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Scoping Studies into the Structure‐Activity Relationship (SAR) of Phenylephrine‐Derived Analogues as Inhibitors of Trypanosoma brucei rhodesiense
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Greene's Protective Groups in Organic Synthesis
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Purification of Laboratory Chemicals
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Dipeptidyl-α,β-epoxyesters as potent irreversible inhibitors of the cysteine proteases cruzain and rhodesain
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Discovery of trypanocidal thiosemicarbazone inhibitors of rhodesain and TbcatB
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SAR of 2-amino and 2,4-diamino pyrimidines with in vivo efficacy against Trypanosoma brucei
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1-Aryl-4-nitro-1H-imidazoles, a new promising series for the treatment of human African trypanosomiasis
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3-(Oxazolo[4,5-b]pyridin-2-yl)anilides as a novel class of potent inhibitors for the kinetoplastid Trypanosoma brucei, the causative agent for human African trypanosomiasis
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3-Nitrotriazole-based piperazides as potent antitrypanosomal agents
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Chemotherapy of trypanosomiases and leishmaniasis
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Nifurtimox-eflornithine combination therapy for second-stage African Trypanosoma brucei gambiense trypanosomiasis: a multicentre, randomised, phase III, non-inferiority trial
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Substituted 2-Phenylimidazopyridines: A New Class of Drug Leads for Human African Trypanosomiasis
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Lead Optimization of a Pyrazole Sulfonamide Series of Trypanosoma brucei N -Myristoyltransferase Inhibitors: Identification and Evaluation of CNS Penetrant Compounds as Potential Treatments for Stage 2 Human African Trypanosomiasis
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Michael Acceptor Based Antiplasmodial and Antitrypanosomal Cysteine Protease Inhibitors with Unusual Amino Acids
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Rearrangement of 1,3-diradicals. Arylcyclopropane photochemistry
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Efficient N-Demethylation of Opiate Alkaloids Using a Modified Nonclassical Polonovski Reaction
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Highly Efficient Stereoconservative Amidation and Deamidation of α-Amino Acids
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High Throughput Screening against the Peroxidase Cascade of African Trypanosomes Identifies Antiparasitic Compounds That Inactivate Tryparedoxin
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Sleeping sickness - human African trypanosomiasis
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New Azasterols against Trypanosoma brucei : Role of 24-Sterol Methyltransferase in Inhibitor Action
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Application of Norphenylephrine Derivatives to the Isoquinoline Syntheses : Studies on the Syntheses of Heterocyclic Compounds. CCCLII
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Fexinidazole – A New Oral Nitroimidazole Drug Candidate Entering Clinical Development for the Treatment of Sleeping Sickness
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SCYX-7158, an Orally-Active Benzoxaborole for the Treatment of Stage 2 Human African Trypanosomiasis
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Naphthoquinone Derivatives Exert Their Antitrypanosomal Activity via a Multi-Target Mechanism
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Epidemiology of human African trypanosomiasis
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1,2-Substituted 4-(1H)-Quinolones: Synthesis, Antimalarial and Antitrypanosomal Activities in Vitro
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An efficient and operationally convenient general synthesis of tertiary amines by direct alkylation of secondary amines with alkyl halides in the presence of Huenig’s base
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Synthesis of Functionalised Indoline and Isoquinoline Derivatives through a Silylcarbocyclisation/Desilylation Sequence
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113861openalex-snapshot
Synthesis and evaluation of tetrahydroisoquinoline derivatives against Trypanosoma brucei rhodesiense
inferred← citeshttps://doi.org/10.1039/d1ra01480copenalex-snapshot
Medicinal chemistry perspectives of 1,2,3,4-tetrahydroisoquinoline analogs – biological activities and SAR studies
inferred← citeshttps://doi.org/10.1155/2017/3789856openalex-snapshot
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Isolation of bioactive compounds from medicinal plants used in traditional medicine: Rautandiol B, a potential lead compound against Plasmodium falciparum
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Synthesis and Investigation of Tricyclic Isoquinoline Derivatives as Antibacterial Agents
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Additional file 1 of Isolation of bioactive compounds from medicinal plants used in traditional medicine: Rautandiol B, a potential lead compound against Plasmodium falciparum
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