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In Vitro Human Dihydroorotate Dehydrogenase Inhibitory, Anti-inflammatory and Cytotoxic Activities of Alkaloids from the Seeds of Nigella glandulifera
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Structural chemistry of polycyclic heteroaromatic compounds. Part 9. Photoelectron spectra and electronic structures of anellated carbazoles. Extension of Clar's aromatic sextet model to hetarenes
inferredcites →https://doi.org/10.1016/0040-4039(95)00210-4openalex-snapshot
Nigellidine — A new indazole alkaloid from the seeds of Nigella sativa
inferredcites →https://doi.org/10.1016/j.bmc.2010.06.106openalex-snapshot
Design, synthesis, and cholesterol-lowering efficacy for prodrugs of berberrubine
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Biaryl analogues of teriflunomide as potent DHODH inhibitors
inferredcites →https://doi.org/10.1016/j.bse.2013.03.003openalex-snapshot
Dolabellane-type diterpene alkaloids from Nigella glandulifera
inferredcites →https://doi.org/10.1016/j.phytol.2013.01.004openalex-snapshot
Acylated dolabellane-type diterpenes from Nigella sativa seeds with triglyceride metabolism-promoting activity in high glucose-pretreated HepG2 cells
inferredcites →https://doi.org/10.1016/j.rvsc.2004.03.002openalex-snapshot
Mechanisms of the hypoglycaemic and immunopotentiating effects of Nigella sativa L. oil in streptozotocin-induced diabetic hamsters
inferredcites →https://doi.org/10.1016/j.tet.2007.01.010openalex-snapshot
Synthesis of 3-substituted indazoles and benzoisoxazoles via Pd-catalyzed cyclization reactions: application to the synthesis of nigellicine
inferredcites →https://doi.org/10.1016/s0031-9422(97)00296-3openalex-snapshot
Flavonol triglycosides from seeds of Nigella sativa
inferredcites →https://doi.org/10.1016/s0162-3109(00)00191-0openalex-snapshot
Leflunomide: an immunomodulatory drug for the treatment of rheumatoid arthritis and other autoimmune diseases
inferredcites →https://doi.org/10.1016/s0378-8741(01)00342-7openalex-snapshot
Effects of Nigella sativa fixed oil on blood homeostasis in rat
inferredcites →https://doi.org/10.1016/s0926-6690(01)00096-6openalex-snapshot
Seed yield, yield components, oil content and essential oil content and composition of Nigella sativa L. and Nigella damascena L.
inferredcites →https://doi.org/10.1021/jf901632jopenalex-snapshot
Tobacco Mosaic Virus (TMV) Inhibitors from Picrasma quassioides Benn
inferredcites →https://doi.org/10.1021/jm300630popenalex-snapshot
Discovery of Diverse Human Dihydroorotate Dehydrogenase Inhibitors as Immunosuppressive Agents by Structure-Based Virtual Screening
inferredcites →https://doi.org/10.1021/np800172xopenalex-snapshot
Nigellidine-4-O-sulfite, the First Sulfated Indazole-Type Alkaloid from the Seeds of Nigella sativa
inferredcites →https://doi.org/10.1021/ol036239copenalex-snapshot
Novel Dolabellane-Type Diterpene Alkaloids with Lipid Metabolism Promoting Activities from the Seeds of Nigella s ativa
inferredcites →https://doi.org/10.1074/jbc.r400007200openalex-snapshot
Mammalian Pyrimidine Biosynthesis: Fresh Insights into an Ancient Pathway
inferredcites →https://doi.org/10.1080/10412905.2004.9698690openalex-snapshot
Essential Oils ofNigella sativaL. andNigella damascenaL. Seed
inferredcites →https://doi.org/10.1089/jmf.2007.0600openalex-snapshot
Evaluation of Antimicrobial and Anti-Inflammatory Activities of Seed Extracts from Six Nigella Species
inferredcites →https://doi.org/10.1248/cpb.52.454openalex-snapshot
A New Alkaloid and Its Artificial Derivative with an Indazole Ring from Nigella glandulifera
inferredcites →https://doi.org/10.1248/cpb.52.494openalex-snapshot
Nigellamines A3, A4, A5, and C, New Dolabellane-Type Diterpene Alkaloids, with Lipid Metabolism-Promoting Activities from the Egyptian Medicinal Food Black Cumin
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.2022.113165zenodo-depositor-declared
The ethnobotany, phytochemistry, and biological properties of Nigella damascena – A review
inferred← citeshttps://doi.org/10.1002/adsc.201901422openalex-snapshot
Selective Synthesis of Indazolo[2,3‐a]quinolines via Rh(III)‐Catalyzed Oxidant‐Free [4+2] or [5+1] Annulation of 2‐Aryl‐2H‐indazoles with α‐Diazo Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/cbdv.202300037openalex-snapshot
Structural Diversity, Spectral Data, and Pharmacological Effects of Genus Nigella
inferred← citeshttps://doi.org/10.1002/open.202400486openalex-snapshot
Unexpected Tellurohalogenation of Terminal N‐Alkynyl (Alkenyl) Derivatives of 4‐Functionalized Pyrazoles
inferred← citeshttps://doi.org/10.1007/s00044-020-02558-9openalex-snapshot
A comprehensive review of ethnopharmacological uses, phytochemistry, biological activities, and future prospects of Nigella glandulifera
inferred← citeshttps://doi.org/10.1007/s10600-025-04823-yopenalex-snapshot
Alkaloid Constituents of Nigella glandulifera
inferred← citeshttps://doi.org/10.1007/s11033-025-10459-6openalex-snapshot
Shikonin a potent phytotherapeutic: a comprehensive review on metabolic reprogramming to overcome drug resistance in cancer
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114714openalex-snapshot
Saponins from Nigella glandulifera seeds attenuate collagen-induced rheumatoid arthritis in rats via the OPG/RANKL/NF-κB and Ang/Tie-2 pathways
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114688openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114693openalex-snapshot
NMR-guided isolation of alkaloids from Nigella glandulifera seeds and their bioactivities
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c01173openalex-snapshot
Phytocompounds Targeting Metabolic Reprogramming in Cancer: An Assessment of Role, Mechanisms, Pathways, and Therapeutic Relevance
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Polysubstituted Cyclopentene Benzamides and Dianthramide Alkaloids from Delphinium anthriscifolium Hance
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Structurally Diverse Labdane Diterpenoids from Leonurus japonicus and Their Anti-inflammatory Properties in LPS-Induced RAW264.7 Cells
inferred← citeshttps://doi.org/10.1039/d0ob02060eopenalex-snapshot
Rhodium-catalyzed oxidative annulation of 1 H -indazoles with alkynes for the synthesis of indazolo[3,2- a ]isoquinolines via C–H bond functionalization
inferred← citeshttps://doi.org/10.1039/d2ra02628gopenalex-snapshot
Chemical constituents from the seeds of Nigella glandulifera and their hypoglycemic activities
inferred← citeshttps://doi.org/10.1080/10286020.2021.1976159openalex-snapshot
Centrantheroside F, a new ionone glycoside from Centranthera grandiflora
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Recent Progress on Chemical Constituents and Pharmacological Effects of the Genus Nigella
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Phytochemical Characterization, Antioxidant, and Anti-Proliferative Activities of Wild and Cultivated Nigella damascena Species Collected in Sicily (Italy)
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Screening of Monoamine Oxidase Inhibitors from Seeds of Nigella glandulifera Freyn et Sint. by Ligand Fishing and Their Neuroprotective Activity
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