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Naturally Occurring Nitrogen–Sulfur Compounds. The Benzothiazole Alkaloids

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What this work says

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

inferredcites →https://doi.org/10.1002/anie.200700728openalex-snapshot
From Amino Acids to Heteroaromatics—Thiopeptide Antibiotics, Nature's Heterocyclic Peptides
inferredcites →https://doi.org/10.1002/cbic.200800438openalex-snapshot
How Nature Morphs Peptide Scaffolds into Antibiotics
inferredcites →https://doi.org/10.1002/hlca.200790086openalex-snapshot
Sesquiterpenoids and Lactone Derivatives from Ligularia dentata
inferredcites →https://doi.org/10.1002/jcp.1030340310openalex-snapshot
Purification of firefly luciferin
inferredcites →https://doi.org/10.1007/bf02466474openalex-snapshot
Gas chromatographic-mass spectrometric analysis of volatile compounds in oak wood used for ageing of wines and spirits
inferredcites →https://doi.org/10.1016/0003-9861(57)90212-6openalex-snapshot
The preparation and properties of crystalline firefly luciferin
inferredcites →https://doi.org/10.1016/0006-291x(68)90036-3openalex-snapshot
The decarboxylation of luciferin in firefly bioluminescence
inferredcites →https://doi.org/10.1016/0040-4020(80)85056-3openalex-snapshot
Thiazo rifamycins—I
inferredcites →https://doi.org/10.1016/j.tetlet.2004.08.137openalex-snapshot
Violatinctamine, a new heterocyclic compound from the marine tunicate Cystodytes cf. violatinctus
inferredcites →https://doi.org/10.1016/j.tetlet.2004.12.134openalex-snapshot
Mevashuntin, a novel metabolite produced by inhibition of the mevalonate pathway in Streptomyces prunicolor
inferredcites →https://doi.org/10.1016/s0040-4020(01)93637-3openalex-snapshot
Studies on firefly bioluminescence—I
inferredcites →https://doi.org/10.1016/s0040-4020(01)93638-5openalex-snapshot
Studies on firefly bioluminescence—II
inferredcites →https://doi.org/10.1016/s0040-4020(97)10153-3openalex-snapshot
Synthetic studies on pentacyclic aromatic alkaloids, kuanoniamine A, 11-hydroxyascididemin, and neocalliactine acetate
inferredcites →https://doi.org/10.1016/s0040-4039(00)93476-2openalex-snapshot
Benzothiazoles from a putatitve bacterial symbiont of the marine sponge
inferredcites →https://doi.org/10.1016/s0040-4039(00)99360-2openalex-snapshot
New cytotoxic acridine alkaloids from two deep water marine sponges of the family
inferredcites →https://doi.org/10.1016/s0304-4165(02)00212-xopenalex-snapshot
Metal ions as potential regulatory factors in the biosynthesis of red hair pigments: a new benzothiazole intermediate in the iron or copper assisted oxidation of 5-S-cysteinyldopa
inferredcites →https://doi.org/10.1016/s0960-894x(99)00205-xopenalex-snapshot
S1319: A novel β2-adrenoceptor agonist from a marine sponge Dysidea sp.
inferredcites →https://doi.org/10.1021/ja00051a062openalex-snapshot
Total synthesis of kuanoniamines and dercitins
inferredcites →https://doi.org/10.1021/ja00155a010openalex-snapshot
A Unified Strategy for the Synthesis of Sulfur-Containing Pyridoacridine Alkaloids: Antitumor Agents of Marine Origin
inferredcites →https://doi.org/10.1021/ja00222a071openalex-snapshot
Dercitine, a new biologically active acridine alkaloid from a deep water marine sponge, Dercitus sp
inferredcites →https://doi.org/10.1021/ja00886a019openalex-snapshot
The Structure and Synthesis of Firefly Luciferin
inferredcites →https://doi.org/10.1021/ja01036a093openalex-snapshot
Chemi- and bioluminescence of firefly luciferin
inferredcites →https://doi.org/10.1021/jf00112a044openalex-snapshot
Identification of some volatile constituents of Aspergillus clavatus
inferredcites →https://doi.org/10.1021/jf072145wopenalex-snapshot
Aging Effects and Grape Variety Dependence on the Content of Sulfur Volatiles in Wine
inferredcites →https://doi.org/10.1021/jf60201a032openalex-snapshot
New volatile constituents of black tea aroma
inferredcites →https://doi.org/10.1021/jf990634topenalex-snapshot
Analysis of Benzothiazole in Italian Wines Using Headspace Solid-Phase Microextraction and Gas Chromatography−Mass Spectrometry
inferredcites →https://doi.org/10.1021/jm00048a017openalex-snapshot
Inhibition of Topoisomerase II Catalytic Activity by Pyridoacridine Alkaloids from a Cystodytes sp. Ascidian: A Mechanism for the Apparent Intercalator-Induced Inhibition of Topoisomerase II
inferredcites →https://doi.org/10.1021/jo00031a035openalex-snapshot
Pyridoacridine alkaloids from deep-water marine sponges of the family Pachastrellidae: structure revision of dercitin and related compounds and correlation with the kuanoniamines
inferredcites →https://doi.org/10.1021/jo00301a040openalex-snapshot
Kuanoniamines A, B, C, and D: pentacyclic alkaloids from a tunicate and its prosobranch mollusk predator Chelynotus semperi
inferredcites →https://doi.org/10.1021/jo960203zopenalex-snapshot
Novel Synthesis of Benzothiazole Derivatives via Directed Lithiation and Aryne-Mediated Cyclization Followed by Quenching with Electrophiles
inferredcites →https://doi.org/10.1021/np010629vopenalex-snapshot
Three New Pyridoacridine Type Alkaloids from a Singaporean Ascidian
inferredcites →https://doi.org/10.1021/np9702704openalex-snapshot
Bioactive Pyridoacridine Alkaloids from the Micronesian SpongeOceanapiasp.
