lrrk2-in-1 suppliers USA

Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.

Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.

Product
LRRK2-IN-1 LRRK2-IN-1 Inhibitor. Uses: Scientific use. Product Category: T2246. CAS No. 1234480-84-2. TARGETMOL CHEMICALS
LRRK2-IN-1 LRRK2-IN-1 is a benzodiazepine based derivative and is known as a selective inhibitor of the Parkinson's disease kinase LRRK2. Group: Biochemicals. Alternative Names: 5, 11-Dihydro-2- [ [2-methoxy-4- [ [4- (4-methyl-1-piperazinyl) -1-piperidinyl] carbonyl] phenyl] amino] -5, 11-dimethyl-6H-pyrimido [4, 5-b] [1, 4] benzodiazepin-6-one. Grades: Highly Purified. CAS No. 1234480-84-2. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 2
Worldwide
LRRK2-IN-1 LRRK2-IN-1 is a potent and selective LRRK2 inhibitor with IC 50 of 6 nM and 13 nM for LRRK2 (G2019S) and LRRK2 (WT), respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 1234480-84-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-10875. MedChemExpress MCE
LRRK2 Inhibitor III, HG-10-102-01 (Leucine-Rich Repeat Kinase 2 Inhibitor III, Mixed-Lineage Kinase 1 Inhibitor I, MLK1 Inhibitor I, MNK Inhibitor III, (4- (5-Chloro-4- (methylamino)pyrimidin-2-ylamino)-3-methoxyphenyl) (morpholino)methanone) A cell-permeable 2,4-diaminopyrimidinyl compound that acts as a potent, ATP-competitive LRRK2-selective inhibitor (IC5050 = 20.3, 3.2, 153.7 and 95.9nM, respectively,against human wt LRRK2 and G2019S, A2016T, G2019S/A2016T LRRK2 mutant; [ATP] = 100uM), displaying much reduced potency against MNK2 and MLK1 (IC50 = 0.6 and 2.1uM, respectively; [ATP] = 100uM) and little activity toward a panel of 136 other kinases. Although both HG-10-102-01 and LRRK2-In-1 inhibit cellular wt and G20195 LRRK2 phosphorylation (Optimal conc. 1 to 3uM), only HG-10-102-01 is effective against cellular A2016T and G2019S/A2016T LRRK2 phosphorylations (IC50 <3uM). And only HG-10-102-01, but not LRRK2-In-1 or CZC-25146, can cross blood-brain-barrier for LRRK2 phosphorylation inhibition in mice (30mg/kg to 50mg/kg i.p.) in vivo. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C??H??ClN?O?. US Biological Life Sciences. USBiological 4
Worldwide

Would you like to list your products on USA Chemical Suppliers?

Our database is helping our users find suppliers everyday.

Add Your Products