Zobrazeno 1 - 10
of 52
pro vyhledávání: '"thiosemicarbazone derivative"'
Autor:
Azmat Ali Khan, Rehan Ahmad, Amer M. Alanazi, Nawaf Alsaif, Maha Abdullah, Tanveer A. Wani, Mashooq A. Bhat
Publikováno v:
Saudi Pharmaceutical Journal, Vol 30, Iss 6, Pp 815-824 (2022)
Thiosemicarbazones have received noteworthy attention due to their numerous pharmacological activities. Various thiosemicarbazone derivatives have been reported to play a key role as potential chemotherapeutic agents for the management of cancer. Her
Externí odkaz:
https://doaj.org/article/5f13549bff2245b99590a6864e785526
Autor:
Qingyun Yuan, Run Cheng, Song Zou, Cheng Ding, Hongxia Liu, Yujie Wang, Di Yang, Xin Xiao, Qiong Jiang, Ruiren Tang, Jingwen Chen
Publikováno v:
Journal of Materials Research and Technology, Vol 9, Iss 5, Pp 11935-11947 (2020)
Five isatin thiosemicarbazone derivatives bearing different substituents (R) at 5-position of the isatin moiety, ISA-R, being R = -H, -CH3, -F, -Cl and -NO2, were synthesized and fully characterized. The corrosion inhibition action of ISA-R on AA6060
Externí odkaz:
https://doaj.org/article/7704c65f917b41e29a927e09a5d6d31f
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Fluorescence. 33:1003-1015
A new simple spectrophotometric method for the determination of Cu2+ ion was developed using an thiosemicarbazone compound, 2-{4-[Bis(2-chloroethyl)amino]benzylidene}-N-[(4-methylthio)phenyl]hydrazinecarbothioamide (TSC). A simultaneous color change
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf38f4c0afb20e2ff2fb632931efed13
https://doi.org/10.1007/s10895-022-03127-6
https://doi.org/10.1007/s10895-022-03127-6
Autor:
Jecika Maciel Velasques, Vanessa Carratu Gervini, Lisliane Kickofel, Renan Lira de Farias, Adriano Bof de Oliveira
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 73, Iss 5, Pp 702-707 (2017)
The acetic acid-catalyzed reaction between 5-chloroisatin and 4-methylthiosemicarbazide yields the title compound, C10H9ClN4OS (I) (common name: 5-chloroisatin-4-methylthiosemicarbazone). The molecule is nearly planar (r.m.s. deviation = 0.047 Å for
Externí odkaz:
https://doaj.org/article/54e0908ea0ca4642adcf1f86aef6c6cb
Autor:
Adriano Bof de Oliveira, Johannes Beck, Christian Landvogt, Renan Lira de Farias, Bárbara Regina Santos Feitoza
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 73, Iss 2, Pp 291-295 (2017)
There are two crystallographically independent molecules in the asymmetric unit of the title compound, C13H17N3S, one of them being disordered over the methyl group [site-occupancy ratio = 0.705 (5):0.295 (5)]. The maximum r.m.s. deviations from the
Externí odkaz:
https://doaj.org/article/0e30bc752ec94b8ca0235e251fb9f8f1
Akademický článek
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Autor:
Gabriela Porto de Oliveira, Leandro Bresolin, Vanessa Senna Nogueira, Priscila Jussiane Zambiazi, Adriano Bof de Oliveira
Publikováno v:
IUCrData, Vol 1, Iss 11, p x161730 (2016)
In the title compound, C17H21N3OS [common nomenclature: (R)-camphor 4-phenylthiosemicarbazone], the N—N—C—(S)—N fragment deviates slightly from planarity, with a maximum deviation of 0.0259 (12) Å for the hydrazinic N atom, and makes an angl
Externí odkaz:
https://doaj.org/article/d78cbc2965554c0ebe8b2edecd90775b
Autor:
Viviane C. D. Bittencourt, Vitor Y. G. Almeida, Davi F. Back, Vanessa C. Gervini, Adriano Bof de Oliveira
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 6, Pp o383-o384 (2015)
In the title compound, C9H7FN4OS, the molecules are almost planar, with an r.m.s. deviation of 0.047 (3) Å from the mean plane defined by the non-H atoms and a maximum deviation of 0.123 (2) Å for the amine N atom. The torsion angle for the N—N
Externí odkaz:
https://doaj.org/article/8b78f41a54b2444bbe73651ca301cf56