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Alkaloids from the Root of Isatis indigotica

https://doi.org/10.1021/np3002833
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What this work says

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

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Chiroptical properties of binuclear rhodium complexes of lanostane alcohols
inferredcites →https://doi.org/10.1002/ejoc.201000284openalex-snapshot
Brasilamides A–D: Sesquiterpenoids from the Plant Endophytic Fungus Paraconiothyrium brasiliense
inferredcites →https://doi.org/10.1002/jlac.19415480112openalex-snapshot
Synthesen in der Oxindolreihe
inferredcites →https://doi.org/10.1002/mrc.1260251016openalex-snapshot
NMR studies of indoles and their N‐carboalkoxy derivatives
inferredcites →https://doi.org/10.1007/bf00798793openalex-snapshot
Synthese von enantiomerenreinem (2R)-1-Oxo-2-methyl-oxazin
inferredcites →https://doi.org/10.1007/bf00809695openalex-snapshot
�ber enantiomerenreines (R)-2-Methyl-3-oxo-perhydro-1,4-oxazin
inferredcites →https://doi.org/10.1007/bf01915408openalex-snapshot
Wachstumsinduktion und Wuchsstoffmetabolismus im Weizenkoleoptilzylinder
inferredcites →https://doi.org/10.1007/s10600-010-9735-xopenalex-snapshot
Indole alkaloids from the roots of Isatis ingigotica and their antiherpes simplex virus type 2 (HSV-2) activity in vitro
inferredcites →https://doi.org/10.1007/s11426-008-0146-9openalex-snapshot
Isolation, structural determination and cytotoxic activity of two new ceramides from the root of Isatis indigotica
inferredcites →https://doi.org/10.1016/0040-4020(89)80133-4openalex-snapshot
Synthesis of various aromatic amide derivatives using nitrile hydratase of J1
inferredcites →https://doi.org/10.1016/j.phytochem.2009.04.019openalex-snapshot
A comprehensive metabolite profiling of Isatis tinctoria leaf extracts
inferredcites →https://doi.org/10.1016/s0031-9422(00)98224-4openalex-snapshot
Brassicanal C and two dioxindoles from cabbage
inferredcites →https://doi.org/10.1016/s0031-9422(03)00441-2openalex-snapshot
Phytoalexins from Thlaspi arvense, a wild crucifer resistant to virulent Leptosphaeria maculans: structures, syntheses and antifungal activity
inferredcites →https://doi.org/10.1016/s0031-9422(99)00112-0openalex-snapshot
Biotransformation of o- and p-aminobenzoic acids and N-acetyl p-aminobenzoic acid by cell suspension cultures of Solanum mammosum
inferredcites →https://doi.org/10.1016/s0040-4020(97)00846-6openalex-snapshot
New alkaloids from Isatis indigotica
inferredcites →https://doi.org/10.1016/s0040-4020(99)00337-3openalex-snapshot
Stereochemical studies on the Uncaria alkaloid, 3-oxo-7-hydroxy-3,7-secorhynchophylline: The absolute configuration of 3-hydroxyoxindole derivatives
inferredcites →https://doi.org/10.1016/s0040-4020(99)01065-0openalex-snapshot
On the Reaction of Isatin with Cyanomethylene(triphenyl)-phosphorane. A Nucleophilic Attack of Alkyl Phosphites on the Carbon–Carbon Double Bond of (E)-Oxindolylideneacetonitrile
inferredcites →https://doi.org/10.1016/s0040-4039(03)01513-2openalex-snapshot
Preparation of cruciferous phytoalexin related metabolites, (−)-dioxibrassinin and (−)-3-cyanomethyl-3-hydroxyoxindole, and determination of their absolute configurations by vibrational circular dichroism (VCD)
inferredcites →https://doi.org/10.1016/s0928-3420(99)80036-6openalex-snapshot
Investigation of functional molecules in African Celosia argentea L.
