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.
Tricyclic benzonaphthyridinone; mTORC1/2 inhibi...
Endogenous quaternary ammonium, required for fa...
Phenylpropanoid found in Castilleja, Verbena, V...
Adenosine A2A antagonist.
Nitroimidazole; hypoxic modifier and radiosensi...
Triazole; 14-α demethylase inhibitor, potentia...
GABA-A antagonist.
Chloramphenicol derivative; protein translation...
Epoxomicin analog; proteasome inhibitor.
Quinazoline; α1-adrenergic antagonist.
ATR inhibitor.
Endogenous steroid hormone involved in immune r...
Isocitrate dehydrogenase inhibitor.
Steroid; glucocorticoid agonist.
Organosulfur found in garlic, binds DNA; inward...
GABA derivative; GABA-B agonist.
Saponin found in Polygala.
Antioxidant, vitamin E derivative found in vege...
Anthracycline, DNA intercalator; topoisomerase ...
Synthetic cytokinin, plant growth regulator; fi...