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ALK

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ALK

Chemical Structure Cat. No. Product Name CAS No.
Belizatinib Chemical Structure
 BCP29521 Belizatinib 1357920-84-3
Belizatinib is an oral, dual, potent inhibitor of ALK and TRKA, TRKB, and TRKC, with IC50 of 0.7 nM for wild-type recombinant ALK kinase.
Ensartinib dihydrochloride Chemical Structure
 BCP29059 Ensartinib dihydrochloride 2137030-98-7
Ensartinib, also known as X-396, is a potent and dual ALK/MET inhibitor with IC50s of <0.4 nM and 0.74 nM, respectively.
LDN-193189 2HCl Chemical Structure
 BCP20431 LDN-193189 2HCl 1435934-00-1
LDN193189 is a highly potent small molecule BMP inhibitor with IC50 of 5 and 30 nM for ALK2 and ALK3, respectively.
Alectinib Hydrochloride Chemical Structure
 BCP09075 Alectinib Hydrochloride 1256589-74-8
CH5424802 Hydrochloride is a potent, selective, and orally available ALK inhibitor with IC50 of 1.9 nM, the dissociation constant (KD) value for ALK in an ATP-competitive manner is 2.4 nM using a competition-bind assay.
ALK inhibitor 1 Chemical Structure
 BCP28167 ALK inhibitor 1 761436-81-1
ALK inhibitor 1 is a novel and selective inhibitor for the ALK kinase.
HG-14-10-04 Chemical Structure
 BCP24835 HG-14-10-04 1356962-34-9
HG-14-10-04 is a potent and specific ALK inhibitor with IC50 of 20 nM.
CEP-28122 Chemical Structure
 BCP15177 CEP-28122 1022958-60-6
CEP-28122 is a highly potent and selective orally active ALK inhibitor with a favorable pharmaceutical and pharmacokinetic profile and robust and selective pharmacologic efficacy against ALK-positive human cancer cells and tumor xenograft models in mice.
CEP-28122 monomesilate hydrochloride salt Chemical Structure
 BCP24832 CEP-28122 monomesilate hydrochloride salt 1354545-57-5
CEP-28122 is a highly potent and selective orally active ALK inhibitor with IC50 of 1.9 ± 0.5 nM in an enzyme-based TRF assay.
KRCA-0008 Chemical Structure
 BCP16229 KRCA-0008 1472795-20-2
KRCA-0008 is a potent dual inhibitor of Ack1 and anaplastic lymphoma kinase (ALK).
TPX-0005 Chemical Structure
 BCP19778 TPX-0005 1802220-02-5
TPX-0005 is a potent ALK/ROS1/TRK inhibitor, with IC50 of 5.3 nM, 1.01 nM, 1.26 nM and 1.08 nM for SRC, WT ALK, ALK G1202R and ALK L1196M, respectively.
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