Maiko Hamada

Construction of 3,5-dinitrated 1,4-dihydropyridines modifiable at 1,4-positions by a reaction of β-formyl-β-nitroenamines with aldehydes

H. Asahara, Maiko Hamada, Y. Nakaike, 2015 .

A phenotypic drug discovery study on thienodiazepine derivatives as inhibitors of T cell proliferation induced by CD28 co-stimulation leads to the discovery of a first bromodomain inhibitor.

H. Sumichika, K. Adachi, K. Iwata, 2016, Bioorganic & medicinal chemistry letters.

Removal of sphingosine 1-phosphate receptor-3 (S1P(3)) agonism is essential, but inadequate to obtain immunomodulating 2-aminopropane-1,3-diol S1P(1) agonists with reduced effect on heart rate.

K. Adachi, K. Sugahara, Mahoko Asayama, 2010, Journal of medicinal chemistry.

Benzoyl methyl phosphate as an efficient reagent for the selective monobenzoylation of N-Bz-FTY720

Hidemasa Hikawa, I. Azumaya, Y. Yokoyama, 2014 .

Efficient Synthesis of the Immunomodulating Compound KRP-203

K. Adachi, Maiko Hamada, M. Kiuchi, 2007 .

Synthesis of a key intermediate for the preparation of FTY720 analogs.

Hidemasa Hikawa, Y. Yokoyama, Maiko Hamada, 2012, Chemical & pharmaceutical bulletin.