42754-71-2

Upstream product

• 949-01-9 1-(morpholin-4-yl)-2-phenylethanethione 
• 111509-98-9 3-Benzyl-2-cyano-3-morpholinoacrylonitrile 
• 476371-60-5 2-phenylacetylmalononitrile 
• 103-80-0 phenylacetyl chloride 
• 42754-59-6 2-(1-Methoxy-2-phenylethylidene)malononitrile 
• 77287-34-4 formamide 
• 42754-64-3 5-Amino-3-benzyl-1H-pyrazole-4-carbonitrile 

Downstream Products

• 476371-80-9 C₁₇H₂₂N₅O₁₃P₃ 
• 476371-76-3 (2S,3R,4S,5R)-2-(4-amino-3-benzylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol 
• 476371-72-9 1-((2S,3R,4S,5R)-3,4-dibenzoyl-5-benzoylmethyltetrahydrofuran-2-yl)-3-benzyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine 

Relevant academic research and scientific papers

Inhibitor scaffolds as new allele specific kinase substrates

The elucidation of protein kinase signaling networks is challenging due to the large size of the protein kinase superfamily (>500 human kinases). Here we describe a new class of orthogonal triphosphate substrate analogues for the direct labeling of analog

Polarized Ethylenes. IV. Synthesis of Polarized Ethylenes Using Thioamides and Methyl Dithiocarboxylates and their Application to Syntheses of Pyrazoles, Pyrimidines, Pyrazolopyrimidines, and 5-Azacyclazines

Polarized ethylenes having both electron-donating (an amino or a methylthio group) and electron-accepting (cyano, carbamoyl, methyl ester) groups on the adjacent two olefinic carbon atoms were prepared by the condensation of S-alkylthioamidinium salts or