2016
DOI: 10.1016/j.bmcl.2016.01.020
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Structural optimization of non-nucleoside DNA methyltransferase inhibitor as anti-cancer agent

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Cited by 7 publications
(5 citation statements)
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“…An assortment of therapeutics have been developed recently targeting epigenetic regulation, including DNA methyltransferase modulators, histone deacetylase modulators, histone acetyltransferase (HAT) modulators, and noncoding miRNAs, exhibiting possible effects against age-related disorders. , Among DNA methyltransferase modulators, 5-azacytidine (azacytidine, CAS RN 320-67-2) and 5-aza-2′-deoxycytidine (decitabine, CAS RN 2353-33-5) are the most thoroughly examined and demonstrate therapeutic potential against certain leukemias. , Histone deacetylase inhibitors include several chemical groups: cyclic peptides, hydroxamic acids, short chain fatty acids, and benzamides . Experimental evidence shows significant life-extending potential of the histone deacetylase inhibitors such as 4-phenylbutyrate (PBA), trichostatin A, sodium butyrate, and suberoylanilide hydroxamic acid (SAHA). , A wide range of histone deacetylase inhibitors are emerging as potential anticancer medications, including belinostat, panobinostat, SAHA and FK228, trichostatin A, sodium butyrate, vorinostat, valproic acid, and romidepsinor demonstrating considerable activity in hematological and solid tumors.…”
Section: Antiaging Drugsmentioning
confidence: 99%
See 1 more Smart Citation
“…An assortment of therapeutics have been developed recently targeting epigenetic regulation, including DNA methyltransferase modulators, histone deacetylase modulators, histone acetyltransferase (HAT) modulators, and noncoding miRNAs, exhibiting possible effects against age-related disorders. , Among DNA methyltransferase modulators, 5-azacytidine (azacytidine, CAS RN 320-67-2) and 5-aza-2′-deoxycytidine (decitabine, CAS RN 2353-33-5) are the most thoroughly examined and demonstrate therapeutic potential against certain leukemias. , Histone deacetylase inhibitors include several chemical groups: cyclic peptides, hydroxamic acids, short chain fatty acids, and benzamides . Experimental evidence shows significant life-extending potential of the histone deacetylase inhibitors such as 4-phenylbutyrate (PBA), trichostatin A, sodium butyrate, and suberoylanilide hydroxamic acid (SAHA). , A wide range of histone deacetylase inhibitors are emerging as potential anticancer medications, including belinostat, panobinostat, SAHA and FK228, trichostatin A, sodium butyrate, vorinostat, valproic acid, and romidepsinor demonstrating considerable activity in hematological and solid tumors.…”
Section: Antiaging Drugsmentioning
confidence: 99%
“…339,340 Among DNA methyltransferase modulators, 5-azacytidine (azacytidine, CAS RN 320-67-2) and 5-aza-2′-deoxycytidine (decitabine, CAS RN 2353-33-5) are the most thoroughly examined and demonstrate therapeutic potential against certain leukemias. 341,342 Histone deacetylase inhibitors include several chemical groups: cyclic peptides, hydroxamic acids, short chain fatty acids, and benzamides. 343 Experimental evidence shows significant life-extending potential of the histone deacetylase inhibitors such as 4-phenylbutyrate (PBA), trichostatin A, sodium butyrate, and suberoylanilide hydroxamic acid (SAHA).…”
Section: Antiaging Drugsmentioning
confidence: 99%
“…602,603 Among DNA methyltransferase modulators, 5-azacytidine (azacytidine, CAS # 320-67-2) and 5-aza-2′deoxycytidine (decitabine, CAS # 2353-33-5) are the most thoroughly examined and demonstrate therapeutic potential against certain leukemias. 604,605 Histone deacetylase inhibitors include several chemical groups: cyclic peptides, hydroxamic acids, short chain fatty acids, and benzamides. 606 Experimental evidence shows significant life-extending potential of the histone deacetylase inhibitors such as 4-phenylbutyrate (PBA), trichostatin A, sodium butyrate, and suberoylanilide hydroxamic acid (SAHA).…”
Section: Epigenetic Drugsmentioning
confidence: 99%
“…305 Another strategy consisted in synthesizing the 3-substituted hydantoin via the cyclization of an ureido intermediate and then to perform Knoevenagel condensation to afford the desired hydantoins. The intermediate was prepared from an isocyanate, 306 commercially available 307 or generated from the corresponding amine with triphosgene 308 or oxalyl chloride. 309 Interestingly, when Hidayat et al performed the condensation reaction of 3-substituted hydantoins and different benzaldehydes under microwave irradiation, the major products obtained were not the expected benzylhydantoins but the corresponding benzylhydantoin alcohols, underlining the fact that microwave conditions favored the formation of the C−C bond but did not accelerated the dehydration step of the reaction.…”
Section: -Substituted 5-alkyl/arylidene Hydantoinsmentioning
confidence: 99%
“…Another strategy consisted in synthesizing the 3-substituted hydantoin via the cyclization of an ureido intermediate and then to perform Knoevenagel condensation to afford the desired hydantoins. The intermediate was prepared from an isocyanate, commercially available or generated from the corresponding amine with triphosgene or oxalyl chloride…”
Section: Alkylidene Hydantoinsmentioning
confidence: 99%