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Cat. No. Product Name Information
PC-28293

UBASHIN-5

UBASH3B inhibitor

UBASHIN-5 (LIT-14-132) is a small-molecule inhibitor targeting UBASH3B 2HP domain, disrupts mitotic localization of UBASH3B and Aurora B, seletively induces arrest and cell death during mitosis without toxicity to normal cells, selectively suppresses breast and colon tumor growth in vivo.
PC-28292

UBASHIN-4

UBASH3B inhibitor

UBASHIN-4 is a small-molecule inhibitor targeting UBASH3B 2HP domain, disrupts mitotic localization of UBASH3B and Aurora B, seletively induces arrest and cell death during mitosis without toxicity to normal cells, selectively suppresses breast and colon tumor growth in vivo.
PC-24004

AAPK-25

DLGAP5 inhibitor

AAPK-25 is a small molecule inhibitor of DLGAP5 with a binding energy of −9.2 Kcal/mol, suppresses proliferation of PRAD cells via inhibiting DLGAP5/E2F1 axis, also is a potent, dual Aurora/PLK coinhibitor.
PC-22957

CAM2602

Aurora A-TPX2 inhibitor

CAM2602 is a potent, selective small molecule inhibitor of Aurora A-TPX2 protein-protein interaction (PPI), binds to Aurora A and displaces TPX2 from Aurora A with a KD of 19 nM,
PC-22868

MK-8745

Aurora A inhibitor

MK-8745 (MK8745) is a potent, specific Aurora kinase A (Aurora A, AURKA) inhibitor with IC50 of 0.6 nM, induces apoptotic cell death in a p53-dependent manner.
PC-22152

JAB-2485

Aurora A inhibitor

JAB-2485 is a potent, highly selective small-molecule Aurora kinase A (AURKA) inhibitor with IC50 of 0.33 nM, with >1500-fold selectivity over AURKB and AURKC.
PC-22141

DBPR728

Aurora A inhibitor

DBPR728 is an oral bioavailable acyl-based prodrug of 6K465, which is a potent selective Aurora A (AURKA) inhibitor, effectively inhibits cancer cells overexpressing c-MYC- and/or N-MYC.
PC-22139

6K465

Aurora A inhibitor

6K465 is a potent selective Aurora A (AURKA) inhibitor, effectively inhibits cancer cells overexpressing c-MYC- and/or N-MYC.
PC-21560

Reversine

Aurora Kinase inhibitor

Reversine is a potent, ATP-competitive Aurora kinases inhibitor with IC50 of 400, 500 and 400 nM for Aurora A, Aurora B and Aurora C, respectively.
PC-21147

Ilorasertib

Aurora Kinase inhibitor

Ilorasertib (ABT-348) is a potent inhibitor of Aurora kinases as well as the VEGF and PDGF families of receptor tyrosine kinases (Aur B IC50=2 nM, PDGFRβ IC50=3 nM).
PC-20713

LXY18

AURKB inhibitor

LXY18 is a potent orally available blocker of AURKB relocation in mitosis with minimum effective concentration (MEC) of 3.5 nM for inducing polyploidy, shows broad-spectrum growth inhibitory and apoptosis-inducing activities with low nanomolar potencies.
PC-49273

PF-03814735

Aurora inhibitor

PF-03814735 is a potent, orally bioavailable, reversible inhibitor of both Aurora A and Aurora B kinases with IC50 values of 0.8 and 5 nM, respectively.

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