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Search Results for " methyl-lysine "

9

Compounds

Cat No. Product Name Synonyms Targets
T32817 L-Lysine, mono(2-(((3-phenyl-1,2,4-oxadiazol-5-yl)methyl)thio)propanoate)
L-Lysine, mono(2-(((3-phenyl-1,2,4-oxadiazol-5-yl)methyl)thio)propanoate) can be used in related research in the field of life sciences. Its product number is T32817 and CAS number is 61560-15-4.
T9221 UNC926 hydrochloride Epigenetic Reader Domain
UNC926 hydrochloride is a methyl-lysine (Kme) reader domain inhibitor.
T4012 UNC926 UNC-926,UNC 926 hydrochloride Epigenetic Reader Domain
UNC926 (UNC-926) inhibits L3MBTL1 (IC50: 3.9 μM). UNC926 also exhibits a low micromolar affinity for L3MBTL3. UNC926 inhibits binding of the 3xMBT domain to H4K20me1. It selectively and dose-dependently inhibits the L3MB...
T24925 UNC-2170 UNC2170 Maleate,UNC-2170 Maleate,UNC 2170 Maleate Others
UNC-2170 (UNC2170 Maleate) is the methyl-lysine binding protein, 53BP1 ligand.
T4705 Aminoadipic acid DL-2-Aminoadipic acid Others , Endogenous Metabolite
Aminoadipic acid (DL-2-Aminoadipic acid) (2-aminoadipate) is a metabolite in the principal biochemical pathway of lysine. It is an intermediate in the metabolism (i.e. breakdown or degradation) of lysine and saccharopine...
T79763 UNC9512 DNA/RNA Synthesis
UNC9512 is a potent antagonist of the methyl-lysine reader protein 53BP1, which can be utilized to investigate the function of 53BP1 in DNA repair, gene editing, and tumorigenesis [1].
T62729 MS31 trihydrochloride
MS31 trihydrochloride is a selective, high-affinity, fragment-like inhibitor of the methyl-lysine read-write protein spindlin 1 (SPIN1). MS31 trihydrochloride effectively disrupts the interaction of SPIN1 with H3K4me3 pr...
T80899 UNC3474
UNC3474, a small molecule ligand, selectively interacts with the aromatic methyl-lysine binding cage of the tumor protein 53BP1 Tudor domain (TT), exhibiting a dissociation constant (Kd) of 1.0±0.3 μM. It impedes 53BP1's...
T36053 D-Lysine lactam
D-Lysine lactam is a chiral building block.1,2It has been used in the synthesis of a chiral antibiotic synthetic intermediate, as well as in the stereoselective synthesis of neurokinin (NK) receptor antagonists. 1.Kumar,...
TargetMol