T1935 |
LDN193189
|
1062368-24-4
|
99.11%
|
|
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 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 is a new-type and selective inhibitor for the ALK kinase.
|
T77726 |
INCB-000928
|
2173389-57-4
|
98.93%
|
|
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 (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 (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 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 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%
|
|
SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5.
|
T3550 |
X-376
|
1365267-27-1
|
98.72%
|
|
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 (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 is a selective ALK kinase inhibitor.
|
T1763 |
SB 525334
|
356559-20-1
|
98.39%
|
|
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 is a potent and specific ALK inhibitor.
|
T13416 |
ZX-29
|
2254805-62-2
|
98.32%
|
|
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 is a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant.
|
T1943 |
ML347
|
1062368-49-3
|
98.3%
|
|
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 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 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 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...
|