The Synthesis of Two New Metabolites of Catecholamines: 3,4-Dihydroxyphenylethyleneglycol and 4-Hydroxy-3-methoxyphenylethyleneglycol1

1963 ◽  
Vol 6 (5) ◽  
pp. 607-608 ◽  
Author(s):  
J. D. Benigni ◽  
Anthony J. Verbiscar
Keyword(s):  
1955 ◽  
Vol 212 (1) ◽  
pp. 449-460 ◽  
Author(s):  
David K. Fukushima ◽  
Norma S. Leeds ◽  
H. Leon Bradlow ◽  
Theodore H. Kritchevsky ◽  
Madeleine B. Stokem ◽  
...  

1996 ◽  
Vol 51 (7-8) ◽  
pp. 493-499 ◽  
Author(s):  
Annette Wunder ◽  
Timm Anke ◽  
Dörte Klostermeyer ◽  
Wolfgang Steglich

Abstract Three known sesquiterpenoids of the lactarane and secolactarane type, deoxylactarorufin A (1), blennin A (2) and blennin C (3), have been obtained from cultures of Lentinellus cochleatus (Basidiomycetes) together with the new metabolites (Z)-2-chloro-3-(4-me-thoxyphenyl)-2-propen-l-ol (4) and lentinellone (5), a protoilludane derivative. The structures were determined by spectroscopic investigations. 1, 2 and 3 are potent inhibitors of leukotriene biosynthesis in rat basophilic leukemia (RBL-1) cells and human peripheral blood leukocytes (PBL).


Microbiology ◽  
2009 ◽  
Vol 78 (4) ◽  
pp. 428-432 ◽  
Author(s):  
S. P. Chetverikov ◽  
O. N. Loginov

1988 ◽  
Vol 41 (10) ◽  
pp. 1316-1330 ◽  
Author(s):  
A. D. ARGOUDELIS ◽  
L. BACZYNSKYJ ◽  
S. A. MIZSAK ◽  
F. B. SHILLIDAY
Keyword(s):  

2014 ◽  
Vol 37 (3) ◽  
pp. 928-935 ◽  
Author(s):  
Ahmed Abdel-Lateff ◽  
Walied M. Alarif ◽  
Hany Z. Asfour ◽  
Seif-Eldin N. Ayyad ◽  
Alaa Khedr ◽  
...  

1991 ◽  
Vol 29 (4) ◽  
pp. 265-274 ◽  
Author(s):  
T. Fujitani ◽  
M. Yoneyama ◽  
A. Ogata ◽  
T. Ueta ◽  
K. Mori ◽  
...  
Keyword(s):  

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3070
Author(s):  
Mariela Gonzalez-Ramirez ◽  
Ivan Limachi ◽  
Sophie Manner ◽  
Juan C. Ticona ◽  
Efrain Salamanca ◽  
...  

In addition to the trichilianones A–D recently reported from Trichilia adolfi, a continuing investigation of the chemical constituents of the ethanol extract of the bark of this medicinal plant yielded the five new limonoids 1–5. They are characterized by having four fused rings and are new examples of prieurianin-type limonoids, having a ε-lactone which in 4 and 5 is α, β- unsaturated. The structures of the isolated metabolites were determined by high field NMR spectroscopy and HR mass spectrometry. The new metabolites were shown to have the ε-lactone fused with a tetrahydrofuran ring which is connected to an oxidized hexane ring joined with a cyclo-pentanone having a 3-furanyl substituent. As the crude extract possesses antileishmanial activity, the compounds were assayed for cytotoxic and antiparasitic activities in vitro in murine macrophage cells (raw 264.7 cells) and in Leishmania amazoniensis as well as L. braziliensis promastigotes. Metabolites 1–3 and 5 showed moderate cytotoxicity (between 30–94 µg/mL) but are not responsible for the antileishmanial effect of the extract.


1984 ◽  
Vol 67 (2) ◽  
pp. 406-412 ◽  
Author(s):  
Perer Mohr ◽  
Christoph Tamm ◽  
Werner Zürcher ◽  
Margareta Zehnder
Keyword(s):  

1998 ◽  
Vol 51 (4) ◽  
pp. 439-441 ◽  
Author(s):  
TRIPTIKUMAR MUKHOPADHYAY ◽  
R. G. BHAT ◽  
KIRITY ROY ◽  
E. K. S. VIJAYAKUMAR ◽  
B. N. GANGULI

Xenobiotica ◽  
1991 ◽  
Vol 21 (5) ◽  
pp. 605-612 ◽  
Author(s):  
J. Tjørnelund ◽  
S. H. Hansen ◽  
C. Cornett

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