AM Madureira

644 total citations
30 papers, 532 citations indexed

About

AM Madureira is a scholar working on Molecular Biology, Plant Science and Food Science. According to data from OpenAlex, AM Madureira has authored 30 papers receiving a total of 532 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Plant Science and 7 papers in Food Science. Recurrent topics in AM Madureira's work include Bioactive Natural Diterpenoids Research (10 papers), Essential Oils and Antimicrobial Activity (7 papers) and Natural product bioactivities and synthesis (5 papers). AM Madureira is often cited by papers focused on Bioactive Natural Diterpenoids Research (10 papers), Essential Oils and Antimicrobial Activity (7 papers) and Natural product bioactivities and synthesis (5 papers). AM Madureira collaborates with scholars based in Portugal, Hungary and Mozambique. AM Madureira's co-authors include Maria‐José U. Ferreira, Joséph Molnár, Aida Duarte, Noélia Duarte, José R. Ascenso, Pedro Abreu, Silva Mulhovo, Nóra Gyémánt, Mariana Reis and Cátia Ramalhete and has published in prestigious journals such as Inorganic Chemistry, Journal of Ethnopharmacology and Phytochemistry.

In The Last Decade

AM Madureira

30 papers receiving 511 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
AM Madureira Portugal 15 285 162 112 110 96 30 532
Sonja Krstin Germany 15 237 0.8× 187 1.2× 79 0.7× 111 1.0× 85 0.9× 17 697
Ana Paula de Almeida Brazil 11 190 0.7× 174 1.1× 65 0.6× 86 0.8× 42 0.4× 13 451
Liang Guang-yi China 14 393 1.4× 157 1.0× 49 0.4× 79 0.7× 110 1.1× 58 699
P. Vijayan India 11 168 0.6× 172 1.1× 52 0.5× 83 0.8× 79 0.8× 21 547
Gabin Thierry M. Bitchagno Cameroon 15 376 1.3× 301 1.9× 36 0.3× 180 1.6× 117 1.2× 63 734
Jennifer K. Schilling United States 18 344 1.2× 202 1.2× 40 0.4× 92 0.8× 50 0.5× 28 627
Giovanna Barbarini Longato Brazil 15 250 0.9× 126 0.8× 28 0.3× 129 1.2× 111 1.2× 41 632
Abdeslam Jaafari Morocco 12 184 0.6× 242 1.5× 34 0.3× 299 2.7× 77 0.8× 14 592
Michel Feussi Tala Cameroon 14 278 1.0× 278 1.7× 27 0.2× 93 0.8× 98 1.0× 32 587
Guy Sedar Singor Njateng Cameroon 16 198 0.7× 186 1.1× 27 0.2× 121 1.1× 147 1.5× 41 590

Countries citing papers authored by AM Madureira

Since Specialization
Citations

This map shows the geographic impact of AM Madureira's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by AM Madureira with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites AM Madureira more than expected).

Fields of papers citing papers by AM Madureira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by AM Madureira. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by AM Madureira. The network helps show where AM Madureira may publish in the future.