inferredcites →https://doi.org/10.1021/ol0518840openalex-snapshot
Synthesis of the Marine Sponge Derived β2-Adrenoceptor Agonist S1319
inferredcites →https://doi.org/10.1039/c3975000042bopenalex-snapshot
A model for firefly luciferin biosynthesis
inferredcites →https://doi.org/10.1039/c39760000032openalex-snapshot
Biosynthesis of firefly luciferin. Probable formation of benzothiazole from p-benzoquinone and cysteine
inferredcites →https://doi.org/10.1039/c39760000153openalex-snapshot
Biosynthesis of luciferin in Pyrophorus pellucens
inferredcites →https://doi.org/10.1073/pnas.33.11.342openalex-snapshot
The Energy Source for Bioluminescence in an Isolated System
inferredcites →https://doi.org/10.1080/14786410601132212openalex-snapshot
Nordehydrocyclodercitin, a hexacyclic pyridoacridine alkaloid from the marine ascidian,Aplidiumsp.
inferredcites →https://doi.org/10.1111/j.1751-1097.2007.00232.xopenalex-snapshot
The “Benzothiazine” Chromophore of Pheomelanins: A Reassessment†
inferredcites →https://doi.org/10.3891/acta.chem.scand.21-2076openalex-snapshot
The Aroma of Cranberries. II. Vaccinium macrocarpon Ait..
inferredcites →https://doi.org/10.3987/com-92-6321openalex-snapshot
Total Synthesis of Kuanoniamine A, 11-Hydroxyascididemin, and Neocalliactine Acetate
inferredcites →https://doi.org/10.7164/antibiotics.33.842openalex-snapshot
Thiazorifamycins. III. Biosynthesis of rifamycins P,Q and verde, novel metabolites from a mutant of Nocardia mediterranea.
inferredcites →https://doi.org/10.7164/antibiotics.53.886openalex-snapshot
New Triene-ansamycins, Thiazinotrienomycins F and G and a Diene-ansamycin, Benzoxazomycin.

What points at this work

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

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Polypyridyl Ruthenium Complexes with Benzothiazole Moiety as Membrane Disruptors and Anti-Resistance Agents for Staphylococcus Aureus
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Use of Molecular Oxygen as a Reoxidant in the Synthesis of 2‐Substituted Benzothiazoles via Palladium‐Catalyzed CH Functionalization/Intramolecular CS Bond Formation
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Synthesis of 2‐Substituted Benzothiazoles by Visible Light‐Driven Photoredox Catalysis
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Transition‐Metal‐Free C‐S Bond Forming Strategy towards Synthesis of Highly Diverse Pyrazole Tethered Benzothiazoles: Investigation of their Photophysical Properties
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Novel metal complexes of 3‐acetylcoumarin‐2‐hydrazinobenzothiazole Schiff base: Design, structural characterizations, DNA binding, DFT calculations, molecular docking and biological studies
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Synthesis and structural characterization of palladium pincer complexes: Sustainable synthesis of benzothiazoles
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Click Chemistry for the Generation of Combination of Triazole Core and Thioether Donor Site in Organosulfur Ligands: Applications of Metal Complexes in Catalysis
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ChemInform Abstract: Naturally Occurring Nitrogen—Sulfur Compounds. The Benzothiazole Alkaloids.
