1. Signaling Pathways
  2. Cell Cycle/DNA Damage
    Epigenetics
  3. Aurora Kinase

Aurora Kinase

Kinase

The Aurora kinases comprise a family of evolutionary conserved serine/threonine kinases (Aurora-A, Aurora-B, and Aurora-C). Aurora kinases control multiple events during cell cycle progression and are essential for mitotic and meiotic bipolar spindle assembly and function.

Aurora-A, Aurora-B, and Aurora-C share a highly conserved kinase domain but have quite different subcellular localizations and functions during mitosis. Aurora-A mostly controls centrosome maturation and bipolar spindle assembly, while Aurora-B and Aurora-C are required for condensation, attachment to kinetochores, and alignment of chromosomes during (pro-)metaphase and cytokinesis. In human tumors, all Aurora kinase members play oncogenic roles related to their mitotic activity and promote cancer cell survival and proliferation. Inhibitors targeting Aurora kinases have attracted attention in cancer research.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-10971
    Alisertib
    Inhibitor 99.84%
    Alisertib (MLN 8237) is an orally active and selective Aurora A kinase inhibitor (IC50=1.2 nM), which binds to Aurora A kinase resulting in mitotic spindle abnormalities, mitotic accumulation. Alisertib (MLN 8237) induces apoptosis and autophagy through targeting the AKT/mTOR/AMPK/p38 pathway in leukemic cells. Antitumor activity.
    Alisertib
  • HY-10126
    Barasertib-HQPA
    Inhibitor 99.47%
    Barasertib-HQPA (AZD2811) is a highly selective Aurora B inhibitor with an IC50 of 0.37 nM in a cell-free assay. Barasertib-HQPA (AZD2811) induces growth arrest and apoptosis in cancer cells.
    Barasertib-HQPA
  • HY-10127
    Barasertib
    Inhibitor 99.62%
    Barasertib (AZD1152), a pro-drug of Barasertib-hQPA, is a highly selective Aurora B inhibitor with an IC50 of 0.37 nM in a cell-free assay. Barasertib (AZD1152) induces growth arrest and apoptosis in cancer cells.
    Barasertib
  • HY-14711
    Reversine
    Inhibitor 99.22%
    Reversine is a novel class of ATP-competitive Aurora kinase inhibitor with IC50s of 400, 500 and 400 nM for Aurora A, Aurora B and Aurora C, respectively.
    Reversine
  • HY-10161
    Tozasertib
    Inhibitor 99.92%
    Tozasertib (VX 680; MK-0457) is an inhibitor of Aurora A/B/C kinases with Kis of 0.6, 18, 4.6 nM, respectively.
    Tozasertib
  • HY-168540
    PROTAC MPS1 degrader 1
    Degrader
    PROTAC MPS1 degrader 1 (Compound 19) is a potent degrader of monopolar spindle 1 (Mps1, TTK), AURKA and AURKB, with DC50s of 17.7, 108.7 and 570.3 nM, respectively. PROTAC MPS1 degrader 1 can be used for the research of acute myeloid leukemia. (Pink: ligand for target protein (HY-168542); Black: linker (HY-W141926); Blue: ligand for E3 ligase (HY-10984).
    PROTAC MPS1 degrader 1
  • HY-169505
    Aurora kinase inhibitor-13
    Inhibitor
    Aurora kinase inhibitor-13 (Compound 2) is an inhibitor of Aurora kinase, with an IC50 value of 2.3 μM against Aurora kinase A.
    Aurora kinase inhibitor-13
  • HY-168543
    PROTAC MPS1 degrader 2
    Degrader
    PROTAC MPS1 degrader 2 (Compound 15) is a potent degrader of monopolar spindle 1 (Mps1,TTK)AURKA and AURKB,with DC50s of 42.0,2.1 and 154.0 nM,respectively. PROTAC MPS1 degrader 1 can be used for the research of acute myeloid leukemia. (Pink: ligand for target protein (HY-168545); Black: linker (HY-N0420); Blue: ligand for E3 ligase (HY-10984).
