Academic Journal
Biological profiling of semisynthetic C19-functionalized ferruginol and sugiol analogues
| العنوان: | Biological profiling of semisynthetic C19-functionalized ferruginol and sugiol analogues |
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| المؤلفون: | González Cardenete, Miguel Ángel., Rivas, Fatima., Bassett, Rachel., Stadler, Marco., Hering, Steffen., Padrón Carrillo, José Manuel., Zaragozá Cardells, Ramón José., Dea Ayuela, María Auxiliadora. |
| المساهمون: | Producción Científica UCH 2021, UCH. Departamento de Farmacia |
| بيانات النشر: | MDPI |
| سنة النشر: | 2021 |
| المجموعة: | Universidad San Pablo CEU Madrid: Repositorio Institucional |
| مصطلحات موضوعية: | Paludismo - Farmacoterapia, Pharmacology, Farmacología, Malaria - Chemotherapy |
| الوصف: | Este artículo se encuentra disponible en la siguiente URL: https://www.mdpi.com/2079-6382/10/2/184 ; Este artículo pertenece al número especial "Search of New Natural Products with Antimicrobial Activity". ; The abietane-type diterpenoids are significant bioactive compounds exhibiting a varied range of pharmacological properties. In this study, the first synthesis and biological investigation of the new abietane-diterpenoid (+)-4-epi-liquiditerpenoid acid (8a) together with several of its analogs are reported. The compounds were generated from the readily available methyl callitrisate (7), which was obtained from callitrisic acid present in Moroccan Sandarac resin. A biological evaluation was conducted to determine the effects of the different functional groups present in these molecules, providing basic structure–activity relationship (SAR) elements. In particular, the ferruginol and sugiol analogs compounds 10–16 were characterized by the presence of a phenol moiety, higher oxidization states at C-7 (ketone), and the hydroxyl, methyl ester or free carboxylic acid at C19. The biological profiling of these compounds was investigated against a panel of six human solid tumor cell lines (HBL-100, A549, HeLa, T-47D, SW1573 and WiDr), four parasitic Leishmania species (L. donovani, L. infantum, L. guyanensis and L. amazonensis) and two malaria strains (3D7 and K1). Furthermore, the capacity of the compounds to modulate gamma-aminobutyric acid type A (GABAA) receptors ( 1 2 2s) is also described. A comparison of the biological results with those previously reported of the corresponding C18-functionalized analogs was conducted. |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English Spanish; Castilian |
| Relation: | Este artículo de investigación ha sido financiada por el Consejo Superior de Investigaciones Científicas (CSIC) (201680I008), por la Austrian Science Fund (FWF W 1232), por la American Lebanese Syrian Associated Charities, por el Banco Santander a través de los grupos consolidados de investigación de la Universidad CEU Cardenal Herrera y por el Ministerio de Ciencia (MICINN) del Gobierno de España a través de la beca PGC2018-094503-B-C22.; UCH. Financiación Universidad; Antibiotics, vol. 10, n. 2 (12 feb. 2021); 201680I008; FWF W 1232; PGC2018-094503-B-C22; González-Cardenete, M.A., Rivas, F., Basset, R., Stadler, M., Hering, S., Padrón, J.M., Zaragozá, R.J. & Dea-Ayuela, M. A. (2021). Biological profiling of semisynthetic C19-functionalized Ferruginol and Sugiol analogues. Antibiotics, vol. 10, i. 2 (12 feb.), art. 184. DOI: https://doi.org/10.3390/antibiotics10020184; 2079-6382 (Electrónico); http://hdl.handle.net/10637/13553; https://doi.org/10.3390/antibiotics10020184 |
| DOI: | 10.3390/antibiotics10020184 |
| الاتاحة: | http://hdl.handle.net/10637/13553 https://doi.org/10.3390/antibiotics10020184 |
| Rights: | http://creativecommons.org/licenses/by/4.0/deed.es |
| رقم الانضمام: | edsbas.D492447E |
| قاعدة البيانات: | BASE |
| DOI: | 10.3390/antibiotics10020184 |
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