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Solid‐Supported Materials‐Based Synthesis of 2‐Substituted Benzothiazoles: Recent Developments and Sanguine Future
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Efficient Single‐Pot Synthesis of Thiazole Derivatives: A Synoptic View
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Physiological, molecular, and environmental insights into plant nitrogen uptake, and metabolism under abiotic stresses
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Two New Proton Transfer Salts of Benzo[d]thiazol-2-amine with Different Aromatic Acids
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Visible light–driven organic synthesis under ruthenium (RuII)-complex photocatalysis
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Metabolites
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.06.028openalex-snapshot
2-S-cysteinylhydroquinone is an intermediate for the firefly luciferin biosynthesis that occurs in the pupal stage of the Japanese firefly, Luciola lateralis
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Synthesis of retinoid enhancers based on 2-aminobenzothiazoles for anti-cancer therapy
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.216677openalex-snapshot
Visible light-mediated synthesis of 1,3-benzothiazoles: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.01.032openalex-snapshot
Synthesis of novel 2-mercapto benzothiazole and 1,2,3-triazole based bis-heterocycles: Their anti-inflammatory and anti-nociceptive activities
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Micro-archaeological indicators for identifying ancient cess deposits: An example from Late Bronze Age Megiddo, Israel
inferred← citeshttps://doi.org/10.1016/j.jcou.2018.03.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2024.112517openalex-snapshot
Polypyridyl ruthenium complexes with benzothiazole moiety as membrane disruptors and anti-resistance agents for Staphylococcus aureus
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2023.115225openalex-snapshot
Role of π-bridge and strong solid-state emission in triphenylamine-benzothiazole based nonlinear optical dyes
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2021.112897openalex-snapshot
Quantifying the release of tyre wear particles to the marine environment via multiple pathways
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.117811openalex-snapshot
Characterisation of tyre wear particle transport from road runoff to sea in coastal environments
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6-(2-Fluorobenzoyl)-3-(2-(4-(4-fluorophenyl)piperazin-1-yl)-2-oxoethyl)benzo[ d ]thiazol-2(3H)-one drug molecule structure and its interaction with atmospheric pressure plasma jet
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Focused library design and synthesis of 2-mercapto benzothiazole linked 1,2,4-oxadiazoles as COX-2/5-LOX inhibitors
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Design, synthesis, biological evaluation and computational study of novel triazolo [4,3-a]pyrazin analogues
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Synthesis, crystal and DFT studies of N-(carboxyethyl)-2-methylbenzothiazolium bromide
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136731openalex-snapshot
Chromogenic sensing, biological, and optical properties of Schiff bases of 2-amino-6-methoxybenzothiazole
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136957openalex-snapshot
Crystal packing of structurally similarand strong dimeric subunits of isomeric N/ -(1,3- benzothiazol-2-yl)nitrobenzenesulfonylhydrazides, influenced by the position of the nitro group
inferred← citeshttps://doi.org/10.1016/j.rechem.2021.100245openalex-snapshot
Synthesis, spectral characterization, antimicrobial evaluation studies and cytotoxic activity of some transition metal complexes with tridentate (N,N,O) donor azo dye ligand
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Structure and vibrational spectra of 6-(4-fluorobenzoyl)-3-(2-(4-methylpiperazin-1-yl)-2-oxoethyl)benzo[d]thiazol-2(3H)-one molecule
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Straightforward convergent access to 2-arylated polysubstituted benzothiazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.042openalex-snapshot
Alkylation of thiols with trichloroacetimidates under neutral conditions
inferred← citeshttps://doi.org/10.1016/s0065-2725(10)10002-6openalex-snapshot
Naturally Occurring Nitrogen–Sulfur Compounds
inferred← citeshttps://doi.org/10.1021/acs.est.1c04422openalex-snapshot
Atmospheric Benzothiazoles in a Coastal Marine Environment
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Thiazole- and Benzothiazole-Based Organoselenium Compounds as Dual-Action Agents: Tyrosinase Inhibitors and Functional Mimics of Glutathione Peroxidase
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Cysteine-Derived Pleurotin Congeners from the Nematode-Trapping Basidiomycete Hohenbuehelia grisea
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00116openalex-snapshot
Brønsted Acid-Catalyzed Asymmetric Friedel–Crafts Alkylation of Indoles with Benzothiazole-Bearing Trifluoromethyl Ketone Hydrates
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00275openalex-snapshot
Tandem Copper-Catalyzed Regioselective N-Arylation–Aza-Michael Addition: Synthesis of Tetracyclic 5H-Benzothiazolo[3,2-a]quinazoline Derivatives
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Cascade Nucleophilic Addition–Cyclic Michael Addition of Arynes and Indoles Bearing Michael Acceptor: A Strategy to Construct Pyrroloacridines and Study of Their Physicochemical Properties
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Synthesis of Arylated Nucleobases by Visible Light Photoredox Catalysis
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Gas Biopsy for Pan-Cancer Mice Early Screening by Untargeted Mass Spectrometry Analysis of Metabolic VOCs
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Divergent S- and C-Difluoromethylation of 2-Substituted Benzothiazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02855openalex-snapshot
Domino Synthesis of 2-Substituted Benzothiazoles by Base-Promoted Intramolecular C–S Bond Formation
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Red Hair Benzothiazines and Benzothiazoles: Mutation-Inspired Chemistry in the Quest for Functionality
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Erythrazoles A–B, Cytotoxic Benzothiazoles from a Marine-DerivedErythrobactersp.
