UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Discovery of new quinolines as potent colchicine binding site inhibitors: design, synthesis, docking studies, and anti-proliferative evaluation

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.640-658

2021

Volltextzugriff (PDF)

Design, synthesis, and anti-cancer evaluation of new pyrido[2,3-d]pyrimidin-4(3H)-one derivatives as potential EGFRWT and EGFRT790M inhibitors and apoptosis inducers

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.1053-1076

2022

Volltextzugriff (PDF)

Synthesis, characterization of some benzazoles bearing pyridine moiety: Search for novel anticancer agents

European journal of medicinal chemistry, 2011-09, Vol.46 (9), p.4025-4034

Elzahabi, Heba S.A.

2011

Volltextzugriff (PDF)

Anticancer evaluation and molecular modeling of multi-targeted kinase inhibitors based pyrido[2,3-d]pyrimidine scaffold

Journal of enzyme inhibition and medicinal chemistry, 2018-01, Vol.33 (1), p.546-557

2018

Volltextzugriff (PDF)

Discovery of new 1H-pyrazolo[3,4-d]pyrimidine derivatives as anticancer agents targeting EGFRWT and EGFRT790M

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.2283-2303

2022

Volltextzugriff (PDF)

An Efficient Synthesis of Novel Bioactive Thiazolyl-Phthalazinediones under Ultrasound Irradiation

Molecules (Basel, Switzerland), 2017-02, Vol.22 (2), p.319-319

2017

Volltextzugriff (PDF)

A convenient synthesis and molecular modeling study of novel purine and pyrimidine derivatives as CDK2/cyclin A3 inhibitors

Bioorganic & medicinal chemistry, 2010-11, Vol.18 (21), p.7639-7650

2010

Volltextzugriff (PDF)

Design, synthesis and evaluation of new quinazolin-4-one derivatives as apoptotic enhancers and autophagy inhibitors with potent antitumor activity

European journal of medicinal chemistry, 2021-10, Vol.222, p.113609-113609, Article 113609

2021

Volltextzugriff (PDF)

Design, Molecular Modeling, MD Simulations, Essential Dynamics, ADMET, DFT, Synthesis, Anti-proliferative, and Apoptotic Evaluations of a New Anti-VEGFR-2 Nicotinamide Analogue

Current pharmaceutical design, 2023-01, Vol.29 (36), p.2902-2920

2023

Volltextzugriff (PDF)

Synthesis and Antitumor Activity of Novel Hybrids of Pyrimidine/Benzimidazole Scaffolds

Polycyclic aromatic compounds, 2022-05, Vol.42 (5), p.2363-2377

2022

Volltextzugriff (PDF)

Discovery of new 1 H -pyrazolo[3,4- d ]pyrimidine derivatives as anticancer agents targeting EGFR WT and EGFR T790M

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.2283-2303

2022

Volltextzugriff (PDF)

Synthesis of New Bis-Spiropyrazoles as Antitumor Agents under Ultrasound Irradiation

Mini reviews in medicinal chemistry, 2018-01, Vol.18 (7), p.631-637

2018

Volltextzugriff (PDF)

A New Theobromine-Based EGFR[sup.WT] and EGFR[sup.T790M] Inhibitor and Apoptosis Inducer: Design, Semi-Synthesis, Docking, DFT, MD Simulations, and In Vitro Studies

Processes, 2022-11, Vol.10 (11)

2022

Volltextzugriff (PDF)

A study of the allosteric inhibition of HCV RNA-dependent RNA polymerase and implementing virtual screening for the selection of promising dual-site inhibitors with low resistance potential

Journal of receptors and signal transduction, 2017-07, Vol.37 (4), p.341-354

2017

Volltextzugriff (PDF)

A New Theobromine-Based EGFRWT and EGFRT790M Inhibitor and Apoptosis Inducer: Design, Semi-Synthesis, Docking, DFT, MD Simulations, and In Vitro Studies

Processes, 2022-11, Vol.10 (11), p.2290

2022

Volltextzugriff (PDF)

Eco-friendly synthesis and 2D-QSAR study of novel pyrazolines as potential anticolon cancer agents

Medicinal chemistry research, 2015-02, Vol.24 (2), p.652-668

2015

Volltextzugriff (PDF)

Virtual screening in drug discovery, a topic between believe and reality?

Biochemistry & pharmacology, 2012, Vol.1 (1)

A. Elzahabi, Heba S.

2012

Volltextzugriff (PDF)

ChemInform Abstract: Synthesis, Characterization of Some Benzazoles Bearing Pyridine Moiety: Search for Novel Anticancer Agents

ChemInform, 2012-01, Vol.43 (5), p.no-no

Elzahabi, Heba S. A.

