The DOI matches its Crossref record.
Comparison of Antimicrobial Properties of Monoterpenes and their Carbonylated Products
Abstract
Some monoterpenes and their carbonylated products were evaluated for their antibacterial and antifungal properties. The carbonylation of tested monoterpenes was shown to increase the bacteriostatic and fungistatic activities specifically by the contact method. Concerning the killing effects, only (1R,2S,5R)-isopulegol, its carbonylated products, and (R)-carvone showed significant bactericidal activities, particularly against Enterococcus faecium and Escherichia coli above a concentration of 10 microliters/ml. A fungicidal efficiency of (1R,2S,5R)-isopulegol and (R)-carvone against Aspergillus niger was also noted. It seems that the presence of an oxygenated function in the framework increases the antimicrobial properties. However, monoterpenes were more active using a micro-atmosphere method.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Monoterpenes (1R, 2S, 5R)-Isopulegol, (R)-carvone and Isolimonene showed good fungistatic activities against C. albicans (Naigre et al. 1996) .”
From Insecticidal, repellent, antimicrobial activity and phytotoxicity of essential oils: With special reference to limonene and its suitability for control of insect pests (2001) · cites this paper as Naigre et al. 1996
Citations
Cites
Still being checked.
Cited by
Sorted by citations
Items 101–132 of 132
da Silva, L. Y. S., Alves, D. S., Ramos, A. G. B., Pessoa, R. T., Neto, J. B. D. A., da Silva, M. M. C., Alcântara, I. S., Neto, L. J. D. L., de Oliveira, M. R. C., Oliveira–Tintino, C. D. D. M., et al. (2024) · Polymer Bulletin · doi:10.1007/s00289-024-05191-3 · Cited by 4
In Vitro Antimicrobial and Antioxidant Activities of Monoterpenes against some Food-Borne Pathogens
Marei, G. I. K., Rabea, E. I., & Badawy, M. E. I. (2019) · Journal of Plant Protection and Pathology /Journal of Plant Protection and Pathology · doi:10.21608/jppp.2019.40594 · Cited by 4
Plant as Potential Resources for Efficacious Essential Oils: Underpinning Aromatherapy Evolution
Misra, P. S. N., Pandey, G., Pandey, S., Singh, A. K., Chaurasia, A. K., Lal, E. P., Agnihotry, S., Srivastav, A. K., & Shukla, P. K. (2024) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815136203124010006 · Cited by 4
Water soluble fractions of caraway (Carum carvi L.) essential oil
Lagunez-Rivera, L., Vilarem, G., Solano, R., Jiménez‐Estrada, M., & Feijoo, J. A. V. (2010) · HAL · Cited by 4
Zahran, E. M., Elfoly, E., Elhamadany, E. Y., Hemied, M. S., Elsayed, T. A., Hisham, M., & Abdelmohsen, U. R. (2025) · Chemistry & Biodiversity · doi:10.1002/cbdv.202402847 · Cited by 3
Molecular docking prediction of carvone and trans‐geraniol inhibitability towards SARS‐CoV ‐2
Quý, P. T., My, T. T. A., Bui, T. Q., Loan, H. T. P., Anh, T. T. V., Triet, N. T., Quang, D. T., & Nhung, N. T. A. (2021) · Vietnam Journal of Chemistry · doi:10.1002/vjch.202000175 · Cited by 3
Analysis of Essential Oils and Antifungal Activity of Cymbopogon Travancorensis Bor.