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Highly Selective Domino Multicyclizations for Forming Polycyclic Fused Acridines and Azaheterocyclic Skeletons
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Bioinspired Oxidative Aromatizations: One-Pot Syntheses of 2-Substituted Benzothiazoles and Pyridines by Aerobic Organocatalysis
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One-pot non-enzymatic formation of firefly luciferin in a neutral buffer from p-benzoquinone and cysteine
inferred← citeshttps://doi.org/10.1039/c005001fopenalex-snapshot
Marine natural products
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Muscarine, imidazole, oxazole, and thiazole alkaloids
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Cu-catalyzed in situ generation of thiol using xanthate as a thiol surrogate for the one-pot synthesis of benzothiazoles and benzothiophenes
inferred← citeshttps://doi.org/10.1039/c3ob42318bopenalex-snapshot
KI-catalyzed arylation of benzothiazoles from the coupling of aryl aldehydes with benzothiazoles in neat water
inferred← citeshttps://doi.org/10.1039/c6nj03103jopenalex-snapshot
Synthesis of 2-acyl-benzo[1,3-d]selenazoles via domino oxidative cyclization of methyl ketones with bis(2-aminophenyl) diselenide
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Transition metal-catalyzed [2 + 2 + 2] cycloaddition of nitrogen-linked 1,6-diynes: a straightforward route to fused pyrrolidine systems
inferred← citeshttps://doi.org/10.1039/c8ra07013jopenalex-snapshot
l -Proline catalyzed one-pot synthesis of polysubstituted pyridine system incorporating benzothiazole moiety via sustainable sonochemical approach
inferred← citeshttps://doi.org/10.1039/c9ob00690gopenalex-snapshot
Photorearrangement of dihetarylethenes as a tool for the benzannulation of heterocycles
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Direct synthesis of triphenylamine-based ordered mesoporous polymers for metal-free photocatalytic aerobic oxidation
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Difluorocarbene as a C–F source for the construction of fluorinated benzothiazoles
inferred← citeshttps://doi.org/10.1039/d5ob00339copenalex-snapshot
Unconventional approaches for synthesis of 2-substituted benzothiazoles
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A chemoenzymatic synthesis of amide-containing quinazolin-4( 3H )-one derivatives
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inferred← citeshttps://doi.org/10.1055/s-0040-1707204openalex-snapshot
Iodine- and TBHP-Promoted Acylation of Benzothiazoles under Metal-Free Conditions
inferred← citeshttps://doi.org/10.1063/5.0303517openalex-snapshot
Synthesis, characterization and antimicrobial activity of nickel(iii), and zinc(II) complexes with novel azo dye ligand (N, N, O) derived from 2-amino benzothiazole
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ORGANIC-08 Research Highlights
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Synthetic Strategies for Fused Benzothiazoles: Past, Present, and Future
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Camphor sulfonic acid catalyzed a simple, facile, and general method for the synthesis of 2-arylbenzothiazoles, 2-arylbenzimidazoles, and 3H-spiro[benzo[d]thiazole-2,3′-indolin]-2′-ones at room temperature
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Synthesis, spectral, and magnetic studies of benzothiazolium tetrachlorocuprate salts: crystal structure and semiconducting behavior of bis[2-(4-methoxyphenyl)benzothiazolium] tetrachlorocuprate(II)
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S-arylation of 2-mercaptobenzazoles: a comprehensive review
inferred← citeshttps://doi.org/10.1080/17568919.2025.2504337openalex-snapshot
Benzothiazole derivatives as inhibitors of chikungunya virus replicative cycle
inferred← citeshttps://doi.org/10.1088/1742-6596/1853/1/012007openalex-snapshot
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inferred← citeshttps://doi.org/10.1248/yakushi.132.887openalex-snapshot
New Sesquiterpenoids from the Rhizomes of Petasites japonicus MAXIM. and the Roots of Ligularia dentata HARA
