Evidence on the Carcinogenicity of Quinoline and Its
Quinoline is a naturally occurring heterocyclic aromatic chemical found in creosote and other products produced from fossil fuels. It is produced by combustion of a variety of substances including tobacco and is used in the chemical industry. Strong acid salts of quinoline, including the hydrochloride,
Isoquinoline alkaloids are not a structurally homogenous group. Based on different degrees of oxygenation, and intramolecular rearrangements, their distribution, and the presence of additional rings connected to the main system, they may be divided into eight subgroups [10]: benzylisoquinoline, aporphine, protoberberine, benzo[c]phenanthridine, protopine,
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Cannabis sativa is one of the world's oldest cultivated plants (Russo, 2007). Although the earliest written records of the human use of cannabis date from the 6th century B.C. (ca. 2,600 cal BP), existing evidence suggests that its use in Europe and East Asia started in the early Holocene (ca. 8,000 cal BP) (Long et al., 2016). Many 19th-century practitioners ascribed medicinal
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applications.16 Merocyanines can be used as probes and markers 40 in chemical analysis, biology and medical applications, non-linear optics, and organic semiconductors16. Many cyanines contain quinoline moiety17 a Department of Chemistry, Institute of Chemical Technology, Matunga, 45 Mumbai-400019, India. E-mail: samantsd@yahoo.
Synthetic antioxidants such as 2,2,4-trime-thyl quinoline (TMQ) have been used widely in polymer formulations to prevent the thermo-oxidative degradation of polymers, but they are not environment-friendly. Also, their manufacture contributes significantly to carbon foot print. From environmental point of view, instead