Results 171 to 180 of about 27,748 (223)
Rosanoid diterpenoids: structural diversity, classification and biological activities. [PDF]
ADMET DMPKIbrahim SRM +5 more
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Enantioselective Synthesis of (+)-Auriculatol A. [PDF]
J Am Chem SocThompson JK +6 more
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Re-sensitization of cancer multidrug resistance through P-gp, MRP1 and BCRP modulation: advances in terpenoids based cancer therapy. [PDF]
Discov OncolPandey P +7 more
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Heterologous Overexpression and Functional Analysis of the <i>Isodon suzhouensis IsKS1</i> Gene in <i>Arabidopsis thaliana</i>. [PDF]
Curr Issues Mol BiolLiu F, Zhai K, Xie D.
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Natural Product Reports, 2010
The lasting attention that researchers have devoted to diterpenoid alkaloids is due to their various bioactivities and toxicities, structural complexity, and intriguing chemistry. From 1998 to the end of 2008, more than 300 new diterpenoid alkaloids were isolated from Nature.
Xiao-Yu Liu
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The lasting attention that researchers have devoted to diterpenoid alkaloids is due to their various bioactivities and toxicities, structural complexity, and intriguing chemistry. From 1998 to the end of 2008, more than 300 new diterpenoid alkaloids were isolated from Nature.
Xiao-Yu Liu
exaly +3 more sources
Natural product reports, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
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AbstractFor Abstract see ChemInform Abstract in Full Text.
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Natural Product Reports, 2002
The review covers the isolation and chemistry of diterpenoids including labdanes, clerodanes, pimaranes, abietanes, kauranes, gibberellins, cembranolides, taxanes and marine diterpenoids. The literature from January to December 2000 is reviewed and 157 references are cited.
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The review covers the isolation and chemistry of diterpenoids including labdanes, clerodanes, pimaranes, abietanes, kauranes, gibberellins, cembranolides, taxanes and marine diterpenoids. The literature from January to December 2000 is reviewed and 157 references are cited.
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2016
Despite a more recent isolation and chemical characterization when compared to phorbol, along with its chemical instability, limited distribution in Nature, and scarce availability, ingenol is the only Euphorbia diterpenoid that has undergone successful pharmaceutical development, with ingenol 3-angelate (ingenol mebutate, Picato(®)) entering the ...
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Despite a more recent isolation and chemical characterization when compared to phorbol, along with its chemical instability, limited distribution in Nature, and scarce availability, ingenol is the only Euphorbia diterpenoid that has undergone successful pharmaceutical development, with ingenol 3-angelate (ingenol mebutate, Picato(®)) entering the ...
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The distribution, chemistry, and molecular bioactivity of tiglianes are reviewed from the very beginning of the studies on these diterpenoids, summarizing their clinical and toxicological literature mostly in its more recent and controversial aspects, and critically analyzing various proposals for their biosynthesis.
Giovanni, Appendino, Simone, Gaeta
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Giovanni, Appendino, Simone, Gaeta
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