Results 91 to 100 of about 203 (114)

Nanangenines: drimane sesquiterpenoids as the dominant metabolite cohort of a novel Australian fungus, Aspergillus nanangensis. [PDF]

Beilstein J Org Chem, 2019
Lacey HJ, Gilchrist CLM, Crombie A, Kalaitzis JA, Vuong D, Rutledge PJ, Turner P, Pitt JI, Lacey E, Chooi YH, Piggott AM.   +10 more
europepmc   +1 more source

Producing Novel Fibrinolytic Isoindolinone Derivatives in Marine Fungus Stachybotrys longispora FG216 by the Rational Supply of Amino Compounds According to Its Biosynthesis Pathway. [PDF]

Mar Drugs, 2017
Yin Y, Fu Q, Wu W, Cai M, Zhou X, Zhang Y.   +5 more
europepmc   +1 more source

Unveiling Drimenol: A Phytochemical with Multifaceted Bioactivities. [PDF]

Plants (Basel)
Yang Z, Chan KW, Abu Bakar MZ, Deng X.
europepmc   +1 more source

In-silico analyses of sesquiterpene-related compounds on selected Leishmania enzyme-based targets. [PDF]

Molecules, 2014
Bernal FA, Coy-Barrera E.
europepmc   +1 more source

Two Decades of Research on Marine-Derived <i>Alternaria</i>: Structural Diversity, Biomedical Potential, and Applications. [PDF]

Mar Drugs
Youssef DTA, Alqarni AS, Shaala LA, Bagalagel AA, Fadil SA, Omar AM, Rateb ME.   +6 more
europepmc   +1 more source

Biogenic trypanocidal sesquiterpenes: lead compounds to design future trypanocidal drugs - a mini review. [PDF]

Daru, 2013
Saeidnia S, Gohari AR, Haddadi A.
europepmc   +1 more source

Unusual Sesquiterpenes from <i>Streptomyces olindensis</i> DAUFPE 5622. [PDF]

J Nat Prod
Chagas FO, Garrido LM, Conti R, Borges RM, Bielinski VA, Padilla G, Pupo MT.   +6 more
europepmc   +1 more source

Drimanes and Other Terpenoids from the FernThelypteris hispidula (Decne.)Reed [PDF]

Chemistry and Biodiversity, 2005
The drimane‐type sesquiterpenoids (−)‐polygodial (1), (−)‐isopolygodial (4), drimenin (5), and isodrimenin (6) were isolated from a pungent Argentine collection of the fern Thelypteris hispidula, along with other terpenoids.
Alicia Bardon
exaly   +2 more sources

Synthesis of Drimanes from (+)-Larixol [PDF]

Synthesis, 2000
The selective transformation of the side chain of larixol 1 to a functionalized one-carbon moiety leads to 6,8-diacetoxydrimenal 13, which was converted to the drimanes (-)-albrassitriol (2), (-)-drimenol (3), (-)-uvidin C (4) and (-)-epi-albrassitriol ...
Aede De Groot, Christophe Morin
exaly   +2 more sources

Synthesis of biologically active drimanes from (−)-sclareol [PDF]

Tetrahedron Letters, 1994
Alejandro Fernández Barrero, Joaquin Altarejos, Sofia Salido   +2 more
exaly   +2 more sources