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MLi-2 - ≥98%, high purity , CAS No.1627091-47-7, Inhibitor of leucine rich repeat kinase 2

  • Moligand™
  • ≥98%
Item Number
M276039
Grouped product items
SKUSizeAvailabilityPrice Qty
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

Basic Description

Synonyms(2R,6S)-2,6-Dimethyl-4-[6-[5-(1-methylcyclopropyl)oxy-1H-indazol-3-yl]pyrimidin-4-yl]morpholine;cis-2,6-Dimethyl-4-(6-(5-(1-methylcyclopropoxy)-1H-indazol-3-yl)pyrimidin-4-yl)morpholine;rel-3-[6-[(2R,6S)-2,6-Dimethyl-4-morpholinyl]-4-pyrimidinyl]-5-[(1-me
Specifications & Purity≥98%
Biochemical and Physiological MechanismsHighly 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 TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of leucine rich repeat kinase 2
NoteRefer 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).

Associated Targets

LRRK2 Tchem Leucine-rich repeat serine/threonine-protein kinase 2 4 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (2R,6S)-2,6-dimethyl-4-[6-[5-(1-methylcyclopropyl)oxy-1H-indazol-3-yl]pyrimidin-4-yl]morpholine
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

Certificates

Certificate of Analysis(COA)

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5 results found

Lot NumberCertificate TypeDateItem
G2412495Certificate of AnalysisJul 02, 2024 M276039
G2412496Certificate of AnalysisJul 02, 2024 M276039
B2215423Certificate of AnalysisAug 10, 2023 M276039
B2215424Certificate of AnalysisAug 10, 2023 M276039
B2215430Certificate of AnalysisAug 10, 2023 M276039

Chemical and Physical Properties

SolubilitySoluble in DMSO to 100 mM

Related Documents

References

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]
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]
3. Fdez E et al..  (2022)  Pathogenic LRRK2 regulates centrosome cohesion via Rab10/RILPL1-mediated CDK5RAP2 displacement..  iScience,  25  (6): (104476).  [PMID:35721463]

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