Mini-Reviews in Organic Chemistry - Volume 16, Issue 7, 2019

Pyridium salts are very valuable compounds with various activities, especially biological, and therefore their preparation can be very useful in the synthesis of various compounds, such as drugs, dyes or surfactants. In this mini-review authors focused mostly on bioactive properties of pyridinium salts, and main preparations of these compounds such, synthesis pyridinium salts from pyrylium salts via nucleophilic substitution SN(ANRORC), obtaining pyridinium salts via directs arylation, and via Addition at Nitrogen atom, and the last method is synthesis of pyridinium salts via ring opening and re-cyclisation.

The malignant neoplasm, which is recognized as cancer, is a serious threat to human health and frequently-occurring disease. Diphenylurea, an important link structure in the design of active substance for treating cancer due to its near-perfect binding with certain acceptors, has demonstrated many activities against several human cancer cell lines. Various novel compounds with diphenyl urea as anticancer agents were constructed with the successful development of sorafenib. Diphenylurea is utilized to treat cancer by inhibiting cell signaling transduction, such as RAS-RAFMEK- ERK signaling pathway and PI3K-Akt-mTOR pathway. In addition, this structure inhibits tumor cell growth by inhibiting receptor tyrosine kinases multiply, such as Vascular Endothelial Growth Factor Receptors (VEGFRs), Platelet-Derived Growth Factor Receptors (PDGFRs), Epidermal Growth Factor Receptors (EGFRs). It regulates the pH value in cells by inhibiting CAIX/XII and to achieve cancer therapeutic effect. Besides, the diphenyl urea structure is applied to the synthesis of reagents like Aurora kinases inhibitors and HDAC inhibitors that affect cell division and differentiation to treat cancer. To reach the goal of treating tumor, this structure is also used as a DNA-directed alkylating agent by affecting the expression of genes. An application of the most representative diphenyl urea derivatives as antitumor agents is summarized in this review, focusing on their mechanisms bound to the targets. Meanwhile, the progress of researches on methods of synthesizing diphenyl urea derivatives is provided.

Quinoline stands out amongst the most essential N-based heterocyclic biologically active compounds. Friedlieb Ferdinand Runge was first to isolate quinoline from coal tar in 1834. Chemical component, quinine found in the bark of cinchona tree was used for treatment of malaria in the year of 1820. Quinoline derivatives have been found to exhibit different therapeutic activities such as antimalarial, antibacterial, antifungal, antiplatelet, anticancer, antitubercular, etc. There are a couple of promising compounds with the Quinoline skeleton like Pamaquine, Chloroquine, Tafenoquine, Bulaquine, Quinine and Mefloquine which show Antimalarial activity. All the methodologies in last decade had been covered to provide a comprehensive review on the development of Quinoline analogs using metal catalyst. Since quinoline and its auxiliaries have extensive pharmacological activities and are moreover utilized as ligands in various metal complexes, various procedures have been now and again reported for their synthesis. We have tried here undertaking to collect a huge part of the procedure that has been represented in the written work by use of metal driving force. This review will be especially profitable to the examiner in quick exploring and developing another ecopleasing, capable and judicious protocol.

Heterocyclic compounds are well known for their different biological activity. The heterocyclic analogs are the building blocks for synthesis of the pharmaceutical active compounds in the organic chemistry. These derivatives show various type of biological activity like anticancer, antiinflammatory, anti-microbial, anti-convulsant, anti-malarial, anti-hypertensive, etc. From the last decade research showed that the quinoline analogs plays a vital role in the development of newer medicinal active compounds for treating various type of disease. Quinoline reported for their antiviral, anticancer, anti-microbial and anti-inflammatory activity. This review will summarize the various synthetic approaches for synthesis of quinoline derivatives and to check their biological activity. Derivatives of quinoline moiety plays very important role in the development of various types of newer drugs and it can be used as lead compounds for future investigation in the field of drug discovery process.

Genus Pandanus belongs to the family Padanaceae, which is widely distributed in old world tropics and subtropics, and has been applied in traditional herbal medicines, pharmacological uses, food chemical products and handicrafts. Original research articles related to this genus are available but an insight account highlighted phytochemical aspects of secondary metabolites is now insufficient. The reliable sources of literature data for this systematic manuscript were obtained from the literatures published from 1960s to now, utilizing data information from ACS journals, Taylor Francis, Springer, IOP Science, SCI-finder, Chemical Abstracts, the Web of Science, Scopus, ScienceDirect, PubMed and Googlescholar. A vast amount of data showed that genus Pandanus contained various classes of the secondary metabolites. Herein, approximately 180 constituents were isolated, comprising alkaloids, phenols, lignans, steroids, terpenoids, lipids, flavonoids, coumarins, lactones and amino acids. In addition, the crucial information involved in food chemistry suggests that Pandanus species can also be a good candidate to provide essential oils and nutrient contents of vitamins and sugars.