Peter Metz - Concepedia

Author

Peter Metz

Technische Universität Dresden ORCID

Also Known As

Metz, P., Metz, Peter, P Metz, P. METZ, P. Metz, Peter Metz, Peter Metz

334

Publications

4.5K

Citations

H-Index

Concepts

All Affiliations

Technische Universität Dresden University of Münster Cairo University International Centre for Diffraction Data

About

Peter Metz is an author at Technische Universität Dresden specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	25	41	1.6K
2	Natural Sciences	23	41	1.4K
3	Biochemistry	20	29	899
4	Medicine	16	19	802
5	Public Health	1	1	81

Peter Metz

104

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
Synthesis and Molluscicidal Activity of New Cinnoline and Pyrano [2,3‐<i>c</i>]pyrazole Derivatives Fathy M. Abdelrazek, Peter Metz, Nadia Hanafy Metwally, Archiv der Pharmazie EngineeringOrganic ChemistryChemistryHeterocycle ChemistryPharmaceutical Chemistry	2006	237
Synthesis and Molluscicidal Activity of New Chromene and Pyrano[2,3‐<i>c</i>]pyrazole Derivatives Fathy M. Abdelrazek, Peter Metz, Olga Kataeva, Archiv der Pharmazie	2007	226
Synthesis of some new pyrazole-based 1,3-thiazoles and 1,3,4-thiadiazoles as anticancer agents Kamal M. Dawood, Taha M. A. Eldebss, Heba S. A. Elzahabi, European Journal of Medicinal Chemistry Medicinal ChemistryEngineeringMedicineDrug DiscoveryOrganic Chemistry	2013	136
An efficient synthesis of the potent phytoestrogens 8-prenylnaringenin and 6-(1,1-dimethylallyl)naringenin by europium(III)-catalyzed Claisen rearrangement Sven Gester, Peter Metz, Oliver Zierau, Tetrahedron Medicinal ChemistryEngineeringClaisen RearrangementOrganic ChemistryEfficient Synthesis	2001	101
Synthesis and Molluscicidal Activity of 5‐oxo‐5,6,7,8‐Tetrahydro‐4<i>H</i>‐Chromene Derivatives Fathy M. Abdelrazek, Peter Metz, Ebtehal K. Farrag Archiv der Pharmazie Derivative (Chemistry)HeterocyclicBiochemistryNatural SciencesOrganic Chemistry	2004	100
Design, efficient synthesis and molecular docking of some novel thiazolyl-pyrazole derivatives as anticancer agents Abdelwahed R. Sayed, Sobhi M. Gomha, Fathy M. Abdelrazek, BMC Chemistry	2019	94
Mechanism of inhibition of human secretory phospholipase A2 by flavonoids: rationale for lead design Jens Lättig, Markus Böhl, Petra Fischer, Journal of Computer-Aided Molecular Design PhytoalexinLead DesignBiochemistryMedicineLipid Peroxidation	2007	91
METABOLISM OF 8-PRENYLNARINGENIN, A POTENT PHYTOESTROGEN FROM HOPS (HUMULUS LUPULUS), BY HUMAN LIVER MICROSOMES Dejan Nikolić, Yongmei Li, Lucas R. Chadwick, Drug Metabolism and Disposition	2004	85
Prenylation has a compound specific effect on the estrogenicity of naringenin and genistein Georg Kretzschmar, Oliver Zierau, Jannette Wober, The Journal of Steroid Biochemistry and Molecular Biology Hormonal ContraceptiveFertilityMedicineHormonal ReceptorGynecology	2009	81
A Total Synthesis of (±)‐Codeine by 1,3‐Dipolar Cycloaddition T. Erhard, Gunnar Ehrlich, Peter Metz Angewandte Chemie International Edition	2011	70

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