Lais Carvalho-De

Tuebingen, BW, Germany

Last Updated: 09/26/2026

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Found 22 publications

The inducible gametocyte producer (iGP1) strain is well-suited to produce both immature and mature gametocytes for subsequent drug sensitivity profiling.

The inducible gametocyte producer (iGP1) strain is well-suited to produce both immature and mature gametocytes for subsequent drug sensitivity profiling.

Journal: Frontiers in cellular and infection microbiology

Published: February 11, 2026

Structure-Activity Relationships of 3-Hydroxypropanamidines (HPAs) with Potent In Vivo Antimalarial Activity.

Structure-Activity Relationships of 3-Hydroxypropanamidines (HPAs) with Potent In Vivo Antimalarial Activity.

Journal: Journal of medicinal chemistry

Published: September 08, 2025

No evidence of molecular markers of piperaquine resistance in southeastern Nigeria.

No evidence of molecular markers of piperaquine resistance in southeastern Nigeria.

Journal: Malaria journal

Published: April 29, 2025

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

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

Journal: Journal of medicinal chemistry

Published: February 13, 2025

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

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

Journal: Journal of medicinal chemistry

Published: December 26, 2024

Exploration of Fluorinated Peptoid-Based Histone Deacetylase Inhibitors as Dual-Stage Antiplasmodial Agents.

Exploration of Fluorinated Peptoid-Based Histone Deacetylase Inhibitors as Dual-Stage Antiplasmodial Agents.

Journal: Archiv der Pharmazie

Published: October 29, 2024

Expanding the Chemical Space of Reverse Fosmidomycin Analogs.

Expanding the Chemical Space of Reverse Fosmidomycin Analogs.

Journal: ACS medicinal chemistry letters

Published: October 17, 2024

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

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

Journal: Cell chemical biology

Published: August 21, 2024

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

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

Journal: Molecules (Basel, Switzerland)

Published: May 31, 2024

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

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

Journal: ACS infectious diseases

Published: April 22, 2024

Discovery of harmiprims, harmine-primaquine hybrids, as potent and selective anticancer and antimalarial compounds.

Discovery of harmiprims, harmine-primaquine hybrids, as potent and selective anticancer and antimalarial compounds.

Journal: Bioorganic & medicinal chemistry

Published: March 17, 2024

Functionalization of Chlorotonils: Dehalogenil as Promising Lead Compound for In Vivo Application.

Functionalization of Chlorotonils: Dehalogenil as Promising Lead Compound for In Vivo Application.

Journal: Angewandte Chemie (International ed. in English)

Published: December 21, 2023

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Last Updated: 09/26/2026