Biologically Active Triterpenoids Usable As Prodrugs
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F15%3A33152706" target="_blank" >RIV/61989592:15310/15:33152706 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61389030:_____/15:00447783 RIV/61989592:15110/15:33152706
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Biologically Active Triterpenoids Usable As Prodrugs
Popis výsledku v původním jazyce
Triterpenoids are a large group of natural compounds, many of which have interesting biological activities. Despite this, only a few derivatives are currently used as therapeutics. The main reason is that the active triterpenes usually have unfavorable pharmacological and physicochemical properties such as solubility and bioavailability. Therefore, many compounds with excellent activity in in vitro tests usually fail during clinical trial. Many research groups have tried to synthesize a variety of prodrugs in order to improve pharmacological properties of the active compound while retaining the desired biological activity. The most commonly chosen functional groups in triterpenes to be modified as prodrugs are hydroxyl and carboxyl. In this chapter, weare going to summarize all of the research that has been done in the area of triterpenoid prodrugs with the main focus on the modifications of hydroxyls and carboxyls. Commonly used types of prodrug groups (such as simple alkyl esters, o
Název v anglickém jazyce
Biologically Active Triterpenoids Usable As Prodrugs
Popis výsledku anglicky
Triterpenoids are a large group of natural compounds, many of which have interesting biological activities. Despite this, only a few derivatives are currently used as therapeutics. The main reason is that the active triterpenes usually have unfavorable pharmacological and physicochemical properties such as solubility and bioavailability. Therefore, many compounds with excellent activity in in vitro tests usually fail during clinical trial. Many research groups have tried to synthesize a variety of prodrugs in order to improve pharmacological properties of the active compound while retaining the desired biological activity. The most commonly chosen functional groups in triterpenes to be modified as prodrugs are hydroxyl and carboxyl. In this chapter, weare going to summarize all of the research that has been done in the area of triterpenoid prodrugs with the main focus on the modifications of hydroxyls and carboxyls. Commonly used types of prodrug groups (such as simple alkyl esters, o
Klasifikace
Druh
C - Kapitola v odborné knize
CEP obor
CC - Organická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název knihy nebo sborníku
Terpenoids and Squalene: Biosynthesis, Functions and Health Implications
ISBN
978-1-63463-656-8
Počet stran výsledku
25
Strana od-do
25-49
Počet stran knihy
90
Název nakladatele
Nova Science Publisher, Inc.
Místo vydání
USA
Kód UT WoS kapitoly
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