Pay in 4 interest-free payments of $30.00 Learn more
Ships within 48 hours · Estimated delivery Aug 4 - Aug 9
Solubility: DMSO up to 25mM
It does not inhibit histone deacetylase (HDAC) or other sirtuin deacetylase family members (IC50 ~20-100 µM)
AGI-6780 was suggested to be used at 1-5 µM final concentration in vitro
inhibition of Aurora kinase activity by ZM-447439 results in abnormalities during mitosis by regulating the phosphorylation of histone H3 serine 10 (H3S10Ph) from G2 to metaphase with different perturbations in each embryonic cycle
Almorexant selectively inhibits the functional consequences of OX1 and OX2 receptor activation
Thalidomide-PEG5-NH2 Catalog No.:M11517-2 Solubility: DMSO up to 25mMThalidomide PEG5 NH2 is a synthesized E3 ligase ligand linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. Product information CAS Number: 2460263 40 3 Molecular Weight: 493. 51 Formula: C23H31N3O9 Chemical Name: 5 [(14 amino 3, 6, 9, 12 tetraoxatetradecan 1 yl)oxy] 2 (2, 6 dioxopiperidin 3 yl) 2, 3 dihydro 1H isoindole 1, 3 dione Smiles: