The antifungal activity of aqueous extract of Cannabis sativa, Parthenium hysterophorus, Urtica dioeca, Polystichum squarrosum and Adiantum venustum was investigated against Alternaria solani, Alternaria zinniae, Curvularia lunata, Rhizoctonia solani and Fusarium oxysporum at different concentrations (5, 10, 15 and 20%). At 20%, maximum antifungal potential was observed with the extracts of C. sativa, which recorded excellent inhibitory activity against C. lunata (100%), A. zinniae (59.68%), followed by leaf extract of P. hysterophorus (50%) against A. solani. The application of botanical extracts for disease management could be less expensive, easily available, non-polluting and eco-friendly.

Plant growth promoting rhizobacteria are key to soil and plant health maintenance. In the present study, two PGPR strains which were identified as spp. (accession number KX650178 and KX650179) with nanozeolite (50 ppm) were applied to the seeds in different combinations and tested on growth profile of maize crop. Various growth related parameters, including plant height, leaf area, number of leaves chlorophyll and total protein were positively increased up to twofold by the nanocompound treatment. GC-MS results reveal increase in total phenolic and acid ester compounds after the treatment of nanozeolite and PGPR, which are responsible for stress tolerance mechanism. Soil physicochemical parameters (organic carbon, phosphorous, potassium, ammoniacal nitrogen and nitrate nitrogen) were assessed qualitatively and a shift towards higher amount was observed. Various biochemical parameters of soil health like dehydrogenase, fluorescein diacetate hydrolysis and alkaline phosphatase activity were significantly enhanced up to threefold with the application of different treatments. The results, for the first time, demonstrate successful use of nanozeolite in enhancing growth of, under controlled conditions and present a viable alternative to GM crop for ensuring food security.

Morphine is a powerful opioid pain medication and commonly used narcotic pain killer and is toxic during overdose or when abused. Compared to conventional analytical techniques, the electroanalytical method has significant advantages viz. low cost, simplicity, ease of operation and facile miniaturization. In the present paper different approaches based on various modifications adopted for effective electrochemical sensing of morphine are reviewed in a comprehensive way. Among different modified electrodes available for the detection of morphine, carbon based materials—CNTs and graphene—display effective quantification and are attractive in terms of cost compared to noble metals. In addition, the performance of reported sensors in terms of their including detection range (LDR), limit of detection (LOD) and technique used are presented. The present review compares various electroanalytical techniques adopted for the determination of morphine.

Cu(I)Cl promoted synthesis of N-propargylated-isatin Mannich mono- and bis-adducts with an extension towards the synthesis of N-propargylated-isatin-7-chloroquinoline conjugates was described. The synthesized scaffolds were evaluated for their in vitro activity against the veterinary protozoal pathogen Tritrichomonas foetus and cytotoxicity against human prostate (PC-3) cancer cell line. The preliminary evaluation data revealed the enhancement in the activity profiles with the introduction of 7-chloroquinoline ring with the most active conjugates 7a, 7c and 7d exhibiting an IC₅₀ of 22.2, 11.3 and 24.5 μM respectively against T. foetus and minimal toxicity against human prostate (PC-3) cell lines.

A series of N-alkyl tethered C-5 functionalized bis-isatins were synthesized and evaluated for antimicrobial activity against pathogenic microorganisms. The preliminary evaluation studies revealed the compound 4t, with an optimal combination of bromo-substituent at the C-5 position of isatin ring along with propyl chain linker being most active among the synthesized series exhibiting an IC50 value of 3.72 μM against Trichomonas vaginalis while 4j exhibited an IC50 value of 14.8 μM against Naegleria fowleri, more effective than the standard drug Miltefosine. The compound 3f with an octyl spacer length was the most potent among the series against Giardia lamblia with an IC50 of 18.4 μM while 3d exhibited an IC50 of 23 μM against Entamoeba histolytica. This library was also screened against the fungal pathogen Aspergillus parasiticus. A number of the compounds demonstrated potency against this fungus, illustrating a possible broad-spectrum activity. Furthermore, an evaluation of these synthesized compounds against a panel of normal flora bacteria revealed them to be non-cytotoxic, demonstrating the selectivity of these compounds. This observation, in combination with previous studies that isatin is non-toxic to humans, presents a new possible scaffold for drug discovery against these important protozoal pathogens of humans and animals.

A series of β-amino alcohol tethered 4-aminoquinoline-isatin conjugates were synthesized with the aim of probing their antimalarial structure activity relationship. Two of the most active conjugates (11b and 11f) exhibited antimalarial efficacy comparable to that of chloroquine, with IC50 values of 11.8 and 13.5 nM, respectively against chloroquine resistant W2 strain of Plasmodium falciparum and are devoid of any cytotoxicity.

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