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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T73300 | AXL-IN-13 | FLT , TAM Receptor , PDGFR , TGF-beta/Smad | |
AXL-IN-13 is a potent and orally active AXL inhibitor with an IC50 value of 1.6 nM and a Kd value of 0.26 nM.AXL-IN-13 exhibits anticancer activity, reverses TGF-β1-induced epithelial-mesenchymal transition (EMT) and inh... | |||
T3S0027 | Picropodophyllotoxin | AXL 1717,Picropodophyllin | IGF-1R |
Picropodophyllotoxin (AXL 1717) is a cyclolignan alkaloid found in the mayapple plant family (Podophyllum peltatum), and a small molecule inhibitor of the insulin-like growth factor 1 receptor (IGF1R) with potential anti... | |||
T63293 | Axl-IN-7 | ||
Axl-IN-7 is a potent inhibitor of AXL. Axl-IN-7 can be used to study Axl-related diseases such as cancer (e.g., acute myeloid leukemia, breast cancer, melanoma, pancreatic cancer, and glial tumors), immune system disorde... | |||
T63683 | Axl-IN-11 | ||
Axl-IN-11 is a potent inhibitor of AXL. Axl-IN-11 can be used to study proliferative diseases, allergic diseases, autoimmune diseases, inflammatory diseases, cancer, transplant rejection, viral infectious diseases or oth... | |||
T63154 | Axl-IN-10 | ||
Axl-IN-10 is a potent inhibitor of AXL (IC50: 5 nM).Axl-IN-10 has good pharmacokinetic properties in animals and excellent transmembrane properties.Axl-IN-10 can be used to study proliferative, allergic, autoimmune, infl... | |||
T79969 | Axl-IN-16 | TAM Receptor | |
Axl-IN-16, a dual Axl/HIF inhibitor, promotes Flammulina velutipes fruiting body formation and suppresses hypoxia-inducible factor activity along with receptor tyrosine kinase expression [1]. | |||
T73310 | AXL-IN-14 | TAM Receptor | |
AXL-IN-14 is a potent, orally active inhibitor of AXL with an IC50 of 0.8 nM that effectively suppresses Gas6/AXL-mediated cell migration and invasion, reduces the expression of p-AXL and p-AKT proteins, and demonstrates... | |||
T63320 | Axl-IN-6 | ||
Axl-IN-6 is an orally active inhibitor of AXL. Axl-IN-6 demonstrated good tolerance and significant inhibition of tumor growth in the MV-4-11 subcutaneous xenograft tumor model. | |||
T63901 | Axl-IN-8 | ||
Axl-IN-8 (NO.1) is a potent inhibitor of AXL (IC50<1 nM) and also inhibits c-MET (IC50: 1-10 nM). : 120.3 nM). | |||
T62778 | Axl-IN-9 | ||
Axl-IN-9 is a potent inhibitor of AXL (IC50: 26 nM) with excellent transmembrane properties.Axl-IN-9 exhibits good pharmacokinetic properties in animals.Axl-IN-9 can be used to study proliferative, autoimmune, allergic, ... | |||
T60259 | Axl-IN-4 | ||
Axl-IN-4 (Compound 24) is an inhibitor of AXL kinase with an IC 50 of 28.8 μM [1]. | |||
T63817 | Axl-IN-5 | ||
Axl-IN-5 (compound 1) is an AXL inhibitor (IC50: 283 nM) that exhibits anticancer activity. | |||
T63888 | Axl-IN-12 | ||
Axl-IN-12 is a potent inhibitor of AXL. Axl-IN-12 can be used to study proliferative, allergic, autoimmune, inflammatory, cancer, transplant rejection, viral infectious diseases or other mammalian diseases. | |||
T62962 | Axl-IN-3 | ||
Axl-IN-3 is a selective, potent and orally active inhibitor of AXL kinase (IC50: 41.5 nM) and has a low inhibitory effect on other kinases. | |||
T79045 | AXL-IN-15 | TAM Receptor | |
AXL-IN-15 (cpd391) is a potent inhibitor of Axl, exhibiting both a dissociation constant (K i) and a half-maximal inhibitory concentration (IC50) of less than 1 nanomolar (nM). It is applicable for cancer research [1]. | |||
T6943 | Picropodophyllin | AXL1717,Picropodophyllin (PPP),Picropodophyllotoxin,PPP | Apoptosis , IGF-1R |
Picropodophyllin (Picropodophyllin (PPP)) (PPP) is a specific IGF-1R inhibitor (IC50: 1 nM). Picropodophyllin specifically inhibits the activity and downregulates the cellular expression of IGF1R without interfering with... | |||
T74353 | PROTAC Axl Degrader 1 | ||
PROTAC Axl Degrader 1 is a potent, selective degrader of PROTAC Axl, exhibiting an IC50 of 0.92 µM. It demonstrates in vitro anti-proliferative and anti-migratory activities and induces mehuosis [1]. | |||
T74354 | PROTAC Axl Degrader 2 | ||
PROTAC Axl Degrader 2, a potent and selective PROTAC Axl degrader, demonstrates an IC50 of 1.61 µM. It exhibits anti-proliferative and anti-migratory activities in vitro and induces mehuosis [1]. | |||
T72574 | Axl/Mer/CSF1R-IN-1 | ||
Axl/Mer-IN-1 is a compound that functions as an inhibitor for Axl/Mer receptor tyrosine kinase (Axl/Mer RTK) and CSF1R, exhibiting dissociation constants (Kds) of less than 0.1 μM. | |||
T6982 | SGI-7079 | FLT , c-Met/HGFR , c-RET , TAM Receptor , Src | |
SGI-7079 is a new selective Axl inhibitor. SGI-7079 can be a dose-dependent manner inhibited growth of tumors. It is also a potential therapeutic target for EGFR inhibitor resistance. |