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7QPM

Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate

Summary for 7QPM
Entry DOI10.2210/pdb7qpm/pdb
DescriptorcAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A, 5,7-dimethyl-2-[(1-methyl-4-phenyl-imidazol-2-yl)sulfanylmethyl]imidazo[1,2-a]pyrimidine, ZINC ION, ... (5 entities in total)
Functional Keywordsphosphodiesterase, pde, pde10a, schizophrenia, basal ganglia disorders, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight80131.40
Authors
Leonard, P.M.,Langgard, M. (deposition date: 2022-01-05, release date: 2023-04-19, Last modification date: 2024-02-07)
Primary citationKehler, J.,Kilburn, J.P.,Langgard, M.,Christoffersen, C.T.,Ritzen, A.,Marigo, M.,Jessing, M.,Bundgaard, C.,Puschl, A.,Feigin, K.,Nielsen, J.
Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate
To Be Published,
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

222415

數據於2024-07-10公開中

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