# LC-ESI-MS/MS Analysis of Echium asperrimum from the Algerian Aurès Region: Antioxidant, Antimicrobial, Cholinesterase Inhibitory, and Antiproliferative Activities

**Authors:** Amina Guetteche, Hamza Fadel, Mohammed Esseddik Toumi, Khawla Kerbab, Aslı Yıldırım Kocaman, İlyas Yıldız, Süleyman Muhammed Çelik, Noor Nayel, Tevfik Ozen, Ibrahim Demirtas, Hichem Hazmoune, Ramazan Erenler, Lahcene Zaiter, Maria D’Elia, Luca Rastrelli

PMC · DOI: 10.3390/molecules31040584 · Molecules · 2026-02-07

## TL;DR

This study identifies bioactive compounds in Echium asperrimum from Algeria and shows they have antioxidant, antimicrobial, and anti-Alzheimer properties.

## Contribution

The paper reports the first comprehensive analysis of Echium asperrimum's phenolic profile and its multiple bioactivities.

## Key findings

- EAAE extract showed higher antioxidant activity than EAEE extract.
- Both extracts inhibited cholinesterase enzymes similarly to the drug galantamine.
- EAAE exhibited antiproliferative effects on cancer cells at specific concentrations.

## Abstract

The aim of the present study was to characterize the phenolic profile of hydroethanolic (EAEE) and ethyl acetate (EAAE) extracts of Echium asperrimum and to evaluate their antibacterial, antioxidant, anti-Alzheimer-related (cholinesterase inhibitory) activity, and antiproliferative activities. The DPPH radical scavenging activity of EAEE and EAAE showed IC50 values of 32.53 ± 1.25 and 97.85 ± 2.31 µg/mL, respectively. In addition, both extracts exhibited phosphomolybdenum reduction capacity, with A0.50 values of 61.60 ± 2.97 µg/mL for EAEE and 23.20 ± 1.55 µg/mL for EAAE. Acetylcholinesterase and butyrylcholinesterase inhibition assays revealed IC50 values comparable to the reference compound galantamine. Both extracts also showed antimicrobial activity against Gram-positive and Gram-negative bacterial strains. LC-ESI-MS/MS analysis indicated that p-coumaric acid (5.12 mg/g), vanillic acid (11.6 mg/g), hydroxybenzaldehyde (3.82 mg/g), and gentisic acid (1.66 mg/g) were the major phenolic constituents of EAAE, whereas p-coumaric acid (0.13 mg/g), salicylic acid (0.141 mg/g), sinapic acid (0.20 mg/g), and trans-ferulic acid (0.20 mg/g) predominated in EAEE. Furthermore, EAAE exhibited dose-dependent antiproliferative activity at concentrations of 50 and 100 µg/mL, with an IC50 value of 83.09 ± 6.50 µg/mL. Taken together, these findings suggest that E. asperrimum represents a promising source of bioactive compounds with potential relevance for future pharmaceutical and nutraceutical research.

## Linked entities

- **Chemicals:** p-coumaric acid (PubChem CID 637542), vanillic acid (PubChem CID 8468), hydroxybenzaldehyde (PubChem CID 6998), gentisic acid (PubChem CID 3469), salicylic acid (PubChem CID 338), sinapic acid (PubChem CID 10743), trans-ferulic acid (PubChem CID 445858), galantamine (PubChem CID 9651)
- **Diseases:** Alzheimer's disease (MONDO:0004975)
- **Species:** Echium asperrimum (taxon 34250)

