# Indene and indole-based compounds as potential antimicrobial agents: synthesis, activity, docking studies and ADME analysis

**Authors:** Vilma Lovrinčević, Monika Šabić Runjavec, Nikica Baričević, Ines Despotović, Jerome Le-Cunff, Dragana Vuk, Marija Vuković Domanovac

PMC · DOI: 10.1039/d5ra08239k · RSC Advances · 2026-02-23

## TL;DR

This paper explores new indene and indole compounds as potential antibiotics, showing effectiveness against some bacteria and fungi.

## Contribution

The study introduces new indene and indole derivatives with antimicrobial activity and validates their mechanism through docking and ADME analysis.

## Key findings

- Most compounds showed antifungal activity and antibacterial activity against Bacillus subtilis.
- Molecular docking revealed strong interactions with DNA gyrase B and 14α-sterol demethylase.
- In silico ADME analysis confirmed favorable physicochemical properties for the compounds.

## Abstract

The excessive use of antibiotics in recent years has led to an accelerated development of resistance in bacterial pathogens and thus to one of the greatest problems of our time: antibiotic resistance. Therefore, despite the large number of available drugs, the development of new and structurally diverse antibiotics is urgently needed. In this study, various indole and indene derivatives were prepared and characterised and their antibacterial activity against Gram-positive bacteria Bacillus subtilis 3020 and Gram-negative bacteria Pseudomonas aeruginosa 3011 was investigated. Two fungal strains, Candida lipolytica 59 and Aspergillus niger 405, were used for antifungal activity. In general, most of the prepared compounds showed potential antifungal activity and antibacterial activity against Bacillus subtilis 3020, while all compounds were inactive against Pseudomonas aeruginosa 3011. The most promising compounds were pyrrole, pyridine and phenol derivatives, which showed antibacterial and antifungal activity. In addition, molecular docking studies showed that the most promising indole and indene derivatives exhibited significant binding interaction networks and binding affinity with DNA gyrase B (GyrB) and 14α-sterol demethylase (CYP51), consistent with their observed antibacterial and antifungal activities. Finally, in silico ADME predictions indicated acceptable physicochemical properties of the newly designed compounds.

Various indene derivatives are presented and their antimicrobial activities against different microbial species are evaluated. To elucidate the plausible inhibitory mechanism in silico molecular docking study was performed for selected molecules.

## Linked entities

- **Chemicals:** indene (PubChem CID 7219), indole (PubChem CID 798), pyrrole (PubChem CID 8027), pyridine (PubChem CID 1049), phenol (PubChem CID 996)

## Full-text entities

- **Diseases:** bacterial infections (MESH:D001424), inflammatory (MESH:D007249)
- **Chemicals:** beta-lactams (MESH:D047090), acetaldehyde (MESH:D000079), H (MESH:D006859), chloramphenicol (MESH:D002701), DMSO (MESH:D004121), Indole (MESH:C030374), bacitracin (MESH:D001414), diethyl ether (MESH:D004986), LiAlH4 (MESH:C042073), fluconazole (MESH:D015725), ATP (MESH:D000255), ampicillin (MESH:D000667), imipenem (MESH:D015378), itraconazole (MESH:D017964), pyrrole (MESH:D011758), sterol (MESH:D013261), THF (MESH:C018674), nystatin (MESH:D009761), KOH (MESH:C029943), amphotericin B (MESH:D000666), amino acid (MESH:D000596), MgSO4 (MESH:D008278), piperacillin and tazobactam (MESH:D000077725), pyrrole-2-carbaldehyde (MESH:C051266), terbinafine (MESH:D000077291), ethyl-acetate (MESH:C007650), 2H (MESH:D003903), 2-((1H-Inden-3-yl)methyl)-5-methylthiophene (-), sulfur (MESH:D013455), pyridine (MESH:C023666), Silica (MESH:D012822), tioconazole (MESH:C020527), n-octanol (MESH:D020003), tetracycline (MESH:D013752), penicillin (MESH:D010406), tobramycin (MESH:D014031), Indanes (MESH:C093582), salicylaldehyde (MESH:C013243), gentamicin (MESH:D005839), erythromycin (MESH:D004917), voriconazole (MESH:D065819), ethanol (MESH:D000431), Amoxicillin (MESH:D000658), aldehyde (MESH:D000447), NaOH (MESH:D012972), 13C (MESH:C000615229), pimaricin (MESH:D010866), phenol (MESH:D019800), indenes (MESH:D007192), Benzene (MESH:D001554), water (MESH:D014867), Indene (MESH:C093581), miconazole (MESH:D008825), clindamycin (MESH:D002981), Indoles (MESH:D007211), ceftazidime (MESH:D002442), tetracyclines (MESH:D013754), clotrimazole (MESH:D003022), meropenem (MESH:D000077731), petroleum ether (MESH:C004544)
- **Species:** Homo sapiens (human, species) [taxon 9606], Fungi (kingdom) [taxon 4751], Pseudomonas aeruginosa (species) [taxon 287], Yarrowia lipolytica (species) [taxon 4952], Aspergillus niger (species) [taxon 5061], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Bacillus subtilis (species) [taxon 1423]
- **Cell lines:** KATMIRA1933 — Homo sapiens (Human), Transformed cell line (CVCL_9I08)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12928186/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928186/full.md

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Source: https://tomesphere.com/paper/PMC12928186