1978
DOI: 10.1002/jps.2600670247
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Synthesis and Antibacterial Evaluation of 2- (Substituted Phenylureido) -4-thiocyanatobenzothiazoles

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1978
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Cited by 22 publications
(6 citation statements)
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“…The same authors used PPA in the condensation of substituted o-ATP with substituted 4-aminobenzoic acids at 220 • C to synthesize the 2-(p-aminophenyl)BTs 6a (Scheme 2) to be evaluated against breast cancer cell lines in vitro and in vivo [46]. ATP was condensed with substituted 4-aminobenzoic acids in PPA to give the 2-substitutedBTs 6b-d (Scheme 2).…”
Section: Condensation With Carboxylic Acidsmentioning
confidence: 99%
See 1 more Smart Citation
“…The same authors used PPA in the condensation of substituted o-ATP with substituted 4-aminobenzoic acids at 220 • C to synthesize the 2-(p-aminophenyl)BTs 6a (Scheme 2) to be evaluated against breast cancer cell lines in vitro and in vivo [46]. ATP was condensed with substituted 4-aminobenzoic acids in PPA to give the 2-substitutedBTs 6b-d (Scheme 2).…”
Section: Condensation With Carboxylic Acidsmentioning
confidence: 99%
“…Moreover, the BT moiety is also found in many functional molecules, such as ratiometric fluorescent pH indicators and ligands for catalytic reactions [18,19]. Since 1991, BT has been a moiety known to play an important role in chemistry, biochemistry, and medicinal chemistry, with a wide array of interesting biological activities and therapeutic functions, such as antimicrobial [20][21][22][23], anticancer [24][25][26][27][28][29], anthelmintic [30], antidiabetic [31,32], antituberculotic [33,34], antitumor [35][36][37][38][39][40][41], antitrypanosomal [42], antiviral [43][44][45], antibacterial [46][47][48][49], antioxidant [50], antiglutamate and antiparkinsonism [51,52], analgesic [53], anti-inflammatory [54,55], antifungal [56,57], antileishmanial [58], anticonvulsant [59], neuroprotective [60], muscle relaxant [61], vasodilator…”
Section: Introductionmentioning
confidence: 99%
“…The benzothiazole ring system was originally found in various marine and terrestrial natural compounds, which is widely used as vulcanization accelerators, antioxidants, plant growth regulators, anti-inflammatory agents, enzyme inhibitors, imaging reagents, fluorescence materials, and electroluminescent devices due to its highly pharmaceutical and biological activity [1][2][3][4]. Especially, benzothiazole plays an important role in the field of medicinal chemistry and renders an extensive range of biological activities including anti-cancer [5,6], anti-bacterial [7,8], anti-tuberculosis [9,10], anti-diabetic [11], anthelmintic [12], anti-tumor [13][14][15], anti-viral [16,17], anti-oxidant [18], anti-inflammatory [19,20], anti-glutamate and anti-parkinsonism [21], anticonvulsant [22], muscle relaxant activities [23], neuroprotective [24], inhibitors of several enzymes and so on [25]. Hence, the synthesis of benzothiazoles is of considerable interest due to their potent and significant biological activities and great pharmaceutical value.…”
Section: Introductionmentioning
confidence: 99%
“…1). 6 The benzothiazole moiety plays an important role in chemistry and is also present in a variety of biologically active applications such as anti-microbial, [7][8][9][10] anti-cancer, [11][12][13][14][15][16] anthelmintic, 17 anti-diabetic, 18,19 anti-tuberculotic, 13,20,21 antitumor, [22][23][24][25][26][27][28] anti-trypanosomal, 29 anti-viral, [30][31][32] antibacterial, [33][34][35][36] anti-oxidant, 37 anti-glutamate and anti-parkinsonism, 38,39 analgesic, 40 anti-inammatory, [41][42][43] antifungal, 44,45 antileishmanial, 46 anticonvulsant, 47 neuroprotective, 48 muscle relaxant activities, 49 vasodilator, 50 orexin receptor,…”
Section: Introductionmentioning
confidence: 99%