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Topics Covered
- Antimalarial drug discovery
- Natural product analogues (Kalinol)
- Drug-resistant Plasmodium falciparum
- Mechanism of action studies
- Apicoplast targeting
- Vesicular trafficking pathways
- Semi-synthetic compound (MED6-189)
- Preclinical development and translational challenges
Biography
Professor Karine Le Roch is a Professor at the University of California, Riverside, whose research focuses on the molecular biology of malaria parasites. Her work explores gene regulation, epigenetics, and chromatin dynamics in Plasmodium falciparum, with the aim of understanding how the parasite progresses through its life cycle and evades host responses. Using advanced genomics and systems biology approaches, her research has contributed to identifying novel targets for antimalarial therapies.
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Talk Citation
Le Roch, K. (2026, May 28). Kalihinol analog MED6-189: a promising pan-antimalarial candidate [Audio file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved May 29, 2026, from https://doi.org/10.69645/RPFK4626.Export Citation (RIS)
Publication History
- Published on May 28, 2026
Financial Disclosures
- Prof. Karine Le Roch has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Playlist: Research Interviews
Transcript
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0:00
Interviewer: The research
group of Prof. Karine Le Roch
at the University of
California, Riverside,
recently published a
paper in Science Journal
detailing the synthesis of
an analog of kalihinol,
a sponge-derived
natural product,
which demonstrates activity
against drug-resistant malaria.
Prof. Roch has kindly
joined us today
to discuss her findings.
Prof. Roch, thank you very
much for joining us today.
Prof. Roch: Thank
you for having me.
Interviewer: Could you
provide some background
on the approach that you
took in this research
and what led you to focus
on kalihinol analogues?
Prof. Roch: So,
I've been working on
natural product
from drug discovery
against malaria for decades.
Over the years, my
work focused on
understanding not only
how the parasite can
survive inside a
human red blood cell,
but also how we can identify
new drugs and drug targets.
So we all know that successful
malaria chemotherapy
still have a strong historical
link to natural products
of which quinine
and artemisinin are
the two most important
antimalarial drugs
extracted from plants.
So why these natural products
are so successful drugs?
They offer a vast source of
chemically diverse compound with
potential therapeutic
properties,
they often exhibit a
unique molecular structure
that can lead to
novel drug candidates
with fewer side effects compared
to purely synthetic molecules,
and they are often very
relevant for tackling
complex disease and fight
mechanisms of drug resistance.
So as I said earlier,
malaria has a very strong
historical link to
natural products, and
I've been interested in
trying to discover new
products that could
actually be efficient
against malaria parasites.