Franz-Josef Meyer-Almes

Franz-Josef Meyer-Almes

Hochschule Darmstadt

H-index: 24

Europe-Germany

About Franz-Josef Meyer-Almes

Franz-Josef Meyer-Almes, With an exceptional h-index of 24 and a recent h-index of 19 (since 2020), a distinguished researcher at Hochschule Darmstadt, specializes in the field of protein-ligand interaction, kinetics, thermodynamic signatures, drug discovery.

His recent articles reflect a diverse array of research interests and contributions to the field:

Design and synthesis of peptides as stabilizers of histone deacetylase 4

Diaryl Pyrazoline, 1, 3, 4-Oxadizole, and 1, 2, 4-Triazole Pharmacophore Hybridization: Design, Synthesis, HDAC Inhibition, and Caspase 3/7 Activation Studies

The catalytic domain of free or ligand bound histone deacetylase 4 occurs in solution predominantly in closed conformation

Selective HDAC8 inhibitors and their uses

Significance of five-membered heterocycles in human histone deacetylase inhibitors

Design, Synthesis, and Biological Evaluation of Novel Quinazolin-4 (3H)-One-Based Histone Deacetylase 6 (HDAC6) Inhibitors for Anticancer Activity

Design, synthesis, and biological evaluation of tetrahydroisoquinoline based hydroxamate derivatives as HDAC 6 inhibitors for cancer therapy

Continuous enzyme activity assay for high-throughput classification of histone deacetylase 8 inhibitors

Franz-Josef Meyer-Almes Information

University

Position

Professor for Biochemistry

Citations(all)

3446

Citations(since 2020)

1115

Cited By

2664

hIndex(all)

24

hIndex(since 2020)

19

i10Index(all)

53

i10Index(since 2020)

32

Email

University Profile Page

Hochschule Darmstadt

Google Scholar

View Google Scholar Profile

Franz-Josef Meyer-Almes Skills & Research Interests

protein-ligand interaction

kinetics

thermodynamic signatures

drug discovery

Top articles of Franz-Josef Meyer-Almes

Title

Journal

Author(s)

Publication Date

Design and synthesis of peptides as stabilizers of histone deacetylase 4

Journal of Peptide Science

Annika Lill

Markus Schweipert

Thomas Nehls

Eva Wurster

Frederik Lermyte

...

2024/4/16

Diaryl Pyrazoline, 1, 3, 4-Oxadizole, and 1, 2, 4-Triazole Pharmacophore Hybridization: Design, Synthesis, HDAC Inhibition, and Caspase 3/7 Activation Studies

Russian Journal of Bioorganic Chemistry

Abdullah Yahya Abdullah Alzahrani

Pratibha Gupta

Vijay Patil

Franz-Josef Meyer-Almes

DV Sokolova

...

2024/4

The catalytic domain of free or ligand bound histone deacetylase 4 occurs in solution predominantly in closed conformation

Protein Science

Markus Schweipert

Thomas Nehls

Anton Frühauf

Cecilé Debarnot

Adarsh Kumar

...

2024/3

Selective HDAC8 inhibitors and their uses

2023/10/31

Significance of five-membered heterocycles in human histone deacetylase inhibitors

Anton Frühauf

Martin Behringer

Franz-Josef Meyer-Almes

2023/7/27

Design, Synthesis, and Biological Evaluation of Novel Quinazolin-4 (3H)-One-Based Histone Deacetylase 6 (HDAC6) Inhibitors for Anticancer Activity

Future Journal of Pharmaceutical Sciences

Iten M Fawzy

Khairia M Youssef

Nasser SM Ismail

Joachim Gullbo

Khaled AM Abouzid

2015/6/1

Design, synthesis, and biological evaluation of tetrahydroisoquinoline based hydroxamate derivatives as HDAC 6 inhibitors for cancer therapy

Journal of Molecular Structure

Yogesh Mahadu Khetmalis

Bakhya Shree

Boddupalli Venkata Siva Kumar

Markus Schweipert

Cécile Debarnot

...