inferredcites →https://doi.org/10.1016/s0957-4166(99)00115-9openalex-snapshot
[Rh2(OCOCF3)4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols
inferredcites →https://doi.org/10.1021/ja017255copenalex-snapshot
Enantioselective Organocatalytic Indole Alkylations. Design of a New and Highly Effective Chiral Amine for Iminium Catalysis
inferredcites →https://doi.org/10.1021/jf802735mopenalex-snapshot
Modified Benzoxazinones in the System Oryza sativa−Echinochloa crus-galli: An Approach to the Development of Biorational Herbicide Models
inferredcites →https://doi.org/10.1021/jm030561bopenalex-snapshot
Generation of New Protein Kinase Inhibitors Utilizing Cytochrome P450 Mutant Enzymes for Indigoid Synthesis
inferredcites →https://doi.org/10.1021/np030505dopenalex-snapshot
Phelligridins C−F: Cytotoxic Pyrano[4,3-c][2]benzopyran-1,6-dione and Furo[3,2-c]pyran-4-one Derivatives from the Fungus Phellinus igniarius
inferredcites →https://doi.org/10.1021/np049662iopenalex-snapshot
Bisindigotin, a TCDD Antagonist from the Chinese Medicinal Herb Isatis indigotica
inferredcites →https://doi.org/10.1021/np060395lopenalex-snapshot
Indole Alkaloids from Cephalanceropsis gracilis
inferredcites →https://doi.org/10.1021/np200117yopenalex-snapshot
Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations
inferredcites →https://doi.org/10.1021/np50122a017openalex-snapshot
Further Brominated Bis- and Tris-Indole Alkaloids from the Deep-Water New Caledonian Marine Sponge Orina sp.
inferredcites →https://doi.org/10.1021/np7007329openalex-snapshot
Glycosides from the Root of Iodes cirrhosa
inferredcites →https://doi.org/10.1021/np900213wopenalex-snapshot
Chemical Constituents of Heteroplexis micocephala
inferredcites →https://doi.org/10.1021/np900504aopenalex-snapshot
Chemical Constituents of the Bark of Machilus wangchiana and Their Biological Activities
inferredcites →https://doi.org/10.1021/ol071274vopenalex-snapshot
[Cp*IrCl2]2-Catalyzed Indirect Functionalization of Alcohols: Novel Strategies for the Synthesis of Substituted Indoles
inferredcites →https://doi.org/10.1021/ol102802uopenalex-snapshot
Spirocurcasone, a Diterpenoid with a Novel Carbon Skeleton from Jatropha curcas
inferredcites →https://doi.org/10.1021/ol203309yopenalex-snapshot
Cationic Ruthenium(II) Catalysts for Oxidative C–H/N–H Bond Functionalizations of Anilines with Removable Directing Group: Synthesis of Indoles in Water
inferredcites →https://doi.org/10.1021/ol300130sopenalex-snapshot
Yaoshanenolides A and B: New Spirolactones from the Bark of Machilus yaoshansis
inferredcites →https://doi.org/10.1021/ol701540yopenalex-snapshot
Isatisine A, a Novel Alkaloid with an Unprecedented Skeleton from Leaves of Isatis indigotica
inferredcites →https://doi.org/10.1055/s-2006-957604openalex-snapshot
Chemical Constituents ofIsatis indigotica
inferredcites →https://doi.org/10.1055/s-2007-971650openalex-snapshot
Isolation of 2-Hydroxy-3-butenyl Thiocyanate, Epigoitrin, and Adenosine from ‘Banlangen’, Isatis indigotica Root
inferredcites →https://doi.org/10.2174/138527210792927717openalex-snapshot
Determination of Absolute Configuration of Natural Products: Theoretical Calculation of Electronic Circular Dichroism as a Tool
inferredcites →https://doi.org/10.3987/com-99-8737openalex-snapshot
Novel Indole-fused, Medium-sized Ring Heterocycles via Chloroacetamide Photochemistry

What points at this work

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

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Application of 7‐Indolylmethanols in Catalytic Asymmetric Arylations with Tryptamines: Enantioselective Synthesis of 7‐indolylmethanes
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Sulfur‐Promoted Synthesis of 2‐Aroylquinazolin‐4(3H)‐ones by Oxidative Condensation of Anthranilamide and Acetophenones
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C7‐Functionalization of Indoles via Organocatalytic Enantioselective Friedel‐Crafts Alkylation of 4‐Amino‐ indoles with 2‐Butene‐1,4‐diones and 3‐Aroylacrylates
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Electrochemical Oxidation of Indoles to Access Tryptanthrins at Room Temperature
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Thermal‐Induced Synthesis of Cyclobute[b]indolines via Intramolecular Formal [2+2] Cycloaddition of Enamines and Triazole‐Derived Ketenimines
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Gold‐katalysierte Synthese von Chinolinen aus Propargylsilylethern und Anthranilen über die Umpolung eines Goldcarben‐Kohlenstoffatoms
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C7‐Indol‐Amidierung und ‐Alkenylierung durch Ruthenium(II)‐ Katalyse
