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5 μM and PAM activity at mGlu6 with a potency of 6
GSK-J1 inhibits the demethylase activity of KDM5C with 8
InChi: InChI=1S/C19H27N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4
The potential activity of Ginsenoside Rh3 is tested on Nrf2 signaling in the retinal pigment epithelium cells (RPEs)
CBR-5884 nib (EGF816) 5 μM and PAM activityCBR 5884 is an active, selective inhibitor of phosphoglycerate dehydrogenase (PHGDH) with an IC50 of 33 M. CBR 5884 inhibits de novo serine synthesis in cancer cells and is selectively toxic to cancer cell lines with high serine biosynthetic activity. CBR 5884 selectively inhibits the proliferation of melanoma and breast cancer lines that have a high propensity for serine synthesis. Product information CAS Number: 681159 27 3 Molecular Weight: 336. 39
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