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Synthesis and evaluation of AKR1C inhibitory properties of A-ring halogenated oestrone derivatives
ID Sinreih, Maša (Avtor), ID Jójárt, Rebeka (Avtor), ID Kele, Zoltán (Avtor), ID Büdefeld, Tomaž (Avtor), ID Paragi, Gábor (Avtor), ID Mernyák, Erzsébet (Avtor), ID Lanišnik-Rižner, Tea (Avtor)

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Izvleček
Enzymes AKR1C regulate the action of oestrogens, androgens, and progesterone at the pre-receptor level and are also associated with chemo-resistance. The activities of these oestrone halides were investigated on recombinant AKR1C enzymes. The oestrone halides with halogen atoms at both C-2 and C-4 positions (13β-, 13α-methyl-17-keto halogen derivatives) were the most potent inhibitors of AKR1C1. The lowest IC$_{50}$ values were for the 13α-epimers 2_2I,4Br and 2_2I,4Cl (IC$_{50}$, 0.7 μM, 0.8 μM, respectively), both of which selectively inhibited the AKR1C1 isoform. The 13α-methyl-17-keto halogen derivatives 2_2Br and 2_4Cl were the most potent inhibitors of AKR1C2 (IC$_{50}$, 1.5 μM, 1.8 μM, respectively), with high selectivity for the AKR1C2 isoform. Compound 1_2Cl,4Cl showed the best AKR1C3 inhibition, and it also inhibited AKR1C1 (Ki: AKR1C1, 0.69 μM; AKR1C3, 1.43 μM). These data show that halogenated derivatives of oestrone represent a new class of potent and selective AKR1C inhibitors as lead compounds for further optimisations.

Jezik:Angleški jezik
Ključne besede:aldo-keto reductases, inhibition, halogenated oestrone derivatives, structure–activity relationships
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2021
Št. strani:Str. 1499–1507
Številčenje:Vol. 36, no. 1
PID:20.500.12556/RUL-144791 Povezava se odpre v novem oknu
UDK:616-006
ISSN pri članku:1475-6366
DOI:10.1080/14756366.2021.1937142 Povezava se odpre v novem oknu
COBISS.SI-ID:67617027 Povezava se odpre v novem oknu
Datum objave v RUL:13.03.2023
Število ogledov:581
Število prenosov:57
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Journal of enzyme inhibition and medicinal chemistry
Skrajšan naslov:J. enzyme inhib. med. chem.
Založnik:Taylor & Francis
ISSN:1475-6366
COBISS.SI-ID:512255001 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC 4.0, Creative Commons Priznanje avtorstva-Nekomercialno 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc/4.0/deed.sl
Opis:Licenca Creative Commons, ki prepoveduje komercialno uporabo, vendar uporabniki ne rabijo upravljati materialnih avtorskih pravic na izpeljanih delih z enako licenco.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:aldo-keto reduktaze, halogenirani derivati estrona, zaviranje

Projekti

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Hungarian Academy of Sciences, János Bolyai Research Scholarship

Financer:Drugi - Drug financer ali več financerjev
Program financ.:National Research, Development and Innovation Office (NKFIH)
Številka projekta:OTKA SNN 124329

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:N1-0066
Naslov:Razvoj novih derivatov estrona kot intrakrinih modulatorjev sinteze in transporta estrogenov

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