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Gold‐Catalyzed Synthesis of Quinolines from Propargyl Silyl Ethers and Anthranils through the Umpolung of a Gold Carbene Carbon
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C7‐Indole Amidations and Alkenylations by Ruthenium(II) Catalysis
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Bioactive Secondary Metabolites From the Marine‐derived Fungus Penicillium steckii SCSIO41025
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Photoinduced Redox Cascade Reaction of Isatins and Aliphatic Carboxylic Acids to Access 6‐Hydroxyindoloquinazolinones
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Photoredox‐Catalyzed Isatin Reactions: Access to Dibenzo‐1,7‐Naphthyridine Carboxylate and Tryptanthrin
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A Diamino Alcohol Catalyzed Enantioselective Crossed Aldol Reaction of Acetaldehyde with Isatins – A Concise Total Synthesis of Antitumor Agents
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Ru(II)‐Catalyzed Regioselective Hydroarylative Coupling of Indolines with Internal Alkynes by C−H Activation
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Metal‐Free Hydroxyalkylative Radical Addition/Cyclization of Unactivated Alkenes for the Synthesis of Hydroxyalkylated Ring‐Fused Quinazolinones
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Brønsted Acid Catalyzed Dehydroxylative Cyanation of Benzylic Alcohols with Trimethylsilyl Cyanide Using 1,1,1,3,3,3‐Hexafluoro‐2‐propanol as a Solvent
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Rhodium‐Catalyzed Synthesis of Polycyclic Spiroindolines via Intramolecular 1,2‐Acyloxy Migration‐Cyclization Cascade
inferred← citeshttps://doi.org/10.1002/fft2.70258openalex-snapshot
Integrative Metabolomic and Transcriptomic Profiling Reveals the Chemical and Molecular Basis for Aroma Divergence in Isatis Fruits
inferred← citeshttps://doi.org/10.1002/jhet.2864openalex-snapshot
Synthesis of Condensed Heterocycles, Containing Partially Saturated Pyrimidine Nuclei, from Aromatic Pyrimidine Derivatives
inferred← citeshttps://doi.org/10.1002/jhet.70102openalex-snapshot
Introduction of the Acyl Group at the C7 Position of Indole via N ‐Acyl Indole Photo‐Fries Rearrangement Under UV ‐C
inferred← citeshttps://doi.org/10.1002/jssc.201301159openalex-snapshot
Comparison of reversed‐phase liquid chromatography and hydrophilic interaction chromatography for the fingerprint analysis of R adix isatidis
inferred← citeshttps://doi.org/10.1002/med.21466openalex-snapshot
Biologically active quinoline and quinazoline alkaloids part I
inferred← citeshttps://doi.org/10.1002/med.21492openalex-snapshot
Biologically active quinoline and quinazoline alkaloids part II
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Development of anti‐influenza agents from natural products
inferred← citeshttps://doi.org/10.1002/tcr.201800079openalex-snapshot
Rapid Generation of Molecular Complexity by Chemical Synthesis: Highly Efficient Total Synthesis of Hexacyclic Alkaloid (−)‐Chaetominine and Its Biosynthetic Implications
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Carbon‐Carbon and Carbon‐Heteroatom Bond Formation Reactions Using Unsaturated Carbon Compounds
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Asymmetric Fluorofunctionalizations with Carboxylate‐Based Phase‐Transfer Catalysts
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Traditional Crude Drugs Against Encephalitis Infection: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies
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Traditional Crude Drugs Against Encephalitis Infection: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies
inferred← citeshttps://doi.org/10.1007/978-3-031-81846-2_6openalex-snapshot
Breeding Strategies of Isatis indigotica (Chinese Woad)
inferred← citeshttps://doi.org/10.1007/s00894-023-05623-3openalex-snapshot
Evidences of noncovalent interactions between indole and dichloromethane under different solvent conditions
inferred← citeshttps://doi.org/10.1007/s11030-025-11222-6openalex-snapshot
De novo synthesis of tryptanthrin and its derivatives from indole: engineering a sustainable photocatalytic strategy
inferred← citeshttps://doi.org/10.1007/s11101-024-10015-3openalex-snapshot
Exploring plant-derived bisindole alkaloids: a comprehensive review of sources, phytochemistry and cytotoxicity
inferred← citeshttps://doi.org/10.1007/s13659-012-0082-4openalex-snapshot
Four new indole alkaloids from Plantago asiatica
inferred← citeshttps://doi.org/10.1007/s43450-022-00282-6openalex-snapshot
