Synthesis and antitumor activity of simplified ecteinascidin–saframycin analogs

ZZ Liu, Y Wang, YF Tang, SZ Chen, XG Chen… - Bioorganic & medicinal …, 2006 - Elsevier
Two series of simplified analogs of the ecteinascidin–saframycin type alkaloids were
prepared from l-DOPA. Their in vitro antitumor activity was tested against three human …

[PDF][PDF] The fight against the ocular cancer

E Guedes - 2022 - researchgate.net
F HN O NH OHN HO HN Page 1 The fight against the ocular cancer By Edigles Guedes
December 3, 2022 Abstract. We suggest the use of the molecule (6S)-6-((3-fluoro-1,2,3,4-tetrahydroquinolin-8-yl)amino)-1,3,2,4-dioxadiazinan-5-ol …

Synthesis of budesonide conjugates and their anti-inflammatory effects: a preliminary study

Y Yan, P Wang, R Li, Y Sun, R Zhang… - Drug Design …, 2019 - Taylor & Francis
Purpose Budesonide (Bud) is a nonhalogenated glucocorticoid with high anti-inflammatory
potency and low systemic side effects. However, the poor water solubility of Bud affects its …

Diosgenin 유도체합성과진통및항고지혈효과

김학순, 마은숙 - 약학회지, 2007 - dbpia.co.kr
Twelve epoxy and hydroxydiosgenin derivatives (DI-1${\sim} $ DI-12) were synthesized from
diosgenin (25 (R)-5-spirosten-3${\beta} $-ol). Diosgenin was epoxidized with m …

Synthesis and biological activity of new anti-inflammatory compounds containing the 1, 4-benzodioxine and/or pyrrole system

Y Harrak, G Rosell, G Daidone, S Plescia… - Bioorganic & medicinal …, 2007 - Elsevier
A series of substituted derivatives containing the 1, 4-benzodioxine or pyrrole nucleus are
described. All the newly synthesized compounds were examined for their in vitro and in vivo …

[HTML][HTML] Synthesis and cytotoxic evaluation of malachite green derived oleanolic and ursolic acid piperazineamides

S Friedrich, I Serbian, S Hoenke, RK Wolfram… - Medicinal Chemistry …, 2020 - Springer
The coupling of acetylated piperazinylamide spacered triterpenoic oleanolic acid and ursolic
acid with meta or para substituted carboxylated malachite green analogs gave conjugates …

Synthesis and anticancer evaluation of complex unsaturated isosteviol-derived triazole conjugates

RN Khaybullin, X Liang, K Cisneros… - Future medicinal …, 2015 - Future Science
Background: For the last two decades, diterpenoid isosteviol and its derivatives have gained
significant attention for novel chemical transformation in the drug discovery field. Results: An …

Proceso para preparar intermedios de compuestos útiles como moduladores de receptores opioides

C Cai, HE Wei, RW Kavash, HJ Breslin - 2015 - Google Patents
First worldwide family litigation filed litigation Critical https://patents. darts-ip. com/? family=
34962827&utm_source= google_patent&utm_medium= platform_link&utm_campaign …

New semi-synthetic analogs of oleuropein show improved anticancer activity in vitro and in vivo

P Samara, N Christoforidou, C Lemus… - European Journal of …, 2017 - Elsevier
Oleuropein is a glucosylated seco-iridoid present in olive fruits and leaves. Due to its broad
spectrum of biological activities, including anticancer properties, oleuropein has attracted …

Fluorescein conjugates of 9-and 10-hydroxystearic acids: synthetic strategies, photophysical characterization, and confocal microscopy applications

C Boga, S Puggioli, M Gherpelli, G Farruggia… - Analytical …, 2004 - Elsevier
Different strategies are presented to conjugate a fluorescein moiety to 9-and 10-
hydroxystearic acids (HSAs). 5-Amino-fluorescein (5-AF) was used as a starting reagent …