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5-dihydro-1H-imidazol-2-yl)-6-methoxy-2-methylpyrimidin-5-amine
It inhibits hypoxia-inducible factor α (HIF-α) prolyl hydroxylase (HIF-PH)
7-dimethyl-2-oxo-1-bicyclo[2
treatment of prenatally stressed rats with Alda-1 significantly increases number of entries into the open arms of the maze and the time spent therein
PLpro inhibitor
Thalidomide D4 - CAS# 1219177-18-0 R40 Activator 1 5-dihydro-1H-imidazol-2-yl)-6-methoxy-2-methylpyrimidin-5-amineThalidomide D4 is a deuterium labeled Thalidomide. Thalidomide is initially promoted as a sedative, inhibits cereblon (CRBN), a part of the cullin 4 E3 ubiquitin ligase complex CUL4 RBX1 DDB1, with a Kd of ~250 nM, and has immunomodulatory, anti inflammatory and anti angiogenic cancer properties. Product information CAS Number: 1219177 18 0 Molecular Weight: 262. 25 Formula: C13H10N2O4 Chemical Name: 2 (2, 6 dioxopiperidin 3 yl) 2, 3 dihydro(H) 1H