Indole Compounds from Raphanus sativus Seeds
inferred← citeshttps://doi.org/10.1007/s44371-026-00782-7openalex-snapshot
Alkaloid isolation methods and applications in agriculture and medicine
inferred← citeshttps://doi.org/10.1016/b978-0-08-099406-2.00014-5openalex-snapshot
Six-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-443-18939-5.00013-5openalex-snapshot
Six-membered ring systems: diazines and benzo derivatives
inferred← citeshttps://doi.org/10.1016/bs.acat.2021.11.003openalex-snapshot
Metal-π-allyl mediated asymmetric cycloaddition reactions
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.08.002openalex-snapshot
Biology of quinoline and quinazoline alkaloids
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.11.001openalex-snapshot
Synthesis of pyrimidine-containing alkaloids
inferred← citeshttps://doi.org/10.1016/j.apsb.2016.01.003openalex-snapshot
Three pairs of alkaloid enantiomers from the root of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.apsb.2016.09.004openalex-snapshot
Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
inferred← citeshttps://doi.org/10.1016/j.apsb.2017.04.003openalex-snapshot
Indole alkaloid sulfonic acids from an aqueous extract of Isatis indigotica roots and their antiviral activity
inferred← citeshttps://doi.org/10.1016/j.apsb.2017.09.006openalex-snapshot
8,4′-Oxyneolignane glucosides from an aqueous extract of “ban lan gen” (Isatis indigotica root) and their absolute configurations
inferred← citeshttps://doi.org/10.1016/j.apsb.2018.08.005openalex-snapshot
Sulfur-enriched alkaloids from the root of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.apsb.2019.09.001openalex-snapshot
Indole alkaloid glycosides with a 1′-(phenyl)ethyl unit from Isatis indigotica leaves
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.102926openalex-snapshot
Discovery of cycloneolignan enantiomers from Isatis indigotica Fortune with neuroprotective effects against MPP+-induced SH-SY5Y cell injury
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Four pairs of alkaloid enantiomers from Isatis indigotica Fortune Ex Land with neuroprotective effects against H2O2-induced SH-SY5Y cell injury
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Dual-target chemical profiling of anti-influenza multi-components from Isatidis Radix via direct binding to neuraminidase and hemagglutinin
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Phenylpropanoids and some nitrogen-containing constituents from the roots of Isatis indigotica Fort. (Cruciferae)
inferred← citeshttps://doi.org/10.1016/j.bse.2020.104089openalex-snapshot
Alkaloids and monoterpenes from the leaves of Isatis tinctoria Linnaeus and their chemotaxonomic significance
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Phytochemical Investigation on Raphanus Sativus L
inferred← citeshttps://doi.org/10.1016/j.bse.2024.104800openalex-snapshot
Alkaloids in Isatis indigotica and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.bse.2026.105326openalex-snapshot
Oxindole alkaloids from Brassica rapa L. and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.05.052openalex-snapshot
Antiviral enantiomers of a bisindole alkaloid with a new carbon skeleton from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.01.042openalex-snapshot
Antiviral stereoisomers of 3,5-bis(2-hydroxybut-3-en-1-yl)-1,2,4-thiadiazole from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.08.006openalex-snapshot
Two pairs of unusual scalemic enantiomers from Isatis indigotica leaves
inferred← citeshttps://doi.org/10.1016/j.cclet.2017.05.019openalex-snapshot
Isatindigodiphindoside, an alkaloid glycoside with a new diphenylpropylindole skeleton from the root of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.cclet.2017.12.001openalex-snapshot
Isatindolignanoside A, a glucosidic indole-lignan conjugate from an aqueous extract of the Isatis indigotica roots
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Review, challenges, and prospects of the process of alkaloid extraction from plants
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Combining network pharmacology and molecular docking to decipher molecular mechanism of Wugen decoction in influenza A prevention
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A review on recent developments of indole-containing antiviral agents
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Discovery, synthesis, and optimization of an N-alkoxy indolylacetamide against HIV-1 carrying NNRTI-resistant mutations from the Isatis indigotica root
