p>Fórmula:C23H23Cl2F3N6O2Cor e Forma:SolidPeso molecular:543.37LRRK2-IN-3
CAS:<p>LRRK2-IN-3: potent, selective oral LRRK2 blocker, BBB-penetrant, IC50 of 0.6 nM in hPBMCs, for Parkinson's research.</p>Fórmula:C25H29ClF2N6O2Cor e Forma:SolidPeso molecular:518.99LRRK2-IN-6
<p>LRRK2-IN-6 is an oral, selective LRRK2 inhibitor crossing the blood-brain barrier, targeting GS (IC50: 4.6μM) and WT LRRK2 (IC50: 49μM).</p>Fórmula:C23H24F2N4O2SCor e Forma:SolidPeso molecular:458.52

