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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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M276039-1mg | 1mg | In stock | $49.90 | |
M276039-5mg | 5mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $119.90 | |
M276039-10mg | 10mg | In stock | $189.90 | |
M276039-50mg | 50mg | In stock | $659.90 |
Potent and selective LRRK2 inhibitor
Specifications & Purity | Moligand™, ≥98% |
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Biochemical and Physiological Mechanisms | Highly effective and selective LRRK2 inhibitors. Inhibition of LRRK2 in cell-free (IC 50 = 0.76 NM) , dephosphorylated cells (IC 50 = 1.4 nM) and radioligand binding (IC 50 = 3.4 nM) assay. |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of leucine rich repeat kinase 2 |
Note | Refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description |
MLi-2 is a structurally novel, highly potent, and selective LRRK2 kinase inhibitor with central nervous system activity. MLi-2 exhibits exceptional potency in a purified LRRK2 kinase assay in vitro (IC50 = 0.76 nM), a cellular assay monitoring dephosphorylation of LRRK2 pSer935 LRRK2 (IC50 = 1.4 nM), and a radioligand competition binding assay (IC50 = 3.4 nM).
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | (2R,6S)-2,6-dimethyl-4-[6-[5-(1-methylcyclopropyl)oxy-1H-indazol-3-yl]pyrimidin-4-yl]morpholine |
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INCHI | InChI=1S/C21H25N5O2/c1-13-10-26(11-14(2)27-13)19-9-18(22-12-23-19)20-16-8-15(28-21(3)6-7-21)4-5-17(16)24-25-20/h4-5,8-9,12-14H,6-7,10-11H2,1-3H3,(H,24,25)/t13-,14+ |
InChi Key | ATUUNJCZCOMUKD-OKILXGFUSA-N |
Canonical SMILES | CC1CN(CC(O1)C)C2=NC=NC(=C2)C3=NNC4=C3C=C(C=C4)OC5(CC5)C |
Isomeric SMILES | C[C@@H]1CN(C[C@@H](O1)C)C2=NC=NC(=C2)C3=NNC4=C3C=C(C=C4)OC5(CC5)C |
PubChem CID | 78319901 |
Molecular Weight | 379.46 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
I2419595 | Certificate of Analysis | Sep 11, 2024 | M276039 |
I2419596 | Certificate of Analysis | Sep 11, 2024 | M276039 |
I2419597 | Certificate of Analysis | Sep 11, 2024 | M276039 |
I2419598 | Certificate of Analysis | Sep 11, 2024 | M276039 |
G2412495 | Certificate of Analysis | Jul 02, 2024 | M276039 |
G2412496 | Certificate of Analysis | Jul 02, 2024 | M276039 |
B2215423 | Certificate of Analysis | Aug 10, 2023 | M276039 |
B2215424 | Certificate of Analysis | Aug 10, 2023 | M276039 |
B2215430 | Certificate of Analysis | Aug 10, 2023 | M276039 |
Solubility | Soluble in DMSO to 100 mM |
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Starting at $139.90
1. Fell MJ, Mirescu C, Basu K, Cheewatrakoolpong B, DeMong DE, Ellis JM, Hyde LA, Lin Y, Markgraf CG, Mei H et al.. (2015) MLi-2, a Potent, Selective, and Centrally Active Compound for Exploring the Therapeutic Potential and Safety of LRRK2 Kinase Inhibition.. J Pharmacol Exp Ther, 355 (3): (397-409). [PMID:26407721] [10.1021/op500134e] |
2. Scott JD, DeMong DE, Greshock TJ, Basu K, Dai X, Harris J, Hruza A, Li SW, Lin SI, Liu H et al.. (2017) Discovery of a 3-(4-Pyrimidinyl) Indazole (MLi-2), an Orally Available and Selective Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitor that Reduces Brain Kinase Activity.. J Med Chem, 60 (7): (2983-2992). [PMID:28245354] [10.1021/op500134e] |
3. Fdez E et al.. (2022) Pathogenic LRRK2 regulates centrosome cohesion via Rab10/RILPL1-mediated CDK5RAP2 displacement.. iScience, 25 (6): (104476). [PMID:35721463] |