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ALK

Anaplastic lymphoma kinase (ALK) also known as ALK tyrosine kinase receptor or CD246 (cluster of differentiation 246) is an enzyme that in humans is encoded by the ALK gene.
Signaling Pathways | Target | TargetMol
Cat. No. Product name CAS No. Purity Chemical Structure
T1935 LDN193189 1062368-24-4 99.11%
LDN193189
LDN193189 (LDN-193189) (DM 3189) is a selective BMP signaling inhibitor, inhibiting the transcriptional activity of ALK2 and ALK3 (IC50s: 0.8/0.8/5.3/16.7 nM for...
T2655 CEP-37440 1391712-60-9 99.01%
CEP-37440
CEP-37440 is an effective and specific Dual FAK/ALK inhibitor with IC50s of 120 nM(ALK cellular in 75% human plasma) and 2.3 nM (FAK).
T3041 ALK inhibitor 2 761438-38-4 99%
ALK inhibitor 2
ALK inhibitor 2 is a new-type and selective inhibitor for the ALK kinase.
T77726 INCB-000928 2173389-57-4 98.93%
INCB-000928
Zilurgisertib (INCB-000928) is a selective and potent ALK 2 inhibitor for the study of cancer and MF anemia.
T6337 RepSox 446859-33-2 98.8%
RepSox
RepSox (ALK5 Inhibitor II) is a TGFβR-1/ALK5 inhibitor that selectively inhibits the binding of ATP to ALK5 and the autophosphorylation of ALK5 (IC50=23/4 nM). R...
T3031 A 83-01 909910-43-6 98.76%
A 83-01
A 83-01 (ALK5 Inhibitor IV) is an inhibitor of the TGF-β type I receptors ALK5, ALK4, and ALK7 (IC50=12/45/7.5 nM). A 83-01 promotes the reprogramming of mouse f...
T38752 EW-7195 1352609-28-9 98.76%
EW-7195
EW-7195 is a selective and potent inhibitor of ALK5 (TGFβR1) with an IC50 value of 4.83 nM.EW-7195 has an affinity for ALK5 that is more than 300-fold higher tha...
T16153 MS4078 2229036-62-6 98.74%
MS4078
MS4078 is an inhibitor and aplastic lymphoma kinase (ALK) PROTAC (degrader) based on Cereblon ligand, with a Kd of 19 nM for binding affinity to ALK.
T2462 SB-505124 694433-59-5 98.74%
SB-505124
SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5.
T3550 X-376 1365267-27-1 98.72%
X-376
X-376 (Ensartinib) is an orally available small molecule inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) with potential antineoplastic...
T8108 Blu-782 2141955-96-4 98.59%
Blu-782
Blu-782 (ALK2-IN-1) is a activin receptor-like kinase-2 (ALK2) inhibitor ( IC50 of <10 nM)
T10285 ALK inhibitor 1 761436-81-1 98.55%
ALK inhibitor 1
ALK inhibitor 1 is a selective ALK kinase inhibitor.
T1763 SB 525334 356559-20-1 98.39%
SB 525334
SB-525334 is a potent and selective inhibitor of the TGF-β1R and ALK5 (IC50: 14.3 nM).
T4015 HG-14-10-04 1356962-34-9 98.36%
HG-14-10-04
HG-14-10-04 is a potent and specific ALK inhibitor.
T13416 ZX-29 2254805-62-2 98.32%
ZX-29
ZX-29 is a potent and selective inhibitor of ALK(IC50 of 2.1 nM, 1.3 nM and 3.9 nM for ALK, ALK L1196M and ALK G1202R mutations, respectively), and also induces ...
T9224 CH5424802 analog 1256577-71-5 98.31%
CH5424802 analog
CH5424802 analog is a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant.
T1943 ML347 1062368-49-3 98.3%
ML347
ML347 (LDN 193719)(DN193719) is a highly specific ALK1/2 inhibitor ( IC50: 46/32 nM), and the selectivity for ALK2 is >300-fold than ALK3.
T35896 AZ 12799734 1117684-36-2 98.23%
AZ 12799734
AZ 12799734 is an orally active, selective and potent dual inhibitor of TGFBR1 and ALK5 with inhibitory effects on BMP and TGFβ for the study of tumours.
