NBS AND NCS APPLIED TO THIOCYANATION OF AROMATIC RINGS

Instead of Br_2 and Cl_2,NBS and NCS are applicable to the thiocyanation of o-nitroaniline and carbendazim.The results show that NBS and NCS are superior to Br_2 and Cl_2 due to their easier operation.

1,3-Dinitro-2-chloro-5-trifluorotoluene and its bridged derivatives Ⅰ.An investigation on the displacement reactions of bidentate nucleophiles towards aromatic rings

The reactions of 1,3-dinitro-2-chloro-5-trifluorotoluene(DNCTT)(1)and its bridged com- pounds with bidentate nucleophiles have been investigated.Primary or secondary diamines and diethylene glycol react with 1 and its bridged derivatives by replacing the substituent grouppara to CF_3, whereas ethanedithiol reacts either by replacing the substituent group para to CF_3 or by displacing both groups and a nitro group.The results have been rationalized in terms of electronic effects and nucleophilicity of the nucleophiles.

One ring is sufficient to inhibit α-synuclein aggregation

Parkinson's disease,the second most prevalent neurodegenerative disorder worldwide,is characterized by a progressive loss of dopaminergic neurons in substantia nigra pars compacta,causing motor symptoms.This disorder's main hallmark is the formation of intraneuronal protein inclusions,named Lewy bodies and neurites.The major component of these arrangements is α-synuclein,an intrinsically disordered and soluble protein that,in pathological conditions,can form toxic and cell-to-cell transmissible amyloid structures.Preventing α-synuclein aggregation has attracted significant effort in the search for a disease-modifying therapy for Parkinson's disease.Small molecules like Synu Clean-D,epigallocatechin gallate,trodusquemine,or anle138 b exemplify this therapeutic potential.Here,we describe a subset of compounds containing a single aromatic ring,like dopamine,ZPDm,gallic acid,or entacapone,which act as molecular chaperones against α-synuclein aggregation.The simplicity of their structures contrasts with the complexity of the aggregation process,yet the block efficiently α-synuclein assembly into amyloid fibrils,in many cases,redirecting the reaction towards the formation of non-toxic off-pathway oligomers.Moreover,some of these compounds can disentangle mature α-synuclein amyloid fibrils.Their simple structures allow structure-activity relationship analysis to elucidate the role of different functional groups in the inhibition of α-synuclein aggregation and fibril dismantling,making them informative lead scaffolds for the rational development of efficient drugs.

<i>In-Silico</i>Identification of Anticancer Compounds;Ligand-Based Pharmacophore Approach against EGFR Involved in Breast Cancer

Objective: Breast cancer is a public health challenge on a global scale that is caused by environmental or genetic factors. Breast cancer is affecting both males and females, but there is still a lack of effective drugs with improved potency and admissibility against breast cancer as many of the breast cancer drugs have severe side effects. Methods: The docking approach has been used to find a new compound for breast cancer with more efficacy and tolerance and with lesser side effects. A ligand-based pharmacophore approach has been generated for 39 anticancer compounds with significance for the development of new drugs. Result: Through docking, the approach found new lead compounds for breast cancer. The proposed pharmacophore model in this study contains two HBAs and one HYD, one hydrophobic domain and two Aromatic rings and the estimated distance range is minimum to maximum of derived pharmacophore features. Conclusion: Based on this research, it is proposed that these two lead compounds may be able to be used against EGFR in breast cancer. New compounds can be identified based on common features in the Pharmacophore model. 3D pharmacophore triangle could be used for further studies because this pharmacophore has better merging and in the future for more studies can suggest the same distance range of pharmacophore features as this pharmacophore.

A comparative study of the aromaticity in some typical conjugated six-membered rings by the method of localized molecular orbital

The localized molecular orbitals and energy levels for four typical conjugated six-membered ring systems C_6H_6, C_3N_3H_3, B_3N_3H_6, and (B_3O_6)^(3-) as well as a non-aromatic reference molecule N_3Cl_6 have been calculated by using Edmiston-Ruedenberg energy localization technique under the CNDO/2 approximation in order to investigate the nature of aromaticity or quasi-aromaticity of the six-membered ring systems studied. The contour maps for π-type localized MO's (LMO) have been plotted to illustrate the bonding characteristics of the five ring systems studied. These LMO calculations show that for all the conjugated six-membered ring systems considered there exists local delocalization of π-bonds or three-centered and occasionally four-centered two-electron π-bonds in our terminology, and the cooperative effect among these π-bonds leading to the formation of a closed continuous x-conjugation system around the ring, which is necessary for the creation of aromaticity in the systems studied. We have been able to discuss the properties of these three-centered π-bonds in terms of the constituent atoms and electrons and the relevant orbitals involved.