Results 141 to 150 of about 1,359 (207)
Vincristine Beyond Mitosis: Uncovering a First Link to G-Quadruplex DNA in Cancer Cells. [PDF]
Di Porzio A +14 more
europepmc +1 more source
UV-B and far-red light shape morphological and phytochemical responses in kratom. [PDF]
Zhang M +6 more
europepmc +1 more source
Biomanufacture of diverse chemicals in yeast. [PDF]
Chen R +5 more
europepmc +1 more source
Asymmetric Formal Synthesis of (+)-Catharanthine via Desymmetrization of Isoquinuclidine
Although (+)-catharanthine is an attractive alkaloid for both clinical research and organic synthetic chemistry, only a limited number of approaches for its catalytic asymmetric synthesis exist. Herein, we describe a novel strategy for synthesizing a chiral intermediate of (+)-catharanthine via phosphoric acid-catalyzed asymmetric desymmetrization of a
Masato Kono +10 more
openaire +4 more sources
Mechanism of interaction of vinca alkaloids with tubulin: catharanthine and vindoline
The interactions of the vinca alkaloid drugs catharanthine and vindoline with tubulin have been investigated and compared with those of vinblastine and vincristine. Both drugs were found to be less effective in bringing about the inhibition of tubulin self-assembly into microtubules than vincristine and vinblastine, the drug to protein molar ratio ...
V, Prakash, S N, Timasheff
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A Rapid Procedure for the Isolation of Catharanthine, Vindoline and Vinblastine
Planta Medica, 1983Null Atta-Ur-Rahman
exaly +3 more sources
Tetrahedron, 1998
Abstract Two new analogs of catharanthine have been synthesized in racemic form. They differ from catharanthine in the fusion of the indole ring to the non-aromatic portion of the iboga skeleton, with the [2,3] fusion present in catharanthine being replaced by [2,1] and [3,2] fusions.
Richard J Sundberg +4 more
openaire +1 more source
Abstract Two new analogs of catharanthine have been synthesized in racemic form. They differ from catharanthine in the fusion of the indole ring to the non-aromatic portion of the iboga skeleton, with the [2,3] fusion present in catharanthine being replaced by [2,1] and [3,2] fusions.
Richard J Sundberg +4 more
openaire +1 more source
ChemInform, 1998
AbstractChemInform 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.
R. J. SUNDBERG +4 more
openaire +1 more source
AbstractChemInform 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.
R. J. SUNDBERG +4 more
openaire +1 more source
Oxidative fragmentation of catharanthine by dichlorodicyanoquinone
The Journal of Organic Chemistry, 1991Oxidation of catharanthine by DDQ leads to formation of products resulting from fragmentation of the C16-C21 bond as well as C3 and C5 dehydrogenation. Among the products are compounds containing a cyclopropane ring formed by bonding between C14 and C16.
Richard J. Sundberg +3 more
openaire +1 more source

