2001
DOI: 10.1016/s0040-4020(01)00894-8
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Brianthein A, a novel briarane-type diterpene reversing multidrug resistance in human carcinoma cell line, from the gorgonian Briareum excavatum

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Cited by 42 publications
(37 citation statements)
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“…collected from the coral reef of Ishigaki Island, Okinawa, Japan, were examined. Ten briarane metabolites, including seven new diepoxybriaranes, briaroxalides A–G ( 15 – 21 ) [14] (Table 3), along with three known analogues, brianthein A [15], violide G [16] and briarlide R [17], were isolated. The absolute configurations of 15 – 21 were further confirmed by chemical conversion and X-ray diffraction analysis [14].…”
Section: Gorgonaceamentioning
confidence: 99%
“…collected from the coral reef of Ishigaki Island, Okinawa, Japan, were examined. Ten briarane metabolites, including seven new diepoxybriaranes, briaroxalides A–G ( 15 – 21 ) [14] (Table 3), along with three known analogues, brianthein A [15], violide G [16] and briarlide R [17], were isolated. The absolute configurations of 15 – 21 were further confirmed by chemical conversion and X-ray diffraction analysis [14].…”
Section: Gorgonaceamentioning
confidence: 99%
“…[18] Brianthein A is known for reversing multidrug resistance in human carcinoma cell lines. [18] In summary, we have successfully developed a new, concise, and efficient strategy for accessing the taxane tricyclic scaffold. These new tricyclic structures are obtained using two key steps: the first step involves a palladiumcatalyzed domino reaction based on methods previously …”
Section: Angewandte Chemiementioning
confidence: 99%
“…Compound 15 represents the basic structure of brianthein A (16), which is a novel brianane-type diterpene recently isolated from the gorgonian Briareum excavatum. [18] Brianthein A is known for reversing multidrug resistance in human carcinoma cell lines. [18] In summary, we have successfully developed a new, concise, and efficient strategy for accessing the taxane tricyclic scaffold.…”
mentioning
confidence: 99%
“…[18] Brianthein A is known for reversing multidrug resistance in human carcinoma cell lines. [18] In summary, we have successfully developed a new, concise, and efficient strategy for accessing the taxane tricyclic scaffold. These new tricyclic structures are obtained using two key steps: the first step involves a palladiumcatalyzed domino reaction based on methods previously developed in our research group.…”
mentioning
confidence: 99%