Results 91 to 100 of about 492 (130)
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ChemInform Abstract: APORPHINES. 31. SYNTHESIS AND ANTITUMOR ACTIVITY OF APORPHINE NITROGEN MUSTARDS
Chemischer Informationsdienst, 1981AbstractDargestellt werden die Verbindungen (I), die Antitumor‐Wirkung besitzen.
J. L. NEUMEYER +4 more
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Topoisomerase II inhibition by aporphine alkaloids
Biochemical Pharmacology, 1999The aporphine alkaloids (+)-dicentrine and (+)-bulbocapnine are non-planar molecules lacking features normally associated with DNA binding by intercalation or minor groove binding. Surprisingly, dicentrine showed significant activity as a topoisomerase II (EC 5.99.1.3) inhibitor and also was active in a DNA unwinding assay.
S H, Woo +3 more
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Antitumor aporphine alkaloids from Thalictrum wangii
Fitoterapia, 2018Nine new isoquinoline alkaloids, including two proaporphine (1-2), three aporphine (3-5), two oxoaporphine (6-7), and two seco-bisbenzylisoquinoline (8-9), together with three known alkaloids (10-12) were isolated from the whole plant of Thalictrum wangii. Their structures were established on the basis of spectroscopic data. The antitumor activities of
Qiong, Jin +11 more
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Chemischer Informationsdienst, 1977
AbstractAus den Morphinen (Ia) und (Ib) entstehen mit HCl die Umlagerungsprodukte (IIa) und (IIb).
F. E. GRANCHELLI +3 more
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AbstractAus den Morphinen (Ia) und (Ib) entstehen mit HCl die Umlagerungsprodukte (IIa) und (IIb).
F. E. GRANCHELLI +3 more
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Journal of Medicinal Chemistry, 1993
The subject compounds were prepared as a part of a continuing structure-activity study of the contrasting actions (agonism-antagonism) of (+)- and (-)-11-hydroxy-10-methylaporphine at serotonin (5-HT1A) receptors. None of the targeted nonoxygenated aporphine derivatives demonstrated significant activity in assays for any effects at serotonin 5-HT1A ...
J G, Cannon +4 more
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The subject compounds were prepared as a part of a continuing structure-activity study of the contrasting actions (agonism-antagonism) of (+)- and (-)-11-hydroxy-10-methylaporphine at serotonin (5-HT1A) receptors. None of the targeted nonoxygenated aporphine derivatives demonstrated significant activity in assays for any effects at serotonin 5-HT1A ...
J G, Cannon +4 more
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Biological Mass Spectrometry, 1979
A series of synthetic, semisynthetic and naturally occurring aporphine alkaloids were converted to the O-trimethylsilyl derivatives, and analyzed by gas chromatography mass spectrometry. A discussion of structurally informative fragment ions along with gas chromatographic data is presented.
J F, Green +3 more
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A series of synthetic, semisynthetic and naturally occurring aporphine alkaloids were converted to the O-trimethylsilyl derivatives, and analyzed by gas chromatography mass spectrometry. A discussion of structurally informative fragment ions along with gas chromatographic data is presented.
J F, Green +3 more
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Dimeric Aporphine-Benzylisoquinoline and Aporphine-Pavine Alkaloids
Journal of Natural Products, 1979Hélène, Guinaudeau +2 more
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Aporphine and Morphinan Alkaloids
1968The aporphine and morphinan alkaloids can be conveniently considered together because they often occur together in the same plant, and also because in terms of structure they can both be derived from a benzylisoquinoline skeleton by additional ring closures:
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Photochemical synthesis of aporphines
The Journal of Organic Chemistry, 1971S M, Kupchan +3 more
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