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Design, Synthesis, Characterization and Molecular Docking Studies of Benzimidazole-2-thione, Benzoxazole-2-thione and Benzothiazole-2-thione Derivatives as Potential HSV and HIV Inhibitors
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Multistep Continuous-Flow Synthesis of Condensed Benzothiazoles
inferred← citeshttps://doi.org/10.2174/1570179419666220330001036openalex-snapshot
A Review on the Design, Synthesis, and Structure-activity Relationships of Benzothiazole Derivatives against Hypoxic Tumors
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Naturally Available Nitrogen-Containing Fused Heterocyclics as Prospective Lead Molecules in Medicinal Chemistry
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Synthesis, Characterization of New Ligand Derived from 4-aminoantipyrine and its Complexes with Few Metallic Ions and Evaluation of their Activity as Anticancer
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A FACILE SYNTHESIS OF BENZAZOLYLSULFONYL PYRIMIDINYL ACETAMIDE DERIVATIVES WITH IONIC LIQUID UNDER ULTRASONIC IRRADIATION
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Synthesis and Preliminary Antibacterial Study of New 2-Mercapto-1, 3- Benzothiazole DerivativesWith Expected Biological Activity
inferred← citeshttps://doi.org/10.3390/cryst14040330openalex-snapshot
Structural Study of N-(1,3-Benzothiazol-2-yl)-4-Halobenzenesulfonylhydrazides: Hirshfeld Surface Analysis and PIXEL Calculations
inferred← citeshttps://doi.org/10.3390/foods7030040openalex-snapshot
Volatile Profile of Raw Lamb Meat Stored at 4 ± 1 °C: The Potential of Specific Aldehyde Ratios as Indicators of Lamb Meat Quality
inferred← citeshttps://doi.org/10.3390/ijms26125901openalex-snapshot
Condensation Reactions of 2-Aminothiophenoles to Afford 2-Substituted Benzothiazoles of Biological Interest: A Review (2020–2024)
inferred← citeshttps://doi.org/10.3390/molecules26216518openalex-snapshot
Benzothiazoles from Condensation of o-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review
inferred← citeshttps://doi.org/10.3390/molecules29020302openalex-snapshot
A Rare Benzothiazole Glucoside as a Derivative of ‘Albedo Bluing’ Substance in Citrus Fruit and Its Antioxidant Activity
inferred← citeshttps://doi.org/10.3390/w17192864openalex-snapshot
Materials in Water Supply Systems: Migration of Organic Compounds from Rubber Materials
inferred← citeshttps://doi.org/10.3762/bjoc.13.61openalex-snapshot
N-Propargylamines: versatile building blocks in the construction of thiazole cores
inferred← citeshttps://doi.org/10.3987/com-13-s(s)65openalex-snapshot
Regioselective Multicomponent Domino Reactions Providing Rapid and Efficient Routes to Fused Acridines
inferred← citeshttps://doi.org/10.4103/ijnpnd.ijnpnd_123_25openalex-snapshot
Nutrients and Drugs in Alzheimer’s Disease: Harnessing Antioxidants
inferred← citeshttps://doi.org/10.5155/eurjchem.13.4.426-434.2315openalex-snapshot
Synthesis, Type II diabetes inhibitory activity, antimicrobial evaluation, and docking studies of N'-arylidene-2-((7-methylbenzo[4,5]thiazolo[2,3-c] [1,2,4]triazol-3-yl)thio)acetohydrazides
inferred← citeshttps://doi.org/10.5194/acp-2021-615-ac1openalex-snapshot
Reply on RC1
inferred← citeshttps://doi.org/10.5194/acp-2021-615-ac2openalex-snapshot
Reply on RC2
inferred← citeshttps://doi.org/10.5194/acp-2021-615-rc1openalex-snapshot
Comment on acp-2021-615
inferred← citeshttps://doi.org/10.5194/acp-2021-615-rc2openalex-snapshot
Comment on acp-2021-615
inferred← citeshttps://doi.org/10.5194/acp-22-1601-2022openalex-snapshot
Marine gas-phase sulfur emissions during an induced phytoplankton bloom
inferred← citeshttps://doi.org/10.59761/rcr5163openalex-snapshot
Benzoannulation of aromatic heterocycles: advances in the 21st century
inferred← citeshttps://doi.org/10.70675/267214e1zb6b9z471bz8a96z55629b86f801openalex-snapshot
Exploiting boron-fluorine bonds for fluorination and synthesis of potential bi-modal imaging agents
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.