scholarly article | Q13442814 |
P50 | author | Alex Domling | Q73024340 |
P2093 | author name string | Haixia Liu | |
Sanaa Botros | |||
Eberhardt Herdtweck | |||
Samia William | |||
P2860 | cites work | The DNA gyrase inhibitors, nalidixic acid and oxolinic acid, prevent iron-mediated repression of catechol siderophore synthesis in Azotobacter vinelandii. | Q53902951 |
The Pictet-Spengler condensation: a new direction for an old reaction | Q53999276 | ||
Neue Darstellungsmethode für Isonitrile | Q54197262 | ||
Über ein neues Kondensations-Prinzip | Q56429957 | ||
Über die Bildung von Isochinolin-derivaten durch Einwirkung von Methylal auf Phenyl-äthylamin, Phenyl-alanin und Tyrosin | Q56434659 | ||
Synthesis and properties of Praziquantel, a novel broad spectrum anthelmintic with excellent activity against Schistosomes and Cestodes | Q56656937 | ||
Cyclizations ofN-Acyliminium Ions | Q56831862 | ||
The use of the Ugi four-component condensation | Q80093506 | ||
One-pot synthesis of highly functionalized seleno amino acid derivatives | Q84457018 | ||
Africa's 32 cents solution for HIV/AIDS | Q21092298 | ||
Association between genital schistosomiasis and HIV in rural Zimbabwean women | Q28296559 | ||
Control of neglected tropical diseases | Q29547285 | ||
Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa | Q29620602 | ||
Multicomponent Reactions with Isocyanides. | Q30940111 | ||
Female genital schistosomiasis: facts and hypotheses | Q34285974 | ||
Recent developments in isocyanide based multicomponent reactions in applied chemistry | Q34482940 | ||
Are Ca2+ channels targets of praziquantel action? | Q35993816 | ||
Praziquantel: mechanisms of action, resistance and new derivatives for schistosomiasis | Q37315241 | ||
Praziquantel and schistosomiasis. | Q37777113 | ||
Female genital schistosomiasis as a risk-factor for the transmission of HIV. | Q38889336 | ||
Recent progress in integrated neglected tropical disease control | Q39078147 | ||
Synthesis, biological evaluation, and molecular docking of Ugi products containing a zinc-chelating moiety as novel inhibitors of histone deacetylases. | Q39864415 | ||
Efficient multicomponent reaction synthesis of the schistosomiasis drug praziquantel. | Q42906063 | ||
Efficient and diverse synthesis of indole derivatives. | Q43296555 | ||
Amino acid derived heterocycles: lewis acid catalyzed and radical cyclizations from peptide acetals | Q44021182 | ||
Effect of praziquantel on the immature stages of Schistosoma haematobium. | Q46588110 | ||
Schistosomiasis control: experiences and lessons from China. | Q51676769 | ||
An Improved Perfusion Technique for Recovering Adult Schistosomes from Laboratory Animals | Q53755844 | ||
P433 | issue | 4 | |
P921 | main subject | praziquantel | Q424145 |
P304 | page(s) | 470-477 | |
P577 | publication date | 2012-01-30 | |
P1433 | published in | Chemical Biology and Drug Design | Q15749458 |
P1476 | title | MCR synthesis of praziquantel derivatives | |
P478 | volume | 79 |
Q28539960 | 'Death and axes': unexpected Ca²⁺ entry phenologs predict new anti-schistosomal agents |
Q46836910 | Artificial Macrocycles by Ugi Reaction and Passerini Ring Closure. |
Q38067995 | Ca²⁺ channels and praziquantel: a view from the free world |
Q89920010 | Current and Novel Therapies Against Helminthic Infections: The Potential of Antioxidants Combined with Drugs |
Q64082229 | Diverse Isoquinoline Scaffolds by Ugi/Pomeranz-Fritsch and Ugi/Schlittler-Müller Reactions |
Q52699502 | Drug Repurposing for Schistosomiasis: Combinations of Drugs or Biomolecules. |
Q28547995 | Ergot Alkaloids (Re)generate New Leads as Antiparasitics |
Q64077252 | MCR Scaffolds Get Hotter with F-Labeling |
Q36522303 | MCR synthesis of a tetracyclic tetrazole scaffold. |
Q34060368 | Modern Multicomponent Reactions for better Drug Syntheses** |
Q27008897 | Novel therapeutic and prevention approaches for schistosomiasis: review |
Q39160696 | Praziquantel derivatives with antischistosomal activity: aromatic ring modification |
Q46081944 | Synthesis and SAR studies of praziquantel derivatives with activity against Schistosoma japonicum. |
Q61802827 | Tetrazoles via Multicomponent Reactions |
Q92815392 | The Pictet-Spengler Reaction Updates Its Habits |
Q42550963 | Tricycles by a new Ugi variation and Pictet-Spengler reaction in one pot. |
Q42612607 | Various cyclization scaffolds by a truly Ugi 4-CR. |
Q45340054 | [(η(6)-Praziquantel)Cr(CO)3] derivatives with remarkable in vitro anti-schistosomal activity |
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