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Niels Heise

Researcher

Martin Luther University Halle-Wittenberg

Germany

Research Interests

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Professors in Germany Professors in Pharmaceutical Chemistry Pharmaceutical Chemistry professors in Germany

Articles (20)

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2026

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Collaborators (10)

Celso Alves

Guest Assistant - Lecturer

Instituto Politécnico de Leiria Escola Superior de Turismo e Tecnologia do Mar de Peniche

PORTUGAL

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Holger B. Deising

Full Professor

Martin Luther University Halle-Wittenberg

GERMANY

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Wolfgang Sippl

Professor

Martin Luther University Halle-Wittenberg

GERMANY

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René Csuk

GERMANY

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Nuno M. Xavier

Assistant Professor (Pharmaceutical and Medicinal Chemistry)

Faculty of Pharmacy, University of Lisbon

PORTUGAL

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Olaf Fuhr

Karlsruher Institut für Technologie

GERMANY

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Matthias Vogt

Wissenschaftlicher Mitarbeiter (Research Associate,Staff Scientist))

Martin Luther University Halle-Wittenberg

GERMANY

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Weiqin Xu

lecturer

Martin Luther University Halle-Wittenberg

GERMANY

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Thomas Mueller

Martin Luther University Halle-Wittenberg

GERMANY

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Ludger A Wessjohann

Full Professor

Martin Luther University Halle-Wittenberg

GERMANY

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Niels Heise

Research Interests

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Articles (20)

Correction: Efficient biotechnological production of N-(Hydroxycinnamoyl) tyramines by utilizing plant-derived enzymes in a bench-scale bioreactor with in situ product precipitation

Efficient biotechnological production of N-(Hydroxycinnamoyl)tyramines by utilizing plant-derived enzymes in a bench-scale bioreactor with in situ product precipitation

Novel Functionalized Pyrrolopyridines to Target Brk

Small Structural Changes in Chili-Derived Capsaicin Resulting in Nonivamide Analogs of Significantly Improved Cytotoxicity and Good Tumor/Non-Tumor Cell Selectivity

Carbon‐Centered Reactivity in Carbodiphosphorane‐Based Ligands Allowing for Redox‐Non‐Innocent Ligand/Ligand Dual Bond‐Activation

Redox Status-Selective Imaging of Iron in Vegetative and Pathogenic Fungal Cells Using Fluorescent Dyes Synthesized Via Simple Chemical Reactions

5′-Guanidino Xylofuranosyl Nucleosides as Novel Types of 5′-Functionalized Nucleosides with Biological Potential

Towards Cytotoxic Derivatives of Cafestol

Kohlenstoffzentrierte Reaktivität von Carbodiphosphoran Liganden ermöglicht nicht‐unschuldige Redoxaktivität, Ligand‐Ligand‐Kooperation und Duale‐Bindungsaktivierungen

(Iso)quinoline amides derived from corosolic acid exhibit high cytotoxicity, and the potential for overcoming drug resistance in human cancer cells

Combination of Betulinic Acid Fragments and Carbonic Anhydrase Inhibitors—A New Drug Targeting Approach

Arylsulfonamido-alkyl-sulfamates act as inhibitors of bovine carbonic anhydrase II

Revisiting capsaicin and nonivamide: Their analogs exert strong inhibitory activity against cholinesterases

Stereochemistry matters: Inhibition of carbonic anhydrase II by amino acid derived sulfamates depends on their absolute configuration

Synthesis and Enzymatic Evaluation of a Small Library of Substituted Phenylsulfonamido-Alkyl Sulfamates towards Carbonic Anhydrase II

Synthesis of Rhodamine-Conjugated Lupane Type Triterpenes of Enhanced Cytotoxicity

Dehydroabietylamine derived bistetrazoles from ultrasound-assisted pseudo-seven-component Ugi reactions act as efficient and selective inhibitors of cholinesterases

Lupane acetates in small molecule drug hybrids: Probing their inhibitory activity for carbonic anhydrase II

Diethoxyphosphoryloxy‐oleanolic acid is a nanomolar‐inhibitor of butyrylcholinesterase

An asiatic acid derived trisulfamate acts as a nanomolar inhibitor of human carbonic anhydrase VA

Collaborators (10)

Celso Alves

Holger B. Deising

Wolfgang Sippl

René Csuk

Nuno M. Xavier

Olaf Fuhr

Matthias Vogt

Weiqin Xu

Thomas Mueller

Ludger A Wessjohann

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