Synthesis and Biological Potentials of Quinoline Analogues: A Review of Literature

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.

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Chemical Diversity and Biological Activity of Secondary Metabolites from Soft Coral Genus Sinularia since 2013

Marine Drugs ◽

10.3390/md19060335 ◽

2021 ◽

Vol 19 (6) ◽

pp. 335

Author(s):

Xia Yan ◽

Jing Liu ◽

Xue Leng ◽

Han Ouyang

Keyword(s):

Biological Activity ◽

Secondary Metabolites ◽

Coral Species ◽

Soft Coral ◽

Biological Activities ◽

Vital Role ◽

Chemical Diversity ◽

Pharmacological Activities ◽

Lead Compounds ◽

Coral Genus

Sinularia is one of the conspicuous soft coral species widely distributed in the world’s oceans at a depth of about 12 m. Secondary metabolites from the genus Sinularia show great chemical diversity. More than 700 secondary metabolites have been reported to date, including terpenoids, norterpenoids, steroids/steroidal glycosides, and other types. They showed a broad range of potent biological activities. There were detailed reviews on the terpenoids from Sinularia in 2013, and now, it still plays a vital role in the innovation of lead compounds for drug development. The structures, names, and pharmacological activities of compounds isolated from the genus Sinularia from 2013 to March 2021 are summarized in this review.

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Synthesis and Antimicrobial Studies of New [Tetrakis (1, 2, 4-Triazole / 1, 3, 4-Oxadiazole / 1, 3, 4-Thiadiazole] [Bis-(Benzene-1, 3, 5-Triyl)] Dioxymethylene Compounds

Iraqi Journal of Science ◽

10.24996/ijs.2020.61.2.1 ◽

2020 ◽

pp. 234-245

Author(s):

Ahmed Neamah Ayyash

Keyword(s):

Biological Activity ◽

Heterocyclic Compounds ◽

Chemical Structure ◽

Acid Hydrazide ◽

Basic Medium ◽

Tosyl Chloride ◽

Antimicrobial Studies ◽

Ft Ir ◽

Concentrated Sulfuric Acid ◽

Derivatives Of

Synthesis of new heterocyclic compounds containing four five-membered rings together was the main goal of this work. The new derivatives of [tetrakis (1,2,4-triazole /1,3,4-thiadiazole /1,3,4-oxadiazole][bis-(benzene-1,3,5-triyl)] dioxymethylene A7-A18 were synthesized by the reaction of [bis-(dimethyl 5-yl-isophthalate)] dioxymethylene compound A1 which was previously prepared from the reaction of 1,2-dibromomethan and dimethyl 5-hydroxyisophthalate, then treated with hydrazine hydrate to yield the corresponding acid hydrazide A2. In the next step, compound A2 was refluxed with 4-substituted isothiocyanate to give substituted thiosemicarbazides A3-A6. The treatment of the latter compounds in basic medium of 2M of NaOH afforded 1,2,4-Triazole derivatives A7-A10. Whereas the reaction of the same compounds with concentrated sulfuric acid gave 1,3,4-thiadiazoles A11-A14. Furthermore, the new derivatives of 1,3,4-oxadiazole A15-A18 were obtained by the reaction of thiosemicarbazides and tosyl chloride in presence of pyridine. (C. H. N.) elemental analysis, FT-IR, and 1HNMR techniques were used to characterize the chemical structure of some of the new synthesized compounds which also exhibited an important biological activity.

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Synthesis and Microbiological Activity of Some Newly Synthesized Derivatives of 2-Oxo-2H-chromen-2-one

E-Journal of Chemistry ◽

10.1155/2011/402975 ◽

2011 ◽

Vol 8 (4) ◽

pp. 1522-1527 ◽

Cited By ~ 2

Author(s):

Majlinda Daci-Ajvazi ◽

Sevdije Govori ◽

Shuhreta Omeragiq

Keyword(s):

Staphylococcus Aureus ◽

Biological Activity ◽

Heterocyclic Compounds ◽

Sulfonyl Chloride ◽

Aeromonas Salmonicida ◽

Significant Activity ◽

Microbiological Activity ◽

Bacillus Spp ◽

New Compounds ◽

Derivatives Of

By the action of 2-amino-5-methylthio-1,3,4-thiadiazole, 3-amino-5-methylisoxazole, 2-amino-6-fluorobenzothiazole, 2-amino-5-chloropyridine, respectively, on 4-chloro-2-oxo-2H-chromene-3-sulfonyl chloride, the corresponding 9-methylthio-7,7-dioxo-7,7a-dihydro-5-oxo-7λ6,10-dithia-8,11-diaza-cyclopenta[b] phenantren-6-one, 9-methyl-7,7-dioxo-7H-5,8-dioxa-7λ6-thia-7a,11-diaza-cyclopenta[b] phenantren-6-one, 9-fluoro-7,7-dioxo-7H-5-oxa-7λ6,12-dithia-7a,13-diaza-indeno[1,2-b] phenantren-6-one and 9-Chloro-7,7-dioxo-7H-5-oxa-7λ6-thia-7a,12-diaza-benzo[α]anthracen -6-one were formed and they have been isolated in satisfying yields. Based on the biological activity of chromene-2-ones and heterocyclic compounds condensed in position 3 and 4, we also studied microbiological activity of these new compounds(5-8), againstStaphylococcus aureusATCC 25923,Streptococcus pneumoniae, Aeromonas Salmonicida, Bacillus sppand some of them exhibited significant activity.

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Pyrazole Carboxylic Acid and Derivatives: Synthesis and Biological Applications

Mini-Reviews in Organic Chemistry ◽

10.2174/1570193x17999200507094857 ◽

2020 ◽

Vol 17 ◽

Author(s):

Adnan Cetin

Keyword(s):

Organic Chemistry ◽

Biological Activity ◽

Carboxylic Acid ◽

Heterocyclic Compounds ◽

Medicinal Chemistry ◽

Biological Activities ◽

Building Blocks ◽

Literature Survey ◽

Synthetic Methods ◽

Biological Applications

: The heterocyclic compounds are the building blocks for synthesis of the different biological active compounds in the organic chemistry. Heterocyclic compounds have versatile synthetic applicability and biological activity. Pyrazole carboxylic acid derivatives are significant scaffold structures in heterocyclic compounds due to biologic activities such as antimicrobial, anticancer, inflammatory, antidepressant, antifungal anti-tubercular and antiviral etc. The aim of this mini-review is an overview synthesis of pyrazole carboxylic acid derivatives and their biologic applications. The summarized literature survey presents in detail biological activities of pyrazole carboxylic acid derivatives and their various synthetic methods. This mini-review can be guide to many scientists in medicinal chemistry.

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