Natural and semi synthetic antimalarial compounds: emphasis on the terpene class (2015)
- Authors:
- Autor USP: EMERY, FLAVIO DA SILVA - FCFRP
- Unidade: FCFRP
- Subjects: ANTIMALÁRICOS; CITOTOXINAS; TERPENOS; SÍNTESE ORGÂNICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Mini-Reviews in Medicinal Chemistry
- ISSN: 1875-5607
- Volume/Número/Paginação/Ano: v. 15, n. 10, p. 809-836, 2015
-
ABNT
SILVA, G. N. S. et al. Natural and semi synthetic antimalarial compounds: emphasis on the terpene class. Mini-Reviews in Medicinal Chemistry, v. 15, n. 10, p. 809-836, 2015Tradução . . Acesso em: 18 fev. 2026. -
APA
Silva, G. N. S., Rezende, L. C. D., Emery, F. da S., Gosmann, G., & Gnoatto, S. C. B. (2015). Natural and semi synthetic antimalarial compounds: emphasis on the terpene class. Mini-Reviews in Medicinal Chemistry, 15( 10), 809-836. -
NLM
Silva GNS, Rezende LCD, Emery F da S, Gosmann G, Gnoatto SCB. Natural and semi synthetic antimalarial compounds: emphasis on the terpene class. Mini-Reviews in Medicinal Chemistry. 2015 ; 15( 10): 809-836.[citado 2026 fev. 18 ] -
Vancouver
Silva GNS, Rezende LCD, Emery F da S, Gosmann G, Gnoatto SCB. Natural and semi synthetic antimalarial compounds: emphasis on the terpene class. Mini-Reviews in Medicinal Chemistry. 2015 ; 15( 10): 809-836.[citado 2026 fev. 18 ] - A review of the synthetic strategies for the development of BODIPY dyes for conjugation with proteins
- On the search for potential anti-Trypanosoma cruzi drugs: synthesis and biological evaluation of 2-hydroxy-3-methylamino and 1,2,3-triazolic naphthoquinoidal compounds obtained by clik chemistry reactions
- On the synthesis of quinone-based BODIPY hybrids: New insights on antitumor activity and mechanism of action in cancer cells
- Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes
- Naftotiazóis inibidores de dihidroorotato desidrogenase potenciais agentes leishmanicidas
- Síntese de análogos heterocíclicos do aripiprazol
- Synthesis of quinoidal molecules: strategies towards bioactive compounds with an emphasis on lapachones
- Oral administration of peptide-based drugs: beyond Lipinski's rule
- Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives
- Claisen rearrangement of hydroxynaphthoquinones: selectivity toward naphthofuran or α-xiloidone using copper salts and iodine
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
