| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V114421 | (Rac)-NRL-1049 dihydrochloride | 863638-93-1 | (Rac)-BA 1049 is a racemic variant of NRL-1049 (BA-1049). |
|
V136770 | Glycerophosphoinositol 4-phosphate disodium | Glycerophosphoinositol 4-phosphate disodium is a metabolite of phospholipase A and an inhibitor of adenylate cyclase. | |
|
V2730 | GSK180736A | 817194-38-0 | GSK180736A (GSK-180736A) is a GRK2 inhibitor thatwasdeveloped as a novel and potent Rho-associated, coiled-coil-containing protein kinase (ROCK) inhibitor whichbinds to GRK2 (G protein-coupled receptor kinase 2) with IC50of 0.77 μM; G protein-coupled receptors (GPCRs) are central to many physiological processes. |
|
V2561 | GSK269962 (GSK269962A) | 850664-21-0 | GSK269962 (also known as GSK269962A) is a novel, potent and selective inhibitor of ROCK (Rho-associated protein kinase) with IC50 values of 1.6 and 4 nM for ROCK1 and ROCK2, respectively. |
|
V1345 | GSK429286A | 864082-47-3 | GSK429286A (also known as RHO15;GSK 429286A;RHO-15;GSK-429286A)is a potent, orally bioactive, andselective inhibitor of ROCK1/2 with antihypertensive effects. |
|
V2563 | Kobe0065 | 436133-68-5 | Kobe0065 (Kobe 0065) is novel and potent inhibitor of the H-Ras-cRaf1 interaction whichexhibits potent activity to competitively inhibit the binding of H-Ras·GTP to c-Raf-1 RBD with a Ki value of 46 ± 13 μM. |
|
V2564 | PD0166285 | 185039-89-8 | PD0166285 (PD-0166285) is a novel and potent Wee1 and Chk1 inhibitor with anticancer activity and enzymatic activity at nanomolar concentrations (IC50s of 24 and 72 nM for WEE1 and Myt1, respectively). |
|
V144104 | Rhodblock 1a | 701226-08-6 | Rhodblock 1a is an inhibitor of the Rho kinase signaling pathway. |
|
V2562 | RK-33 | 1070773-09-9 | RK-33 is a potent and first-in-class small molecule inhibitor of DDX3 (a RNA helicase) and causes G1 cell cycle arrest, induces apoptosis, and promotes radiation sensitization in DDX3-overexpressing cells. |
|
V1346 | RKI-1447 | 1342278-01-6 | RKI-1447 (ROCK Inhibitor XIII; RKI 1447; RKI1447) is a potent small molecule inhibitor of ROCK1 and ROCK2 with potential antitumor activities againstbreast cancer. |
|
V88764 | ROCK-IN-10 | 1038549-25-5 | ROCK-IN-10 (compound 50) is a potent ROCK inhibitor with IC50 values of 6 nM and 4 nM for ROCK1 and ROCK2, respectively. |
|
V144266 | ROCK-IN-11 | 445267-51-6 | ROCK-IN-11 is a potent inhibitor of ROCK1 and ROCK2, with an IC50 ≤ 5 μM. |
|
V144267 | ROCK-IN-12 | ROCK-IN-12 is a selective ROCK inhibitor. | |
|
V144264 | ROCK/HDAC-IN-2 | ROCK/HDAC-IN-2 is a ROCK/HDAC inhibitor with IC50 values of 0.185 µM, 0.8 µM, and 0.7 µM for HDAC6, ROCK1, and ROCK2, respectively. | |
|
V144265 | ROCK2-IN-14 | 3115784-59-0 | ROCK2-IN-14 is an orally effective selective ROCK2 inhibitor (IC50 = 4.8 nM) with 212 times greater selectivity for ROCK1 than ROCK1 (IC50 = 1.01 μM). |
|
V2558 | ZINC00881524 (ROCK inhibitor) | 557782-81-7 | ZINC00881524 is a novel, potent and selectiveROCK inhibitor. |
|
V2556 | SAR-020106 | 1184843-57-9 | SAR-020106 is a potent,ATP-competitive, and selective CHK1 inhibitor with an IC50 of 13.3 nM on isolated human enzyme. |
|
V2951 | SR-3677 | 1072959-67-1 | SR-3677 (SR3677) is a potent and selective Rho-kinase/ROCK2 inhibitor with anticancer activity. |
|
V2557 | THZ1 | 1604810-83-4 | THZ1 (THZ-1) is a novel, potent, selective and covalent/irreversible CDK7 inhibitor (IC50 = 3.2 nM) with anticancer activity. |
|
V1184 | Wogonin | 632-85-9 | Wogonin (Vogonin), a naturally occurring and pharmacologically-active flavonoid found in plants, has been reported to exhibit anticancer effects against various cancer cell types such as osteosarcoma, leukemia, breast cancer and glioma. |