Results 161 to 170 of about 1,758 (205)
Seven diarylheptanoids and three 3-keto-steroids were detected in the acetone extract obtained from Zostera marina L. collected at the coast of the German Baltic Sea.
Alfonso Mangoni, Christian Zidorn
exaly +2 more sources
Diarylheptanoids from Alnus incana
Thirteen known (1–13) and a previously undescribed diarylheptanoid 14, named cis-oregonoyl A, were isolated from Alnus incana bark using standard dry column flash silica gel chromatography followed by reversed-phase semipreparative HPLC. Structure elucidation was performed on the basis of 1H and 13C, COSY, NOESY, HSQC, and HMBC NMR experiments ...
Novaković, Miroslav +6 more
openaire +3 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Phytochemistry Letters, 2021
Abstract Two pairs of enantiomeric diarylheptanoid-phenylpropanoid adducts bearing a cyclohexenone core, (±)-saccardianones A and B (1 and 2), an alkaloidal diarylheptanoid-phenylpropanoid adduct bearing a 4-piperidone core, (±)-saccardianine A (3), a pair of enantiomeric dimeric diarylheptanoid alkaloids bearing a tetrahydropyridine core ...
Zi-Yang Chan +9 more
openaire +1 more source
Abstract Two pairs of enantiomeric diarylheptanoid-phenylpropanoid adducts bearing a cyclohexenone core, (±)-saccardianones A and B (1 and 2), an alkaloidal diarylheptanoid-phenylpropanoid adduct bearing a 4-piperidone core, (±)-saccardianine A (3), a pair of enantiomeric dimeric diarylheptanoid alkaloids bearing a tetrahydropyridine core ...
Zi-Yang Chan +9 more
openaire +1 more source
Chemopreventive potential of cyclic diarylheptanoids
Bioorganic & Medicinal Chemistry, 2002Eleven cyclic diarylheptanoids and seven related compounds were screened as potential antitumor promoters by using the in vitro short-term 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced Epstein-Barr virus early antigen (EBV-EA) activation assay. In addition, the cyclic diarylheptanoid myricanone (2) was examined for antitumor initiating activity in
Junko, Ishida +6 more
openaire +2 more sources
Antihepatotoxic actions of gingerols and diarylheptanoids
Journal of Ethnopharmacology, 1985The antihepatotoxic effects of gingerols, shogaols, diarylheptanoids and related analogues were assessed utilizing carbon tetrachloride- and galactosamine-induced cytotoxicity in primary cultured rat hepatocytes. Most congeners exhibited significant actions in these assay methods.
H, Hikino +8 more
openaire +2 more sources
Diarylheptanoids of Centrolobium species
Phytochemistry, 1970Abstract The heartwoods of two Centrolobium species (Leguminosae) were examined. C. robustum Mart. was found to contain piceatannol, (-)-centrolobine (VIIa), (-)-de- O -methylcentrolobine (VIIb) and (-)-centrolobol (VI). C. tomentosum Benth. was found to contain (+)-centrolobine (IXa), (+)-de- O -methylcentrolobine (IXb) and (+)-centrolobol ...
A. Aragão Craveiro +3 more
openaire +1 more source
Synthesis of a diarylheptanoid, (+)-centrolobine
Tetrahedron: Asymmetry, 2010A chiron approach for the total synthesis of (+)-centrolobine has been described from the commercially available aldehyde 3 employing an acid-catalyzed stereoselective formation of tetrahydropyran ring as the key step. The desired molecule was accomplished in eight steps with 62% overall yield.
Ch. Raji Reddy +2 more
openaire +1 more source
Diarylheptanoid: A privileged structure in drug discovery
Fitoterapia, 2020Privileged structures are widely used in the process of drug design, and provide an effective template in medicinal chemistry. Diarylheptanoids are a class of structurally distinctive compounds with a wide variety of bioactivity, raising keenly interest in the past decades.
De-Juan, Sun +6 more
openaire +2 more sources
Synthesis of gingerol and diarylheptanoids
Tetrahedron: Asymmetry, 2011Abstract The synthesis of gingerol 1 and related compounds 2 – 5 along with diarylheptanoids 6 – 8 has been accomplished using a Keck allylation, Crimmins’ aldol reaction, aldehyde coupling with acetylene, and chelation controlled reductions as the key reactions.
Gowravaram Sabitha +4 more
openaire +1 more source
Journal of Natural Products, 2002
Two new diarylheptanoids (1, 2) and seven new diarylheptanoid glucosides (3-9) were isolated from the rhizomes of Tacca chantrieri. Their structures were determined by spectroscopic analysis, including 2D NMR data, and the results of hydrolytic cleavage.
Akihito, Yokosuka +3 more
openaire +2 more sources
Two new diarylheptanoids (1, 2) and seven new diarylheptanoid glucosides (3-9) were isolated from the rhizomes of Tacca chantrieri. Their structures were determined by spectroscopic analysis, including 2D NMR data, and the results of hydrolytic cleavage.
Akihito, Yokosuka +3 more
openaire +2 more sources

