About: Tetraphenylporphyrin-cobalt(III) Bis(1,2-dicarbollide) Conjugates: From the Solution Characteristics to Inhibition of HIV Protease     Goto   Sponge   NotDistinct   Permalink

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  • Práce popisuje syntézu a detailní spektroskopickou charakterizaci metallakarboranových konjugátů tetrafenylporfyrinu. Je vysvětlena závislost fenoménu molekulární asociace konjugátů na pH roztoku a prokázána inhibice HIV proteasy. (cs)
  • Tetraphenylporphyrin conjugates with four (PB4) and one (PB1) cobalt(III)bis(1,2-dicarbollide) substituents were synthesized. The physico-chemical and photophysical properties as well as inhibition of HIV-1 protease are described. In methanol, both PB4 and PB1 are monomeric and form the triplet states and singlet oxygen after excitation. We observed protonation of the triplet states and only a small decrease of quantum yields of the singlet oxygen formation (17 % for PB4 and 13% for PB1) as compared with 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin. On the contrary, no singlet oxygen was detected in aqueous solutions due to strong aggregation. Light scattering and AFM measurements show that the behavior of aggregates in aqueous solutions is fairly complex and depends on pH, concentration and aging. The aggregation in neutral solutions starts with the formation of spherical species. In acidic solutions, an extended aggregation occurs due to slow protonation of the porphyrin pyrrole nitrogens. Both P
  • Tetraphenylporphyrin conjugates with four (PB4) and one (PB1) cobalt(III)bis(1,2-dicarbollide) substituents were synthesized. The physico-chemical and photophysical properties as well as inhibition of HIV-1 protease are described. In methanol, both PB4 and PB1 are monomeric and form the triplet states and singlet oxygen after excitation. We observed protonation of the triplet states and only a small decrease of quantum yields of the singlet oxygen formation (17 % for PB4 and 13% for PB1) as compared with 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin. On the contrary, no singlet oxygen was detected in aqueous solutions due to strong aggregation. Light scattering and AFM measurements show that the behavior of aggregates in aqueous solutions is fairly complex and depends on pH, concentration and aging. The aggregation in neutral solutions starts with the formation of spherical species. In acidic solutions, an extended aggregation occurs due to slow protonation of the porphyrin pyrrole nitrogens. Both P (en)
Title
  • Tetraphenylporphyrin-cobalt(III) Bis(1,2-dicarbollide) Conjugates: From the Solution Characteristics to Inhibition of HIV Protease
  • Tetraphenylporphyrin-cobalt(III) Bis(1,2-dicarbollide) Conjugates: From the Solution Characteristics to Inhibition of HIV Protease (en)
  • Konjugáty kobalt(3+) bis(1,2-dikarbolidu) s tetrafenylporfyrinem: od vlastností roztoků k inhibici HIV proteasy. (cs)
skos:prefLabel
  • Tetraphenylporphyrin-cobalt(III) Bis(1,2-dicarbollide) Conjugates: From the Solution Characteristics to Inhibition of HIV Protease
  • Tetraphenylporphyrin-cobalt(III) Bis(1,2-dicarbollide) Conjugates: From the Solution Characteristics to Inhibition of HIV Protease (en)
  • Konjugáty kobalt(3+) bis(1,2-dikarbolidu) s tetrafenylporfyrinem: od vlastností roztoků k inhibici HIV proteasy. (cs)
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  • RIV/60461373:22340/07:00020926!RIV09-MSM-22340___
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  • P(1M0508), P(GA203/04/0426), P(GA203/04/0490), P(GA203/07/1424), P(KAN100500652), R, S, Z(AV0Z40320502), Z(AV0Z40400503), Z(AV0Z40550506), Z(MSM0021620857)
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  • 17
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  • 454901
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  • RIV/60461373:22340/07:00020926
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  • porphyrin; metallacarborane; cobalt(III) bis(1,2-dicarbollide); HIV protease; association (en)
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  • US - Spojené státy americké
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  • [7C51E9587AC4]
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  • JOURNAL OF PHYSICAL CHEMISTRY B
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  • 111
http://linked.open...iv/tvurceVysledku
  • Cígler, Petr
  • Král, Vladimír
  • Kubát, Pavel
  • Kožíšek, Milan
  • Lang, Kamil
  • Matějíček, Pavel
  • Zelinger, Zdeněk
  • Janda, Pavel
  • Procházka, Karel
http://linked.open...ain/vavai/riv/wos
  • 000245954800034
http://linked.open...n/vavai/riv/zamer
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  • 1520-6106
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  • 22340
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