Results 91 to 100 of about 436 (127)
Some of the next articles are maybe not open access.

Cytotoxic and Antitumor Constituents in Pericarps ofMallotus japonicus

Planta Medica, 1990
A variety of phloroglucinol derivatives isolated from the pericarps of Mallotus japonicus were assessed for growth inhibiting activity against human larynx (HEp-2) and lung (PC-13) carcinoma cells as well as mouse B16 melanoma, leukemia P388, and L5178Y cells. Most of these derivatives were proved to be significantly cytotoxic in culture.
M, Arisawa   +3 more
openaire   +2 more sources

Studies on Cytotoxic Constituents in Pericarps of Mallotus japonicus, Part II

Journal of Natural Products, 1985
Two new phloroglucinol derivatives, mallotolerin (8) and mallotochromanol (9), were isolated from the cytotoxic fraction of the pericarps of Mallotus japonicus. The new derivatives were identified as 3-(3-methyl-2-hydroxybut-3-enyl)-5-(3-acetyl-2,4-dihydroxy-5-me thy l-6- methoxybenxyl)-phlorbutyrophenone (8) and 8-acetyl-5,7-dihydroxy-6-(3-acetyl-2,4 ...
M, Arisawa   +6 more
openaire   +3 more sources

Phloroglucinol derivatives from fruits of Mallotus japonicus

Phytochemistry, 1983
Abstract Two new rottlerin-like phloroglucinol derivatives were isolated from the fruits of Mallotus japonicus and identified by chemical and spectral data as 3-(3, 3-dimethylallyl)-5-(3-acetyl-2, 4-dihydroxy-5-methyl-6-methoxybenzyl)-phloracetophenone and 3-(3-methyl-2-hydroxybut-3-enyl)-5-(3-acetyl-2, 4-dihydroxy-5-methyl-6-methoxybenzyl ...
Nobuharu Shigematsu   +2 more
openaire   +1 more source

Phenol glucoside gallates from Mallotus japonicus

Phytochemistry, 1989
Abstract Five phenol glucoside gallates were isolated from Mallotus japonicus , and their structures characterized by chemical and spectroscopic means as 4-hydroxy-2-methoxyphenol 1- O -β- d -(6′- O -galloyl)glucoside, 4-hydroxy-3-methoxyphenol 1- O -β- d -(2′,6′-di- O -galloyl)glucoside, 4-hydroxy-3-methoxyphenol 1- O -β- d -2′,3′,6′-tri- O ...
Reiko Saijo   +2 more
openaire   +1 more source

Further phloroglucinol derivatives in the fruits of Mallotus japonicus

Phytochemistry, 1985
Abstract Two new rottlerin-like phloroglucinol derivatives were detected from the fruits of Mallotus japonicus and identified as 3-(3,3-dimethylallyl)-5-(3-acetyl-2,4-dihydroxy-5-methyl-6-methoxybenzyl)-phlorobutyrophenone and -phloroisobutyrophenone by spectral studies.
Isao Kouno   +3 more
openaire   +1 more source

Structure and biosynthesis of malloprenols from Mallotus japonicus

Phytochemistry, 1980
Abstract The mallo prenol isolated from the leaves of Mallotus japonicus was elucidated to be a mixture of (2Z,6Z, 10Z, 14Z, 18Z, 22Z, 26E, 30E, 34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaen-1-ol and its C45- and C55-homologues and not the previously reported structure.
Takayuki Suga   +2 more
openaire   +1 more source

Glucosylation of salicylic acid by cell suspension cultures of Mallotus japonicus

Plant Cell Reports, 1990
Salicylic acid was converted into its O-glucoside when administered to cell suspension cultures of Mallotus japonicus. The efficiency of the glucosylation was highest in the cells grown in Linsmaier-Skoog medium containing 1 μM 2,4-dichlorophenoxy-acetic acid at any scale of culture (7 ml - 3 1).
Y, Umetani   +4 more
openaire   +2 more sources

A review of the biological activity and chemistry of Mallotus japonicus (Euphorbiaceae)

Phytomedicine, 1994
Biological and pharmacological activities of Mallotus japonicus (Euphorbiaceae) are reviewed. Chemical constituents, biological and pharmacological activities of tannins and related compounds, cardenolides, cytotoxicity, antitumor and antitumor-promoting effects, antiviral activity, and inhibition of HIV-RT activity of this plant are described.
openaire   +2 more sources

ent-Labdane Diterpenes from the Stems of Mallotus japonicus

Journal of Natural Products, 2013
Eight new ent-labdane diterpenoids, mallonicusins A-H (1-8), were isolated from the stems of Mallotus japonicus. Their structures, including the absolute configurations, were determined by extensive analyses of spectroscopic data and the ECD spectra of the Pr(FOD)₃ complex of substrates in CCl₄. The absolute configuration of compound 1 was confirmed by
Li, De-Zheng   +6 more
openaire   +3 more sources

Antitumor-Promoting Activity of Mallotojaponin, a Major Constituent of Pericarps of Mallotus japonicus

Oncology, 2009
Mallotojaponm, a major constituent of the pericarps of Mallotus japonicus (Euphorbiaceae), inhibited the action of tumor promoter in vitro and in vivo; it inhibited tumor promoter-enhanced phospholipid metabolism in cultured cells, and also suppressed the promoting effect of 12-O-tetradecanoylphorbol-13-acetate on skin tumor formation in mice initiated
Y, Satomi   +3 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy