
JH-II-127
CAS No. 1700693-08-8
JH-II-127( JH-II-127 | JH-II 127 | JH-II127 )
Catalog No. M12597 CAS No. 1700693-08-8
A potent and selective inhibitor of both wild-type and G2019S mutant LRRK2 with IC50 of 6.6 and 2.2 nM, respectively.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 74 | In Stock |
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5MG | 120 | In Stock |
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10MG | 185 | In Stock |
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25MG | 332 | In Stock |
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50MG | 494 | In Stock |
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100MG | 709 | In Stock |
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Biological Information
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Product NameJH-II-127
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NoteResearch use only, not for human use.
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Brief DescriptionA 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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DescriptionA potent and selective inhibitor of both wild-type and G2019S mutant LRRK2 with IC50 of 6.6 and 2.2 nM, respectively; also inhibits LRRK2 A2016T with IC50 of 47.7 nM; substantially inhibits Ser910 and Ser935 phosphorylation of both wild-type LRRK2 and G2019S mutant at 0.1-0.3 uM in a variety of cell types; inhibits Ser935 phosphorylation in mouse brain; orally active.Parkinson's Disease Preclinical.
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In VitroJH-II-127 (0.03, 0.1, 0.3, 1, 3 μM; 90 min) inhibits LRRK2 in HEK293 cells.JH-II-127 (0.3, 1, 3 μM; 90 min) inhibits endogenously expressed LRRK2 in mouse Swiss 3T3 cells.Western Blot Analysis Cell Line:HEK293 cells (expressing GFP-LRRK2, GFP-LRRK2[G2019S], GFP-LRRK2[G2019S + A2016T], and GFP-LRRK2[A2016T], respectively )Concentration:0.03, 0.1, 0.3, 1, 3 μMIncubation Time:90 min Result:Induced a dose-dependent inhibition of Ser910 and Ser935 phosphorylation in both wild-type LRRK2 and LRRK2[G2019S] stably transfected into HEK293 cells.Inhibited phosphorylation of Ser910 and Ser935 at approximately 0.3 μM for wild-type LRRK2 and LRRK2[G2019S].Induced dephosphorylation of Ser910 and Ser935 at a concentration of 0.3-1 μM in the drug-resistant LRRK2[A2016T + G2019S] and LRRK2[A2016T] mutants.Western Blot Analysis Cell Line:Mouse Swiss 3T3 cellsConcentration:0.03, 0.1, 0.3, 1, 3 μM Incubation Time:90 min Result:Induced similar dose-dependent Ser935 dephosphorylation of endogenous LRRK2.
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In VivoJH-II-127 (100 mg/kg; i.p.; single) results in near complete dephosphorylation of Ser935 of LRRK2 in all tissues including brain.Pharmacokinetic Parameters of JH-II-127 in Wild type male C57BL/6 mice.Animal Model:Wild type male C57BL/6 mice.Dosage:2 mg/kg (for i.v.); 10 mg/kg (for p.o.); 10, 30, 100 mg/kg (for i.p.)Administration:Intravenous and intraperitoneal injection; oral administration; single.Result:Led to near complete dephosphorylation of Ser935 of LRRK2 in all tissues including brain when at 100 mg/kg of i.p. and near complete inhibition in all tissues at 30 mg/kg but only partial inhibition in brain at the 10 mg/kg dose.
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SynonymsJH-II-127 | JH-II 127 | JH-II127
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PathwayAutophagy
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TargetLRRK2
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RecptorLRRK2
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Research AreaNeurological Disease
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IndicationParkinson Disease
Chemical Information
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CAS Number1700693-08-8
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Formula Weight416.8615
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Molecular FormulaC19H21ClN6O3
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 30 mg/mL
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SMILESClC1=CNC2=C1C(NC)=NC(NC3=C(OC)C=C(C(N4CCOCC4)=O)C=C3)=N2
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Chemical NameMethanone, [4-[[5-chloro-4-(methylamino)-7H-pyrrolo[2,3-d]pyrimidin-2-yl]amino]-3-methoxyphenyl]-4-morpholinyl-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Hatcher JM, et al. ACS Med Chem Lett. 2015 Apr 7;6(5):584-9.
molnova catalog



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