Xu J, Dong L, Sun H, Huang P, Zhang R, Wang X
PLoS Negl Trop Dis. 2023; 17(7):e0011215.
PMID: 37410790
PMC: 10353801.
DOI: 10.1371/journal.pntd.0011215.
Yaremenko I, Radulov P, Belyakova Y, Fomenkov D, Tsogoeva S, Terentev A
Pharmaceuticals (Basel). 2022; 15(4).
PMID: 35455469
PMC: 9025639.
DOI: 10.3390/ph15040472.
Park S, Friedrich L, Yahya N, Rohr C, Chulkov E, Maillard D
Sci Transl Med. 2021; 13(625):eabj5832.
PMID: 34936384
PMC: 8855674.
DOI: 10.1126/scitranslmed.abj5832.
Dziwornu G, Attram H, Gachuhi S, Chibale K
RSC Med Chem. 2021; 11(4):455-490.
PMID: 33479649
PMC: 7593896.
DOI: 10.1039/d0md00062k.
Zorn K, Sun S, McConnon C, Ma K, Chen E, Foil D
ACS Infect Dis. 2021; 7(2):406-420.
PMID: 33434015
PMC: 7887754.
DOI: 10.1021/acsinfecdis.0c00754.
Three monthly doses of 60 mg/kg praziquantel for Schistosoma haematobium infection is a safe and effective treatment regimen.
Darko S, Hanson H, Twumasi-Ankrah S, Baffour-Awuah S, Adjei-Kusi P, Yar D
BMC Infect Dis. 2020; 20(1):323.
PMID: 32375658
PMC: 7204294.
DOI: 10.1186/s12879-020-05053-z.
Structure-Activity Relationship of Antischistosomal Ozonide Carboxylic Acids.
Wu J, Wang X, Chiu F, Haberli C, Shackleford D, Ryan E
J Med Chem. 2020; 63(7):3723-3736.
PMID: 32134263
PMC: 7182039.
DOI: 10.1021/acs.jmedchem.0c00069.
In vitro and in vivo activities of DW-3-15, a commercial praziquantel derivative, against Schistosoma japonicum.
Wang X, Yu D, Li C, Zhan T, Zhang T, Ma H
Parasit Vectors. 2019; 12(1):199.
PMID: 31053083
PMC: 6500042.
DOI: 10.1186/s13071-019-3442-7.
Progress in antischistosomal N,N'-diaryl urea SAR.
Wu J, Wang C, Leas D, Vargas M, White K, Shackleford D
Bioorg Med Chem Lett. 2018; 28(3):244-248.
PMID: 29317164
PMC: 6026081.
DOI: 10.1016/j.bmcl.2017.12.064.
Praziquantel for Schistosomiasis: Single-Drug Metabolism Revisited, Mode of Action, and Resistance.
Vale N, Gouveia M, Rinaldi G, Brindley P, Gartner F, Costa J
Antimicrob Agents Chemother. 2017; 61(5).
PMID: 28264841
PMC: 5404606.
DOI: 10.1128/AAC.02582-16.
Pharmacokinetics of the Antischistosomal Lead Ozonide OZ418 in Uninfected Mice Determined by Liquid Chromatography-Tandem Mass Spectrometry.
Leonidova A, Vargas M, Huwyler J, Keiser J
Antimicrob Agents Chemother. 2016; 60(12):7364-7371.
PMID: 27697760
PMC: 5119018.
DOI: 10.1128/AAC.02394-15.
Oxadiazole-2-oxides may have other functional targets, in addition to SjTGR, through which they cause mortality in Schistosoma japonicum.
Song L, Luo H, Fan W, Wang G, Yin X, Shen S
Parasit Vectors. 2016; 9:26.
PMID: 26791563
PMC: 4721062.
DOI: 10.1186/s13071-016-1301-3.
An artemisinin derivative of praziquantel as an orally active antischistosomal agent.
Dong L, Duan W, Chen J, Sun H, Qiao C, Xia C
PLoS One. 2014; 9(11):e112163.
PMID: 25386745
PMC: 4227710.
DOI: 10.1371/journal.pone.0112163.
Tetrasubstituted pyrazinones derived from the reaction of praziquantel with -bromosuccinimide.
Zhao Q, Wang C, Ezell E, Dong Y, Vennerstrom J
Tetrahedron Lett. 2014; 55(32):4463-4465.
PMID: 25125709
PMC: 4128413.
DOI: 10.1016/j.tetlet.2014.06.083.
Metabolic profiling of praziquantel enantiomers.
Wang H, Fang Z, Zheng Y, Zhou K, Hu C, Krausz K
Biochem Pharmacol. 2014; 90(2):166-78.
PMID: 24821110
PMC: 4168258.
DOI: 10.1016/j.bcp.2014.05.001.
Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products.
Terentev A, Borisov D, A Vil V, Dembitsky V
Beilstein J Org Chem. 2014; 10:34-114.
PMID: 24454562
PMC: 3896255.
DOI: 10.3762/bjoc.10.6.
Synthesis and SAR studies of praziquantel derivatives with activity against Schistosoma japonicum.
Wang W, Song L, Chen X, Yin X, Fan W, Wang G
Molecules. 2013; 18(8):9163-78.
PMID: 23912271
PMC: 6269691.
DOI: 10.3390/molecules18089163.
APPLICATIONS OF MULTICOMPONENT ASSEMBLY PROCESSES TO THE FACILE SYNTHESES OF DIVERSELY FUNCTIONALIZED NITROGEN HETEROCYCLES.
Donald J, Granger B, Hardy S, Sahn J, Martin S
Heterocycles. 2012; 84(2):1089-1112.
PMID: 22451742
PMC: 3311471.
DOI: 10.3987/COM-11-S(P)92.
Resolution of praziquantel.
Woelfle M, Seerden J, de Gooijer J, Pouwer K, Olliaro P, Todd M
PLoS Negl Trop Dis. 2011; 5(9):e1260.
PMID: 21949890
PMC: 3176743.
DOI: 10.1371/journal.pntd.0001260.
Polycyclic compounds by Ugi-Pictet-Spengler sequence.
Wang W, Ollio S, Herdtweck E, Domling A
J Org Chem. 2010; 76(2):637-44.
PMID: 21190371
PMC: 3101332.
DOI: 10.1021/jo102058s.