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ROCK

ROCK

ROCK related products

Structure Cat No. Product Name CAS No. Product Description
(Rac)-NRL-1049 dihydrochloride V114421 (Rac)-NRL-1049 dihydrochloride 863638-93-1 (Rac)-BA 1049 is a racemic variant of NRL-1049 (BA-1049).
Glycerophosphoinositol 4-phosphate disodium V136770 Glycerophosphoinositol 4-phosphate disodium Glycerophosphoinositol 4-phosphate disodium is a metabolite of phospholipase A and an inhibitor of adenylate cyclase.
GSK180736A 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.
GSK269962 (GSK269962A) 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.
GSK429286A 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.
N-(3-氯-4-甲基苯基)-2-[2,6-二硝基-4-(三氟甲基)苯基]-肼硫代甲酰胺 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.
PD0166285 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).
Rhodblock 1a V144104 Rhodblock 1a 701226-08-6 Rhodblock 1a is an inhibitor of the Rho kinase signaling pathway.
RK-33 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.
RKI-1447 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.
ROCK-IN-10 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.
ROCK-IN-11 V144266 ROCK-IN-11 445267-51-6 ROCK-IN-11 is a potent inhibitor of ROCK1 and ROCK2, with an IC50 ≤ 5 μM.
ROCK-IN-12 V144267 ROCK-IN-12 ROCK-IN-12 is a selective ROCK inhibitor.
ROCK/HDAC-IN-2 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.
ROCK2-IN-14 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).
ROCK抑制剂 V2558 ZINC00881524 (ROCK inhibitor) 557782-81-7 ZINC00881524 is a novel, potent and selectiveROCK inhibitor.
SAR-020106 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.
SR-3677 V2951 SR-3677 1072959-67-1 SR-3677 (SR3677) is a potent and selective Rho-kinase/ROCK2 inhibitor with anticancer activity.
THZ1 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.
汉黄芩素 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.
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