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Highly Conjugated Norditerpenoid and Pyrroloquinoline Alkaloids with Potent PTP1B Inhibitory Activity from Nigella glandulifera
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Pharmacological and toxicological properties of Nigella sativa
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Nigellidine — A new indazole alkaloid from the seeds of Nigella sativa
inferredcites →https://doi.org/10.1016/j.bse.2013.03.003openalex-snapshot
Dolabellane-type diterpene alkaloids from Nigella glandulifera
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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.phytol.2013.07.002openalex-snapshot
Indazole-type alkaloids from the seeds of Nigella glandulifera
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Sesquiterpene xylosides from Iphiona scabra
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Isolation and structure determination of nigellicine, a novel alkaloid from the seeds of
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Small Molecule Interactions with Protein−Tyrosine Phosphatase PTP1B and Their Use in Inhibitor Design
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Determination of the Absolute Configurations of Pharmacological Natural Products via Density Functional Theory Calculations of Vibrational Circular Dichroism: The New Cytotoxic Iridoid Prismatomerin
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/10.1021/ol202994copenalex-snapshot
Dysidavarones A–D, New Sesquiterpene Quinones from the Marine Sponge Dysidea avara
inferredcites →https://doi.org/10.1039/b515476fopenalex-snapshot
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
inferredcites →https://doi.org/10.1111/j.1745-7254.2008.00737.xopenalex-snapshot
Discovery of a novel competitive inhibitor of PTP1B by high-throughput screening
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
inferredcites →https://doi.org/10.1248/cpb.60.213openalex-snapshot
Rupestines F-M, New Guaipyridine Sesquiterpene Alkaloids from Artemisia rupestris
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Phytochemicals and their effective role in the treatment of diabetes mellitus: a short review
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Protein tyrosine phosphatase 1B inhibitors as antidiabetic agents – A brief review
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Recent updates on development of protein-tyrosine phosphatase 1B inhibitors for treatment of diabetes, obesity and related disorders
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Anti-diabetic effect of three new norditerpenoid alkaloids in vitro and potential mechanism via PI3K/Akt signaling pathway
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New phenolic compounds from the seeds of Nigella glandulifera and their inhibitory activities against human cancer cells
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Optimization of microwave-assisted extraction using response surface methodology and the potential anti-diabetic efficacy of Nigella glandulifera Freyn determined using the spectrum–effect relationship
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NMR-guided isolation of alkaloids from Nigella glandulifera seeds and their bioactivities
inferred← citeshttps://doi.org/10.1016/j.phytol.2016.12.024openalex-snapshot
Pyrrolo-isoquinoline and glycosylated pyrrolidine alkaloids from Nigella glandulifera and their anti-PTP1B activity
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Nigegladines A–C, Three Thymoquinone Dimers from Nigella glandulifera
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