T15572 IN-1130 868612-83-3 98.08%
IN-1130
IN-1130 is a selective inhibitor of ALK5 with IC50 values of 5.3 nM, 36 nM, and 4.3 μM for phosphorylation of ALK5-mediated Smad3, ALK5 phosphorylation of casein...
T15612 JH-VIII-157-02 1639422-97-1 98.02%
JH-VIII-157-02
JH-VIII-157-02 is an inhibitor of ALK and inhibits echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) with IC50s of 2 nM for EML4-ALK G1202R, EML4-A...
LDN193189
T1935
LDN193189 (LDN-193189) (DM 3189) is a selective BMP signaling inhibitor, inhibiting the transcriptional activity of ALK2 and ALK3 (IC50s: 0.8/0.8/5.3/16.7 nM for...
CEP-37440
T2655
CEP-37440 is an effective and specific Dual FAK/ALK inhibitor with IC50s of 120 nM(ALK cellular in 75% human plasma) and 2.3 nM (FAK).
ALK inhibitor 2
T3041
ALK inhibitor 2 is a new-type and selective inhibitor for the ALK kinase.
INCB-000928
T77726
Zilurgisertib (INCB-000928) is a selective and potent ALK 2 inhibitor for the study of cancer and MF anemia.
RepSox
T6337
RepSox (ALK5 Inhibitor II) is a TGFβR-1/ALK5 inhibitor that selectively inhibits the binding of ATP to ALK5 and the autophosphorylation of ALK5 (IC50=23/4 nM). R...
A 83-01
T3031
A 83-01 (ALK5 Inhibitor IV) is an inhibitor of the TGF-β type I receptors ALK5, ALK4, and ALK7 (IC50=12/45/7.5 nM). A 83-01 promotes the reprogramming of mouse f...
EW-7195
T38752
EW-7195 is a selective and potent inhibitor of ALK5 (TGFβR1) with an IC50 value of 4.83 nM.EW-7195 has an affinity for ALK5 that is more than 300-fold higher tha...
MS4078
T16153
MS4078 is an inhibitor and aplastic lymphoma kinase (ALK) PROTAC (degrader) based on Cereblon ligand, with a Kd of 19 nM for binding affinity to ALK.
SB-505124
T2462
SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5.
X-376
T3550
X-376 (Ensartinib) is an orally available small molecule inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) with potential antineoplastic...
Blu-782
T8108
Blu-782 (ALK2-IN-1) is a activin receptor-like kinase-2 (ALK2) inhibitor ( IC50 of <10 nM)
ALK inhibitor 1
T10285
ALK inhibitor 1 is a selective ALK kinase inhibitor.
SB 525334
T1763
SB-525334 is a potent and selective inhibitor of the TGF-β1R and ALK5 (IC50: 14.3 nM).
HG-14-10-04
T4015
HG-14-10-04 is a potent and specific ALK inhibitor.
ZX-29
T13416
ZX-29 is a potent and selective inhibitor of ALK(IC50 of 2.1 nM, 1.3 nM and 3.9 nM for ALK, ALK L1196M and ALK G1202R mutations, respectively), and also induces ...
CH5424802 analog
T9224
CH5424802 analog is a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant.
ML347
T1943
ML347 (LDN 193719)(DN193719) is a highly specific ALK1/2 inhibitor ( IC50: 46/32 nM), and the selectivity for ALK2 is >300-fold than ALK3.
AZ 12799734
T35896
AZ 12799734 is an orally active, selective and potent dual inhibitor of TGFBR1 and ALK5 with inhibitory effects on BMP and TGFβ for the study of tumours.
IN-1130
T15572
IN-1130 is a selective inhibitor of ALK5 with IC50 values of 5.3 nM, 36 nM, and 4.3 μM for phosphorylation of ALK5-mediated Smad3, ALK5 phosphorylation of casein...
JH-VIII-157-02
T15612
JH-VIII-157-02 is an inhibitor of ALK and inhibits echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) with IC50s of 2 nM for EML4-ALK G1202R, EML4-A...
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TargetMol