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| Cat.No. | Product name | Product Description |
| R10032 | SLx-2119 (KD-025) | 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 |
| R10262 | LY294002 | LY294002 is the first synthetic molecule known to inhibit PI3Kα/δ/β with IC50 of |
| R10378 | Erlotinib Hydrochloride (CP-358774 Hydrochloride; NSC 718781 Hydrochloride; OSI-774 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 f |
| 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 | CZC54252;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 and brain penetrant LRRK2 inhibitor wi |
| R11628 | GSK2578215A | GSK2578215A is a potent and selective LRRK2 kinase inhibitor with IC50 of 8.9 nM |
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