Results 131 to 140 of about 1,327 (175)
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Diarylheptanoids: Potent Anticancer Agents
Clinical Cancer Drugs, 2021Abstract: Diarylheptanoids are widely distributed among species belonging to the family Betulaceae. Being highly polar in nature, they can either be isolated from plants by using sophisticated chromatographic techniques or can be synthesized in the laboratory.
Rabia Hameed
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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
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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
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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
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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
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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
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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
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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
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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
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Diarylheptanoids from the rhizomes of Zingiber officinale
Phytochemistry, 2004Seven new diarylheptanoids, i.e., (3S,5S)-3,5-diacetoxy-1,7-bis(4-hydroxy-3-methoxyphenyl)heptane, (3R,5S)-3-acetoxy-5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)heptane, (3R,5S)-3,5-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)heptane, (5S)-5-acetoxy-1,7-bis(4-hydroxy-3-methoxyphenyl)heptan-3-one, 5-hydroxy-1-(3,4-dihydroxy ...
Jianping, Ma +3 more
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Diarylheptanoids from Alpinia officinarum
Journal of Asian Natural Products Research, 2006A new diarylheptanoid, along with five known diarylheptanoids, was isolated from the rhizomes of Alpinia officinarum (Zingiberaceae). The structure of the new compound was determined to be trans,trans-1(3'-methoxy-4'-hydroxyphenyl)-7-phenyl-5-ol-4,6-dien-3-heptanone on the basis of spectral and chemical evidence.
N, An, L-Z, Xu, Z-M, Zou, S-L, Yang
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