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Quassinoids: Phytochemistry and antitumor prospect
Phytochemistry, 2021Quassinoids, originating from the oxidative degradation of tetracyclic tirucallane triterpene, are a diverse class of secondary metabolites identifying from nature mostly in Simaroubaceae family. The crucial pharmacological activities and structural complexity of quassinoids have long fascinated scientists due to their medicinal uses, infamous toxicity,
Shu-Hui Dong +2 more
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Quassinoids from Eurycoma longifolia
Phytochemistry, 2002Three quassinoids, eurycolactone D (1), eurycolactone E (2) and eurycolactone F (3) were isolated from the roots of Eurycoma longifolia Jack. The structures of 1-3 were elucidated by spectroscopic methods, and that of 3 was further confirmed by X-ray crystallography.
Hooi Hoon Ang +2 more
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Quassinoids from Ailanthus excelsa
Phytochemistry, 2003Three quassinoids, 1, 2 and 3, 4-dihydro excelsin 3 were isolated from the stem bark of Ailanthus excelsa, along with five known quassinoids excelsin, glaucarubine, ailanthinone, glaucarubinone and glaucarubolone. The glaucarubolone has been isolated for the first time from this plant.
Ram Prakash Sharma
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Quassinoids from Eurycoma harmandiana
Phytochemistry, 2001Three quassinoids, iandonosides A and B and iandonone, were isolated from the root of Eurycoma harmandiana, along with five known quassinoids, casteloside B, 13 beta, 21-dihydroeurycomanone, chaparrinone, glaucarubolone and ailanquassin B as well as the coumarin, scopoletin. The structural elucidations were based on analyses of spectroscopic data.
Tripetch Kanchanapoom, Ryoji Kasai
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Cytotoxic quassinoids from Ailanthus altissima
Bioorganic and Medicinal Chemistry Letters, 2013Two new quassinoids, altissinol A (1) and B (7), together with 12 known quassinoids, were isolated from the 95% ethanol extract of the barks of Ailanthus altissima. The structures of the new compounds (1 and 7) were determined on the basis of the spectroscopic methods including UV, IR, HR-ESI-MS, 1D and 2D NMR.
Wen-Jing Wang +2 more
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Antifeedant activity of quassinoids
Journal of Chemical Ecology, 1984The antifeedant activity of 13 quassinoids of different structural types has been studied against the Mexican bean beetle (Epilachna varivestis Mulsant) 4th instar larvae and the southern armyworm (Spodoptera eridania Crawer) 5th instar larvae. All quassinoids tested displayed significant activity against the Mexican bean beetle and, thus, do not ...
V, Leskinen, J, Polonsky, S, Bhatnagar
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Quassinoids from Picrasma Crenata
Natural Product Research, 2003From woods of Picrasma crenata, a new stereoisomer dihydronorneoquassin was obtained together with others well knowns dihydronorneoquassin, parain, alpha-neoquassin, beta-neoquassin and quassin. The structures were determined by spectroscopic data and chemical evidence.
Claudio R, Novello +3 more
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Synthesis of cytotoxic fluorinated quassinoids
Bioorganic & Medicinal Chemistry, 1997The C-15 senecioyl side chain of brusatol was interchanged with fluorinated acyl groups, and the C-3 hydroxy group of bruceolide was esterified with fluorinated acyl chlorides. These fluorinated quassinoids 11, 12, 13, and 17 showed significant cytotoxic activity against eight human cancer cell lines including small and non-small cell lung, colon, CNS,
N, Ohno +4 more
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Tetrahedron Letters, 1982
Abstract Inactive chaparrin 1 has been converted in seven steps and in 16% overall yield to castelanone 3 which is known to inhibit significantly growth of the murine lymphocytic leukemia P-388 cell line. The methodology developed has been applied to the preparation of quassinoid analogs 15 , 16 and 17 .
Andrew J. Caruso +2 more
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Abstract Inactive chaparrin 1 has been converted in seven steps and in 16% overall yield to castelanone 3 which is known to inhibit significantly growth of the murine lymphocytic leukemia P-388 cell line. The methodology developed has been applied to the preparation of quassinoid analogs 15 , 16 and 17 .
Andrew J. Caruso +2 more
openaire +1 more source

