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Isolation, Total Synthesis, and Absolute Configuration Determination of Renoprotective Dimeric N-Acetyldopamine–Adenine Hybrids from the Insect Aspongopus chinensis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Absolute configuration determination of chiral molecules in the solution state using vibrational circular dichroism
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Optically Pure Isoproterenol Analogues With Side Chains Containing an Amide Bond: Synthesis and biological properties
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Vibrational Circular Dichroism Absolute Configuration Determination of Natural Products
inferredcites →https://doi.org/10.1016/j.bmcl.2014.09.083openalex-snapshot
Bioactive compounds from the insect Aspongopus chinensis
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Inverse electron demand hetero-Diels–Alder reaction in preparing 1,4-benzodioxin from o-quinone and enamine
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Tyrosinase-catalyzed unusual oxidative dimerization of 1,2-dehydro-N-acetyldopamine.
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New polycyclic pyrimidine derivatives with antiplatelet in vitro activity: synthesis and pharmacological screening
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Total Syntheses of (−)-Mersicarpine, (−)-Scholarisine G, (+)-Melodinine E, (−)-Leuconoxine, (−)-Leuconolam, (−)-Leuconodine A, (+)-Leuconodine F, and (−)-Leuconodine C: Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon for Scholarisine G and Leuconodines A and C
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Absolute Configurations of Fungal and Plant Metabolites by Chiroptical Methods. ORD, ECD, and VCD Studies on Phyllostin, Scytolide, and Oxysporone
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Shorter Synthesis of Trifunctionalized Cryptophane-A Derivatives
inferredcites →https://doi.org/10.1021/ol3016463openalex-snapshot
Epicatechin B-Ring Conjugates: First Enantioselective Synthesis and Evidence for Their Occurrence in Human Biological Fluids
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Spiro Fused Diterpene–Indole Alkaloids from a Creek-Bottom-Derived Aspergillus terreus
inferredcites →https://doi.org/10.1021/ol403409vopenalex-snapshot
(±)-Aspongamide A, an N-Acetyldopamine Trimer Isolated from the Insect Aspongopus chinensis, Is an Inhibitor of p-Smad3
inferredcites →https://doi.org/10.1023/b:cohc.0000018339.22815.13openalex-snapshot
Synthesis of 2-(β-Hetarylaminoethyl)-3,5,6-trichloro-1,4-benzoquinones
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Insects and their chemical weaponry: New potential for drug discovery
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Recent advances in the use of vibrational chiroptical spectroscopic methods for stereochemical characterization of natural products
inferredcites →https://doi.org/10.1039/c5np00121hopenalex-snapshot
The use of isolated natural products as scaffolds for the generation of chemically diverse screening libraries for drug discovery
inferredcites →https://doi.org/10.1071/ch9842545openalex-snapshot
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The Renaissance of Natural Products as Drug Candidates
inferredcites →https://doi.org/10.1248/cpb.48.1749openalex-snapshot
Optically Active N-Acetyldopamine Dimer of the Crude Drug "Zentai", the Cast-off Shell of the Cicada, Cryptotympana sp.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Aspongpyridiniums A−J, amino acid-derived pyridinium salts from insect species Aspongopus chinensis
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133395openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2026.135138openalex-snapshot
Diastereoselective synthesis of N-acyl dopamine dimers in Aspongopus
inferred← citeshttps://doi.org/10.1016/s1875-5364(23)60483-2openalex-snapshot
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Multioxidized polyketides from an endophytic Penicillium sp. YUD17006 associated with Gastrodia elata
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