About: Thiazine is a research topic. Over the lifetime, 1541 publications have been published within this topic receiving 11572 citations. The topic is also known as: thiazines.
TL;DR: The thiazine dyes were the most uniformly potent structural class tested, and among the dyes in this class, methylene blue was notable for both its high antimalarial potency and selectivity.
Abstract: In 1891 Guttmann and Ehrlich (P. Guttmann and P. Ehrlich, Berlin Klin. Wochenschr. 28:953-956, 1891) were the first to report the antimalarial properties of a synthetic, rather than a natural, material when they described the clinical cure of two patients after oral administration of a thiazine dye, methylene blue. Since that time, sporadic reports of the antimalarial properties of several xanthene and azine dyes related to methylene blue have been noted. We report here the results from a reexamination of the antimalarial properties of methylene blue. Janus green B, and three rhodamine dyes and disclose new antimalarial data for 16 commercially available structural analogs of these dyes. The 50% inhibitory concentrations for the chloroquine-susceptible D6 clone and SN isolate and the chloroquine-resistant W2 clone of Plasmodium falciparum were determined by the recently described parasite lactate dehydrogenase enzyme assay. No cross-resistance to chloroquine was observed for any of the dyes. For the 21 dyes tested, no correlation was observed between antimalarial activity and cytotoxicity against KB cells. No correlation between log P (where P is the octanol/water partition coefficient) or relative catalyst efficiency for glucose oxidation and antimalarial activity or cytotoxicity was observed for the dyes as a whole or for the thiazine dyes. The thiazine dyes were the most uniformly potent structural class tested, and among the dyes in this class, methylene blue was notable for both its high antimalarial potency and selectivity.
TL;DR: In this paper, 1,2,4,thiadiazine and 1,4-thiazine derivatives represented by formula (I) are defined in the description, compositions thereof and methods for preparing the compounds are described.
Abstract: 1,2,4-thiadiazine and 1,4-thiazine derivatives represented by formula (I) wherein A, B, D, R?1, R2, R3 and R4? are defined in the description, compositions thereof and methods for preparing the compounds are described. The compounds are useful in the treatment of diseases of the central nervous system, the cardiovascular system, the pulmonary system, the gastrointestinal system and the endocrinological system.
TL;DR: The chemistry of leuco triarylmethanes is discussed in this paper, where the authors also present a synthesis and properties of Phthalide-type color formers.
Abstract: Spiropyran Leuco Dyes H. Nakazumi. Leuco Quinone Dyes M. Matsuoka. Thiazine, Oxazine, and Phenazine Leuco Dyes T. Van Thien. Synthesis and Properties of Phthalide-Type Color Formers I.J. Fletcher, R. Zink. The Chemistry of Leuco Triarylmethanes R. Muthyala, X. Lan. The Chemistry of Fluoran Leuco Dyes Y. Hatano. The Chemistry of Tetrazolium Salts D.S. Daniel. Conclusions. Index.
TL;DR: In this paper, electrochemical impedance spectroscopy (EIS) and Tafel polarization techniques were used to investigate the reactivities and selectivities of azine and thiazine dyes.
Abstract: The inhibition performances of some selected azine and thiazine dyes, namely, Neutral Red (NR), Azure A Eosinate (AAE), Toluidine Blue (TB), phenosafranin (PS), and Rhodanile Blue (RB), on mild steel corrosion in hydrochloric acid solution was studied the using electrochemical impedance spectroscopy (EIS) and Tafel polarization techniques. Quantum chemical calculations based on the density functional theory (DFT) and semiempirical (PM3) methods were used to investigate the reactivities and selectivities of the studied cationic dyes. The effects of inhibitor concentration on the inhibition efficiency have been studied. Inhibition efficiency increased with increase in concentration of all the studied cationic dyes within the concentration range 100–500 ppm. Potentiodynamic studies revealed that all the inhibitors are of mixed type. The results obtained from the EIS studies showed good agreement with the results from potentiodynamic polarization techniques. The quantitative structure–activity relationship (Q...