Description
JH-II-127 is a selective inhibitor of leucine-rich repeat kinase 2 (LRRK2), a potential therapeutic target for neurodegenerative disease. It inhibits phosphorylation of Ser910 and Ser935 in both wild-type LRRK2 and the G2019S mutant.
| Product Unit Size | Cost | Quantity | Stock |
|---|
JH-II-127 is a selective inhibitor of leucine-rich repeat kinase 2 (LRRK2), a potential therapeutic target for neurodegenerative disease. It inhibits phosphorylation of Ser910 and Ser935 in both wild-type LRRK2 and the G2019S mutant.
| Cas No. | 1700693-08-8 |
|---|---|
| Purity | ≥98% |
| Formula | C19H21ClN6O3 |
| Formula Wt. | 416.87 |
| IUPAC Name | (4-{[5-Chloro-4-(methylamino)-3H-pyrrolo[2,3-d]pyrimidin-2-yl]amino}-3-methoxyphenyl)(4-morpholinyl)methanone |
| Synonym | Pyrrolopyrimidine |
| Solubility | DMSO |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Hatcher J., Zhang J., et al. Discovery of a Pyrrolopyrimidine (JH-II-127), a Highly Potent, Selective, and Brain Penetrant LRRK2 Inhibitor. ACS Med Chem Lett. 6(5):584-9 (2015). PMID: 26005538.
Neuropeptide hormone found in insects, involved...
Camptothecin analog; topoisomerase I inhibitor,...
Caffeic acid derivative.
TRPA1 agonist, xanthine oxidase inhibitor.
Steroid hormone involved in stress signaling; g...
Endogenous steroid hormone involved in immune r...
Aromatase inhibitor.
Benzimidazole; microtubule polymerization inhib...
β2-adrenergic agonist.
AR antagonist.
Vitamin B1
Endogenous calcitonin-family peptide, involved ...
Non-fluorescent halogenated A23187 analog, Ca2+...
BH3 mimetic; Bcl-2 and Bcl-xl inhibitor.
Dihydropyridine, FIASMA; L-type Ca2+ channel bl...
BHA derivative, antioxidative food and cosmetic...
Endogenous proneurotensin peptide, involved in ...
Benzimidazole; microtubule polymerization inhib...
Used for in vitro fertilization; FIASMA, SERM.<...
Fluoroquinolone; topoisomerase IV and bacterial...