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Published in 2020 at "Archiv der Pharmazie"
DOI: 10.1002/ardp.202000006
Abstract: A series of new benzofuran/oxadiazole hybrids (8a–n) was synthesized from 2H‐chromene‐3‐carbonitriles (3a–c) through the multistep synthetic methodology, and these hybrids are known to exhibit anticancer activities. All the compounds were evaluated for their in vitro…
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Keywords:
synthesis cytotoxicity;
cytotoxicity molecular;
docking substituted;
activity ... See more keywords
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Published in 2019 at "ChemMedChem"
DOI: 10.1002/cmdc.201900180
Abstract: Octahydroepoxyisoindole analogues of norcantharidin were accessed through a Diels–Alder reaction of an amine‐substituted furan with maleic anhydride and subsequent reduction of the bicyclo[2.2.1]heptene olefin. Despite retention of the carboxylate and the ether bridgehead known to…
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Keywords:
norcantharidin analogues;
synthesis cytotoxicity;
carboxylic acids;
cytotoxicity octahydroepoxyisoindole ... See more keywords
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Published in 2018 at "Chemistry of Natural Compounds"
DOI: 10.1007/s10600-018-2270-x
Abstract: Using a reported pharmacophore, 4-[N,N-bis(2-chloroethyl)-amino]phenol, and pentacyclic triterpenes, pharmacologically and structurally diverse components of natural products, six pentacyclic triterpene-4-[N,N-bis(2-chloroethyl)-amino]phenol conjugates were synthesized by click chemistry. Their cytotoxicities against the BEL-7404 and NCI-H460 tumor cell lines…
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Keywords:
synthesis cytotoxicity;
phenol;
chemistry;
pentacyclic triterpene ... See more keywords
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Published in 2018 at "Chemistry of Natural Compounds"
DOI: 10.1007/s10600-018-2565-y
Abstract: Conjugates of betulinic acid with 2-(fluoroacyl)cycloalkane-1,3-dione motifs were synthesized by reacting 3-chloro-2-(fluoroacyl)-2-cycloalkene-1-ones with an equivalent amount of betulinic acid aminoalkylamide hydrochlorides in the presence of Et3N in CHCl3. Reduction of betulonic acid conjugates with 2-trifluoroacetylcyclopentane-1,3-dione…
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Keywords:
synthesis cytotoxicity;
conjugates betulinic;
cytotoxicity conjugates;
betulinic acid ... See more keywords
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Published in 2020 at "Chemistry of Natural Compounds"
DOI: 10.1007/s10600-020-03064-5
Abstract: 28-Oxo-allobetulone derivatives that were newly synthesized or prepared earlier by modification of ring A (3- and 4-pyridylidene, furfurylidene, azepane, lactam, quinolone, spiroindole, pyrazole, isoxazole, and tetraoxane derivatives) and 3 β ,19 β ,28-oleantriol were tested…
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Keywords:
synthesis cytotoxicity;
oxo allobetulone;
cytotoxicity oxo;
cytotoxicity ... See more keywords
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Published in 2017 at "Research on Chemical Intermediates"
DOI: 10.1007/s11164-017-3060-y
Abstract: A novel series of α-aminophosphonates containing the trifluoromethyl aniline moiety were obtained in high yields by condensation of 2-methyl-3-trifluoromethyl aniline, aryl/heteroaryl aldehydes and dimethylphosphite in the presence of chitosan as a catalyst. The molecular modeling…
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Keywords:
synthesis cytotoxicity;
pot green;
green synthesis;
one pot ... See more keywords
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Published in 2018 at "Russian Chemical Bulletin"
DOI: 10.1007/s11172-018-2111-x
Abstract: Regioselective synthesis of new dispiro indolinones combining both an indolinone and an oxazolone fragment in their structure comprised the 1,3-dipolar cycloaddition of azomethine ylides, generated in situ from isatin and sarcosine, at 2-aryl-5-arylmethylidene-substituted 1,3-oxazol-5(4H)-ones. When…
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Keywords:
protein;
synthesis cytotoxicity;
cytotoxicity;
dispiro derivatives ... See more keywords
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Published in 2019 at "Comptes Rendus Chimie"
DOI: 10.1016/j.crci.2018.11.002
Abstract: Abstract Synthetically, 1-(benzo[c]phenanthren-2-yl)ethanol and 1-(benzo[c]phenanthren-2-yl)-3-phenylpropane-1,3-diol were successfully obtained from 2-acetylbenzo[c]phenanthrene and methyl benzo[c]phenanthrene-2-carboxylate, respectively, and fully characterized. The desired compounds were purified by silica gel column chromatography, and their structures were characterized by melting points,…
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Keywords:
two novel;
cytotoxicity;
benzo phenanthrene;
synthesis cytotoxicity ... See more keywords
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Published in 2019 at "Journal of Organometallic Chemistry"
DOI: 10.1016/j.jorganchem.2019.06.024
Abstract: Abstract Two new platinum(II) complexes incorporating acridine ligands with aniline moieties were successfully synthesised and characterised. The acridine-based ligands were synthesised by means of Ullmann's condensation. The reaction of cis -[PtCl 2 (DMSO) 2 ]…
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Keywords:
cytotoxicity;
acridine based;
synthesis cytotoxicity;
platinum ... See more keywords
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Published in 2019 at "Mendeleev Communications"
DOI: 10.1016/j.mencom.2019.07.004
Abstract: For the development of new antitumor agents, novel dibenzo-1,7-diaza-14-crown-4 ethers containing γ-piperidone moiety were synthesized by a domino condensation of new podands, ketones and ammonium acetate. The crystal structure of one Ts of them was…
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Keywords:
crown ethers;
synthesis cytotoxicity;
dibenzo diaza;
piperidone ... See more keywords
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Published in 2020 at "Natural product research"
DOI: 10.1080/14786419.2020.1736060
Abstract: Simple and efficient method was established for the synthesis of a new family of 14α-O-(andrographolide-3-subsitutedisoxazole-5-carboxylate) derivatives (10a-j) from naturally occurring andrographolide (1) by selective esterification with propiolic acid at C-14 using protection and deprotection strategy…
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Keywords:
synthesis cytotoxicity;
subsitutedisoxazole carboxylate;
andrographolide subsitutedisoxazole;
cytotoxicity ... See more keywords