Study on impact of parasite (Nosema species) on characters of tropical tasar silkworm Anthereae mylitta drury.

Infection of the pebrine disease has been found to be highly virulent and harm the cocoon yield as well as characters of silkworm Anthereae mylitta. Therefore, an attempt was made to evaluate the impact of parasite Nosema species on the ecorace (Sukinda) of A. mylitta in respect of transovarial transmitted (T1), secondary infection (T2) and healthy silkworm (T3). In comparison to T3, the number of larval mortality was 16 and 11 in T1 and T2 respectively; whereas as number of pupal mortality was 6 and 5 in T1 and T2 respectivelyThe larval weight, number of moths emerged, number of eggs laid and percent hatchability were reduced in T1 and T2 in comparison to T3.The infected layings were high in T1 (51%) and T2 (42%) as against T3 (0%). Similarly, the infected moths were 34% in T1 and 15% in T2 as against 0 percent in T3. All the characteristics parameters of cocoon were reduced in T1 and T2 against T3. The study explains that there was no significant variation between T1 and T2 on different parameters of larva, pupa and cocoon characters.

Synthesis of privileged scaffolds by using diversity-oriented synthesis.

An elegant reagent-controlled strategy has been developed for the generation of a diverse range of biologically active scaffolds from a chiral bicyclic lactam. Reduction of the chiral lactam with LAH or alkylation with LHMDS to trigger different cyclization reactions have been shown to generate privileged scaffolds, such as pyrrolidines, indolines, and cyclotryptamines. Their amenability to substitution allows us to create various compound libraries by using these scaffolds. In silico studies were used to estimate the drug-like properties of these compounds. Selected compounds were subjected to anticancer screening by using three different cell lines. In addition, all these compounds were subjected to antibacterial screening to gauge the spectrum of biological activity that was conferred by our DOS methodology. Gratifyingly, with no additional iterative cycles, our method directly generated anticancer compounds with potency at low nanomolar concentrations, as represented by spiroindoline 14.