    PROTAC MPS1 degrader 2
  • HY-B0712B
    Ceftriaxone sodium salt
    Inhibitor 99.90%
    Ceftriaxone sodium salt (Ro 13-9904) is a broad spectrum β-lactam third-generation cephalosporin antibiotic, which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone sodium salt is a covalent inhibitor of GSK3β with IC50 value of 0.78 μM. Ceftriaxone sodium salt is an inhibitor of Aurora B. Ceftriaxone sodium salt has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone sodium salt can be used in the study of bacterial infections and meningitis.
    Ceftriaxone sodium salt
  • HY-10329
    JNJ-7706621
    Inhibitor 99.91%
    JNJ-7706621 is a potent aurora kinase inhibitor, and also inhibits CDK1 and CDK2, with IC50s of 9 nM, 3 nM, 11 nM, and 15 nM for CDK1, CDK2, aurora-A and aurora-B, respectively.
    JNJ-7706621
  • HY-12054
    Hesperadin
    Inhibitor 98.89%
    Hesperadin is an ATP competitive indolinone inhibitor of Aurora A and B. Hesperadin inhibits Aurora B with an IC50 of 250 nM. Hesperadin inhibits the growth of Trypanosoma brucei by blocking nuclear division and cytokinesis. Hesperadin also is a broad-spectrum influenza antiviral.
    Hesperadin
  • HY-50514
    AT9283
    Inhibitor 99.67%
    AT9283 is a multi-targeted kinase inhibitor with potent activity against Aurora A/B, JAK2/3, Abl (T315I) and Flt3 (IC50s ranging from 1 to 30 nM). AT9283 inhibits growth and survival of multiple solid tumors in vitro and in vivo.
    AT9283
  • HY-10339
    KW-2449
    Inhibitor 99.69%
    KW-2449 is a multi-targeted kinase inhibitor of FLT3, ABL, ABLT315I and Aurora kinase with IC50s of 6.6, 14, 4 and 48 nM, respectively.
    KW-2449
  • HY-13252
    MK-5108
    Inhibitor 99.89%
    MK-5108 is a highly potent and specific inhibitor of Aurora A kinase with an IC50 value of 0.064 nM.
    MK-5108
  • HY-13253
    AMG 900
    Inhibitor 99.05%
    AMG 900 is a potent and highly selective pan-Aurora kinases inhibitor with IC50 of 5 nM, 4 nM and 1 nM for Aurora A, B and C, respectively.
    AMG 900
  • HY-N0110
    Palmatine chloride
    Inhibitor 99.81%
    Palmatine chloride is an orally active and irreversible indoleamine 2,3-dioxygenase 1 (IDO-1) inhibitor with IC50s of 3 μM and 157μM against HEK 293-hIDO-1 and rhIDO-1, respectively. Palmatine chloride can also inhibit West Nile virus (WNV) NS2B-NS3 protease in an uncompetitive manner with an IC50 of 96 μM. Palmatine chloride shows anti-cancer, anti-oxidation, anti-inflammatory, neuroprotection, antibacterial, anti-viral activities.
    Palmatine chloride
  • HY-10128
    ZM-447439
    Inhibitor 99.19%
    ZM-447439 is an aurora kinase inhibitor with IC50s of 110 and 130 nM for aurora A and B, respectively.
    ZM-447439
  • HY-70044
    GSK-1070916
    Inhibitor 99.55%
    GSK-1070916 is a potent and selective ATP-competitive inhibitor of aurora B and aurora C with Kis of 0.38 and 1.5 nM, respectively, and is >250- fold selective over Aurora A.
    GSK-1070916
  • HY-114258
    LY3295668
    Inhibitor 99.48%
    LY3295668 (AK-01) is a potent, orally active and highly specific Aurora-A kinase inhibitor, with Ki values of 0.8 nM and 1038 nM for AurA and AurB, respectively.
    LY3295668
  • HY-10179
    Danusertib
    Inhibitor 99.44%
    Danusertib is a pyrrolo-pyrazole and aurora kinase inhibitor with IC50 of 13, 79, and 61 nM for Aurora A, B, and C, respectively.
    Danusertib
Cat. No. Product Name / Synonyms Application Reactivity