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Indole alkaloids from the roots of Isatis indigotica and their inhibitory effects on nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.05.001openalex-snapshot
Pharmaceutical prospects of naturally occurring quinazolinone and its derivatives
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.05.025openalex-snapshot
N-acylanthranilic acid derivatives with anti-Aβ1–42 aggregation activity from the leaves of Isatis indigotica fortune
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104189openalex-snapshot
Lignans from Isatis indigotica roots and their inhibitory effects on nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104654openalex-snapshot
Bisindole alkaloids with nitric oxide inhibitory activities from an alcohol extract of the Isatis indigotica roots
inferred← citeshttps://doi.org/10.1016/j.indcrop.2012.12.050openalex-snapshot
Microwave-assisted aqueous enzymatic extraction of oil from Isatis indigotica seeds and its evaluation of physicochemical properties, fatty acid compositions and antioxidant activities
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Fatty acid and glucosinolate patterns of seed from Isatis indigotica Fortune as bioproducts for green chemistry
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110884openalex-snapshot
A synthetic derivative of bioactive constituents from Isatis indigotica ameliorates hypersensitivity and arthritis by inhibiting JAK2-STAT3 pathway in mice
inferred← citeshttps://doi.org/10.1016/j.jafr.2025.102200openalex-snapshot
Comparative analysis of the chemical composition and cytotoxic activity of broccoli by-products as an alternative source of bioactive compounds
inferred← citeshttps://doi.org/10.1016/j.jep.2015.08.037openalex-snapshot
Lariciresinol-4-O-β-D-glucopyranoside from the root of Isatis indigotica inhibits influenza A virus-induced pro-inflammatory response
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114648openalex-snapshot
Isatidis Radix and Isatidis Folium: A systematic review on ethnopharmacology, phytochemistry and pharmacology
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2014.05.011openalex-snapshot
Useful procedures for fluorocyclization of tryptamine and tryptophol derivatives to 3a-fluoropyrrolo[2,3-b]indoles and 3a-fluorofuro[2,3-b]indoles
inferred← citeshttps://doi.org/10.1016/j.phymed.2022.153930openalex-snapshot
Role of medicinal plants in inhibiting SARS-CoV-2 and in the management of post-COVID-19 complications
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.02.016openalex-snapshot
Alkaloids with neuroprotective effects from the leaves of Isatis indigotica collected in the Anhui Province, China
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112337openalex-snapshot
Four undescribed sulfur-containing indole alkaloids with nitric oxide inhibitory activities from Isatis tinctoria L. roots
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.01.015openalex-snapshot
α-Furanones, secondary metabolites from the fungus Cephalotrichum microsporum and their antibacterial activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.08.005openalex-snapshot
Three new indole alkaloid glycosides with unusual structural features from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.023openalex-snapshot
One-pot, three-component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium-catalyzed intramolecular Heck reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.025openalex-snapshot
Protecting group-free syntheses of natural products and biologically active compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134858openalex-snapshot
Solvent-controlled selective synthesis of quinazolinones and 2-arylquinazolinones via copper-catalyzed [5 + 1] annulation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.07.113openalex-snapshot
One-pot synthesis of tryptanthrin by the Dakin oxidation of indole-3-carbaldehyde
inferred← citeshttps://doi.org/10.1016/s1875-5364(21)60093-6openalex-snapshot
Discovery of alkaloids from the leaves of Isatis indigotica Fortune with neuroprotective activity
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00800openalex-snapshot
Catalyst-Free Synthesis of Polycyclic Spiroindolines by Cascade Reaction of 3-(2-Isocyanoethyl)indoles with 1-Sulfonyl-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00654openalex-snapshot
Synthesis of Pyrimido[1,2-a]indolediones and Pyrimidinediones via [4+2] Annulation of 2H-Azirine-2-carbaldehydes
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00512openalex-snapshot
DBU-Mediated Diastereoselective Aldol-Type Cyanomethylation of Isatins
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02026openalex-snapshot
