R2032454 |
ML167;CID44968231;NCGC00188654) |
ML167 is a highly selective Cdc2-like kinase 4 (Clk4) inhibitor with IC50 of 136
|
R2032455 |
ML323 |
ML-323 is a reversible, potent USP1-UAF1 inhibitor with IC50 of 76 nM in a Ub-Rh
|
R2032456 |
ML-347(LDN-193719) |
ML347(DN193719) is a highly selective ALK1/ALK2 inhibitor with IC50s of 46/32 nM
|
R2032457 |
Mocetinostat(MGCD0103) |
Mocetinostat (MGCD0103) is a potent, orally active and isotype-selective HDAC (C
|
R2032458 |
Mps1-IN-2 |
Mps1-IN-2 is a potent, selective and ATP-competitive dual Mps1/Plk1 inhibitor, w
|
R2032459 |
MS436 |
MS436 is a new class of bromodomain inhibitor, exhibits potent affinity of an es
|
R2032460 |
N6022 |
N6022 is a potent, selective, reversible, and efficacious S-Nitrosoglutathione r
|
R2032461 |
Necrostatin-1 |
Necrostatin-1 (Nec-1) is a potent, selective and cell-permeable necroptosis inhi
|
R2032462 |
Nepicastat hydrochloride(SYN-117 hydrochloride) |
Nepicastat hydrochloride (SYN-117 hydrochloride) is a selective, potent, and ora
|
R2032463 |
Nesbuvir;HCV-796) |
Nesbuvir is a nonnucleoside inhibitor of the hepatitis C virus (HCV) nonstructur
|
R2032464 |
NMS-873 |
NMS-873 is a potent, selective allosteric VCP/p97 inhibitor with IC50 value of 3
|
R2032465 |
NMS-P715 |
NMS-P715 analog is an inhibitor of MPS1, with an IC50 of 84 nM.
|
R2032466 |
NSC319726 |
NSC319726 (ZMC1) is a mutant p53R175 reactivator; inhibits growth of fibroblasts
|
R2032467 |
NU-7441;KU-57788 |
KU-57788 is a potent and selective inhibitor of DNA-PK with an IC50 of 13 nM, wi
|
R2032468 |
Nutlin-3 |
Nutlin-3 is a potent and selective Mdm2 (RING finger-dependent ubiquitin protein
|
R2032469 |
Nutlin-3b |
Nutlin (3b) is a p53/MDM2 inhibitor with an IC50 of 13.6 μM.Nutlin (3b) is 150 t
|
R2032470 |
NVP-ADW742(ADW742;GSK 552602A ) |
NVP-ADW742(ADW742; GSK 552602A ) is an selective IGF-1R inhibitor with IC50 of 0
|
R2032471 |
NVP-BEP800;ER-82576 |
VER-82576 (NVP-BEP800) is a potent, orally available and selective Hsp90 inhibit
|
R2032472 |
NVP-BVU972 |
NVP-BVU972 is a selective and potent Met inhibitor (IC50 = 14 nM).Antitumor agen
|
R2032473 |
OG-L002 |
OG-L002 is a potent and highly selective LSD1 inhibitor with an IC50 of 0.02 μM.
|
R2032474 |
ONX0914(PR-957) |
ONX-0914 (PR-957) is a potent and selective inhibitor of immunoproteasome subuni
|
R2032475 |
OSI027 |
OSI-027 is an ATP-competitive mTOR kinase activity inhibitor with an IC50 of 4 n
|
R2032476 |
OSI930 |
OSI-930 is a potent inhibitor of Kit, KDR and CSF-1R with IC50 of 80 nM, 9 nM an
|
R2032477 |
OSU-03012 |
OSU-03012 is a PDK-1 inhibitor with an IC50 of 5 μM.
|
R2032478 |
OTSSP167 hcl |
OTSSP167 is a highly potent MELK inhibitor with IC50 value of 0.41 nM.
|