68701-32-6Relevant articles and documents
A highly selective fluorogenic substrate for imaging glutathione S-transferase P1: Development and cellular applicability in epigenetic studies
Mori, Masaya,Fujikawa, Yuuta,Kikkawa, Manami,Shino, Moeho,Sawane, Mei,Sato, Shiho,Inoue, Hideshi
supporting information, p. 8122 - 8125 (2019/07/15)
Pi-class glutathione S-transferase (GSTP1) is a molecular marker enzyme whose expression level is altered in various malignant tumour tissues. Herein, we report the first highly selective fluorogenic GSTP1 substrate, Ps-TG, and its membrane-permeable deri
Design, synthesis and insecticidal activities of novel anthranilic diamides containing fluorinated groups as potential ryanodine receptors activitors
Wu, Chang-Chun,Wang, Bao-Lei,Liu, Jing-Bo,Wei, Wei,Li, Yu-Xin,Liu, Yang,Chen, Ming-Gui,Xiong, Li-Xia,Yang, Na,Li, Zheng-Ming
supporting information, p. 1248 - 1251 (2017/06/19)
In order to search for novel potent and environmentally benign insecticides, a series of anthranilic diamides containing various fluorinated groups were designed and synthesized. Their structures were confirmed by 1H NMR, 13C NMR, s
Compositions and Methods for the Inhibition of Methyltransferases
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Paragraph 0193, (2015/03/04)
Methods and compositions disclosed herein relate to detecting, analyzing, isolating and inhibiting methyltransferases, methyltransferase substrates, S-adenosyl-methionine-binding proteins and RNA, including for the treatment of disease.
POTENT SMALL MOLECULE INHIBITORS OF AUTOPHAGY, AND METHODS OF USE THEREOF
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Page/Page column 104, (2014/09/29)
Certain aspects of the invention relate to small molecule autophagy inhibitors, and their use for treatment and prevention of cancers and acute pancreatitis. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity.
Novel phenylalanine derivatives
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Page/Page column 32, (2010/02/14)
Specific phenylalanine derivatives and analogues thereof have an antagonistic activity to α4 integrin. They are used as therapeutic agents for various diseases concerning α4 integrin.
Piperidyindoles as serotonin receptor ligands
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Page 9, (2010/02/05)
A pharmaceutical compound of the formula (I) in which R1 and R2 are each hydrogen or C1-6 alkyl, R3 is —SR10, —SOR10, —SO2R10, —COR10, —CH2OH or —CONHR11, where R10 is C1-6 alkyl and R11 is hydrogen or C1-6 alkyl, R4, R5, R6 and R7 are each hydrogen or C1-6 alkyl, provided that at least one of R4, R5, R6 and R7 is C1-6 alkyl, R8 and R9 are each hydrogen, halo, C1-6 alkyl or cyano, n is 0 or 1 and m is 2 or 3, x is a (a) or (b), and y is (c) or (d), wherein R12 and R13 are each hydrogen, C1- alkyl, cyclopropyl or cyclopropyl-C1-6 alkyl; and salts thereof.
Synthesis and antinephritic activities of quinoline-3-carboxamides and related compounds
Tsuji, Kiyoshi,Spears, Glen W.,Nakamura, Katsuya,Tojo, Takashi,Seki, Nobuo,Sugiyama, Aiko,Matsuo, Masaaki
, p. 85 - 88 (2007/10/03)
A series of linomide-related quinoline-3-carboxamides and their analogues was prepared and evaluated for antinephritic activities. The 6-MeS derivative 7a was highly effective in two nephritis models, namely chronic graft-versus-host disease and autoimmune MRL/l mice.
Reactions of 2H-3,1-Benzoxazine-2,4-(1H)dione (Isatoic Anhydride) (1) with Anions of 1,4-Dihydro-5H-Pyrazol-5-ones: Synthesis of Pyrazoloquinazolin-9-ones
Sircar, Jagadish C.,Capiris, Thomas,Kesten, Stephen J.
, p. 117 - 121 (2007/10/02)
Reactions of 2H-3,1-benzoxazine-2,4-(1H)dione (isatoic anhydride) (1) with anions of 1,4-dihydro-5H-pyrazol-5-ones (2) gave pyrazoloquinazolin-9-ones (3) via the nucleophilic attack of the anion 2b rather than 2a.However, in the case of 5-methoxyis
Pyrazolo[5,1-b]quinazolin-9-(4H)-ones and anti-allergic pharmaceutical compositions containing them
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, (2008/06/13)
Certain pyrazolo[5,1-b]quinazolin-9-(4H)-ones are disclosed. These compounds prevent the allergic response in mammals. Novel alkylthioanthranilic acids, useful as intermediates, are also disclosed.