81979-35-3Relevant academic research and scientific papers
New donor-acceptor stenhouse adducts as visible and near infrared light polymerization photoinitiators
Bonardi, Aude-Héloise,Dumur, Frédéric,Duval, Sylvain,Gigmes, Didier,Lalevée, Jacques,Noirbent, Guillaume,Xu, Yangyang
supporting information, (2020/05/28)
Polymerization photoinitiators that can be activated under low light intensity and in the visible range are being pursued by both the academic and industrial communities. To efficiently harvest light and initiate a polymerization process, dyes with high molar extinction coefficients in the visible range are ideal candidates. In this field, Donor-acceptor Stenhouse Adducts (DASA) which belong to a class of recently discovered organic photochromic molecules still lack practical applications. In this work, a series of DASA-based dyes are proposed as photoinitiators for the free radical polymerization of (meth)acrylates upon exposure to a near infrared light (laser diode at 785 nm).
Acetylcholinesterase and butyrylcholinesterase inhibitory activities of 5-arylidene-N, N-diethylthiobarbiturates
Khan, Momin,Rehman, Munir Ur,Qadir, Naveed,Ashraf, Muhammad,Ismail, Tayaba,Ismail, Muhammad,Kanwal,Salar, Uzma,Khan, Khalid Mohammed,Perveen, Shahnaz
, p. 134 - 140 (2020/02/13)
5-Arylidene-N,N-diethylthiobarbiturates 1-25 were evaluated for their potential against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes and displayed varying degree of inhibition. Based on the IC50 values, compound 6 (ICsu
Antiglycation activity of N, N-diethylthiobarbiturates derivatives
Ahad, Ghulam,Kanwal,Khan, Ajmal,Khan, Khalid Mohammed,Khan, Momin,Salar, Uzma,Salman, Syed Muhammad,Shah, Sana
, p. 409 - 515 (2020/04/17)
Background: Previous identification of N,N-diethylthiobarbiturates as potential α-glucosidase inhibitory potential prompted us to investigate the antiglycation activity of these synthetic compounds (1-25) in order to identify the lead candidates for their
Synthesis, molecular modeling and biological evaluation of 5-arylidene- N,N-diethylthiobarbiturates as potential α-glucosidase Inhibitors
Ashraf, Muhammad,Hameed, Abdul,Hussain, Zahid,Khan, Abbas,Khan, Iltaf,Khan, Khalid M.,Khan, Momin,Khan, Sehrish,Perveen, Shahnaz,Rahman, Jameel,Shams, Sulaiman,Ul Mulk, Amir,Ur Rahman, Anis,Wadood, Abdul,Zaman, Khair
, p. 175 - 185 (2019/07/12)
Background: Barbituric acid derivatives are a versatile group of compounds which are identified as potential pharmacophores for the treatment of anxiety, epilepsy and other psychiatric disorders. They are also used as anesthetics and have sound effects on
A sulfur on behalf of the barbituric acid derivative for the probe molecule detecting secondary amine method and its preparation
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Paragraph 0047; 0048; 0049; 0050; 0051; 0052; 0053; 0054, (2018/01/19)
The invention discloses a method for detecting secondary amine with thiobarbituric acid derivatives (TBAs) serving as ultraviolet-visible light (UV-vis) spectrophotometric method probe molecules and preparation of the thiobarbituric acid derivatives for detecting secondary amine. The probe molecules are prepared from primary amine through a preparation line of a system. The probe molecules are provided with a furan ring (or thiophene ring) for recognizing secondary amine, an independent probe molecule solution is yellow, and along with addition of secondary amine, the solution becomes red from yellow. A molecular probe is high in selectivity and sensitivity to secondary amine, the response range to secondary amine is 100 micrometers to 400 micrometers, and the limit of detection (LOD) is 12 micrometers. Test paper can be prepared from the probe molecules, and qualitative detection on secondary amine can be achieved fast with low cost. The method can be widely applied to fast and sensitive detection such as online detection of secondary amine compounds, food analysis and environmental monitoring in the industrial process.
