T16855 |
SB-772077B dihydrochloride
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SB-772077B dihydrochloride is an aminofurazan-based Rho kinase inhibitor (IC50s: 5.6 nM and 6 nM toward ROCK1 and ROCK2, respectively).
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T13972 |
Y-9738
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Y-9738 is an agent of hypolipidemic.
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T1606 |
Fasudil
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Fasudil is a potent inhibitor of ROCK1, PKA, PKC, and MLCK.
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T13364 |
YAP/TAZ inhibitor-1
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YAP/TAZ inhibitor-1 is an inhibitor of YAP/TAZ (IC50 of <0.100 μΜ in firefly luciferase assay).
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T23308 |
SAR407899 hydrochloride
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ATP-competitive ROCK inhibitor
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T15808 |
Merestinib dihydrochloride
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Merestinib dihydrochloride is an effective and orally bioavailable c-Met inhibitor (Ki=2 nM). It has anti-tumor activities and also has potent activity against M...
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T35328 |
H-1152 dihydrochloride
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H-1152 dihydrochloride is a specific inhibitor of Rho-associated protein kinase (ROCK) with an IC50 of 12 nM and a Ki of 1.6 nM. H-1152 dihydrochloride inhibits ...
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T67748 |
ROCK-IN-5
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ROCK-IN-5 (compound I-B-37) is a potent inhibitor of protein kinases, including ROCK, ERK, GSK, and AGC. ROCK-IN-5 exhibits the potential for cardiac, proliferat...
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TN1533 |
Cucurbitacin A
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Cucurbitacin I, cytotoxic triterpenoid sterols isolated from plants, elicits the formation of actin/phospho-myosin II co-aggregates by stimulation of the RhoA/RO...
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T23888 |
CID-5056270
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CID-5056270 is a ROCK2 enzyme inhibitor that is novel and potent.
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T7552 |
H-1152
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H-1152 is a potent, specific, ATP-competitive, and cell permeable ROCK inhibitor (Ki = 1.6 nM).
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T22037 |
AS 1892802
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AS 1892802 is a potent and selective inhibitor of ROCK. AS 1892802 exibits IC50 values of 52nM, 57nM and 122 nM for human ROCK2, rat ROCK2 and human ROCK1, respe...
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T7492 |
Ripasudil free base
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Ripasudil free base is a selective and potent ROCK inhibitor, is a novel and potent antiglaucoma agent.
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T12747 |
ROCK2-IN-2
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ROCK2-IN-2 is a selective inhibitor of ROCK2 (IC50 of <1 μM).
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T9652 |
SB-747651A Dihydrochloride
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SB-747651A Dihydrochloride is an ATP-competitive mitogen- and stress-activated kinase 1 (MSK1) inhibitor with an IC50 of 11 nM. SB-747651A Dihydrochloride also i...
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TQ0183 |
Narciclasine
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Narciclasine, a natural product, modulates the Rho/Rho-kinase/LIM kinase/cofilin signaling pathway, greatly increasing GTPase RhoA activity.
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T7885 |
Afuresertib hydrochloride
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Afuresertib hydrochloride is an inhibitor of Akt kinase (Kis of 0.08/2/2.6 nM for Akt1/Akt2/Akt3 respectively)
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T19913 |
CKI-7
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CKI-7 2HCl is an inhibitor of casein kinase 1 (CK1).
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TQ0110 |
ROCK-IN-2
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Azaindole 1 is a selective and ATP-competitive ROCK inhibitor with IC50 of 0.6 and 1.1 nM for human ROCK-1 and ROCK-2.
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T7301 |
BDP5290
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BDP5290 is a potent inhibitor of both ROCK and MRCK(IC50s of 5 nM, 50 nM, 10 nM and 100 nM for ROCK1, ROCK2, MRCKα and MRCKβ, respectively.)
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T2482 |
AT13148
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AT13148 is an oral-active and ATP-competitive, multi-AGC kinase inhibitor for Akt1/2/3, p70S6K, PKA, and ROCKI/II.
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T2633 |
GSK429286A
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GSK429286A is a specific inhibitor of ROCK1/2 (IC50: 14/63 nM).
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T3513 |
GSK180736A
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GSK180736A is an effective and selective GRK2 inhibitor (IC50: 0.77 μM) and >100-fold selectivity over other GRKs. It is a weak inhibitor of PKA (IC50: 30 μM), b...
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T6867 |
Belumosudil
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KD025 is an orally available, and specific ROCK2 inhibitor (IC50/Ki: 60/41 nM).
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T2155 |
Thiazovivin
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Thiazovivin, a ROCK inhibitor (IC50: 0.5 μM), increases the survival rate of hESC.
