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New natural product carbonic anhydrase inhibitors incorporating phenol moieties
被引:44
|作者:
Karioti, Anastasia
[1
]
Ceruso, Mariangela
[2
]
Carta, Fabrizio
[2
]
Bilia, Anna-Rita
[3
]
Supuran, Claudiu T.
[2
,4
]
机构:
[1] Aristotle Univ Thessaloniki, Sch Pharm, Lab Pharmacognosy, Thessaloniki 54124, Greece
[2] Univ Florence, Lab Chim Bioinorgan, I-50019 Florence, Italy
[3] Univ Florence, PHYTOLAB, Dept Chim Ugo Schiff, I-50019 Florence, Italy
[4] Univ Florence, Polo Sci, Dipartimento NEUROFARBA, Sez Sci Farmaceut & Nutraceut, I-50019 Florence, Italy
关键词:
Carbonic anhydrase inhibitors (CAIs);
Metalloenzymes;
Phenol;
Polyphenols;
Natural products;
THERAPEUTIC APPLICATIONS;
SALVIA-MILTIORRHIZA;
ANTIOXIDANT;
REQUIREMENTS;
ISOFLAVONES;
POLYPHENOLS;
DERIVATIVES;
GLYCOSIDES;
COUMARINS;
CANCER;
D O I:
10.1016/j.bmc.2015.10.018
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Carbonic anhydrases (CAs, EC 4.2.1.1) catalyze the fundamental reaction of CO2 hydration in all living organisms, being actively involved in the regulation of a plethora of patho/physiological conditions. They represent a typical example of enzyme convergent evolution, as six genetically unrelated families of such enzymes were described so far. The need to find selective CA inhibitors (CAIs) triggered the investigation of natural product libraries, which proved to be a valid source of agents with such an activity, as demonstrated for the phenols, polyamines and coumarins. Herein we report an in vitro inhibition study of human (h) CA isoforms hCAs I, II, IV, VII and XII with a panel of natural polyphenols including flavones, flavonols, flavanones, flavanols, isoflavones and depsides, some of which extracted from Quercus ilex and Salvia miltiorrhiza. Several of the investigated derivatives showed interesting inhibition activity and selectivities for inhibiting some important isoforms over the off-target ones hCA I and II. (C) 2015 Elsevier Ltd. All rights reserved.
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页码:7219 / 7225
页数:7
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