Aurora Kinase

Aurora A

Aurora B

Aurora C

Your Search Returned No Results.

Sorry. There is currently no product that acts on isoform together.

Please try each isoform separately.

Aurora Kinase Degraders & Inhibitors
Product NameAurora KinaseAurora AAurora BAurora CPurity    
Alisertib 
Aurora A, IC50: 1.2 nM
Aurora B, IC50: 396.5 nM
 99.84%
Barasertib-HQPA  
Aurora B, IC50: 0.37 nM
 99.47%
Barasertib  
Aurora B, IC50: 0.37 nM
 99.62%
Reversine 
Aurora A, IC50: 400 nM
Aurora B, IC50: 500 nM
Aurora C, IC50: 400 nM
99.22%
Tozasertib 
Aurora A, Ki: 0.6 nM
Aurora B, Ki: 18 nM
Aurora C, Ki: 4.6 nM
99.92%
PROTAC MPS1 degrader 1 
Aurora A, DC50: 108.7 nM
Aurora B, DC50: 570.3 nM
 
Aurora kinase inhibitor-13 
Aurora A, IC50: 2.3 μM
  
JNJ-7706621 
Aurora A, IC50: 11 nM
Aurora B, IC50: 15 nM
 99.91%
Hesperadin  
Aurora B, IC50: 250 nM
 98.89%
AT9283 
Aurora A, IC50: 3 nM
Aurora B, IC50: 3 nM
 99.67%
KW-2449 
Aurora A, IC50: 48 nM
  99.69%
MK-5108 
Aurora A, IC50: 64 pM
  99.89%
AMG 900 
Aurora A, IC50: 5 nM
Aurora B, IC50: 4 nM
Aurora C, IC50: 1 nM
99.05%
ZM-447439 
Aurora A, IC50: 110 nM
Aurora B, IC50: 130 nM
 99.19%
GSK-1070916  
Aurora B, Ki: 0.38 nM
Aurora C, Ki: 1.5 nM
99.55%
LY3295668 
Aurora A, IC50: 0.8 nM
  99.48%
Danusertib 
Aurora A, IC50: 13 nM
Aurora B, IC50: 79 nM
Aurora C, IC50: 61 nM
99.44%
PF 477736 
Aurora-A, IC50: 23 nM
  99.21%
MLN8054 
Aurora A, IC50: 4 nM
  99.54%
PF-03814735 
Aurora 1, IC50: 0.8 nM
Aurora 2, IC50: 5 nM
 99.58%
TAK-632  
Aurora B, IC50: 66 nM
 98.84%
SNS-314 mesylate 
Aurora A, IC50: 9 nM
Aurora B, IC50: 31 nM
Aurora C, IC50: 6 nM
99.53%
JB170 
Aurora A, DC50: 28 nM
Aurora A, Kd: 99 nM
Aurora A, EC50: 193 nM
  98.97%
ENMD-2076 
Aurora A, IC50: 14 nM
  99.99%
XL228 
Aurora A, IC50: 3.1 nM
  99.64%
Ilorasertib hydrochloride 
Aurora A, IC50: 120 nM
Aurora B, IC50: 7 nM
Aurora B (Y156H), IC50: 12 nM
Aurora C, IC50: 1 nM
98.48%
Cenisertib 
Aurora-A
Aurora-B
 99.86%
TCS7010 
Aurora A, IC50: 3.4 nM
Aurora B, IC50: 3.4 μM
 99.82%
SP-96 
Aurora A, IC50: 18.975 nM
Aurora B, IC50: 0.316 nM
 99.42%
TAK-901 
Aurora A, IC50: 21 nM
Aurora B, IC50: 15 nM
 99.84%
CCT129202 
Aurora A, IC50: 42 nM
Aurora B, IC50: 198 nM
Aurora C, IC50: 227 nM
≥98.0%
BI-847325   
Aurora C, IC50: 15 nM
98.15%
CCT 137690 
Aurora A, IC50: 15 nM
Aurora B, IC50: 25 nM
Aurora C, IC50: 19 nM
99.54%
GRK2 Inhibitor 2 
Aurora A, IC50: 137 nM
  98.88%
CYC-116 
Aurora A, Ki: 8 nM
Aurora B, Ki: 9.2 nM
 99.03%
SCH-1473759 hydrochloride 
Aurora A, IC50: 4 nM
Aurora B, IC50: 13 nM
 99.79%
GW779439X 
Aurora A
  99.85%
NU6140 
Aurora A, IC50: 67 nM
Aurora B, IC50: 35 nM
 99.07%
CD532 
Aurora A, IC50: 45 nM
  98.78%
MK-8745 
Aurora A, IC50: 0.6 nM
  99.08%
TAS-119 
Aurora A, IC50: 1 nM
Aurora B, IC50: 95 nM
 98.03%
Chiauranib  
Aurora B, IC50: 9 nM
 99.28%
DB0614
Aurora Kinase
   98.80%
PHA-680632 
Aurora A, IC50: 27 nM
Aurora B, IC50: 135 nM
Aurora C, IC50: 120 nM
98.07%
Aurora kinase inhibitor-3 
Aurora A, IC50: 42 nM
  99.05%
dAURK-4 hydrochloride 
Aurora A
  99.44%
GSK2646264 
Aurora A, pIC50: <4.3
Aurora B, pIC50: <4.6
 98.39%
Aurkin A 
Aurora A, Kd: 3.77 μM
  ≥98.0%
ENMD-2076 Tartrate 
Aurora A, IC50: 1.86 nM
  99.42%
Ilorasertib 
Aurora A, IC50: 120 nM
Aurora B, IC50: 7 nM
Aurora B (Y156H), IC50: 12 nM
Aurora C, IC50: 1 nM
99.86%
SCH-1473759 
Aurora A, IC50: 4 nM
Aurora B, IC50: 13 nM
 98.20%
Aurora kinase inhibitor-2 
Aurora A, IC50: 310 nM
Aurora B, IC50: 240 nM
 99.08%
CCT241736 
Aurora-A, IC50: 38 nM
Aurora-A, Kd: 7.5 nM
Aurora-B, Kd: 48 nM
 99.88%
AKI603 
Aurora A, IC50: 12.3 nM
  98.03%
TC-A 2317 hydrochloride 
Aurora A, Ki: 1.2 nM
Aurora B, Ki: 101 nM
 99.57%
Phthalazinone pyrazole 
Aurora-A, IC50: 0.031 μM
  ≥98.0%
AurkA allosteric-IN-1 
Aurora A, IC50: 6.5 μM ([1])
  