2023/4/15

Continuous enzyme activity assay for high-throughput classification of histone deacetylase 8 inhibitors

Exploration of Targeted Anti-tumor Therapy

Markus Schweipert

Anuja Amurthavasan

Franz-Josef Meyer-Almes

2023

Electrophilic MiniFrags Revealed Unprecedented Binding Sites for Covalent HDAC8 Inhibitors

Journal of Medicinal Chemistry

Aaron B Keeley

Aleksandra Kopranovic

Vincenzo Di Lorenzo

Péter Ábrányi-Balogh

Niklas Jänsch

...

2023/12/19

3‐Chloro‐5‐Substituted‐1, 2, 4‐Thiadiazoles (TDZs) as Selective and Efficient Protein Thiol Modifiers

ChemBioChem

Niklas Jänsch

Anton Frühauf

Markus Schweipert

Cécile Debarnot

Miriam Erhardt

...

2022/11/4

Synthesis and Characterization of Reversible Covalent HDAC4 Inhibitors

Anton Frühauf

Benjamin Wolff

Markus Schweipert

Franz-Josef Meyer-Almes

2022/10/19

Methionine 274 is not the determining factor for selective inhibition of histone deacetylase 8 (HDAC8) by L-shaped inhibitors

International Journal of Molecular Sciences

Niklas Jänsch

Kim Leoni Lang

Franz-Josef Meyer-Almes

2022/10/4

Synthesis and HDAC inhibitory activity of pyrimidine-based hydroxamic acids

Beilstein journal of organic chemistry

Virginija Jakubkiene

Gabrielius Ernis Valiulis

Markus Schweipert

Asta Zubriene

Daumantas Matulis

...

2022/7/13

Transcriptomic and genomic studies classify NKL54 as a histone deacetylase inhibitor with indirect influence on MEF2-dependent transcription

Nucleic acids research

Martina Minisini

Eros Di Giorgio

Emanuela Kerschbamer

Emiliano Dalla

Massimo Faggiani

...

2022/3/21

Multi-target weapons: diaryl-pyrazoline thiazolidinediones simultaneously targeting VEGFR-2 and HDAC cancer hallmarks

RSC Medicinal Chemistry

Neha Upadhyay

Kalpana Tilekar

Sabreena Safuan

Alan P Kumar

Markus Schweipert

...

2021

HDAC4 Inhibitors with Cyclic Linker and Non‐hydroxamate Zinc Binding Group: Design, Synthesis, HDAC Screening and in vitro Cytotoxicity evaluation.

ChemistrySelect

Kalpana Tilekar

Jessica D Hess

Neha Upadhyay

Markus Schweipert

Felix Flath

...

2021/7/13

Development and investigation of thiazolidinedione and pyrazoline compounds as antiangiogenic weapons targeting VEGFR-2

Future medicinal chemistry

Neha Upadhyay

Kalpana Tilekar

Sabreena Safuan

Alan P Kumar

Markus Schweipert

...

2021/11

Thiazolidinedione “Magic Bullets” Simultaneously Targeting PPARγ and HDACs: Design, Synthesis, and Investigations of their In Vitro and In Vivo Antitumor Effects

Journal of Medicinal Chemistry

Kalpana Tilekar

Jessica D Hess

Neha Upadhyay

Alessandra Lo Bianco

Markus Schweipert

...

2021/5/18

Double-edged swords: diaryl pyrazoline thiazolidinediones synchronously targeting cancer epigenetics and angiogenesis

Bioorganic chemistry

Neha Upadhyay

Kalpana Tilekar

Sabreena Safuan

Alan P Kumar

Markus Schweipert

...

2021/11/1

Discovery of dihydro-1, 4-benzoxazine carboxamides as potent and highly selective inhibitors of sirtuin-1

Journal of Medicinal Chemistry

Martin Spinck

Matthias Bischoff

Philipp Lampe

Franz-Josef Meyer-Almes

Sonja Sievers

...

2021/4/20

See List of Professors in Franz-Josef Meyer-Almes University(Hochschule Darmstadt)