Asymmetric Dearomatizing Fluoroamidation of Indole Derivatives with Dianionic Phase-Transfer Catalyst
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01315openalex-snapshot
Switching of Enantioselectivity in the Cu-Catalyzed Asymmetric Decarboxylative Aldol Reaction of Tryptanthrin with β-Keto Acids: An Unexpected Counteranion Effect
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c04266openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Regio- and Enantioselective C7-Alkylation of 4-Aminoindoles with α-Bromoenals
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03987openalex-snapshot
The Cascade Reaction Chemistry of Diazo Compounds with Intentionally Designed Alkene to Access Esterified Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02891openalex-snapshot
Direct Catalytic Asymmetric Synthesis of β-Hydroxy Acids from Malonic Acid
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01428openalex-snapshot
Enantioselective Construction of gem-Difluorinated Tetrahydroindolo[2,1-b]quinazolines via CPA-Catalyzed Asymmetric [4 + 2]-Annulation
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03009openalex-snapshot
Synthesis of Tryptanthrins by Organocatalytic and Substrate Co-catalyzed Photochemical Condensation of Indoles and Anthranilic Acids with Visible Light and O2
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00408openalex-snapshot
Synthesis of Chiral (hydro)Indoloquinazolinones via Enantioselective Copper-Catalyzed Borylative Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02676openalex-snapshot
Synthesis of C3-Alkynyl Pyrroloindolines via Intermolecular Cascade Dearomatization/1,2-Migration of Tryptamine Derivatives with Alkynyliodonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01336openalex-snapshot
Catalytic Asymmetric Construction of the Tryptanthrin Skeleton via an Enantioselective Decarboxylative [4 + 2] Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01321openalex-snapshot
Total Synthesis of an Isatis indigotica-Derived Alkaloid Using a Biomimetic Thio-Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1021/jacs.3c01667openalex-snapshot
Enantioselective Copper-Catalyzed Fukuyama Indole Synthesis from 2-Vinylphenyl Isocyanides
inferred← citeshttps://doi.org/10.1021/jacs.4c13535openalex-snapshot
Selective Synthesis of Cyclopeptides with a 2-Oxindole or 3a-Hydroxy-hexahydropyrrolo-[2,3-b]indole Structure by Cytochrome P450 Enzymes
inferred← citeshttps://doi.org/10.1021/jo502062zopenalex-snapshot
C7-Derivatization of C3-Alkylindoles Including Tryptophans and Tryptamines
inferred← citeshttps://doi.org/10.1021/np400202fopenalex-snapshot
Guaiane-Type Sesquiterpenes from Curcuma phaeocaulis and Their Inhibitory Effects on Nitric Oxide Production
inferred← citeshttps://doi.org/10.1021/ol302660topenalex-snapshot
Enantiomers of an Indole Alkaloid Containing Unusual Dihydrothiopyran and 1,2,4-Thiadiazole Rings from the Root of Isatis indigotica
inferred← citeshttps://doi.org/10.1021/ol400644mopenalex-snapshot
Indium/TFA-Catalyzed Synthesis of Tetracyclic [6,5,5,6] Indole Ring, via a Tandem Cycloannulation of β-Oxodithioester with Tryptamine
inferred← citeshttps://doi.org/10.1021/ol401709topenalex-snapshot
Total Synthesis of a Pyrroloindoloquinazoline Alkaloid
inferred← citeshttps://doi.org/10.1021/ol4018062openalex-snapshot
Aryne Insertion Reactions Leading to Bioactive Fused Quinazolinones: Diastereoselective Total Synthesis of Cruciferane
inferred← citeshttps://doi.org/10.1021/ol4023936openalex-snapshot
I2/TBHP-Catalyzed Chemoselective Amination of Indoles
inferred← citeshttps://doi.org/10.1038/s41438-020-0240-5openalex-snapshot
A chromosome-scale genome assembly of Isatis indigotica, an important medicinal plant used in traditional Chinese medicine
inferred← citeshttps://doi.org/10.1038/srep24945openalex-snapshot
Plasiatine, an Unprecedented Indole–Phenylpropanoid Hybrid from Plantago asiatica as a Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2
inferred← citeshttps://doi.org/10.1039/c4ra10309bopenalex-snapshot
Total synthesis of cruciferane via epoxidation/tandem cyclization sequence
inferred← citeshttps://doi.org/10.1039/c5np00032gopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c5ob00601eopenalex-snapshot
Ruthenium-catalyzed oxidative coupling of 2-aryl-4-quinazolinones with olefins: synthesis of pyrrolo[2,1-b]quinazolin-9(1H)-one motifs
inferred← citeshttps://doi.org/10.1039/c5ob00964bopenalex-snapshot
Natural nitric oxide (NO) inhibitors from the rhizomes of Curcuma phaeocaulis
inferred← citeshttps://doi.org/10.1039/c5ob01560jopenalex-snapshot
An efficient aldol-type direct reaction of isatins with TMSCH 2 CN
