Thalidomide-NH-amido-PEG1-C2-NH2 hydrochloride 13176 69(2):86-95

69(2):86-95

Inhibition of aFGF-stimulated MM cell growth by PD173074 is highly correlated with the expression of FGFR3

Smiles: CC1C=NC(=CC=1)S(=O)(=O)NC1=NC(=NC(OC)=C1OC1=CC=CC=C1OC)C1C=CN=CC=1

moDC differentiated in the presence of adenosine showed a decreased ability to stimulate IFN-γ secretion from allogenic CD4+ T-cells in a MLR

specifically activates the cholesterol efflux arm of the LXR pathway without stimulating triglyceride synthesis

Thalidomide-NH-amido-PEG1-C2-NH2 hydrochloride 13176 69(2):86-95Thalidomide NH amido PEG1 C2 NH2 hydrochloride is a synthesized E3 ligase ligand linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. Product information Molecular Weight: 453. 88 Formula: C19H24ClN5O6 Chemical Name: N [2 (2 aminoethoxy)ethyl] 2 {[2 (2,6 dioxopiperidin 3 yl) 1,3 dioxo 2,3 dihydro 1H isoindol 4 yl]amino}acetamide; chlorohydrogen Smiles: Cl.