Results 131 to 140 of about 624 (180)
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A total synthesis of chelidonine
Tetrahedron Letters, 1980Abstract Condensation of homophthalic anhydride 3 with the Schiff base 4 is exploited as the key step in a total synthesis of the benzophenanthridine alkaloid (±)-chelidonine (8).
Mark Cushman +3 more
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ChemInform Abstract: TOTAL SYNTHESIS OF (.+‐.)‐CHELIDONINE
Chemischer Informationsdienst, 1981AbstractAus Piperonal (Ia) entstehen die Imine (Ib) und (Ic).
M. CUSHMAN +3 more
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Toxicology Letters, 2013
Poor oral bioavailability of chelidonine, a bio-active ingredient of Chelidonium majus, showing anti-cancer potentials against cancer cells with multidrug resistance, makes its optimal use rather limited. To address this problem, we encapsulated chelidonine in biodegradable poly(lactide-co-glycolide) (PLGA) polymers and evaluated nano-chelidonine's ...
Asmita Samadder +2 more
exaly +3 more sources
Poor oral bioavailability of chelidonine, a bio-active ingredient of Chelidonium majus, showing anti-cancer potentials against cancer cells with multidrug resistance, makes its optimal use rather limited. To address this problem, we encapsulated chelidonine in biodegradable poly(lactide-co-glycolide) (PLGA) polymers and evaluated nano-chelidonine's ...
Asmita Samadder +2 more
exaly +3 more sources
Modulation of multidrug resistance in cancer cells by chelidonine and Chelidonium majus alkaloids
Phytomedicine, 2013Cancer cells often develop multidrug resistance (MDR) which is a multidimensional problem involving several mechanisms and targets. This study demonstrates that chelidonine and an alkaloid extract from Chelidonium majus, which contains protoberberine and benzo[c]phenanthridine alkaloids, has the ability to overcome MDR of different cancer cell lines ...
Mahmoud Zaki El-Readi +2 more
exaly +3 more sources
The Solid‐State and Solution Conformations of (+)‐Chelidonine
Helvetica Chimica Acta, 1990AbstractThe solid‐state and solution conformations of (+)‐chelidonine (1), a biologically active alkaloid, were determined by X‐ray diffraction and 1H‐NMR spectroscopy, X‐Ray diffraction analysis revealed a conformer with B/C ‘anti‐type’ cis conjunction, a half‐chair of ring B, and a twist half‐chair of ring C.
Miyoko Kamigauchi +8 more
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In vitro and in vivo studies of the metabolic activation of chelidonine
Chemico-Biological Interactions, 2019Chelidonium majus L. is a herbal medicine widely employed in Europe and Western Asia. Chelidonine (CHE) is a major constituent of the herb and has been reported to be an inhibitor of the cytochrome P450 enzymes (CYP). The major objective of the present study was to study the metabolic pathways of CHE in order to identify potential reactive metabolites ...
Yuyang Liu +5 more
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ChemInform Abstract: TOTALSYNTHESE VON DL‐CHELIDONIN
Chemischer Informationsdienst. Organische Chemie, 1971AbstractBei Umsetzung des Na‐Salzes des Urethans (I) mit dem Benzylbromid (II) in Gegenwart von NaJ entsteht das Styrol (IIIa), das durch Bromierung und anschließende Behandlung mit K‐tert.‐butoxid und 1,5‐Diaza‐bicyclo[5 .4.0]undecen‐(5) in Hexamethylphosphorsäureamid in das Acetylen (IIIb) umgewandelt wird.
W. OPPOLZER, K. KELLER
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Mechanism‐based inactivation of cytochrome P450 2D6 by chelidonine
Journal of Biochemical and Molecular Toxicology, 2018Abstract Chelidonine (CHE) is a major bioactive constituent of greater celandine, a plant used in traditional herbal medicines. CHE has widely been used as an analgesic in clinical settings. We evaluated the inhibitory effects of CHE on human cytochrome P450 enzymes.
Yuyang Liu +4 more
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ChemInform Abstract: Crystal and Molecular Structure of Chelidonine
ChemInform, 1991AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
B. RIBAR +4 more
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Nature, 1958
IN connexion with the chromatographic separation of alkaloids of Chelidonium maius L.1, I found alkaloids giving rather big spots with a tendency to form tails. This is connected, among other things, with the dissociation constant (K B), the value of which influences the course of the chromatographic process, organic electrolytes having different ...
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IN connexion with the chromatographic separation of alkaloids of Chelidonium maius L.1, I found alkaloids giving rather big spots with a tendency to form tails. This is connected, among other things, with the dissociation constant (K B), the value of which influences the course of the chromatographic process, organic electrolytes having different ...
openaire +2 more sources

