2017
DOI: 10.1016/j.msec.2017.01.001
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Nanofibrous matrixes with biologically active hydroxybenzophenazine pyrazolone compound for cancer theranostics

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Cited by 14 publications
(5 citation statements)
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“…Numerous reports are devoted to the preparation of materials by solvent casting or compression molding of PHB blends with poly(ε-caprolactone) (PCL) [16][17][18][19]. The electrospinning of mixed PHB/PCL solutions has been reported [20,21]. However, there are still no reports on the simultaneous electrospinning of separate PHB and PCL spinning solutions.…”
Section: Introductionmentioning
confidence: 99%
“…Numerous reports are devoted to the preparation of materials by solvent casting or compression molding of PHB blends with poly(ε-caprolactone) (PCL) [16][17][18][19]. The electrospinning of mixed PHB/PCL solutions has been reported [20,21]. However, there are still no reports on the simultaneous electrospinning of separate PHB and PCL spinning solutions.…”
Section: Introductionmentioning
confidence: 99%
“…Initially there occurs condensation between 3 with 2 to give the intermediate benzo[ a ]phenazin-5-ol 245, the second step is an aldol-type condensation that takes place between aromatic aldehyde with 245, resulting in situ C C bond formation of intermediate 246, which on further reaction undergoes Michael-type addition with another molecule of 3-methyl-1-phenyl-1 H -pyrazol-5(4 H )-one 247 keto–enol tautomerism under the influence of the Fe( iii )Y-zeolite solid state catalyst to furnish the desired product 244( Scheme 74 ). 105 …”
Section: Synthesis Of Benzo[ a ]Phenazin-5-olsmentioning
confidence: 99%
“…Initially there occurs condensation between 3 with 2 to give the intermediate benzo[a]phenazin-5-ol 245, the second step is an aldoltype condensation that takes place between aromatic aldehyde with 245, resulting in situ C]C bond formation of intermediate 246, which on further reaction undergoes Michael-type addition with another molecule of 3-methyl-1-phenyl-1H-pyrazol-5(4H)one 247 keto-enol tautomerism under the inuence of the Fe(III) Y-zeolite solid state catalyst to furnish the desired product 244(Scheme 74). 105 In 2018, for the synthesis of pyrazolo-fused benzophenazines 248 in 78-87% yields, Mohebat and co-workers developed a multi-component condensation reaction involving 3, 2a, aromatic aldehydes, and 4-methylbenzenesulfonohydrazide in the presence of phosphotungstic acid (H 3 PW 12 O 40 ) under microwave irradiation (180 W, max. 70 C) in EtOH within 15-20 min.…”
Section: Synthesis Of Benzooxazinophenazinesmentioning
confidence: 99%
“…It results in the fabrication of nanofibers as nanostructured scaffolds mimicking microporosity, intricate morphology of extracellular matrix (ECM), and the possession of beneficial characteristics for tissue healing, tissue growth, disease theranostics, etc. [ 32 , 33 , 34 , 35 , 36 , 37 ]. Numerous scaffolds made of synthetic/natural polymers and their hybrids have been developed for these applications.…”
Section: Introductionmentioning
confidence: 99%