inferred← citeshttps://doi.org/10.1039/c7qo00882aopenalex-snapshot
Indium( iii )-catalyzed intramolecular dearomative cycloaddition of N -sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons
inferred← citeshttps://doi.org/10.1039/c8ob02046aopenalex-snapshot
Bioactive spiropyrrolizidine oxindole alkaloid enantiomers from Isatis indigotica Fortune
inferred← citeshttps://doi.org/10.1039/c9ob01243eopenalex-snapshot
Stereoselective construction of deoxy-cruciferane alkaloids by NHC-catalyzed intramolecular annulation of homoenolate with quinazolinone
inferred← citeshttps://doi.org/10.1039/d0cs00530dopenalex-snapshot
Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis
inferred← citeshttps://doi.org/10.1039/d0nj04395hopenalex-snapshot
Synthesis of 6-substituted indoloquinazolinones from arynes and 2-acyl-4-quinazolinones: a transition-metal free C–N and C–C bond formation strategy
inferred← citeshttps://doi.org/10.1039/d1ob02215fopenalex-snapshot
An iron-catalyzed domino reaction of donor–acceptor cyclopropanes: a diastereoselective approach towards diversely functionalized pyrrolo-quinazolines
inferred← citeshttps://doi.org/10.1039/d1qo01543eopenalex-snapshot
Palladium-catalysed stereoselective [3 + 2] annulation of vinylethylene carbonates and tryptanthrin-based ketones
inferred← citeshttps://doi.org/10.1039/d2nj01428aopenalex-snapshot
DMSO as a dual carbon synthon in one-pot tandem synthesis of N -alkylated quinazolinones from anthranilamides and acetophenones
inferred← citeshttps://doi.org/10.1039/d3cc02673fopenalex-snapshot
An efficient Selectfluor-mediated condensation of indoles and anthranilates for the synthesis of indoloquinazolinones
inferred← citeshttps://doi.org/10.1039/d4qo01685hopenalex-snapshot
A general photocatalytic strategy for the synthesis of β-hydroxy acid derivatives from alkenes
inferred← citeshttps://doi.org/10.1039/d4qo02362eopenalex-snapshot
Enantioselective modular synthesis of α-aryl-α-heteroaryl aminonitriles with parts per million organocatalyst loading: mechanistic investigation for stereochemical origins
inferred← citeshttps://doi.org/10.1039/d4ra01834fopenalex-snapshot
Exploring the synthetic potential of epoxide ring opening reactions toward the synthesis of alkaloids and terpenoids: a review
inferred← citeshttps://doi.org/10.1039/d5ra10073aopenalex-snapshot
NHC-catalyzed asymmetric synthesis of natural products and pharmaceutical drugs
inferred← citeshttps://doi.org/10.1055/a-1023-8940openalex-snapshot
Alkaloid Enantiomers from Isatis tinctoria with Neuroprotective Effects against H2O2-Induced SH-SY5Y Cell Injury
inferred← citeshttps://doi.org/10.1080/10286020.2015.1055729openalex-snapshot
Antiviral glycosidic bisindole alkaloids from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1080/10286020.2015.1117452openalex-snapshot
Indole alkaloid glucosides from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1080/10286020.2017.1320547openalex-snapshot
Diglycosidic indole alkaloid derivatives from an aqueous extract of Isatis indigotica roots
inferred← citeshttps://doi.org/10.1080/10286020.2022.2064284openalex-snapshot
Sulfonated alkaloids from an aqueous extract of Isatis indigotica roots
inferred← citeshttps://doi.org/10.1080/10286020.2022.2089979openalex-snapshot
Lignans and a neolignan from an aqueous extract of Isatis indigotica roots
inferred← citeshttps://doi.org/10.1080/10286020.2025.2483810openalex-snapshot
Sulfonated and sulfated lignans/neolignans from an aqueous extract of Isatis indigotica roots
inferred← citeshttps://doi.org/10.1080/14786419.2018.1482892openalex-snapshot
New adenine analogues and a pyrrole alkaloid from Selaginella delicatula
inferred← citeshttps://doi.org/10.1080/14786419.2019.1624960openalex-snapshot
Indole alkaloid glycosides from Isatis tinctoria roots
inferred← citeshttps://doi.org/10.1080/14786419.2019.1644632openalex-snapshot
Isatisindigoticanine A, a novel indole alkaloid with an unpresented carbon skeleton from the roots of Isatis tinctoria
inferred← citeshttps://doi.org/10.1080/14786419.2020.1779716openalex-snapshot
Four new indole alkaloids from the roots of Isatis tinctoria
inferred← citeshttps://doi.org/10.1080/14786419.2024.2348667openalex-snapshot
Natural 3,4-dihydro-2(1 H )-quinolinones- Part I: plant sources
inferred← citeshttps://doi.org/10.1080/14786419.2026.2683917openalex-snapshot
2-oxotetrahydroquinoline derivatives from Abelmoschus sagittifolius flowers
inferred← citeshttps://doi.org/10.1134/s1021443717020121openalex-snapshot
Role of 5-aminolevulinic acid on growth, photosynthetic parameters and antioxidant enzyme activity in NaCl-stressed Isatis indigotica Fort.
