Wnt family ligands

Omtriptolide (PG490-88) is a derivative proagent of triptolide purified from the Chinese herb.In VitroTriptolide, a traditional Chinese medicine, has anti-inflammatory, antiproliferative, and proapoptotic properties. MCE has not independently

OSM-SMI-10B a derivative of OSM-SMI-10. OSM-SMI-10B significantly reduces OSM-induced STAT3 phosphorylation in cancer cells upon co-incubation with OSM (Oncostatin M).Appearance:SolidIC50&amp Target:p-STAT3Biological Activity:OSM-SMI-10B a

OSM-SMI-10B a derivative of OSM-SMI-10. OSM-SMI-10B significantly reduces OSM-induced STAT3 phosphorylation in cancer cells upon co-incubation with OSM (Oncostatin M).Appearance:SolidIC50&amp Target:p-STAT3Biological Activity:OSM-SMI-10B a

OSM-SMI-10B a derivative of OSM-SMI-10. OSM-SMI-10B significantly reduces OSM-induced STAT3 phosphorylation in cancer cells upon co-incubation with OSM (Oncostatin M).Appearance:SolidIC50&amp Target:p-STAT3Biological Activity:OSM-SMI-10B a

OSM-SMI-10B a derivative of OSM-SMI-10. OSM-SMI-10B significantly reduces OSM-induced STAT3 phosphorylation in cancer cells upon co-incubation with OSM (Oncostatin M).Appearance:SolidIC50&amp Target:p-STAT3Biological Activity:OSM-SMI-10B a

Pachymic acid is a lanostrane-type triterpenoid from P. cocos . Pachymic acid inhibits Akt and ERK signaling pathways.In VitroPachymic acid (PA) is able to inhibit gallbladder cancer tumorigenesis involving affection of Akt and ERK signaling

Pachymic acid is a lanostrane-type triterpenoid from P. cocos . Pachymic acid inhibits Akt and ERK signaling pathways.In VitroPachymic acid (PA) is able to inhibit gallbladder cancer tumorigenesis involving affection of Akt and ERK signaling

Pachymic acid is a lanostrane-type triterpenoid from P. cocos . Pachymic acid inhibits Akt and ERK signaling pathways.In VitroPachymic acid (PA) is able to inhibit gallbladder cancer tumorigenesis involving affection of Akt and ERK signaling

Pachymic acid is a lanostrane-type triterpenoid from P. cocos . Pachymic acid inhibits Akt and ERK signaling pathways.In VitroPachymic acid (PA) is able to inhibit gallbladder cancer tumorigenesis involving affection of Akt and ERK signaling

PF-04802367 (PF-367) is a highly selective GSK-3 inhibitor with an IC 50 of 2.1 nM based on a recombinant human GSK-3β enzyme assay and 1.1 nM based on ADP-Glo assay. PF-04802367 shows desirable central nervous system (CNS) properties and potency.

PF-04802367 (PF-367) is a highly selective GSK-3 inhibitor with an IC 50 of 2.1 nM based on a recombinant human GSK-3β enzyme assay and 1.1 nM based on ADP-Glo assay. PF-04802367 shows desirable central nervous system (CNS) properties and potency.

PF-04802367 (PF-367) is a highly selective GSK-3 inhibitor with an IC 50 of 2.1 nM based on a recombinant human GSK-3β enzyme assay and 1.1 nM based on ADP-Glo assay. PF-04802367 shows desirable central nervous system (CNS) properties and potency.