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ArticleMedicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents2026

Structure-based discovery of acridone alkaloids as disruptors of the HEG1-KRIT1 protein-protein interaction in cerebral cavernous malformation signaling.

Emadeldin M Kamel, May Bin-Jumah, Haifa E Alfassam, Raghad A Alotaibi, Ahmed A Allam, Fahad M Alshabrmi, Faris F Aba Alkhayl, Al Mokhtar Lamsabhi

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Article in Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Emadeldin M KamelChemistry Department, Faculty of Science, Beni-Suef University, Beni-Suef, 62514, Egypt. emad.abdelhameed@science.bsu.edu.eg.ORCID http://orcid.org/0000-0002-1279-9564
May Bin-JumahDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P.O. BOX 84428, Riyadh, 11671, Saudi Arabia.
Haifa E AlfassamDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P.O. BOX 84428, Riyadh, 11671, Saudi Arabia.
Raghad A AlotaibiDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P.O. BOX 84428, Riyadh, 11671, Saudi Arabia.
Ahmed A AllamDepartment of Biology, Faculty of Science, Beni-suef University, 65211, Beni Suef, Egypt.
Fahad M AlshabrmiDepartment of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, 51452, Saudi Arabia.
Faris F Aba AlkhaylDepartment of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, 51452, Saudi Arabia.
Al Mokhtar LamsabhiDepartamento de Química and Institute for advanced research in chemical Science (IAdChem), Facultad de Ciencias, Universidad Autónoma de Madrid, Módulo 13, Madrid, 28049, Spain.

Funding

Deanship of Scientific Research, Princess Nourah Bint Abdulrahman University PNURSP2026R400Ministerio de Ciencia, Innovación y Universidades PID2023-150717NB-I00 (MICINN)
6 · The paper itself

Abstract

The HEG1-KRIT1 interaction is essential for endothelial cerebral cavernous malformation complex localization and signaling, making this interface a relevant target for chemical disruption. This study aimed to identify acridone alkaloids capable of inhibiting HEG1 binding to KRIT1 through integrated virtual screening, molecular simulations, binding-energy analysis, drug-likeness prediction, and experimental validation. Screening of 2,449 acridone alkaloids prioritized five candidates: 5-hydroxynoracronycine, acronycine, arborinine, glycocitrine I, and rutacridone. Computational analyses showed stable binding within the HEG1-recognition pocket of KRIT1 and predicted interface weakening, with rutacridone and 5-hydroxynoracronycine producing the strongest destabilizing effects. A bead-based flow-cytometry competition assay confirmed concentration-dependent inhibition, with half-maximal inhibitory concentration values of 2.21 ± 0.31 µM for rutacridone, 2.30 ± 0.30 µM for arborinine, and 2.90 ± 0.35 µM for 5-hydroxynoracronycine. These findings identify rutacridone, arborinine, and 5-hydroxynoracronycine as promising acridone-based starting points for developing HEG1-KRIT1 interaction disruptors. The image explains the difference between normal and disrupted HEG1-KRIT1 protein interactions affecting CCM signaling. On the left, the homeostatic HEG1-KRIT1 complex forms at the endothelial cell membrane, where HEG1 and VE-cadherin proteins connect with KRIT1 (FERM domain) and CCM2 and CCM3 proteins. This complex activates a signaling cascade through MEKK3, MEK5, ERK5, MEF2, and KLF2/4, resulting in regulated CCM signaling. On the right, a small-molecule protein-protein interaction disruptor blocks the binding between HEG1 and KRIT1, shown by a red cross. This disruption prevents the normal complex formation, leading to dysregulated CCM signaling and an altered KLF2/4 transcriptional response. A predicted binding model illustrates the small molecule at the HEG1-KRIT1 interface, with HEG1 cytoplasmic tail and KRIT1 FERM domain labeled.

Indexed as

Acridone alkaloidsCerebral cavernous malformationHEG1–KRIT1 interactionMolecular dynamics simulationProtein–protein interaction inhibitors.

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.