Alisertib sodium 
Aurora A, IC50: 12.5 nM
Aurora B, IC50: 396.5 nM
 
AT9283 lactic acid 
Aurora A, IC50: 3 nM
Aurora B, IC50: 3 nM
 
Hesperadin hydrochloride  
Aurora B, IC50: 250 nM
 
Aurora inhibitor 1 
Aurora A, IC50: 4 nM
Aurora B, IC50: 13 nM
 
dAURK-4 
Aurora A
  
FAK-IN-22  
Aurora B, IC50: 0.49 nM
 
Aurora A inhibitor 2 
Aurora A, IC50: 21.94 nM
Aurora B, IC50: 273.18 nM
 
RET-IN-19 
Aurora A, IC50: 0.242 ± 0. μM
Aurora B, IC50: 0.536 ± 45 μM
 
SNS-314 
Aurora A, IC50: 9 nM
Aurora B, IC50: 31 nM
Aurora C, IC50: 6 nM
Aurora kinase inhibitor-10  
Aurora B, IC50: 8 nM
 
Glycyl H-1152 hydrochloride 
Aurora A, IC50: 2.35 μM
  
Aurora A/PKC-IN-1 
Aurora A, IC50: 6.9 nM
  
Aurora kinase-IN-5 
Aurora A, IC50: 5.6 nM
Aurora B, IC50: 18.4 nM
Aurora C, IC50: 24.6 nM
Aurora kinase-IN-2 
Aurora A, IC50: 90 nM
Aurora B, IC50: 152 nM
 
Aurora kinase inhibitor-9 
Aurora A, IC50: 0.093 μM
Aurora B, IC50: 0.09 μM
 
BRD-7880 
Aurora A, IC50: 2153 nM
Aurora B, IC50: 7 nM
Aurora C, IC50: 12 nM
SAR156497 
Aurora A, IC50: 0.6 nM
Aurora B, IC50: 1 nM
 
TAK-901 hydrochloride 
Aurora A, IC50: 21 nM
Aurora B, IC50: 15 nM
 
(Rac)-Aurora A/PKC-IN-1 
Aurora A, IC50: 6.9 nM
  
Benzo[c][1,8]naphthyridin-6(5H)-one 
Aurora A, IC50: 5.5 μM
  
TY-011 
Aurora A
Aurora B
 
Binucleine 2  
Aurora B
 
Aurora A inhibitor 4 
Aurora A
  
Aurora B inhibitor 1  
Aurora B, Ki: 0.01 μM