Products for Aurora Kinase

  1. Cat.No. Product Name Information
  2. BCC2176 MK-5108 (VX-689) MK-5108 is a highly potent and specific inhibitor of Aurora A kinase with an IC50 value of 0.064 nM. MK-5108 (VX-689)
  3. BCC2166 MLN8237 (Alisertib) 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. MLN8237 (Alisertib)
  4. BCC1934 SCH-1473759 SCH-1473759 is an aurora inhibitor with IC50s of 4 and 13 nM for aurora A and B, respectively. SCH-1473759
  5. BCC2188 CCT137690 CCT 137690 is a potent and orally available aurora kinase inhibitor with IC50s of 15, 25, and 19 nM for aurora A, B and C, respectively. CCT137690
  6. BCC2177 SNS-314 Mesylate SNS-314 is a potent and selective aurora kinase inhibitor with IC50s of 9, 31, and 6 nM for aurora A, B and C, respectively. SNS-314 Mesylate
  7. BCC2418 TC-A 2317 hydrochloride Potent, selective Aurora kinase A inhibitor TC-A 2317 hydrochloride
  8. BCC2185 ENMD-2076 L-(+)-Tartaric acid ENMD-2076 Tartrate is a multi-targeted kinase inhibitor with IC50s of 1.86, 14, 58.2, 15.9, 92.7, 70.8, 56.4 nM for Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα, respectively. ENMD-2076 L-(+)-Tartaric acid
  9. BCN2483 Ginkgolic acid C15:0 Anacardic Acid, extracted from cashew nut shell liquid, is a histone acetyltransferase inhibitor, inhibits HAT activity of p300 and PCAF, with IC50s of ∼8.5 μM and ∼5 μM, respectively. Ginkgolic acid C15:0
  10. BCC2169 ZM 447439 ZM-447439 is an aurora kinase inhibitor with IC50s of 110 and 130 nM for aurora A and B, respectively. ZM 447439
  11. BCC2178 PHA-680632 PHA-680632 is an aurora kinase inhibitor with IC50s of 27, 135 and 120 nM for aurora A, B and C, respectively. PHA-680632
  12. BCC2174 Hesperadin Hesperadin is an ATP-competitive inhibitor of aurora B kinase with an IC50 of 250 nM. Hesperadin
  13. BCC2171 JNJ-7706621 JNJ-7706621 is a potent aurora kinase inhibitor, and also inhibits CDK1 and CDK2, with IC50s of 9, 3, 11, and 15 nM for CDK1, CDK2, Aurora-A and Aurora-B, respectively. JNJ-7706621
  14. BCC2167 VX-680 (MK-0457,Tozasertib) Tozasertib (VX 680; MK-0457) is an inhibitor of Aurora A/B/C kinases with Kis of 0.6, 18, 4.6 nM, respectively. VX-680 (MK-0457,Tozasertib)
  15. BCC1892 Reversine 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
  16. BCC2181 CYC116 CYC-116 is a potent aurora A and aurora B inhibitor with Kis of 8 and 9 nM, respectively. CYC116
  17. BCC1393 AZD1152 AZD1152 is a pro-drug of Barasertib-hQPA, which is a highly selective Aurora B inhibitor with IC50 of 0.37 nM in a cell-free assay. AZD1152
  18. BCC2168 Barasertib (AZD1152-HQPA) Barasertib-HQPA (AZD2811) is a highly selective Aurora B inhibitor with an IC50 of 0.37 nM in a cell-free assay, and shows 3700-fold selectivity for Aurora B over Aurora A. Barasertib (AZD1152-HQPA)
  19. BCC2170 MLN8054 MLN8054 is a potent, selective and orally available aurora A kinase inhibitor with an IC50 of 4 nM. MLN8054
  20. BCC2173 AT9283 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
  21. BCC2058 XL228 XL228 is a multi-targeted tyrosine kinase inhibitor with IC50s of 5, 3.1, 1.6, 6.1, 2 nM for Bcr-Abl, Aurora A, IGF-1R, Src and Lyn, respectively. XL228
  22. BCC2186 ENMD-2076 ENMD-2076 is a multi-targeted kinase inhibitor with IC50s of 1.86, 14, 58.2, 15.9, 92.7, 70.8, 56.4 nM for Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα, respectively. ENMD-2076
  23. BCC2180 TAK-901 TAK-901 is a multi-targeted aurora inhibitor with IC50s of 21 and 15 nM for aurora A and B, respectively. TAK-901
  24. BCC2184 PF-03814735 PF-03814735 is a potent, orally available and reversible aurora A and aurora B inhibitor with IC50s of 0.8 and 0.5 nM, respectively. PF-03814735
  25. BCC2183 GSK1070916 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. GSK1070916
  26. BCC2187 CCT129202 CCT129202 is an aurora kinase inhibitor with IC50s of 42, 198, and 227 nM for aurora A, B and C, respectively. CCT129202
  27. BCC2175 AMG-900 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

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