Co-authorship network of co-authors of AM Madureira

This figure shows the co-authorship network connecting the top 25 collaborators of AM Madureira. A scholar is included among the top collaborators of AM Madureira based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with AM Madureira. AM Madureira is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Gonçalves, Bruno M. F., et al.. (2024). Monoterpene indole alkaloids with anticancer activity from Tabernaemontana species. Phytochemistry Reviews. 24(3). 2271–2307. 7 indexed citations
2.
Freitas, Elisabete B., Maria Manuela Gaspar, Rita Capela, et al.. (2023). Structural Optimization of Antimycobacterial Azaaurones Towards Improved Solubility and Metabolic Stability. ChemMedChem. 18(24). e202300410–e202300410. 3 indexed citations
3.
Coelho, Jaime A. S., Raquel F. M. Frade, AM Madureira, et al.. (2023). Functionalized Cyclopentenones with Low Electrophilic Character as Anticancer Agents. ChemMedChem. 18(13). e202300104–e202300104. 2 indexed citations
4.
Fontinha, Diana, Vera L. M. Silva, Filipe A. Almeida Paz, et al.. (2023). Facile Access to Structurally Diverse Antimalarial Indoles Using a One‐Pot A3 Coupling and Domino Cyclization Approach. ChemMedChem. 18(17). e202300264–e202300264. 1 indexed citations
5.
Madureira, AM, Fátima Nogueira, Diana Fontinha, et al.. (2020). Half-Sandwich Cyclopentadienylruthenium(II) Complexes: A New Antimalarial Chemotype. Inorganic Chemistry. 59(17). 12722–12732. 11 indexed citations
6.
Gonçalves, Marta, AM Madureira, Aida Duarte, et al.. (2019). Zanthoxylum zanthoxyloides and Zanthoxylum leprieurii : a micromorphological, phytochemical and antibacterial evaluation. Annals of Medicine. 51(sup1). 81–81. 1 indexed citations
7.
8.
Madureira, AM, et al.. (2015). Cleistochlamys kirkii chemical constituents: Antibacterial activity and synergistic effects against resistant Staphylococcus aureus strains. Journal of Ethnopharmacology. 178. 180–187. 26 indexed citations
9.
Pereira, Fillipe de Oliveira, et al.. (2015). Evaluation of the antibacterial activity of some African medicinal plants. Planta Medica. 81(16). 1 indexed citations
10.
Baptista, Rafael, AM Madureira, Aida Duarte, et al.. (2015). Antioxidant and Antimycotic Activities of Two NativeLavandulaSpecies from Portugal. Evidence-based Complementary and Alternative Medicine. 2015. 1–10. 39 indexed citations
11.
Duarte, Noélia, Mariana Reis, Gabriella Spengler, et al.. (2014). Improving the MDR reversal activity of 6,17-epoxylathyrane diterpenes. Bioorganic & Medicinal Chemistry. 22(22). 6392–6400. 33 indexed citations
12.
Madureira, AM, Aida Duarte, & Generosa Teixeira. (2012). Antimicrobial activity of selected extracts from Hakea salicifolia and H. sericeae (Proteaceae) against Staphylococcus aureus multiresistant strains. South African Journal of Botany. 81. 40–43. 9 indexed citations
13.
Reis, Mariana, Ricardo J. Ferreira, Julianna Serly, et al.. (2012). Colon Adenocarcinoma Multidrug Resistance Reverted by Euphorbia Diterpenes: Structure-Activity Relationships and Pharmacophore Modeling. Anti-Cancer Agents in Medicinal Chemistry. 12(9). 1015–1024. 20 indexed citations
14.
Anes, Elsa, et al.. (2007). Screening for antimycobacterial activity of plants used in traditional medicine. Planta Medica. 73(9). 1 indexed citations
15.
Ferreira, Maria‐José U., Nóra Gyémánt, AM Madureira, et al.. (2006). The effects of jatrophane derivatives on the reversion of MDR1- and MRP-mediated multidrug resistance in the MDA-MB-231 (HTB-26) cell line.. PubMed. 25(6B). 4173–8. 25 indexed citations
16.
Madureira, AM, Maria‐José U. Ferreira, Nóra Gyémánt, et al.. (2004). Rearranged Jatrophane-Type Diterpenes fromEuphorbiaSpecies. Evaluation of their Effects on the Reversal of Multidrug Resistance. Planta Medica. 70(1). 45–49. 18 indexed citations
17.
Madureira, AM, et al.. (2004). A New Sesquiterpene-Coumarin Ether and a New Abietane Diterpene and their Effects as Inhibitors of P-Glycoprotein. Planta Medica. 70(9). 828–833. 38 indexed citations
18.
Madureira, AM, M. Teresa Duarte, M. Fátima M. Piedade, José R. Ascenso, & Maria‐José U. Ferreira. (2004). Isoprenoid compounds from Euphorbia portlandica. X-ray structure of lupeportlandol, a new lupane triterpene. Journal of the Brazilian Chemical Society. 15(5). 742–747. 11 indexed citations
19.
Madureira, AM, José R. Ascenso, Aida Duarte, et al.. (2003). Evaluation of the Antiviral and Antimicrobial Activities of Triterpenes Isolated fromEuphorbia segetalis. Natural Product Research. 17(5). 375–380. 60 indexed citations
20.
Ferreira, Maria‐José U., AM Madureira, & José R. Ascenso. (1998). A Tetracyclic diterpene and triterpenes from euphorbia segetalis. Phytochemistry. 49(1). 179–183. 8 indexed citations

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