Cholinesterases Inhibition, Anticancer and Antioxidant Activity of Novel Benzoxazole and Naphthoxazole Analogs.
acetylcholinesterase
antioxidant
antiproliferative activity
benzoxazole
butyrylcholinesterase
naphthoxazole
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
03 Dec 2022
03 Dec 2022
Historique:
received:
31
10
2022
revised:
29
11
2022
accepted:
01
12
2022
entrez:
11
12
2022
pubmed:
12
12
2022
medline:
15
12
2022
Statut:
epublish
Résumé
Benzoxazole and naphthoxazole fused systems are found in many biologically active molecules. Novel benzoxazole and naphthoxazole analogs functionalized by the 2,4-dihydroxyphenyl moiety were designed, obtained and evaluated as a broad spectrum of biological potency compounds. Sulfinylbis[(2,4-dihydroxyphenyl)methanethione] or its analogs and 2-aminophenols or 1-amino-2-naphthol were used as starting reagents. 4-(Naphtho[1,2-
Identifiants
pubmed: 36500605
pii: molecules27238511
doi: 10.3390/molecules27238511
pmc: PMC9738531
pii:
doi:
Substances chimiques
Benzoxazoles
0
Cholinesterase Inhibitors
0
Antioxidants
0
Oxazoles
0
Acetylcholinesterase
EC 3.1.1.7
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Références
Bioorg Med Chem. 2007 May 1;15(9):3201-7
pubmed: 17350846
Biomolecules. 2019 Dec 12;9(12):
pubmed: 31842463
Bioorg Med Chem Lett. 2016 Jul 1;26(13):3067-3072
pubmed: 27209235
Bioorg Chem. 2017 Oct;74:82-90
pubmed: 28772160
J Antibiot (Tokyo). 2001 Jan;54(1):102-4
pubmed: 11269707
Bioorg Chem. 2022 Jul;124:105832
pubmed: 35500502
Mol Med Rep. 2019 Aug;20(2):1479-1487
pubmed: 31257471
Molecules. 2018 Sep 25;23(10):
pubmed: 30257495
Bioorg Chem. 2021 Feb;107:104617
pubmed: 33444983
Bioorg Med Chem Lett. 2010 Apr 15;20(8):2609-13
pubmed: 20231096
Bioorg Med Chem Lett. 2004 Jun 21;14(12):3221-6
pubmed: 15149679
Molecules. 2021 Nov 26;26(23):
pubmed: 34885751
J Enzyme Inhib Med Chem. 2013 Aug;28(4):816-23
pubmed: 22630076
Molecules. 2020 Jun 03;25(11):
pubmed: 32503288
Chem Biol Drug Des. 2017 Nov;90(5):987-994
pubmed: 28544428
J Med Chem. 2006 Nov 30;49(24):6958-71
pubmed: 17125249
Eur J Med Chem. 2013 Apr;62:311-9
pubmed: 23376249
Molecules. 2012 Jan 17;17(1):873-83
pubmed: 22252503
Org Lett. 1999 Aug 12;1(3):527-30
pubmed: 10822593
Eur J Med Chem. 2000 Apr;35(4):393-404
pubmed: 10858600
Bioorg Chem. 2019 Feb;82:211-223
pubmed: 30326403
Eur J Med Chem. 2021 Jan 15;210:112979
pubmed: 33183865
Int J Mol Sci. 2022 Aug 25;23(17):
pubmed: 36077036
Bioorg Med Chem. 2006 Jul 1;14(13):4483-9
pubmed: 16517170
J Chem Inf Comput Sci. 1987 Feb;27(1):21-35
pubmed: 3558506
J Mol Graph Model. 2000 Aug-Oct;18(4-5):512-24, 541
pubmed: 11143566
Eur J Med Chem. 2018 Jan 1;143:970-982
pubmed: 29232587
Bioorg Med Chem. 2002 Dec;10(12):3997-4004
pubmed: 12413851
Chem Biol Drug Des. 2017 May;89(5):783-789
pubmed: 27863021
PLoS One. 2014 Sep 03;9(9):e106186
pubmed: 25184280
Molecules. 2022 Apr 11;27(8):
pubmed: 35458662
Molecules. 2021 Apr 20;26(8):
pubmed: 33924091
Bio Protoc. 2016 Nov 5;6(21):
pubmed: 28573164
JAMA Netw Open. 2019 Jun 5;2(6):e196167
pubmed: 31225887
Biochim Biophys Acta. 2014 Aug;1842(8):1240-7
pubmed: 24189435
Arch Pharm Res. 2011 Oct;34(10):1639-47
pubmed: 22076764
Eur J Med Chem. 2019 Feb 1;163:116-135
pubmed: 30503937
Arch Pharm (Weinheim). 2011 Apr;344(4):224-30
pubmed: 21469171
Bioorg Med Chem. 2006 Sep 1;14(17):6106-19
pubmed: 16714116
Food Chem. 2013 May 1;138(1):414-20
pubmed: 23265506
Eur J Med Chem. 2017 Sep 29;138:761-773
pubmed: 28728108
Z Naturforsch C J Biosci. 2016 Nov 1;71(11-12):409-413
pubmed: 27505087
J Org Chem. 2006 Mar 3;71(5):1802-8
pubmed: 16496964
J Med Chem. 1971 Jun;14(6):546-9
pubmed: 4326401
J Bacteriol. 1934 Apr;27(4):325-40
pubmed: 16559703
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Jan 24;118:448-53
pubmed: 24080575
Pharmacol Res. 2004 Oct;50(4):433-40
pubmed: 15304240
Bioorg Med Chem. 2008 Feb 15;16(4):1775-83
pubmed: 18037301