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1.
Chem Biodivers ; 20(8): e202300560, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37477067

ABSTRACT

QSAR analysis of previously synthesized and nature-inspired virtual isoflavone-cytisine hybrids against the HEp-2 laryngeal carcinoma cell lines was performed using the OCHEM web platform. The validation of the models using an external test set proved that the models can be used to predict the activity of newly designed compounds such as 8-cytisinylmethyl derivatives of 5,7- and 6,7-dihydroxyisoflavones. The synthetic procedure for selective aminomethylation of 5,7-dihydroxyisoflavones with cytisine was developed. In vitro testing identified compound 7 f with cisplatin-level cytotoxicity against HEp-2 cell lines and compound 10 which was twice active than cisplatin after 72 h of incubation.


Subject(s)
Alkaloids , Antineoplastic Agents , Carcinoma , Isoflavones , Humans , Cisplatin , Antineoplastic Agents/pharmacology , Isoflavones/pharmacology , Mannich Bases , Structure-Activity Relationship , Alkaloids/pharmacology , Cell Line, Tumor
2.
J Med Chem ; 63(7): 3538-3551, 2020 04 09.
Article in English | MEDLINE | ID: mdl-32134266

ABSTRACT

The overaccumulation of glycogen appears as a hallmark in various glycogen storage diseases (GSDs), including Pompe, Cori, Andersen, and Lafora disease. Accumulating evidence suggests that suppression of glycogen accumulation represents a potential therapeutic approach for treating these GSDs. Using a fluorescence polarization assay designed to screen for inhibitors of the key glycogen synthetic enzyme, glycogen synthase (GS), we identified a substituted imidazole, (rac)-2-methoxy-4-(1-(2-(1-methylpyrrolidin-2-yl)ethyl)-4-phenyl-1H-imidazol-5-yl)phenol (H23), as a first-in-class inhibitor for yeast GS 2 (yGsy2p). Data from X-ray crystallography at 2.85 Å, as well as kinetic data, revealed that H23 bound within the uridine diphosphate glucose binding pocket of yGsy2p. The high conservation of residues between human and yeast GS in direct contact with H23 informed the development of around 500 H23 analogs. These analogs produced a structure-activity relationship profile that led to the identification of a substituted pyrazole, 4-(4-(4-hydroxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)pyrogallol, with a 300-fold improved potency against human GS. These substituted pyrazoles possess a promising scaffold for drug development efforts targeting GS activity in GSDs associated with excess glycogen accumulation.


Subject(s)
Enzyme Inhibitors/chemistry , Glycogen Synthase/antagonists & inhibitors , Imidazoles/chemistry , Pyrazoles/chemistry , Animals , Caenorhabditis elegans/enzymology , Crystallography, X-Ray , Drug Discovery , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/metabolism , Glycogen Synthase/chemistry , Glycogen Synthase/metabolism , HEK293 Cells , Humans , Imidazoles/chemical synthesis , Imidazoles/metabolism , Kinetics , Molecular Structure , Protein Binding , Pyrazoles/chemical synthesis , Pyrazoles/metabolism , Saccharomyces cerevisiae/enzymology , Structure-Activity Relationship
3.
J Org Chem ; 84(11): 7138-7147, 2019 06 07.
Article in English | MEDLINE | ID: mdl-31090415

ABSTRACT

A reliable method for the synthesis of B-ring hydroxylated homoisoflavonoids and 3-hetarylmethyl chromones has been developed. The method involves an initial oxa-Diels-Alder reaction of ortho-quinone methides generated from aryl/hetaryl-substituted ortho-( N, N-dimethylaminomethyl)phenols with (2 E)-3-( N, N-dimethylamino)-1-(2-hydroxyphenyl)prop-2-en-1-ones and the subsequent cascade of reactions. This synthetic strategy avoids conventional multistep protocols and does not require the protection of hydroxyl groups, thus allowing the facile synthesis of a library of various aromatic and heterocyclic analogues of naturally occurring homoisoflavonoids.

4.
ChemMedChem ; 11(6): 600-11, 2016 Mar 17.
Article in English | MEDLINE | ID: mdl-26889756

ABSTRACT

The regioselective condensations of various 7-hydroxyisoflavonoids with bis(N,N-dimethylamino)methane in a Mannich reaction provided C-8 N,N-dimethylaminomethyl-substituted isoflavonoids in good yield. Similar condensations of 7-hydroxy-8-methylisoflavonoids led to the C-6-substituted analogs. Thermal eliminations of dimethylamine from these C-6 or C-8 N,N-dimethylaminomethyl-substituted isoflavonoids generated ortho-quinone methide intermediates within isoflavonoid frameworks for the first time. Despite other potential competing outcomes, these ortho-quinone methide intermediates trapped dienophiles including 2,3-dihydrofuran, 3,4-dihydro-2H-pyran, 3-(N,N-dimethylamino)-5,5-dimethyl-2-cyclohexen-1-one, 1-morpholinocyclopentene, and 1-morpholinocyclohexene to give various inverse electron-demand Diels-Alder adducts. Several adducts derived from 8-N,N-dimethylaminomethyl-substituted isoflavonoids displayed good activity in the 1-10 µm concentration range in an in vitro proliferation assay using the PC-3 prostate cancer cell line.


Subject(s)
Antineoplastic Agents/chemical synthesis , Isoflavones/chemical synthesis , Mannich Bases/chemistry , Pyrans/chemical synthesis , Xanthenes/chemical synthesis , Antineoplastic Agents/pharmacology , Cell Line, Tumor , Cell Proliferation/drug effects , Cycloaddition Reaction , Humans , Isoflavones/pharmacology , Pyrans/pharmacology , Stereoisomerism , Xanthenes/pharmacology
5.
Org Biomol Chem ; 13(46): 11292-301, 2015 Dec 14.
Article in English | MEDLINE | ID: mdl-26416505

ABSTRACT

The regiospecific Mannich aminomethylation of 7-hydroxyisoflavonoids using bis(N,N-dimethylamino)methane afforded C-8 substituted N,N-dimethylaminomethyl adducts, and the regioselective aminomethylation of 5-hydroxy-7-methoxyisoflavonoids afforded predominantly the C-6 substituted N,N-dimethylaminomethyl adducts. Acetylation of these C-6 or C-8 Mannich bases with potassium acetate in acetic anhydride provided access to the corresponding acetoxymethyl derivatives that were subsequently converted to hydroxymethyl- and methoxymethyl-substituted 5-hydroxy- or 7-hydroxyisoflavonoids related to naturally occurring flavonoids. The C-8 acetoxymethyl, hydroxymethyl or methoxymethyl-substituted isoflavonoids possessed promising inhibitory potency in the low micromolar range in a prostate cancer PC-3 cell proliferation assay.


Subject(s)
Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Cell Proliferation/drug effects , Isoflavones/chemical synthesis , Isoflavones/pharmacology , Mannich Bases/chemistry , Antineoplastic Agents/chemistry , Cell Line, Tumor , Humans , Hydroxylation , Isoflavones/chemistry , Male , Mannich Bases/chemical synthesis , Methylation , Prostate/drug effects , Prostatic Neoplasms/drug therapy
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