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Phytomedicine
BACKGROUND Chelidonium majus l., a traditional herbal medicine listed in the Pharmacopoeia of China (2025), has remarkable anticancer properties. Chelidonine (CHE), its primary bioactive alkaloid, can inhibit the proliferation of breast cancer (BC) cells;
Kaili Liu +7 more
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BACKGROUND Chelidonium majus l., a traditional herbal medicine listed in the Pharmacopoeia of China (2025), has remarkable anticancer properties. Chelidonine (CHE), its primary bioactive alkaloid, can inhibit the proliferation of breast cancer (BC) cells;
Kaili Liu +7 more
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Chemico-Biological Interactions
Chelidonium majus L. (C. majus) is a notable medicinal plant, esteemed for its antispasmodic and analgesic properties. The principal bioactive compound, chelidonine, acts similarly to morphine as an anesthetic analgesic and inhibits tumor growth by ...
Jin Gu +6 more
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Chelidonium majus L. (C. majus) is a notable medicinal plant, esteemed for its antispasmodic and analgesic properties. The principal bioactive compound, chelidonine, acts similarly to morphine as an anesthetic analgesic and inhibits tumor growth by ...
Jin Gu +6 more
semanticscholar +1 more source
Design, synthesis and apoptosis-related antiproliferative activities of chelidonine derivatives.
Bioorganic & Medicinal Chemistry Letters, 2019To get chelidonine derivatives with enhanced antiproliferative activity and selectivity, a series of nitric oxide donating derivatives (10a-f and 11a-j) were designed, synthesized and biologically evaluated.
Xue-Yan Huang +9 more
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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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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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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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Absolute configuration and chiroptical properties of chelidonine and tetrahydroberberine alkaloids
Tetrahedron, 1970Abstract The CD within the 1 L b band of tetrahydroberberine alkaloids is rationalized with the aid of a rule taking into account the chirality of the second sphere, a sector rule for third (fourth, …) sphere contributions. Extension to the 1 L a , band CD is proposed.
G. Snatzke +4 more
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Preliminary pharmacological evaluation of chelidonine in rodents.
Polish journal of pharmacology and pharmacy, 1990Our studies showed that the chelidonine administered intraperitoneally (ip) exerted an inhibitory effect on the central nervous system of the rodents. It was shown that chelidonine depressed the spontaneous and explorative motor activities, decreased body temperature, potentiated the action of hypnotics and increased sedation in reserpinized mice ...
E, Jagiełło-Wójtowicz +3 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