2012

Volltextzugriff (PDF)

Discovery of new 1H-pyrazolo3,4-dpyrimidine derivatives as anticancer agents targeting EGFRWT and EGFRT790M

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.2283

2022

Volltextzugriff (PDF)

Modifying the lipophilic part of phenylthiazole antibiotics to control their drug-likeness

European journal of medicinal chemistry, 2020-01, Vol.185, p.111830-111830, Article 111830

2020

Volltextzugriff (PDF)

Modified pyrido[2,3-d]pyrimidin-4(3H)-one derivatives as EGFRWT and EGFRT790M inhibitors: Design, synthesis, and anti-cancer evaluation

Journal of molecular structure, 2022-12, Vol.1270, p.133971, Article 133971

2022

Volltextzugriff (PDF)

Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation

Azhar International Journal of Pharmaceutical and Medical Sciences, 2023-01, Vol.3 (1), p.112-119

2023

Volltextzugriff (PDF)

1 – 22 von 22

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(19)
Mit Volltextzugriff
(17)

Publikationsform

Artikel
(22)

Sprache

Englisch
(22)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Discovery of new quinolines as potent colchicine binding site inhibitors: design, synthesis, docking studies, and anti-proliferative evaluation

Design, synthesis, and anti-cancer evaluation of new pyrido[2,3-d]pyrimidin-4(3H)-one derivatives as potential EGFRWT and EGFRT790M inhibitors and apoptosis inducers

Synthesis, characterization of some benzazoles bearing pyridine moiety: Search for novel anticancer agents

Anticancer evaluation and molecular modeling of multi-targeted kinase inhibitors based pyrido[2,3-d]pyrimidine scaffold

Discovery of new 1H-pyrazolo[3,4-d]pyrimidine derivatives as anticancer agents targeting EGFRWT and EGFRT790M

An Efficient Synthesis of Novel Bioactive Thiazolyl-Phthalazinediones under Ultrasound Irradiation

A convenient synthesis and molecular modeling study of novel purine and pyrimidine derivatives as CDK2/cyclin A3 inhibitors

Design, synthesis and evaluation of new quinazolin-4-one derivatives as apoptotic enhancers and autophagy inhibitors with potent antitumor activity

Design, Molecular Modeling, MD Simulations, Essential Dynamics, ADMET, DFT, Synthesis, Anti-proliferative, and Apoptotic Evaluations of a New Anti-VEGFR-2 Nicotinamide Analogue

Synthesis and Antitumor Activity of Novel Hybrids of Pyrimidine/Benzimidazole Scaffolds

Discovery of new 1 H -pyrazolo[3,4- d ]pyrimidine derivatives as anticancer agents targeting EGFR WT and EGFR T790M

Synthesis of New Bis-Spiropyrazoles as Antitumor Agents under Ultrasound Irradiation

A New Theobromine-Based EGFR[sup.WT] and EGFR[sup.T790M] Inhibitor and Apoptosis Inducer: Design, Semi-Synthesis, Docking, DFT, MD Simulations, and In Vitro Studies

A study of the allosteric inhibition of HCV RNA-dependent RNA polymerase and implementing virtual screening for the selection of promising dual-site inhibitors with low resistance potential

A New Theobromine-Based EGFRWT and EGFRT790M Inhibitor and Apoptosis Inducer: Design, Semi-Synthesis, Docking, DFT, MD Simulations, and In Vitro Studies

Eco-friendly synthesis and 2D-QSAR study of novel pyrazolines as potential anticolon cancer agents

Virtual screening in drug discovery, a topic between believe and reality?

ChemInform Abstract: Synthesis, Characterization of Some Benzazoles Bearing Pyridine Moiety: Search for Novel Anticancer Agents

Discovery of new 1H-pyrazolo3,4-dpyrimidine derivatives as anticancer agents targeting EGFRWT and EGFRT790M

Modifying the lipophilic part of phenylthiazole antibiotics to control their drug-likeness

Modified pyrido[2,3-d]pyrimidin-4(3H)-one derivatives as EGFRWT and EGFRT790M inhibitors: Design, synthesis, and anti-cancer evaluation

Novel Pyrido-Thiazolo-Pyrimidinone Hybrids targeting EGFRWT and EGFRT790M: Design, Synthesis, Anticancer Activity and docking simulation

Suchergebnisse filtern