71149-52-5Relevant articles and documents
Fragment-based lead discovery to identify novel inhibitors that target the ATP binding site of pyruvate dehydrogenase kinases
Akaki, Tatsuo,Bessho, Yuki,Ito, Takashi,Fujioka, Shingo,Ubukata, Minoru,Mori, Genki,Yamanaka, Kenji,Orita, Takuya,Doi, Satoki,Iwanaga, Tomoko,Ikegashira, Kazutaka,Hantani, Yoshiji,Nakanishi, Isao,Adachi, Tsuyoshi
, (2021/07/21)
A fragment-based lead discovery approach was applied to Pyruvate Dehydrogenase Kinases (PDHKs) to discover inhibitors against the ATP binding site with novel chemotypes. X-ray fragment screening toward PDHK4 provided a fragment hit 1 with a characteristic
SUBSTITUTED CARBONUCLEOSIDE DERIVATIVES USEFUL AS ANTICANCER AGENTS
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Page/Page column 220; 221, (2018/05/29)
Compounds of the general formula:processes for the preparation of these compounds, compositions containing these compounds, and the uses of these compounds.
PIPERIDINE SUBSTITUTED PYRAZOLO[1,5-A]PYRIMIDINE DERIVATIVES WITH INHIBITORY ACTIVITY ON THE REPLICATION OF THE RESPIRATORY SYNCYTIAL VIRUS (RSV)
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Page/Page column 36, (2016/11/07)
The invention concerns novel substituted bicyclic pyrazolo pyrimidine compounds of formula (I) having antiviral activity, in particular, having an inhibitory activity on the replication of the respiratory syncytial virus (RSV). The invention further conce