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Opium Alkaloids VII. Isolation of a New Benzylisoquinoline Alkaloid. Synthesis and NMR Studies of Papaveroline Trimethyl Ethers
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ardp.19562890705openalex-snapshot
Synthese einiger β‐Aryl‐β‐methoxy‐äthylamine
inferredcites →https://doi.org/10.1002/jps.2600560621openalex-snapshot
Opium alkaloids IV. Isolation of isoboldine
inferredcites →https://doi.org/10.1007/bf00903594openalex-snapshot
Die Synthese desdl-Codamins,dl-Pseudocodamins und verwandter 1-Benzyl-isochinoline
inferredcites →https://doi.org/10.1039/jr9310002893openalex-snapshot
CCCCV.—Experiments on the synthesis of phenolic aporphines. Part IV. Laurotetanine
inferredcites →https://doi.org/10.1039/jr9310003163openalex-snapshot
CCCCXXXVIII.—Preliminary synthetical experiments in the morphine group. Part I
inferredcites →https://doi.org/10.1515/znb-1965-1103openalex-snapshot
NMR-spektroskopische Untersuchungen an Benzylisochinolin-Derivaten
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112598zenodo-depositor-declared
Biotransformation of papaverine and in silico docking studies of the metabolites on human phosphodiesterase 10a
inferred← citeshttps://doi.org/10.1002/9780470187111.ch2openalex-snapshot
Synthetic and Natural Sources of the Isoquinoline Nucleus
inferred← citeshttps://doi.org/10.1002/hlca.19810640310openalex-snapshot
Aromatization of 1‐Benzyltetrahydroisoquinolines: Racemization of (−)‐(S)‐(N‐nor)‐Reticuline
inferred← citeshttps://doi.org/10.1002/jps.2600601108openalex-snapshot
Total Synthesis of (±)-Bisnorargemonine
inferred← citeshttps://doi.org/10.1002/jps.2600601118openalex-snapshot
Opium Alkaloids X: Biosynthesis of 1-Benzylisoquinolines
inferred← citeshttps://doi.org/10.1002/jps.2600610239openalex-snapshot
A New Benzylisoquinoline Alkaloid:N-Methylpalaudinium Chloride
inferred← citeshttps://doi.org/10.1016/0021-9673(64)80112-6openalex-snapshot
Über alkaloide der gattung papaver 31. Mitteilung, dünnschichtchromatographische charakterisierung von alkaloiden der gattung papaver
inferred← citeshttps://doi.org/10.1016/b978-0-444-59530-0.00003-4openalex-snapshot
Recent Asymmetric Syntheses of Tetrahydroisoquinolines Using “Named” and Some Other Newer Methods
inferred← citeshttps://doi.org/10.1016/j.nucmedbio.2009.12.012openalex-snapshot
Carbon-11 labeled papaverine as a PET tracer for imaging PDE10A: radiosynthesis, in vitro and in vivo evaluation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.10.114openalex-snapshot
Enantioselective syntheses and X-ray structures of (S)- and (R)-N-norlaudanidine: trace opium constituents
inferred← citeshttps://doi.org/10.1016/s0065-2164(08)70150-3openalex-snapshot
Microbial Models for Drug Metabolism
inferred← citeshttps://doi.org/10.1016/s1876-0813(08)60104-9openalex-snapshot
Chapter 5 Papaverceae Alkaloids
inferred← citeshttps://doi.org/10.1016/s1876-0813(08)60105-0openalex-snapshot
Chapter 6 Alkaloids Unclassified and of Unknown Structure
inferred← citeshttps://doi.org/10.1016/s1876-0813(08)60265-1openalex-snapshot
Chapter 13 Alkaloids Unclassified and of Unknown Structure
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c03360openalex-snapshot
Papaverine-Derived Dual-Active Modulator Ameliorates Alzheimer’s Disease Pathology in Aged APP/PSEN1 Transgenic Mice
inferred← citeshttps://doi.org/10.1039/c5ob00926jopenalex-snapshot
A divergent approach to benzylisoquinoline-type and oxoaporphine alkaloids via regioselective direct ring metalation of alkoxy isoquinolines
inferred← citeshttps://doi.org/10.1186/s13104-021-05762-xopenalex-snapshot
Alkaloid profiling and antimicrobial activities of Papaver glaucum and P. decaisnei
inferred← citeshttps://doi.org/10.3109/00498257509056111openalex-snapshot
Metabolism of Papaverine I. Identification of Metabolites in Rat Bile
inferred← citeshttps://doi.org/10.3109/00498257709036245openalex-snapshot
Microbial Models of Mammalian MetabolismO-Demethylations of Papaverine
inferred← citeshttps://doi.org/10.3390/molecules28041583openalex-snapshot
Papaverinol-N-Oxide: A Microbial Biotransformation Product of Papaverine with Potential Antidiabetic and Antiobesity Activity Unveiled with In Silico Screening
inferred← citeshttps://doi.org/10.6084/m9.figshare.16590501openalex-snapshot
Additional file 2 of Alkaloid profiling and antimicrobial activities of Papaver glaucum and P. decaisnei
inferred← citeshttps://doi.org/10.6084/m9.figshare.16590504openalex-snapshot
Additional file 3 of Alkaloid profiling and antimicrobial activities of Papaver glaucum and P. decaisnei
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