Results 41 to 50 of about 1,566 (134)

Design, synthesis, and biological evaluation of novel 3,5-disubstituted-1,2,6-thiadiazine-1,1-dione derivatives as HIV-1 NNRTIs

open access: yes, 2013
On the basis of structural features, binding mode, and structure-activity relationship studies of two pyrimidine-derived non-nucleoside reverse-transcriptase inhibitors, DABOs, and diaryl pyrimidines, a novel class of 1,2,6-thiadiazine-1,1-dione ...
Zhan, Peng   +7 more
core   +1 more source

Design, synthesis, and biological evaluation of novel 4-aminopiperidinyl-linked 3,5-disubstituted-1,2,6-thiadiazine-1,1-dione derivatives as HIV-1 NNRTIs

open access: yes, 2015
Based on the hybridization of the privileged fragments in DABO and DAPY-typed HIV-1 NNRTIs, a novel series of 4-aminopiperidinyl-linked 3,5-disubstituted-1,2,6-thiadiazine-1,1-dione derivatives were designed, synthesized, and evaluated for their in vitro
Liang, Xin   +9 more
core   +1 more source

Una nueva familia de antichagásicos derivados de 2,2-dióxido de imidazo [4,5-c] [1,2,6] tiadiazina [PDF]

open access: yes, 2009
[EN] Compounds derived from imidazo[4,5-c][1,2,6]thiadiazine 2,2-dioxides for use as medicament or pharmaceutical composition for treatment of parasitic diseases, preferably of diseases caused by parasites of the genus Trypanosome, and more preferably ...
Cerecetto, Hugo   +5 more
core  

Acid-Catalyzed Hydrolysis and Intramolecular Cyclization of NCyano Sulfoximines for the Synthesis of Thiadiazine 1Oxides

open access: yes, 2022
Herein, we describe a novel approach for the practical synthesis of thiadiazine 1-oxides 10. The first example of an intramolecular cyclization with 2-N-cyano-sulfonimidoyl amides 9 to form the desired thiadiazine 1-oxides 10 was developed.
Seong Jun Park (7388279)   +11 more
core   +1 more source

Effect of thiadiazine derivatives on intracellular amastigotes of Leishmania amazonensis

open access: yes, 2004
Current therapy for leishmaniasis is not satisfactory. We describe the in vitro antiproliferative effects of new thiadiazine derivatives against Leishmania amazonensis.
Lianet Monzote Fidalgo   +11 more
core   +1 more source

Synthesis and Evaluation of Novel 1,2,6-Thiadiazinone Kinase Inhibitors as Potent Inhibitors of Solid Tumors. [PDF]

open access: yesMolecules, 2021
Kalogirou AS   +9 more
europepmc   +1 more source

thiadiazine‐4‐thiones

open access: yes, 1994
Thiation of N‐(1‐tert‐butyl‐3‐methylpyrazol‐5‐yl)carboxamides 2 with the Lawesson reagent afforded the corresponding thiocarboxamides 3. Heating of 3 in formic acid gave the N‐dealkylated thiocarboxamides 4 which were cyclized into 4H‐pyrazolo[1,5‐c][1,3,
C. B. Vicentini   +11 more
core   +1 more source

New chemistry of isothiazoles and 1,2,6-thiadiazines

open access: yes, 2011
This thesis begins with a short introduction on heterocyclic chemistry as well as the known chemistry of isothiazoles and 1,2,6-thiadiazines. The main part is then divided into 3 parts (Chapters 2, 3 and 4 are Part 1, Chapters 5, 6 and 7 are part 2 and part 3 is chapter 8). In the first part, the regioselective dehalogenation of 3,5-dihaloisothiazole-4-
Ioannidou, Heraklidia A.   +1 more
openaire   +1 more source

Fungitoxicity of 6H-Pyrazolo[3,4-c] [1,2,5]thiadiazine 2,2-Dioxides

open access: yes, 1990
A base‐promoted cyclisation of 4‐nitroso‐5‐benzylsulphonamidopyrazoles (VII) afforded 6H‐pyrazolo[3,4‐c][1,2,5]thiadiazine‐2,2‐dioxides (VIII). They were tested in vitro for antifungal activity against a series of phytopathogenic fungi of different ...
GIORI, Paolo   +5 more
core   +1 more source

Synthesis of 3,4-Dihydropyrimidin(thio)one Containing Scaffold: Biginelli-like Reactions. [PDF]

open access: yesPharmaceuticals (Basel), 2022
Sánchez-Sancho F   +6 more
europepmc   +1 more source

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