Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid

Extensive research has been carried out on bisindole compounds due to their potent activities. Modifying the structures of bisindoles has been proven to be useful in the search for new therapeutic agents. Since varying substituents is a common method for drug design in medicinal chemistry, 66 deriva...

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Main Author:	Abid, Obaidurahman
Format:	Thesis
Language:	English
Published:	2019
Subjects:	RM Therapeutics Pharmacology
Online Access:	https://ir.uitm.edu.my/id/eprint/89241/1/89241.pdf
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id	my-uitm-ir.89241
record_format	uketd_dc
spelling	my-uitm-ir.892412024-04-29T02:49:01Z Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid 2019 Abid, Obaidurahman RM Therapeutics. Pharmacology Extensive research has been carried out on bisindole compounds due to their potent activities. Modifying the structures of bisindoles has been proven to be useful in the search for new therapeutic agents. Since varying substituents is a common method for drug design in medicinal chemistry, 66 derivatives of bisindolylmethane bearing hydrazide-hydrazone, sulfonylhydrazide, and carbothioamide moieties were synthesized and evaluated for their β-glucuronidase and α-glucosidase inhibition potential. As the first step, acid-catalyzed reaction of 5-bromo and 5-cyano, substituted indole with methyl 4-formylbenzoate was carried out. The products were reacted with hydrazine hydrate forming two key-intermediates which were further derivatized into three series of target compounds (37-102). Synthesized compounds were characterized using 1H-NMR, 13C-NMR, FT-IR, and EI-MS spectroscopic techniques. Bisindolylmethanehydrazide-hydrazone derivatives 37-66 were evaluated for their in- vitro β-glucuronidase inhibition potential while the sulfonohydrazides 67-83 and carbothioamide analogs 84-102 were tested for α-glucosidase inhibitory activity. The results are stated as IC50 values and the structure-activity relationships were established based on the presence and location of different substituents, i.e., hydroxyl, methyl, methoxy, nitro, cyano, bromine, chlorine, and fluorine. Among the bisindolylmethanehydrazide-hydrazone derivatives, trihydroxylated compounds such as 6 (0.60 µM), 20 (1.50 µM), and 25 (0.50 µM) were found to be the most active. Comparing the IC50 values, compound 25 was approximately 100 times more active than the standard D-saccharic acid 1,4-lactone (IC50 = 48.40 µM). The results from SAR reveal that the presence of hydroxyl, fluorine, and chlorine groups significantly contributes to the activity, while methyl and methoxy substituents, or replacing the benzene ring with pyridine diminishes the activity. 2019 Thesis https://ir.uitm.edu.my/id/eprint/89241/ https://ir.uitm.edu.my/id/eprint/89241/1/89241.pdf text en public masters Universiti Teknologi MARA (UiTM) Faculty of Applied Sciences Ismail, Nor Hadiani
institution	Universiti Teknologi MARA
collection	UiTM Institutional Repository
language	English
advisor	Ismail, Nor Hadiani
topic	RM Therapeutics Pharmacology
spellingShingle	RM Therapeutics Pharmacology Abid, Obaidurahman Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid
description	Extensive research has been carried out on bisindole compounds due to their potent activities. Modifying the structures of bisindoles has been proven to be useful in the search for new therapeutic agents. Since varying substituents is a common method for drug design in medicinal chemistry, 66 derivatives of bisindolylmethane bearing hydrazide-hydrazone, sulfonylhydrazide, and carbothioamide moieties were synthesized and evaluated for their β-glucuronidase and α-glucosidase inhibition potential. As the first step, acid-catalyzed reaction of 5-bromo and 5-cyano, substituted indole with methyl 4-formylbenzoate was carried out. The products were reacted with hydrazine hydrate forming two key-intermediates which were further derivatized into three series of target compounds (37-102). Synthesized compounds were characterized using 1H-NMR, 13C-NMR, FT-IR, and EI-MS spectroscopic techniques. Bisindolylmethanehydrazide-hydrazone derivatives 37-66 were evaluated for their in- vitro β-glucuronidase inhibition potential while the sulfonohydrazides 67-83 and carbothioamide analogs 84-102 were tested for α-glucosidase inhibitory activity. The results are stated as IC50 values and the structure-activity relationships were established based on the presence and location of different substituents, i.e., hydroxyl, methyl, methoxy, nitro, cyano, bromine, chlorine, and fluorine. Among the bisindolylmethanehydrazide-hydrazone derivatives, trihydroxylated compounds such as 6 (0.60 µM), 20 (1.50 µM), and 25 (0.50 µM) were found to be the most active. Comparing the IC50 values, compound 25 was approximately 100 times more active than the standard D-saccharic acid 1,4-lactone (IC50 = 48.40 µM). The results from SAR reveal that the presence of hydroxyl, fluorine, and chlorine groups significantly contributes to the activity, while methyl and methoxy substituents, or replacing the benzene ring with pyridine diminishes the activity.
format	Thesis
qualification_level	Master's degree
author	Abid, Obaidurahman
author_facet	Abid, Obaidurahman
author_sort	Abid, Obaidurahman
title	Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid
title_short	Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid
title_full	Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid
title_fullStr	Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid
title_full_unstemmed	Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid
title_sort	synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / obaidurahman abid
granting_institution	Universiti Teknologi MARA (UiTM)
granting_department	Faculty of Applied Sciences
publishDate	2019
url	https://ir.uitm.edu.my/id/eprint/89241/1/89241.pdf
_version_	1804889808058712064

Synthesis, α-glucosidase and β-glucuronidase inhibitory activities of bisindolylmethane bearing hydrazide-hydrazone, sulfonohydrazide and carbothioamide moieties / Obaidurahman Abid

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