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Home > Products > Autophagy
Cat.No. Product name Product Description
R10032 SLX2119 SLx-2119(KD-025) is a small molecule and selective inhibitor of ROCK2 with IC50
R10046 TORIN1 Torin 1 is a potent inhibitor of mTORC1/2 with IC50 of 2 nM/10 nM in cell-free a
R10230 Y27632 Y-27632 2HCl is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM in a ce
R10240 ABT737 ABT-737 is a BH3 mimetic inhibitor of Bcl-xL, Bcl-2 and Bcl-w with EC50 of 78.7
R10262 LY294002 LY294002 is the first synthetic molecule known to inhibit PI3Kα/δ/β with IC50 of
R10378 Erlotinib hydrochloride Erlotinib HCl (OSI-744) is an EGFR inhibitor with IC50 of 2 nM in cell-free assa
R10430 Rapamycin; Sirolimus Rapamycin (Sirolimus) is a specific mTOR inhibitor with IC50 of ~0.1 nM HEK293 c
R10450 Erlotinib; NSC718781; OSI744; R1415 Erlotinib is an EGFR inhibitor with IC50 of 2 nM, >1000-fold more sensitive for
R10550 Vorinostat Vorinostat (suberoylanilide hydroxamic acid, SAHA) is an HDAC inhibitor with IC5
R10599 3-Methyladenine; 3-MA 3-Methyladenine (3-MA) is a selective PI3K inhibitor for Vps34 and PI3Kγ with IC
R10706 MHY1485 MHY1485 is a potent, and cell-permeable mTOR activator, and also potently inhibi
R10716 CZC-54252 CZC-54252 is a potent inhibitor of LRRK2 with IC50s of 1.28 nM and 1.85 nM for w
R10726 PF-06447475 PF-06447475 is a highly potent, selective, brain penetrant LRRK2 inhibitor with
R11628 GSK2578215A GSK2578215A is a potent and selective LRRK2 kinase inhibitor with IC50 of 8.9 nM
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