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UNC569
CAS No. : 1350547-65-7
Biological Activity：UNC569 is a potent, reversible, ATP-competitive and orally active Mer kinase inhibitor with an IC50 of 2.9 nM and a Ki of 4.3 nM. UNC569 also inhibits Axl and Tyro3 with IC50s of 37 nM and 48 nM, respectively. UNC569 can be used for acute lymphoblastic leukemia (ALL) and atypical teratoid/rhabdoid tumors research[2]
Research Area：Cancer
Targets：TAM Receptor
Related Screening Libraries:Bioactive Compound Library Plus;Kinase Inhibitor Library;Protein Tyrosine Kinase Compound Library;Anti-Cancer Compound Library;Orally Active Compound Library;Anti-Blood Cancer Compound Library;Targeted Diversity Library;
Related Small Molecules:Axl-IN-5;PROTAC Axl Degrader 2;UNC2250;R916562;XL092;Axl-IN-3;Gilteritinib-d8;UNC1062;Bemcentinib;Axl-IN-6;ONO-7475;RU-302;TAM-IN-2;SGI-7079;Axl-IN-8;AZ14145845;NPS-1034;Ningetinib Tosylate;UNC2541;Gilteritinib hemifumarate;UNC4203;BMS 777607;Axl-IN-7;Axl-IN-12;RU-301;TAM&Met-IN-1
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