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T7764 |
CCG-222740
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CCG-222740 is an inhibitor of Rho/MRTF pathway
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T4276L |
Hydroxyfasudil
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Hydroxyfasudil is a ROCK inhibitor(IC50s of 0.73 and 0.72 μM for ROCK1 and ROCK2, respectively).
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T14989 |
CMPD101
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CMPD101 is a membrane-permeable small-molecule inhibitor of GRK2/3 (IC50: 18 nM and 5.4 nM). Which can be used for the study of heart failure. CMPD101 exhibits ...
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T2011 |
RKI1313
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RKI-1313 was a selective inhibitor for ROCK-dependent signaling, cytoskeletal changes, anchorage-independent colony formation, migration, and invasion.
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T4488 |
GSK-25
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GSK-25 maintains good selectivity against a panel of 31 kinases, as well as RSK1 and p70S6K (RSK1 IC50 of 398 nM, p70S6K IC50 of 1000nM), and a dramatically impr...
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TQ0319 |
Ripasudil
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Ripasudil (K-115) hydrochloride dihydrate is a specific ROCK inhibitor (IC50s: 51/19 nM for ROCK1/ROCK2).
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T6057 |
URMC-099
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URMC-099 is an orally bioavailable, brain penetrant MLK inhibitor (IC50: 19/42/14/150 nM, for MLK1/MLK2/MLK3/DLK), and also inhibits LRRK2 activity (IC50: 11 nM)...
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T13384L |
Y-33075 dihydrochloride
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Y-33075 dihydrochloride is a selective inhibitor of ROCK(IC50 of 3.6 nM).
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T4095 |
ZINC00881524
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ZINC00881524 is an effective and specific ROCK inhibitor.
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T12721 |
Rho-Kinase-IN-1
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Rho-Kinase-IN-1 is an inhibitor of ROCK with Kis of 30.5 nM and 3.9 nM for ROCK1 and ROCK2, respectively. Rho-Kinase-IN-1 can be used in studies about excessive ...
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T3518 |
GSK269962A
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GSK269962 is a selective ROCK(Rho-associated protein kinase) inhibitor with IC50 values of 1.6 and 4 nM for ROCK1 and ROCK2, respectively.
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T1898 |
RKI-1447
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RKI-1447 is a potent inhibitor of ROCK1 and ROCK2. It has anti-invasive and antitumor activities.
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T6321 |
Tofacitinib
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Tofacitinib is an oral, small molecule inhibitor of Janus kinases that is used to treat moderate-to-severe rheumatoid arthritis.
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T1911 |
Afuresertib
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Afuresertib is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity.
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T4276 |
Hydroxyfasudil Hydrochloride
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Hydroxyfasudil hydrochloride is a ROCK1/2 inhibitor (IC50s: 0.73/0.72 μM).
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T1870 |
Y-27632
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Y-27632 is a selective ATP-competitive inhibitor of ROCK-I and ROCK-II.
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T12746 |
ROCK inhibitor-2
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ROCK inhibitor-2 is a selective dual inhibitor of ROCK1 and ROCK2 (IC50s of 17 nM and 2 nM, respectively).
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TQ0187 |
SR-3677
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SR-3677 is an effective and specific inhibitor of ROCK2 (IC50: 3 nM).
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T14960 |
Chroman 1
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Chroman 1 is an inhibitor of ROCK2 (IC50: 1 nM).
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T7391 |
SAR407899
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SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.
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T1725 |
Y-27632 dihydrochloride
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Y-27632 is a selective inhibitor of ROCKs including p160ROCK (Ki: 140 nM) and ROCK2 (IC50: 800 nM).
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T3060 |
Fasudil hydrochloride
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Fasudil Hydrochloride is a potent inhibitor of ROCK1, PKA, PKC, and MLCK with Ki of 0.33 μM, 1.0 μM, 9.3 μM and 55 μM, respectively.
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T10358 |
Netarsudil Dihydrochloride
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Netarsudil hydrochloride is an inhibitor of Rho-associated protein kinase (ROCK) and norepinephrine transporter (NET) with effective in intraocular pressure (IOP...
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T9431 |
Y-39983 hydrochloride
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Y-39983 hydrochloride is a selective Rho-associated coiled coil-forming protein kinase (ROCK) inhibitor.
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T15798 |
LX7101
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LX7101 is an effective inhibitor of LIMK and ROCK2 (IC50: 24, 1.6, and 10 nM for LIMK1, LIMK2, and ROCK2, respectively). It also inhibits PKA (IC50 <1 nM).
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