Dr. Lauro Figueroa

Professor
Faculty of Chemical Biological Sciences, Autonomus University of Campeche, Mexico

Highest Degree
Ph.D. in Biological Sciences from University of Autonomous Metropolitan, Mexico

My URL
https://livedna.org/52.35184

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Area of Interest:

Pharmacology

Selected Publications

  1. Figueroa-Valverde Lauro, Lopez-Ramos Maria, Diaz-Cedillo Francisco, Rosas-Nexticapa Marcela and Mateu-Armad M. Virginia et al., 2022. Synthesis and biological activity of the pyridine-hexacyclic-steroid derivative on a heart failure model. Anti-Inflammatory Anti-Allergy Agents Med. Chem., 21: 34-45.
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  2. Figueroa‐Valverde, L., D.C. Francisco, Lopez‐Ramos Maria, Rosas‐Nexticapa Marcela, Mateu‐Armand Virginia, Lopez‐Gutierrez Tomas and Alvarez‐Ramirez Magdalena, 2021. Design and synthesis of two epoxide derivatives from 3‐ethynylaniline. J. Heterocyclic. Chem., 58: 1154-1163.
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  3. Figueroa‐Valverde Lauro, D.C. Francisco, Rosas‐Nexticapa Marcela, Lopez‐Ramos Maria, Mateu‐Armand Virginia, Garcimarero‐Espino E. Alejandra and Ortiz‐Ake Yazmin, 2021. Facile synthesis of two oxocan derivatives using some chemical strategies. J. Heterocyclic. Chem., 58: 515-522.
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  4. Figueroa‐Valverde Lauro, D.C. Francisco, Lopez‐Ramos Maria, Garcia‐Martinez Rolando and Rosas‐Nexticapa Marcela et al., 2020. Design and synthesis of a bismethylsulfanyl‐steroid‐azetyl butanol derivative from 2‐nitroestradiol. J. Heterocycl. Chem., 57: 1737-1747.
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  5. Figueroa-Valverde Lauro, Rosas-Nexticapa Marcela, Lopez-Ramos Maria, Diaz Cedillo Francisco and Mateu-Armand Virginia et al., 2019. Synthesis of a new dioxaspiro[bicyclo[3.3.1]nonane-oxabicyclo[6.2.0]deca- 1(10),8-dien-4-one derivative using some chemical strategies. Lett. Org. Chem., 17: 393-402.
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  6. Figueroa-Valverde, L., F. Diaz-Cedillo, E. Garcia-Cervera, E. Pool-Gomez, M. Rosas-Nexticapa, M. Lopez-Ramos and M.I. Vera-Escobedo, 2018. Design and synthesis of two triazonine-carbaldehyde derivatives using several chemical tools. J. Saudi Chem. Soc., 22: 183-197.
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  7. Figueroa-Valverde Lauro, Rosas-Nexticapa Marcela, Mateu-Armand Virginia, Herrera-Meza Socorro and Diaz-Cedillo Francisco, 2018. Evaluation of biological activity exerted by an aza-bicyclocarboxylic acid derivative using anischemia-reperfusion injury modela. Biomed. Pharmacol. J., 11: 1865-1877.
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  8. Figueroa-Valverde Lauro, Rosas-Nexticapa Marcela, Mateu-Armand Virginia, Diaz-Cedillo Francisco and Hau-Heredia Lenin et al., 2018. Preparation of two cyclobutadiene-steroid derivatives theoretical analysis of its interaction with the μ, d, and k opiod-receptors. Orient. J. Chem., 34: 2689-2702.
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  9. Lopez-Ramos, M., L. Figueroa-Valverde, S. Herrera-Meza, M. Rosas-Nexticapa and F. Diaz-Cedillo et al., 2017. Design and synthesis of a new steroid-macrocyclic derivative with biological activity. J. Chem. Biol., 10: 69-84.
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  10. Lopez-Ramos Maria, Figueroa-Valverde Lauro, Rosas-Nexticapa Marcela, Herrera-Meza Maria Del Socorro and Cervantes-Ortega Catalina et al., 2017. Design and synthesis of new dioxa diazaspiro[bicyclo [9.4.2] heptadecane-steroid-dienyne derivative from estrone and otbs-estrone. Orient. J. Chem., 33: 1061-1070.
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  11. Hau-Heredia Lenin, Figueroa-Valverde Lauro, Garcia-Cervera Elodia, Lopez-Ramos Maria and Diaz-Cedillo Francisco, 2017. Antibacterial activity exerted by some diazabicyclo-steroid derivatives against Staphylococcus aureus and Streptococcus pneumoniae. Orient. J. Chem., 33: 2647-2667.
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  12. Figueroa-Valverde, L., M. Rosas-Nexticapa, c. cervantes-ortega, F. Diaz-Cedillo, E. Garcia-Cervera and E. Pool-Gomez, 2017. Design and synthesis of two steroid-pyrrolo-triazecin derivatives using estrone and pregnenolone as chemical tools. Orient. J. Chem., 33: 52-65.
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  13. Figueroa-Valverde, L., F. Diaz-Cedillo, E. Garcia-Cervera, E. Pool-Gomez and M. Lopez-Ramos et al., 2016. Design and synthesis of naphthalene-pregnen derivative using some strategies. Asian J. Chem., 28: 1-5.
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  14. Figueroa-Valverde, L., E. Garcia-Cervera, F. Diaz-Cedillo, L. Hau-heredia and M. Rosas-Nexticapa et al., 2016. Design and synthesis of new steroid-derivatives with antibacterial activity on Salmonella typhi. Asian J. Chem., 28: 2357-2364.
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Member since December, 2020