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Pregled bibliografske jedinice broj: 1143024

Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists


Bednarska-Szczepaniak, Katarzyna; Mieczkowski, Adam; Kierozalska, Aleksandra; Pavlović Saftić, Dijana; Głąbała, Konrad; Przygodzki, Tomasz; Stańczyk, Lidia; Karolczak, Kamil; Watała, Cezary; Rao, Harsha et al.
Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists // European journal of medicinal chemistry, 223 (2021), 113607-113631 doi:10.1016/j.ejmech.2021.113607 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1143024 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists
(Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists)

Autori
Bednarska-Szczepaniak, Katarzyna ; Mieczkowski, Adam ; Kierozalska, Aleksandra ; Pavlović Saftić, Dijana ; Głąbała, Konrad ; Przygodzki, Tomasz ; Stańczyk, Lidia ; Karolczak, Kamil ; Watała, Cezary ; Rao, Harsha ; Gao, Zhan-Guo ; Jacobson, Kenneth A. ; Leśnikowski, Zbigniew J.

Izvornik
European journal of medicinal chemistry (0223-5234) 223 (2021); 113607-113631

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Adenosine ; Boron cluster ; Agonists ; Antagonists ; Selectivity ; Nucleosides ; Purinergic receptors

Sažetak
A series of adenosine and 2′-deoxyadenosine pairs modified with a 1, 12-dicarba-closo-dodecaborane cluster or alternatively with a phenyl group at the same position was synthesized, and their affinity was determined at A1, A2A, A2B and A3 adenosine receptors (ARs). While AR affinity differences were noted, a general tendency to preferentially bind A3 AR over other ARs was observed for most tested ligands. In particular, 5′-ethylcarbamoyl-N6-(3-phenylpropyl)adenosine (18), N6-(3-phenylpropyl)-2-chloroadenosine (24) and N6-(3-phenylpropyl)adenosine (40) showed nanomolar A3 affinity (Ki 4.5, 6.4 and 7.5 nM, respectively). Among the boron cluster-containing compounds, the highest A3 affinity (Ki 206 nM) was for adenosine derivative 41 modified at C2. In the matched molecular pairs, analogs bearing boron clusters were found to show lower binding affinity for adenosine receptors than the corresponding phenyl analogs. Nevertheless, interestingly, several boron cluster modified adenosine ligands showed significantly higher A3 receptor selectivity than the corresponding phenyl analogs: 7 vs. 8, 15 vs. 16, 17 vs. 18.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Profili:

Avatar Url Dijana Pavlović Saftić (autor)

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com doi.org

Citiraj ovu publikaciju:

Bednarska-Szczepaniak, Katarzyna; Mieczkowski, Adam; Kierozalska, Aleksandra; Pavlović Saftić, Dijana; Głąbała, Konrad; Przygodzki, Tomasz; Stańczyk, Lidia; Karolczak, Kamil; Watała, Cezary; Rao, Harsha et al.
Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists // European journal of medicinal chemistry, 223 (2021), 113607-113631 doi:10.1016/j.ejmech.2021.113607 (međunarodna recenzija, članak, znanstveni)
Bednarska-Szczepaniak, K., Mieczkowski, A., Kierozalska, A., Pavlović Saftić, D., Głąbała, K., Przygodzki, T., Stańczyk, L., Karolczak, K., Watała, C. & Rao, H. (2021) Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists. European journal of medicinal chemistry, 223, 113607-113631 doi:10.1016/j.ejmech.2021.113607.
@article{article, author = {Bednarska-Szczepaniak, Katarzyna and Mieczkowski, Adam and Kierozalska, Aleksandra and Pavlovi\'{c} Safti\'{c}, Dijana and G\l\k{a}ba\la, Konrad and Przygodzki, Tomasz and Sta\'{n}czyk, Lidia and Karolczak, Kamil and Wata\la, Cezary and Rao, Harsha and Gao, Zhan-Guo and Jacobson, Kenneth A. and Le\'{s}nikowski, Zbigniew J.}, year = {2021}, pages = {113607-113631}, DOI = {10.1016/j.ejmech.2021.113607}, keywords = {Adenosine, Boron cluster, Agonists, Antagonists, Selectivity, Nucleosides, Purinergic receptors}, journal = {European journal of medicinal chemistry}, doi = {10.1016/j.ejmech.2021.113607}, volume = {223}, issn = {0223-5234}, title = {Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists}, keyword = {Adenosine, Boron cluster, Agonists, Antagonists, Selectivity, Nucleosides, Purinergic receptors} }
@article{article, author = {Bednarska-Szczepaniak, Katarzyna and Mieczkowski, Adam and Kierozalska, Aleksandra and Pavlovi\'{c} Safti\'{c}, Dijana and G\l\k{a}ba\la, Konrad and Przygodzki, Tomasz and Sta\'{n}czyk, Lidia and Karolczak, Kamil and Wata\la, Cezary and Rao, Harsha and Gao, Zhan-Guo and Jacobson, Kenneth A. and Le\'{s}nikowski, Zbigniew J.}, year = {2021}, pages = {113607-113631}, DOI = {10.1016/j.ejmech.2021.113607}, keywords = {Adenosine, Boron cluster, Agonists, Antagonists, Selectivity, Nucleosides, Purinergic receptors}, journal = {European journal of medicinal chemistry}, doi = {10.1016/j.ejmech.2021.113607}, volume = {223}, issn = {0223-5234}, title = {Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists}, keyword = {Adenosine, Boron cluster, Agonists, Antagonists, Selectivity, Nucleosides, Purinergic receptors} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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