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TitleDesign, synthesis and biological evaluations of N-Hydroxy thienopyrimidine-2,4-diones as inhibitors of HIV reverse transcriptase-associated RNase H.
Journal, issue, pagesEur J Med Chem, Vol. 141, Page 149-161, Year 2017
Publish dateAug 15, 2017 (structure data deposition date)
AuthorsKankanala, J. / Kirby, K.A. / Huber, A.D. / Casey, M.C. / Wilson, D.J. / Sarafianos, S.G. / Wang, Z.
External linksEur J Med Chem / PubMed:29031062
MethodsX-ray diffraction
Resolution1.8 Å
Structure data

PDB-6aoc:
Crystal Structure of an N-Hydroxythienopyrimidine-2,4-dione RNase H Active Site Inhibitor with Multiple Binding Modes to HIV Reverse Transcriptase
Method: X-RAY DIFFRACTION / Resolution: 1.8 Å

Chemicals

ChemComp-MN:
Unknown entry

ChemComp-ZW2:
6-benzyl-3-hydroxythieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

ChemComp-PGE:
TRIETHYLENE GLYCOL

ChemComp-EDO:
1,2-ETHANEDIOL

ChemComp-HOH:
WATER

Source
  • human immunodeficiency virus type 1 group m subtype b (isolate bh10)
KeywordsTRANSFERASE / TRANSFERASE INHIBITOR / HIV-1 / TRANSFERASE - TRANSFERASE INHIBITOR complex

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