Marine Drugs · 2012 · 68 citations · 26 references
Life SciencesBiochemistryPharmacologyCancer PharmacologyCoral Reef BiologyStructure-activity RelationshipsMarine Bioactive CompoundsMarine Natural ProductsMarine PharmacologyReef-building CoralsBioactive Compounds From Marine CoralsBioactive Marine MetabolitesEpoxide Hydrolase ActivityGlutathione S-transferasesMarine-derived AntioxidantsRelative Configuration DeterminationSoft Coral MetabolitesX-ray Diffraction Analysis
A chemical investigation of an ethyl acetate extract of the Red Sea soft coral Sarcophyton glaucum has led to the isolation of two peroxide diterpenes, 11(S) hydroperoxylsarcoph-12(20)-ene (1), and 12(S)-hydroperoxylsarcoph-10-ene (2), as well as 8-epi-sarcophinone (3). In addition to these three new compounds, two known structures were identified including: ent-sarcophine (4) and sarcophine (5). Structures were elucidated by spectroscopic analysis, with the relative configuration of 1 and 2 confirmed by X-ray diffraction. Isolated compounds were found to be inhibitors of cytochrome P₄₅₀ 1A activity as well as inducers of glutathione S-transferases (GST), quinone reductase (QR), and epoxide hydrolase (mEH) establishing chemo-preventive and tumor anti-initiating activity for these characterized metabolites.
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Measurement of protein using bicinchoninic acid
Pam Smith, Randall I. Krohn, Greg T. Hermanson et al. · Analytical Biochemistry · 1985 · 18.4K citations
William H. Habig, M. Pabst, William B. Jakoby · Journal of Biological Chemistry · 1974 · 18.1K citations · Full text
<i>International Tables for X-ray Crystallography</i>
Acta Crystallographica Section B · 1976 · 14.2K citations · Full text