Eight new phenethoxy derivatives, trichoasperellins A-H (-), were isolated from the endophytic fungus G10 isolated from the medicinal plant L. The structures of these compounds were elucidated from spectroscopic data, -based configurational analysis, and Mosher's methods. Compounds - and - bear one or two multioxidized C moieties with the same carbon skeleton. The carbon skeletons of compounds - are new, all containing three moieties connected via two acetal carbons similar to those of disaccharide glycosides. Compound inhibited nitric oxide production with an IC value of 48.3 μM, comparable to that of the positive control indomethacin (IC, 42.3 μM).
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http://dx.doi.org/10.1021/acs.jnatprod.1c00813 | DOI Listing |
J Nat Prod
May 2022
Hainan Institute for Tropical Agricultural Resources, Haikou Key Laboratory for Research and Utilization of Tropical Natural Products, Institute of Tropical Bioscience and Biotechnology, CATAS, Haikou 571101, People's Republic of China.
Eight new phenethoxy derivatives, trichoasperellins A-H (-), were isolated from the endophytic fungus G10 isolated from the medicinal plant L. The structures of these compounds were elucidated from spectroscopic data, -based configurational analysis, and Mosher's methods. Compounds - and - bear one or two multioxidized C moieties with the same carbon skeleton.
View Article and Find Full Text PDFHeliyon
January 2020
Department of Chemistry, Ahmadu Bello University, Zaria, Nigeria.
Quantitative Structure Activity Relationship studies were carried out on arylpiperazine derivatives to investigate their anti-proliferate activity against prostate PC-3 cancer cell lines. The built model with statistical parameters; R = 0.8483, R = 0.
View Article and Find Full Text PDFBioorg Med Chem
November 2015
Università degli Studi di Firenze, Polo Scientifico, Laboratorio di Chimica Bioinorganica, Rm. 188, Via della Lastruccia 3, 50019 Sesto Fiorentino (Florence), Italy; Università degli Studi di Firenze, Polo Scientifico, Dipartimento NEUROFARBA, Sezione di Scienze Farmaceutiche e Nutraceutiche, Via Ugo Schiff 6, 50019 Sesto Fiorentino (Firenze), Italy. Electronic address:
A series of phenolic acid esters incorporating caffeic, ferulic, and p-coumaric acid, and benzyl, m/p-hydroxyphenethyl- as well as p-hydroxy-phenethoxy-phenethyl moieties were investigated for their inhibitory effects against the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.
View Article and Find Full Text PDFJ Pharm Biomed Anal
January 2015
Institute of Pharmaceutical Chemistry, Goethe-University, Max-von-Laue Str. 9, D-60438 Frankfurt, Germany. Electronic address:
Alzheimer's disease (AD) is the most common cause of dementia. Since no causative treatment is available, new therapeutic options are utmost needed. Several pirinixic acid derivatives, including MH84 (2-((4,6-bis(4-(trifluoromethyl)phenethoxy)pyrimidin-2-yl)thio)hexanoic acid), have shown promising in vitro results as γ-secretase modulators as well as PPARγ activators as potential pharmacological compounds against AD.
View Article and Find Full Text PDFBioorg Med Chem
May 1998
Dipartimento di Scienze Chimiche, Università di Camerino, Italy.
In the present study an investigation of the structure-activity relationships in 9-ethylpurine derivatives, aimed at preparing A1, A2A, A2B, and A3 selective adenosine receptor antagonists, was undertaken. Our synthetic approach was to introduce various substituents (amino, alkoxy and alkynyl groups) into the 2-, 6-, or 8-positions of the purine ring. The starting compounds for each series of derivatives were respectively: 2-iodo-9-ethyladenine (9), obtained from 2-amino-6-chloropurine (5); 9-ethyl-6-iodo-9H-purine (11), 8-bromo-9-ethyl-adenine (3) and 8-bromo-9-ethyl-6-iodo-9H-purine (13), obtained from 9-ethyl-adenine (2).
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