Synthesis of 8-chloro-benzo[c]quinolizin-3-ones as potent and selective inhibitors of human steroid 5α-reductase 1
- DOI
- 10.1016/s0960-894x(99)00698-8
- Published
- 2000-02
- Container
- Bioorganic & Medicinal Chemistry Letters
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/s0960-894x-99-00698-8,
title = {Synthesis of 8-chloro-benzo[c]quinolizin-3-ones as potent and selective inhibitors of human steroid 5α-reductase 1},
author = {Antonio Guarna and Ernesto G. Occhiato and Dina Scarpi and Chiara Zorn and Giovanna Danza and Alessandra Comerci and Rosa Mancina and Mario Serio},
year = {2000},
journal = {Bioorganic \& Medicinal Chemistry Letters},
doi = {10.1016/s0960-894x(99)00698-8},
url = {https://doi.org/10.1016/s0960-894x(99)00698-8}
}RIS
TY - JOUR TI - Synthesis of 8-chloro-benzo[c]quinolizin-3-ones as potent and selective inhibitors of human steroid 5α-reductase 1 AU - Antonio Guarna AU - Ernesto G. Occhiato AU - Dina Scarpi AU - Chiara Zorn AU - Giovanna Danza AU - Alessandra Comerci AU - Rosa Mancina AU - Mario Serio PY - 2000 JO - Bioorganic & Medicinal Chemistry Letters DO - 10.1016/s0960-894x(99)00698-8 UR - https://doi.org/10.1016/s0960-894x(99)00698-8 ER -
APA
Guarna, A., Occhiato, E. G., Scarpi, D., Zorn, C., Danza, G., Comerci, A., Mancina, R., & Serio, M. (2000). Synthesis of 8-chloro-benzo[c]quinolizin-3-ones as potent and selective inhibitors of human steroid 5α-reductase 1. Bioorganic & Medicinal Chemistry Letters. https://doi.org/10.1016/s0960-894x(99)00698-8
Source records
- crossref · retrieved 2026-09-26T16:27:33.955Z