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Structure-Guided Optimization and Biological Validation of 1,3,4-Thiadiazole-Based SIRT2 Inhibitors Reinforcing Channel Entrance Interactions. [PDF]
Aksel AB +9 more
europepmc +1 more source
Lipophilic Ligand Efficiency-Monitored Discovery of Potent, Achiral, and Bioavailable Apo-IDO1 Inhibitors. [PDF]
Kazmierski WM +15 more
europepmc +1 more source
Synthesis and antifungal activity of thiadiazole-functionalized chitosan derivatives
A groups of novel water soluble chitosan derivatives containing 1,3,4-thiadiazole group were synthesized including 1,3,4-thiadiazole (TPCTS), 2-methyl-1,3,4-thiadiazole (MTPCTS), and 2-phenyl-1,3,4-thiadiazole (PTPCTS).
Qing Li, Zhanyong Guo, Guodong Gu
exaly +2 more sources
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A 1,2,3-thiadiazole–1,2,3-thiadiazole rearrangement
J. Chem. Soc., Chem. Commun., 1983During its preparation, 4-ethoxycarbonyl-5-diazomethyl-1,2,3-thiadiazole (4), undergoes a ring transformation into the isomeric structure (5), but when the ester function in (4) is replaced by a phenyl group, no isomerization is observed.
Gerrit L'abbé +2 more
openaire +1 more source
1968
Publisher Summary This chapter presents the review of organic and physical chemistry of monocyclic 1, 2, 5-thiadiazoles up to the early part of 1967. Reference is made to the 2, 1, 3-benzothiadiazoles and related compounds only as they contribute to the chemistry of the basic ring system. The 1, 2, 5-thiadiazole nucleus is numbered as in 4.
L M, Weinstock, P I, Pollak
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Publisher Summary This chapter presents the review of organic and physical chemistry of monocyclic 1, 2, 5-thiadiazoles up to the early part of 1967. Reference is made to the 2, 1, 3-benzothiadiazoles and related compounds only as they contribute to the chemistry of the basic ring system. The 1, 2, 5-thiadiazole nucleus is numbered as in 4.
L M, Weinstock, P I, Pollak
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SYNTHESIS AND METHYLATION OF SOME 1,2,4-THIADIAZOLE-5-THIONES
3,4-Disubstituted-1,2,4-thiadiazole-5(4H)-thiones (4) have been prepared by the treatment of 3,4-di-substituted-1,2,4-thiadiazole-5(4H)-ones (3) with P4S10.
Yaşar Dürüst, Hikmet Agirbas
exaly +2 more sources
Journal of Molecular Spectroscopy, 1962
Abstract The microwave spectra of 1, 3, 4-thiadiazole (I) and [ 34 S] 1, 3, 4-thiadiazole (II) have been recorded in the 15,000–30,000 Mc/sec region. Twelve and ten transitions, respectively, were assigned. The rotational constants of (I) are, A = 8907.51 ± 0.10, B = 5569.27 ± 0.02, and C = 3424.80 ± 0.03 Mc/sec. For (II), A = 8908.15 ± 0.20,
Børge Bak +4 more
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Abstract The microwave spectra of 1, 3, 4-thiadiazole (I) and [ 34 S] 1, 3, 4-thiadiazole (II) have been recorded in the 15,000–30,000 Mc/sec region. Twelve and ten transitions, respectively, were assigned. The rotational constants of (I) are, A = 8907.51 ± 0.10, B = 5569.27 ± 0.02, and C = 3424.80 ± 0.03 Mc/sec. For (II), A = 8908.15 ± 0.20,
Børge Bak +4 more
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Heterocycles containing nitrogen, oxygen and sulfur have been under investigation for a long time because of their important medicinal properties. The literature survey has described that thiadiazole moieties serve as analgesic, anti-inflammatory, anti-microbial activities, antihypertensive,anticancer, antituberculosis and vasodilator and this ...
G. Nagendra +3 more
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G. Nagendra +3 more
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ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
D. J. Wilkins, P. A. Bradley
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AbstractFor Abstract see ChemInform Abstract in Full Text.
D. J. Wilkins, P. A. Bradley
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