1357192-32-5Relevant articles and documents
Design and synthesis of potent and selective pyridazin-4(1H)-one-based PDE10A inhibitors interacting with Tyr683 in the PDE10A selectivity pocket
Yoshikawa, Masato,Hitaka, Takenori,Hasui, Tomoaki,Fushimi, Makoto,Kunitomo, Jun,Kokubo, Hironori,Oki, Hideyuki,Nakashima, Kosuke,Taniguchi, Takahiko
, p. 3447 - 3455 (2016/07/21)
Utilizing structure-based drug design techniques, we designed and synthesized phosphodiesterase 10A (PDE10A) inhibitors based on pyridazin-4(1H)-one. These compounds can interact with Tyr683 in the PDE10A selectivity pocket. Pyridazin-4(1H)-one derivative
FUSED HETEROCYCLIC RING COMPOUND
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, (2013/06/05)
Provided is a compound having a PDE10A inhibitory action, and useful as a medicament for the prophylaxis or treatment of mental diseases such as schizophrenia and the like, and the like. A compound represented by the formula (I): wherein each symbol is as defined in the DESCRIPTION, or a salt thereof.
RADIOLABELED COMPOUNDS AND THEIR USE AS RADIOTRACERS FOR QUANTITATIVE IMAGING OF PHOSPHODIESTERASE (PDE10A) IN MAMMALS
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Paragraph 0409, (2013/03/26)
The present invention provides radiolabeled compounds useful as radiotracers for quantitative imaging of PDE10A in mammals. The compound of the present invention is represented by the formula (I): wherein each symbols are as defined in the specification.