## Full-text entities

- **Genes:** ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, MCL1 (MCL1 apoptosis regulator, BCL2 family member) [NCBI Gene 4170] {aka BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1}, HSPA5 (heat shock protein family A (Hsp70) member 5) [NCBI Gene 3309] {aka BIP, GRP78, HEL-S-89n}, H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, FASLG (Fas ligand) [NCBI Gene 356] {aka ALPS1B, APT1LG1, APTL, CD178, CD95-L, CD95L}, BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Liver cancer (MESH:D006528), breast cancer (MESH:D001943), cardiovascular and other chronic diseases (MESH:D002318), cytotoxic (MESH:D064420), kidney stones (MESH:D007669), snakebites (MESH:D012909), colon cancer (MESH:D015179), fever (MESH:D005334), hand fissures (MESH:D003750), Alzheimer (MESH:D000544), cancer (MESH:D009369), asthma (MESH:D001249), inflammatory (MESH:D007249), injury to (MESH:D014947), skin melanoma (MESH:D008545), skin abrasions (MESH:D012871)
- **Chemicals:** anthocyanins (MESH:D000872), hydrogen (MESH:D006859), caffeic acid (MESH:C040048), flavonoid (MESH:D005419), syringic acid (MESH:C001945), DMSO (MESH:D004121), Chloramphenicol (MESH:D002701), chlorogenic acid (MESH:D002726), ROS (MESH:D017382), ofloxacin (MESH:D015242), polyphenols (MESH:D059808), protocatechuic acid (MESH:C009091), butyrylcholine chloride (MESH:C017100), L-glutamine (MESH:D005973), CO2 (MESH:D002245), lipid (MESH:D008055), ABTS (MESH:C002502), CHCl3 (MESH:D002725), p-coumaric acid (MESH:C495469), lignans (MESH:D017705), sodium sulfate (MESH:C012036), isoflavone (MESH:D007529), GLA (MESH:D017965), acetylshikonin (MESH:C073944), EAEE (-), homogentisic acid (MESH:D006713), EAAE (MESH:C007650), naphthoquinones (MESH:D009285), Thiazolyl Blue Tetrazolium Bromide (MESH:C022616), ammonium molybdate (MESH:C022175), gentisic acid (MESH:C010925), n-butanol (MESH:D020001), glycerol (MESH:D005990), CaCl2 (MESH:D002122), 4-hydroxybenzoic acid (MESH:C038193), Ascorbic acid (MESH:D001205), DTNB (MESH:D004228), quinic acid (MESH:D011801), ethanol (MESH:D000431), sinapic acid (MESH:C073734), water (MESH:D014867), galantamine (MESH:D005702), 5-fluorouracil (MESH:D005472), carotenoids (MESH:D002338), free radical (MESH:D005609), ferulic acid (MESH:C004999), phenolic acids (MESH:C017616), vanillin (MESH:C100058), BHT (MESH:D002084), trans-cinnamic acid (MESH:C029010), terpenoids (MESH:D013729), echimidine (MESH:C000615871), nordihydroguaiaretic acid (MESH:D009637), acetylcholine iodide (MESH:D000109), homovanillic acid (MESH:D006719), nitrogen (MESH:D009584), agar (MESH:D000362), 2,2-diphenyl-1-picrylhydrazyl (MESH:C004931), acetonitrile (MESH:C032159), rutin (MESH:D012431)
- **Species:** Echium vulgare (species) [taxon 34253], Listeria ivanovii (species) [taxon 1638], Staphylococcus aureus (species) [taxon 1280], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Erodium chium (species) [taxon 337363], Homo sapiens (human, species) [taxon 9606], Listeria monocytogenes (species) [taxon 1639], Meleagris gallopavo (common turkey, species) [taxon 9103], Echium asperrimum (species) [taxon 34250], Enterococcus faecalis (species) [taxon 1351], Electrophorus electricus (electric eel, species) [taxon 8005], Echium amoenum (species) [taxon 701470], Pseudomonas aeruginosa (species) [taxon 287], Bacillus cereus (species) [taxon 1396], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** ATCC 15442 — Homo sapiens (Human), Transformed cell line (CVCL_5Z21), A431 cell line — Homo sapiens (Human), Skin squamous cell carcinoma, Cancer cell line (CVCL_0037), T47D — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0553), MCF-7 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0031), RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), CCM 99 — Homo sapiens (Human), Anaplastic astrocytoma, Cancer cell line (CVCL_2613), ATCC 25213 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942907/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942907/full.md

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Source: https://tomesphere.com/paper/PMC12942907