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Active compounds against tinea pedis dermatophytes from Ageratina pichinchensis var. bustamenta
B Aguilar-Guadarrama, V Navarro… - Natural Product …, 2009 - Taylor & Francis
Secondary metabolites 5-acetyl-3β-angeloyloxy-2β-(1-hydroxyisopropyl)-2, 3-
dihydrobenzofurane (1), 5-acetyl-3β-angeloyloxy-2β-(1-hydroxyisopropyl)-6-methoxy-2, 3 …
dihydrobenzofurane (1), 5-acetyl-3β-angeloyloxy-2β-(1-hydroxyisopropyl)-6-methoxy-2, 3 …
Encecalol angelate, an unstable chromene from Ageratum conyzoides L.: total synthesis and investigation of its antiprotozoal activity
D Harel, SA Khalid, M Kaiser, R Brun, B Wünsch… - Journal of …, 2011 - Elsevier
ETHNOPHARMACOLOGICAL RELEVANCE: In agreement with ethnomedicinal reports, the
dichloromethane extract of Ageratum conyzoides L.(Asteraceae) was recently shown to be …
dichloromethane extract of Ageratum conyzoides L.(Asteraceae) was recently shown to be …
Carboxymethylcellulose–tetrahydrocurcumin conjugates for colon-specific delivery of a novel anti-cancer agent, 4-amino tetrahydrocurcumin
T Plyduang, L Lomlim, S Yuenyongsawad… - European Journal of …, 2014 - Elsevier
Several curcumin derivatives are now becoming increasingly of interest because of their
bioactive attributes, especially their action as antioxidants and anti-carcinogenic activities …
bioactive attributes, especially their action as antioxidants and anti-carcinogenic activities …
Molecular docking studies and synthesis of a new class of chroman-4-one fused 1, 3, 4-thiadiazole derivatives and evaluation for their anticancer potential
Abstract γ-Secretase inhibitors (GSIs) are repurposed as cancer therapeutics based on the
promising inhibition of NOTCH1 signalling pathway in various cancers. GSIs are a class of …
promising inhibition of NOTCH1 signalling pathway in various cancers. GSIs are a class of …
Isochaihulactone analogues: Synthesis and anti-proliferative activity of novel dibenzylbutyrolactones
A series of dibenzyl-γ-butyrolactones bearing a hydroxyl group at the benzylic position of 3-
benzyl group were synthesized as hydrated analogue of isochaihulactone and evaluated …
benzyl group were synthesized as hydrated analogue of isochaihulactone and evaluated …
[HTML][HTML] New chroman-4-one/thiochroman-4-one derivatives as potential anticancer agents
S Demirayak, L Yurttas, N Gundogdu-Karaburun… - Saudi Pharmaceutical …, 2017 - Elsevier
Abstract The synthesis of 3-[3/4-(2-aryl-2-oxoethoxy) arylidene] chroman/thiochroman-4-one
derivatives (1–34) and evaluation of their anticancer activities were aimed in this work. Final …
derivatives (1–34) and evaluation of their anticancer activities were aimed in this work. Final …
New chromanone derivatives containing thiazoles: Synthesis and antitumor activity evaluation on A549 lung cancer cell line
Abstract Novel 2‐[2‐(chroman‐4‐ylidene) hydrazinyl]‐4/5‐substituted thiazole derivatives
(2a–i) were synthesized and investigated for their anticancer activity. Cytotoxic activity on …
(2a–i) were synthesized and investigated for their anticancer activity. Cytotoxic activity on …
Synthesis of chromeno [3, 4-b] quinoline derivatives by heterogeneous [Cu (II) BHPPDAH] catalyst without being immobilized on any support under mild conditions …
The efficient synthesis of chromeno [3, 4-b] quinoline derivatives by condensation of O-
propargylated salicylaldehyde, or corresponding compounds and primary aromatic amine …
propargylated salicylaldehyde, or corresponding compounds and primary aromatic amine …
Facile eco-friendly synthesis of novel chromeno [4, 3-b] pyridine-2, 5-diones and evaluation of their antimicrobial and antioxidant properties
SR Jaggavarapu, AS Kamalakaran, VP Jalli… - Journal of Chemical …, 2014 - Springer
Rapid and facile access to novel chromeno [4, 3-b] pyridine-2, 5-dione derivatives was
achieved by a mild base catalysed reaction of 4-chloro-3-formylcoumarin and …
achieved by a mild base catalysed reaction of 4-chloro-3-formylcoumarin and …
[HTML][HTML] Synthesis, TD-DFT, and optical properties study of a chromeno-quinoline (acceptor) and mirror-less laser action enabled by energy transfer from a conjugated …
Structurally interesting chromeno-quinolines were constructed via the cyclization reaction of
O-propargylated naphthaldehyde and substituted anilines in good yields. We explored …
O-propargylated naphthaldehyde and substituted anilines in good yields. We explored …