Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4-aryl group.
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Antiproliferative and apoptosis inducing properties of pyrano[3,2-c]pyridones accessible by a one-step multicomponent synthesisStructural simplification of bioactive natural products with multicomponent synthesis. 2. antiproliferative and antitubulin activities of pyrano[3,2-c]pyridones and pyrano[3,2-c]quinolones.Anticancer properties of an important drug lead podophyllotoxin can be efficiently mimicked by diverse heterocyclic scaffolds accessible via one-step synthesis.Anti-proliferative and apoptotic effects of the derivatives from 4-aryl-4H-chromene family on human leukemia K562 cells.Synthesis and cytotoxic activity of some 2-amino-4-aryl-3-cyano-7-(dimethylamino)-4H-chromenes.Biological evaluation of structurally diverse amaryllidaceae alkaloids and their synthetic derivatives: discovery of novel leads for anticancer drug designCytotoxicity and Apoptosis Inducing Activities of 2-Amino-4H-chromene-3-carbonitrile Derivatives Loaded on Gold Nanoparticles Against Human Breast Cancer Cell Line T47D.Up regulation of Bax and down regulation of Bcl2 during 3-NC mediated apoptosis in human cancer cells.(4R,7S)-2-Amino-4-(3,4-dimeth-oxy-phen-yl)-5-oxo-7-phenyl-5,6,7,8-tetra-hydro-4H-chromene-3-carbonitrile monohydrateDesign, Synthesis and Biological Evaluation of Novel 5H-Chromenopyridines as Potential Anti-Cancer Agents.Microtubule inhibitor, SP-6-27 inhibits angiogenesis and induces apoptosis in ovarian cancer cells.4-Cyano-N-ethyl-spiro-[chromene-2,4'-piperidine]-1'-carboxamide.New substituted 4H-chromenes as anticancer agents.Exploring natural product chemistry and biology with multicomponent reactions. 5. Discovery of a novel tubulin-targeting scaffold derived from the rigidin family of marine alkaloids.Chromenes: potential new chemotherapeutic agents for cancer.Current molecular imaging positron emitting radiotracers in oncology.Microwave-assisted synthesis of chromenes: biological and chemical importance.Toxicity of Cisplatin-Loaded Poly Butyl Cyanoacrylate Nanoparticles in a Brain Cancer Cell Line: Anionic Polymerization ResultsCatalysis of Cascade and Multicomponent Reactions of Carbonyl Compounds and CH Acids by Electricity.Organocatalyzed enantioselective synthesis of 2-amino-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carboxylates.2-Amino-3-cyano-4-(5-arylisoxazol-3-yl)-4H-chromenes: synthesis and in vitro cytotoxic activity.QSAR study of 4-aryl-4H-chromenes as a new series of apoptosis inducers using different chemometric tools.Structure-activity relationships and molecular docking studies of chromene and chromene based azo chromophores: A novel series of potent antimicrobial and anticancer agents.Facile synthesis of 4H-chromene derivatives via base-mediated annulation of ortho-hydroxychalcones and 2-bromoallyl sulfones."One-pot" access to dihydrofurans via tandem oxidative difunctionalization and ring contraction of aminopyrans.Evaluation the Anti-Cancer Effect of PEGylated Nano-Niosomal Gingerol, on Breast Cancer Cell lines (T47D), In-VitroAn expeditious and greener one-pot synthesis of 4H-chromenes catalyzed by Ba(OTf)2in PEG-water
P2860
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P2860
Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4-aryl group.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Discovery of 4-aryl-4H-chromen ...... tionships of the 4-aryl group.
@en
type
label
Discovery of 4-aryl-4H-chromen ...... tionships of the 4-aryl group.
@en
prefLabel
Discovery of 4-aryl-4H-chromen ...... tionships of the 4-aryl group.
@en
P2093
P356
P1476
Discovery of 4-aryl-4H-chromen ...... tionships of the 4-aryl group.
@en
P2093
Charles Blais
David Bouffard
Denis Labreque
Giorgio Attardo
Henriette Gourdeau
Hong Zhang
Jianghong Zhao
John Drewe
John Herich
P304
P356
10.1021/JM049640T
P407
P577
2004-12-01T00:00:00Z