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TitleAn insight into the pharmacophores of phosphodiesterase-5 inhibitors from synthetic and crystal structural studies
Journal, issue, pagesBIOCHEM. PHARM., Vol. 75, Page 1717-1728, Year 2008
Publish dateDec 3, 2007 (structure data deposition date)
AuthorsChen, G. / Wang, H. / Robinson, H. / Cai, J. / Wan, Y. / Ke, H.
External linksBIOCHEM. PHARM. / PubMed:18346713
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-3bjc:
Crystal structure of the PDE5A catalytic domain in complex with a novel inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-MG:
Unknown entry

ChemComp-WAN:
5-ethoxy-4-(1-methyl-7-oxo-3-propyl-6,7-dihydro-1H-pyrazolo[4,3-d]pyrimidin-5-yl)thiophene-2-sulfonamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / PDE5 / erectile dysfunction / inhibitor design / Allosteric enzyme / Alternative splicing / cGMP / cGMP-binding / Magnesium / Metal-binding / Nucleotide-binding / Phosphoprotein / Polymorphism / Zinc

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