Laís Pessanha de Carvalho

University of Tübingen

Germany

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Articles (10)

Year:

2025

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2025

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2025

Year:

2024

Year:

2024

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2024

Year:

2024

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2024

Year:

2024

Year:

2024

Collaborators (6)

Jana Held

Eberhard Karls Universität Tübingen

GERMANY

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Thomas Kurz

Heinrich Heine University Düsseldorf

GERMANY

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Felix Deschner

Helmholtz Institute for Pharmaceutical Research Saarland

GERMANY

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Daniel Stopper

University of Bonn

GERMANY

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Daniel Ramsbeck

Anhalt University of Applied Sciences

GERMANY

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Elizabeth Winzeler

Professor

University of California, San Diego

UNITED STATES

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Laís Pessanha de Carvalho

Research Interests

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Contact this professor

Articles (10)

Natural products chlorotonils exert a complex antibacterial mechanism and address multiple targets

Exploring Alternative Zinc-Binding Groups in Histone Deacetylase (HDAC) Inhibitors Uncovers <b>DS-103</b> as a Potent Ethylhydrazide-Based HDAC Inhibitor with Chemosensitizing Properties.

Multicomponent syntheses enable the discovery of novel quisinostat-derived chemotypes as histone deacetylase inhibitors

Reverse <i>N</i>-Substituted Hydroxamic Acid Derivatives of Fosmidomycin Target a Previously Unknown Subpocket of 1-Deoxy-<scp>d-</scp>xylulose 5-Phosphate Reductoisomerase (DXR)

Development of peptoid-based heteroaryl-decorated histone deacetylase (HDAC) inhibitors with dual-stage antiplasmodial activity

Design, Synthesis, Antitumor, and Antiplasmodial Evaluation of New 7-Chloroquinoline–Benzimidazole Hybrids

Towards Novel Antiplasmodial Agents—Design, Synthesis and Antimalarial Activity of Second-Generation β-Carboline/Chloroquine Hybrids

Expanding the Chemical Space of Reverse Fosmidomycin Analogs

TKK130 is a 3-Hydroxy-Propanamidine (HPA) with Potent Antimalarial <i>In Vivo</i> Activity and a High Barrier to Resistance

Targeting the <i>Plasmodium falciparum</i> IspE Enzyme

Collaborators (6)

Jana Held

Thomas Kurz

Felix Deschner

Daniel Stopper

Daniel Ramsbeck

Elizabeth Winzeler

Make your next move.

Laís Pessanha de Carvalho

Research Interests

Explore related searches

Contact this professor

Articles (10)

Natural products chlorotonils exert a complex antibacterial mechanism and address multiple targets

Exploring Alternative Zinc-Binding Groups in Histone Deacetylase (HDAC) Inhibitors Uncovers &lt;b&gt;DS-103&lt;/b&gt; as a Potent Ethylhydrazide-Based HDAC Inhibitor with Chemosensitizing Properties.

Multicomponent syntheses enable the discovery of novel quisinostat-derived chemotypes as histone deacetylase inhibitors

Reverse <i>N</i>-Substituted Hydroxamic Acid Derivatives of Fosmidomycin Target a Previously Unknown Subpocket of 1-Deoxy-<scp>d-</scp>xylulose 5-Phosphate Reductoisomerase (DXR)

Development of peptoid-based heteroaryl-decorated histone deacetylase (HDAC) inhibitors with dual-stage antiplasmodial activity

Design, Synthesis, Antitumor, and Antiplasmodial Evaluation of New 7-Chloroquinoline–Benzimidazole Hybrids

Towards Novel Antiplasmodial Agents—Design, Synthesis and Antimalarial Activity of Second-Generation β-Carboline/Chloroquine Hybrids

Expanding the Chemical Space of Reverse Fosmidomycin Analogs

TKK130 is a 3-Hydroxy-Propanamidine (HPA) with Potent Antimalarial <i>In Vivo</i> Activity and a High Barrier to Resistance

Targeting the <i>Plasmodium falciparum</i> IspE Enzyme

Collaborators (6)

Jana Held

Thomas Kurz

Felix Deschner

Daniel Stopper

Daniel Ramsbeck

Elizabeth Winzeler

Make your next move.

Exploring Alternative Zinc-Binding Groups in Histone Deacetylase (HDAC) Inhibitors Uncovers <b>DS-103</b> as a Potent Ethylhydrazide-Based HDAC Inhibitor with Chemosensitizing Properties.