BP13469
|
ROCK2-IN-2
|
|
|
|
ROCK2-IN-2 is a selective inhibitor of ROCK2 (IC50 of <1 μM).
|
BP13470
|
Roniciclib
|
|
|
|
Roniciclib is a potent pan-CDK inhibitor and a novel oral cytotoxic agent. Roniciclib inhibits the activity of cell-cycle CDKs CDK1, CDK2, CDK3, CDK4, and of transcriptional CDKs CDK7 and CDK9 with IC(50) values in the range between 5 and 25 nmol/L.
|
BP13471
|
Seliciclib
|
|
|
|
Roscovitine is a potent inhibitor of Cdk2/cyclin E (IC50: 0.1 μM). It also inhibits Cdk7/cyclin H, Cdk5/p35, and Cdc2/cyclin B (IC50s: 0.49/0.16/0.65 μM).
|
BP13472
|
RX-3117
|
|
|
|
RX-3117 is a novel a cytidine analog. RX-3117 displays anticancer activity in several cancer cell lines, including gemcitabine-resistant variants.
|
BP13473
|
sAJM589
|
|
|
|
sAJM589 is a Myc inhibitor(IC50: 1.8 μM).
|
BP13474
|
Sanggenol L
|
|
|
|
Sanggenol L shows higher cytotoxicity against human oral tumor cell lines (HSC-2 and HSG) than against normal human gingival fibroblasts (HGF), it induces apoptosis via caspase activation and inhibition of NF-κB/IκBα± phosphorylation as a potent chemotherapeutic agent for ovarian cancers.
|
BP13475
|
Sangivamycin
|
|
|
|
Sangivamycin is an effective inhibitor of protein kinase C (PKC, Ki = 10 μM). Sangivamycin exhibits antiproliferative activity against a variety of human cancers.
|
BP13476
|
Sapacitabine
|
|
|
|
Sapacitabine is a nucleoside analog prodrug with antitumor activity.
|
BP13477
|
SAR-020106
|
|
|
|
SAR-020106 is a potent, ATP-competitive, and selective CHK1 inhibitor with an IC50 of 13.3 nmol/L on the isolated human enzyme.
|
BP13478
|
SAR407899 hydrochloride
|
|
|
|
SAR407899 hydrochloride is a selective, potent and ATP-competitive ROCK inhibitor, with an IC50 of 135 nM for ROCK-2, and Kis of 36 nM and 41 nM for human and rat ROCK-2, respectively.
|
BP13479
|
SAR407899
|
|
|
|
SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.
|
BP13480
|
SB-218078
|
|
|
|
SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM). SB-218078 is a potent, ATP-competitive, and cell-permeable checkpoint kinase 1 inhibitor that inhibits Chk1 phosphorylation of cdc25C (IC50: 15 nM).
|
BP13481
|
SB-743921 hydrochloride
|
|
|
|
SB-743921 is an effective inhibitor of kinesin spindle protein, KSP, (Ki =0.1 nM).
|
BP13482
|
SB-772077B dihydrochloride
|
|
|
|
SB-772077B dihydrochloride is an aminofurazan-based Rho kinase inhibitor (IC50s: 5.6 nM and 6 nM toward ROCK1 and ROCK2, respectively).
|
BP13483
|
SBC-110736
|
|
|
|
SBC-110736 is a proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitor
|
BP13484
|
SBC-115076
|
|
|
|
SBC-115076 is a potent extracellular proprotein convertase subtilisin kexin type 9 (PCSK9) antagonist.
|
BP13485
|
SBC-115337
|
|
|
|
SBC-115337 is a PCSK9 inhibitor.
|
BP13486
|
SC-514
|
|
|
|
SC-514 is a selective, orally active, ATP-competitive IKK-2 inhibitor (IC50=11.2±4.7 μM), obstructs NF-κB-dependent gene expression.
|
BP13487
|
SCH-1473759 hydrochloride
|
|
|
|
SCH-1473759 hydrochloride is an inhibitor of aurora(aurora A and B with IC50s of 4 and 13 nM, respectively).
|
BP13488
|
SCH-1473759
|
|
|
|
SCH-1473759 is an inhibitor of the aurora (IC50s: 4 and 13 nM for Aurora A and B, respectively).
|