Maridass, M. (2008) · Cited by 3
Zhang, J., Chen, Q., Xiong, Q., Liang, Y., & Zhang, J. (2025) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2025.106823 · Cited by 2
Santos, P. H., Marciano, J. S., da Silva, D. J., Camani, P. H., Ferreira, G. D. S., Duran, A. F. A., Camillo, L. D. M. B., Bueno, R. D. F., & Rosa, D. D. S. (2025) · South African Journal of Botany · doi:10.1016/j.sajb.2025.12.011 · Cited by 2
Fezea, A. F., Al-Zobaidy, H. N., & Alquraishi, M. F. (2017) · IOSR Journal of Agriculture and Veterinary Science · doi:10.9790/2380-1006023640 · Cited by 2
Morrish, J. L. E. (2008) · QSpace (Queen's University Library) · Cited by 2
Bioprospecção dos constituintes voláteis de espécies do gênero Croton l. do Delta do Parnaíba
Cavalcante, Y. P., Amaro, B. O., & Filho, F. A. E. S. (2022) · Research Society and Development · doi:10.33448/rsd-v11i7.29639 · Cited by 1
Paré, D., N’do, J. Y.-P., KABRE, V. N., Nikièma, M., Zongo, E., Meda, R. N.-T., & Hilou, A. (2025) · South African Journal of Botany · doi:10.1016/j.sajb.2025.03.039 · Cited by 1
Monoterpenoids: A Neuropharmacological Approach
Buch, P., Airao, V., Sharma, T., & Parmar, S. K. (2020) · American Journal Of Pharmacy And Health Research · doi:10.46624/ajphr.2020.v8.i11.002 · Cited by 1
Hadaček, F. (2008) · Soil biology · doi:10.1007/978-3-540-74543-3_10 · Cited by 1
Subramanyam, B. (2023) · Modern Concepts & Developments in Agronomy · doi:10.31031/mcda.2023.12.000791 · Cited by 1
Lagunez-Rivera, L., Vilarem, G., Solano, R., & Jiménez‐Estrada, M. (2010)
The metabolism of terprenoides in caprins
Malecky, M. (2008) · HAL
de Sousa, J. P. (2012) · Americanae (AECID Library)
Aladejana, A. E., Bradley, G., & Afolayan, A. J. (2020) · Asian Journal of Chemistry · doi:10.14233/ajchem.2020.22698
Pande, K. K., Pandey, B., Pande, L., Paliwal, A., & Kumar, T. (2024) · Journal of Mountain Research · doi:10.51220/jmr.v19-i1.29
Aguilar‐Galvez, A., Rivadeneira-Mallqui, C., García‐Ríos, D., Figueroa‐Merma, A., Chirinos, R., Pedreschi, R., & Campos, D. (2025) · International Journal of Food Science & Technology · doi:10.1093/ijfood/vvaf223
Highly selective methoxycarbonylation of (R)-carvone with N-Xantphos-modified Pd-catalyst
Chen, C., Peng, P.-Y., Hu, L.-G., Hua, Y.-X., & Liu, Y. (2025) · Molecular Catalysis · doi:10.1016/j.mcat.2025.115595
Mécanisme d’action antibactérienne des huiles essentielles
Goetz, P. W., & Ghedira, K. (2012) · Phytothérapie pratique · doi:10.1007/978-2-8178-0058-5_9
Hlila, M. B., Jilani, S., Hamdi, A., Dbeibia, A., Rich, S., Horchani, M., Al-Shammari, W. B., Alardan, D., Alshammari, A. A., Ghorbel, M., et al. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1772426
Kačániová, M., Ban, Z., Li, L., Lou, J., Elizondo‐Luévano, J. H., Hsouna, A. B., Saad, R. B., Bianchi, A., & Garzoli, S. (2026) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2026.104205
Ghouti, A., & Meddah, A. T. T. (2026) · Pharmaceutical Chemistry Journal · doi:10.1007/s11094-026-03573-7
Metadata
- Authors
- Naigre, R., Kalck, P., Roques, C., Roux, I., & Michel, G.
- Affiliations
- Université Toulouse III - Paul Sabatier (FR)
- Venue
- Planta Medica
- Publisher
- Georg Thieme Verlag KG
- Published
- 1996-06
- Volume
- 62
- Issue
- 03
- Pages
- 275-277
- ISSN
- 0032-0943 (ISSN-L)
- 1439-0221
- OpenAlex
- W1973167128
- Cited by
- 133
- References
- 0
- Citations by year
- 2026: 3 · 2025: 6 · 2024: 3 · 2023: 3 · 2022: 3 · 2021: 6 · 2020: 6 · 2019: 7 · 2018: 6 · 2017: 5 · 2016: 2 · 2015: 9 · 2014: 4 · 2013: 7 · 2012: 10
- FWCI
- 2.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Planta Medica (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Food Science › Essential Oils and Antimicrobial Activity
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Antimicrobial agents and applications
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Insect Pest Control Strategies
- Keywords
- monoterpenes, antimicrobial activity, antibacterial activity, antifungal activity, isopulegol, carvone, bactericidal activity, fungicidal activity, Enterococcus faecium, Escherichia coli, Aspergillus niger, oxygenated compounds
- MeSH terms
- Anti-Infective Agents, Anti-Bacterial Agents, Antifungal Agents, Aspergillus niger, Bacteria, Candida albicans, Escherichia coli, Microbial Sensitivity Tests, Pseudomonas aeruginosa, Staphylococcus aureus, Structure-Activity Relationship, Terpenes, Enterococcus faecium
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
