2013
DOI: 10.22146/ijc.21279
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A NEW CYTOTOXIC DOLABELLANE FROM THE INDONESIAN SOFT CORAL <i>Anthelia</i> sp.

Abstract: One new dolabellane (1) and two known diterpenoids stolonidiol (2)

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Cited by 4 publications
(14 citation statements)
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“…Therefore, the current primary issues in marine conservation, such as the loss of biodiversity through over-exploitation and habitat degradation, can be overcome. Additional information can be found in the Supplementary Materials [95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,148,149,150,151,152,153,154,…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, the current primary issues in marine conservation, such as the loss of biodiversity through over-exploitation and habitat degradation, can be overcome. Additional information can be found in the Supplementary Materials [95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,148,149,150,151,152,153,154,…”
Section: Discussionmentioning
confidence: 99%
“…In another chemical investigation, one new dolabellane ( 119 ) and two known diterpenoids (stolonidiol ( 120 ) and clavinflol B ( 121 )) (Figure 15) were isolated from the coral Anthelia sp. Among them, compound 119 exhibited cytotoxicity against NBT-T2 cells at 10 μg/mL (31.25 µM), while known compounds 120 and 121 showed stronger cytotoxicity at 1.0 and 0.5 μg/mL (2.98 and 1.34 µM), respectively [108]. Chao et al [109] isolated three new steroidal carboxylic acids, paraminabic acids A–C, from the coral Paraminabea acronocephala .…”
Section: Bioactive Compounds From Coralmentioning
confidence: 99%
“…Stolonidiol showed cytotoxicity at 1 g/mL and was identified from its 1 H NMR spectrum and specific rotation. Further chromatographic separation resulted in the isolation of the known clavinflol B [18] and a dolabellane [3], and a new minor constituent 1, whose structure ( Figure 1) is the subject of this note. hydroxyl groups.…”
mentioning
confidence: 97%
“…Most of them lack physical defense and therefore have been known to develop chemical defense [1]. The metabolites within the soft corals have been extensively studied resulting in the identification of a diverse array of structurally unique and biologically active terpenoids including eunicellin [2], dolabellane [3], cembrane [4], casbane [5],…”
mentioning
confidence: 99%
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