Nucleic Acid Synthesis

A single enantiomer of a potent and selective inactivator of KIAA1363, a MAGE hydrolase an enzyme that is upregulated in aggressive cancers from various tissues (IC50 = 150 nM when tested as a racemic mixture in SK0V-3 cells) activity of the

Hill Formula: C₁₉H₂₂N₂O CAS Number: 118-10-5

Hill Formula: C₁₉H₂₂N₂O CAS Number: 118-10-5

(+)-Di-p-anisoyl-D-tartaric Acid.

(+)-Di-p-anisoyl-D-tartaric Acid.

(+)-Di-p-anisoyl-D-tartaric Acid.

(+)-Di-p-anisoyl-D-tartaric Acid.

Displaces BET proteins from chromatin by competitively binding to the acetyl-lysine recognition pocket of BET bromodomains binds BRD4 bromodomains 1 and 2 with Kd values of ~50 and 90 nM, respectively.

Displaces BET proteins from chromatin by competitively binding to the acetyl-lysine recognition pocket of BET bromodomains binds BRD4 bromodomains 1 and 2 with Kd values of ~50 and 90 nM, respectively.

Other NotesStarting material for the synthesis of chiral building blocks: L-Ascorbic acid, review.

Other NotesStarting material for the synthesis of chiral building blocks: L-Ascorbic acid, review.

Application (±)-&#945:-Methoxyphenylacetic acid can be used as a reactant to synthesize:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp:&nbsp: N -(Cyclohexylmethyl)-2-methoxy-2-phenylethylamine by reacting with cyclohexylmethylamine in the presence