inferred← citeshttps://doi.org/10.1142/s0192415x1350050xopenalex-snapshot
Research Progress of Chinese Herbal MedicineRadix isatidis(Banlangen)
inferred← citeshttps://doi.org/10.1155/2014/516904openalex-snapshot
Evolution of New Variants/Mutants of JE Virus, Its Effect on Neurovirulence, Antigenicity, Host Immune Responses and Disease Transmission in Endemic Areas
inferred← citeshttps://doi.org/10.1177/1934578x20953289openalex-snapshot
Multigram Scale Synthesis and Anti-Influenza Activity of 3-Indoleacetonitrile Glucosides
inferred← citeshttps://doi.org/10.1186/s12906-023-03916-xopenalex-snapshot
Antiviral and ROS scavenging potential of Carica papaya Linn and Psidium guajava leaves extract against HIV-1 infection
inferred← citeshttps://doi.org/10.1186/s43897-021-00021-wopenalex-snapshot
Isatis indigotica: from (ethno) botany, biochemistry to synthetic biology
inferred← citeshttps://doi.org/10.1371/journal.pone.0119022openalex-snapshot
Establishment of Hairy Root Cultures by Agrobacterium Rhizogenes Mediated Transformation of Isatis Tinctoria L. for the Efficient Production of Flavonoids and Evaluation of Antioxidant Activities
inferred← citeshttps://doi.org/10.1371/journal.pone.0173058openalex-snapshot
Transcriptome profiling of influenza A virus-infected lung epithelial (A549) cells with lariciresinol-4-β-D-glucopyranoside treatment
inferred← citeshttps://doi.org/10.21203/rs.3.rs-874471/v1openalex-snapshot
Theoretical Investigation of the Modeling of Indole –dichlormethane Hydrogen Bonding in Different Solvents
inferred← citeshttps://doi.org/10.2174/1385272824999200818181531openalex-snapshot
Recent Achievements in Nucleophilic Decarboxylative Addition Reactions
inferred← citeshttps://doi.org/10.2174/1573412916999200526120449openalex-snapshot
Determination of Free Amino Acids in Banlangen Granule and its Fractions by Solid Phase Extraction Combined with Ion-pair Hig-h Perfor mance Liquid Chromatography using a Corona-charged Aerosol Detector (SPE-HPLC-CAD)
inferred← citeshttps://doi.org/10.3389/fchem.2022.1005360openalex-snapshot
Research progress on the antiviral activities of natural products and their derivatives: Structure–activity relationships
inferred← citeshttps://doi.org/10.3389/fphar.2021.685575openalex-snapshot
Microscopic Mass Spectrometry Imaging Reveals the Distribution of Phytochemicals in the Dried Root of Isatis tinctoria
inferred← citeshttps://doi.org/10.3389/fphar.2022.928106openalex-snapshot
Chinese herbal prescriptions for COVID-19 management: Special reference to Taiwan Chingguan Yihau (NRICM101)
inferred← citeshttps://doi.org/10.3389/fphar.2025.1542061openalex-snapshot
Indirubin attenuates sepsis by targeting the EGFR/SRC/PI3K and NF-κB/MAPK signaling pathways in macrophages
inferred← citeshttps://doi.org/10.3390/molecules23061390openalex-snapshot
Synthesis of 2-Mercapto-(2-Oxoindolin-3-Ylidene)Acetonitriles from 3-(4-Chloro-5H-1,2,3-Dithiazol-5-Ylidene)Indolin-2-ones
inferred← citeshttps://doi.org/10.3390/molecules24173140openalex-snapshot
Alkaloid Enantiomers from the Roots of Isatis indigotica
inferred← citeshttps://doi.org/10.3390/molecules24224033openalex-snapshot
Alkaloids with Nitric Oxide Inhibitory Activities from the Roots of Isatis tinctoria
inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
inferred← citeshttps://doi.org/10.3390/molecules27217558openalex-snapshot
Eight Indole Alkaloids from the Roots of Maerua siamensis and Their Nitric Oxide Inhibitory Effects
inferred← citeshttps://doi.org/10.3390/toxins7114507openalex-snapshot
Cytotoxic Indole Alkaloids against Human Leukemia Cell Lines from the Toxic Plant Peganum harmala
inferred← citeshttps://doi.org/10.3987/rev-18-sr(t)3openalex-snapshot
β-Amino Alcohol Organocatalysts for Asymmetric Additions
inferred← citeshttps://doi.org/10.4103/2225-4110.126635openalex-snapshot
Anti-inflammatory and Antimicrobial Effects of Heat-clearing Chinese Herbs: A Current Review
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.76.802openalex-snapshot
Synthesis of Indoloquinazoline Alkaloids Using Cascade Reactions
inferred← citeshttps://doi.org/10.58837/chula.the.2022.299openalex-snapshot
Chemical constituents and nitric oxide inhibitory activity of capparis micracantha and maerua siamensis
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