Coumarin-based drugs: a patent review (2008–present)

C Kontogiorgis, A Detsi… - Expert opinion on …, 2012 - Taylor & Francis
Introduction: Coumarins are a group of plant-derived polyphenolic compounds. They belong
to the benzopyrones family and possess a wide variety of cytoprotective and modulatory …

Design and validation of specific inhibitors of 17β-hydroxysteroid dehydrogenases for therapeutic application in breast and prostate cancer, and in endometriosis

JM Day, HJ Tutill, A Purohit… - Endocrine-related …, 2008 - erc.bioscientifica.com
Advanced medullary thyroid cancers (MTCs) are now being treated with drugs that inhibit
receptor tyrosine kinases, many of which involved in angiogenesis. Response rates vary …

Recent Advancement in Palladium-Catalyzed C–C Bond Activation of Strained Ring Systems: Three-and Four-Membered Carbocycles as Prominent C3/C4 Building …

T Nanda, M Fastheem, A Linda, BV Pati… - ACS …, 2022 - ACS Publications
In recent years, transition metal-catalyzed strong C–C bond activation has significantly
attracted the attention of synthetic chemists. This protocol enables simultaneous and direct …

Antifungal and antibacterial metabolites from a French poplar type propolis

S Boisard, AM Le Ray, A Landreau… - Evidence‐Based …, 2015 - Wiley Online Library
During this study, the in vitro antifungal and antibacterial activities of different extracts
(aqueous and organic) obtained from a French propolis batch were evaluated. Antifungal …

[HTML][HTML] Synthesis of cinnamic acid ester derivatives with antiproliferative and antimetastatic activities on murine melanoma cells

JA do Vale, MP Rodrigues, ÂMA Lima… - Biomedicine & …, 2022 - Elsevier
Melanoma is the most aggressive skin cancer, and its incidence has continued to rise during
the past decades. Conventional treatments present severe side effects in cancer patients …

Study on the constituents of Mexican propolis and their cytotoxic activity against PANC-1 human pancreatic cancer cells

F Li, S Awale, Y Tezuka, H Esumi… - Journal of natural …, 2010 - ACS Publications
Three new flavonoids,(2 R, 3 R)-3, 5-dihydroxy-7-methoxyflavanone 3-(2-methyl) butyrate
(1),(7′′ R)-8-[1-(4′-hydroxy-3′-methoxyphenyl) prop-2-en-1-yl] chrysin (2), and (7 …

Antifungal activity of cinnamic acid derivatives involves inhibition of benzoate 4‐hydroxylase (CYP53)

B Korošec, M Sova, S Turk, N Kraševec… - Journal of applied …, 2014 - academic.oup.com
Aims CYP53A15, from the sorghum pathogen Cochliobolus lunatus, is involved in
detoxification of benzoate, a key intermediate in aromatic compound metabolism in fungi …

Synthesis of (E)-cinnamyl ester derivatives via a greener Steglich esterification

AB Lutjen, MA Quirk, AM Barbera… - Bioorganic & Medicinal …, 2018 - Elsevier
Cinnamic acid derivatives are known antifungal, antimicrobial, antioxidant, and anticancer
compounds. We have developed a facile and mild methodology for the synthesis of (E) …

Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for Aedes aegypti L. Control

MO Araújo, Y Pérez-Castillo, LHG Oliveira, FC Nunes… - Molecules, 2020 - mdpi.com
The mosquito Aedes aegypti transmits the virus that causes dengue, yellow fever, Zika and
Chikungunya viruses, and in several regions of the planet represents a vector of great …

Synthesis of cinnamic acid derivatives and leishmanicidal activity against Leishmania braziliensis

MP Rodrigues, DC Tomaz, LA de Souza… - European journal of …, 2019 - Elsevier
Leishmania braziliensis is one of the pathogenic agents of cutaneous and mucocutanoeous
leishmaniasis. There are no validated vaccines to prevent the infection and the treatment …