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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10415 | Autotaxin-IN-3 | PDE | |
Autotaxin-IN-3 is an inhibitor of Autotaxin (IC50 = 2.4 nM) which is responsible for the increase in lysophosphatidic acid in ascites and plasma. | |||
T22086 | HA 155 | Autotaxin Inhibitor IV | PDE |
HA 155 (Autotaxin Inhibitor IV) is a boronic acid-based compound, inhibiting ATX with IC50 of 5.7 nM by selectively binding to its catalytic threonine. | |||
T10418 | Autotaxin modulator 1 | PDE | |
Autotaxin modulator 1 is a new modulator of Autotaxin. | |||
T10416 | Autotaxin-IN-4 | PDE | |
Autotaxin-IN-4 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis. | |||
T10417 | Autotaxin-IN-5 | PDE | |
Autotaxin-IN-5 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis. | |||
T14352 | Autotaxin-IN-1 | PDE | |
Autotaxin-IN-1 is a potent autotaxin inhibitor, which has favorable potency (IC50=2.2 nM), PK properties, and a robust PK/PD relationship and it is used in treatment of osteoarthritis pain[1]. | |||
T72837 | Autotaxin-IN-6 | ||
Autotaxin-IN-6 (compound 23) is a potent inhibitor of autotaxin (ATX), exhibiting an IC50 of 30 nM, and is capable of attenuating cell migration with potential applications in anticancer research [1]. | |||
T11533 | Z-HA155 | CS-963 | PDE |
Z-HA155 (CS-963) selectively and potently inhibits autotaxin with an IC50 of 5.7 nM. | |||
T10545 | BIO-32546 | PDE | |
BIO-32546 (S-isomer) is a highly potent regulator of autotaxin (ATX) with an IC50 value of 1 nM. | |||
T2646 | HA130 | PDE | |
HA130 is a selective ATX (autotaxin) inhibitor. | |||
T31101 | CRT0273750 | CRT 0273750,CRT-0273750 | PDE |
CRT0273750 regulates plasma LPA levels and is suitable for in vivo studies. CRT0273750 is an autotaxin (ATX) inhibitor with IC50 of 0.014 μM. | |||
T63190 | Cudetaxestat | BLD-0409 | PDE |
Cudetaxestat (BLD-0409) is a potent inhibitor of orally active autotaxin. | |||
T4041 | Ziritaxestat | GLPG1690 | PDE |
Ziritaxestat (GLPG1690), an autotaxin inhibitor, currently being evaluated in an exploratory phase 2 study in idiopathic pulmonary fibrosis patients. | |||
T3631 | PF-8380 | PDE | |
PF-8380 is an effective and orally available autotaxin inhibitor (IC50: 2.8 nM, in isolated enzyme assay; 101 nM, in the human whole blood). It modulates lysophosphatidic acid (LPA) levels in vivo/vitro by directly inhib... | |||
T38759 | ONO-8430506 | PDE | |
ONO-8430506 is an orally available, potent autotaxin (ATX)/ENPP2 inhibitor (IC90: 100 nM) that inhibits ATX activity in mouse plasma. | |||
T10409 | ATX inhibitor 5 | PDE | |
ATX inhibitor 5 is a potent and orally active autotaxin (ATX) inhibitor (IC50 : 15.3 nM) that reduces the level of CCl4-induced hepatic fibrosis and has anti-hepatic fibrosis effects,. | |||
T12372 | PAT-505 | EGFR | |
PAT-505 is an orally available, selective and potent inhibitor of autologous epidermal growth factor (IC50 2 nM in Hep3B cells, 9.7 nM in human blood, 62 nM in mouse plasma). | |||
T23293 | S32826 disodium | S 32826 | Others |
autotaxin inhibitor | |||
T28299 | PAT-078 | PAT078,PAT 078 | |
PAT-078 is an inhibitor of type II autotaxin. | |||
T28301 | PAT-494 | PAT 494,PAT494 | |
PAT-494 is an inhibitor of type II Autotaxin. |