[17]
Lai, P.H.; Tian, G.H.; Ji, X.H.; Liu, C.F.; Guo, Y.M. Synthesis and antimicrobial activity of novel 2′-hydroxy-4′-methoxy-3-nitrochalcone. Chin. J. Synth. Chem., 2010, 18(4), 465-467.
[39]
Safina, B.S.; Baker, S.; Baumgardner, M.; Blaney, P.M.; Chan, B.K.; Chen, Y.H.; Cartwright, M.W.; Castanedo, G.; Chabot, C.; Cheguillaume, A.J.; Goldsmith, P.; Goldstein, D.M.; Goyal, B.; Hancox, T.; Handa, R.K.; Iyer, P.S.; Kaur, J.; Kondru, R.; Kenny, J.R.; Krintel, S.L.; Li, J.; Lesnick, J.; Lucas, M.C.; Lewis, C.; Mukadam, S.; Murray, J.; Nadin, A.J.; Nonomiya, J.; Padilla, F.; Palmer, W.S.; Pang, J.; Pegg, N.; Price, S.; Reif, K.; Salphati, L.; Savy, P.A.; Seward, E.M.; Shuttleworth, S.; Sohal, S.; Sweeney, Z.K.; Tay, S.; Tivitmahaisoon, P.; Waszkowycz, B.; Wei, B.; Yue, Q.; Zhang, C.; Sutherlin, D.P. Discovery of novel PI3-kinase δ specific inhibitors for the treatment of rheumatoid arthritis: taming CYP3A4 time-dependent inhibition.
J. Med. Chem., 2012,
55(12), 5887-5900.
[
http://dx.doi.org/10.1021/jm3003747] [PMID:
22626259]
[51]
Nevagi, R.J. Biological and medicinal significance of 2-aminothiazoles. Der. Pharm. Lett., 2014, 6, 134-150.
[64]
Blanquicett, C.; Roman, J.; Hart, C.M. Thiazolidinediones as anti-cancer agents. Cancer Ther., 2008, 6(1), 501-534.
[71]
Huang, Y.P.; Shih, H.P.; Liang, Y.C.; Lin, H.H.; Lin, M.C.; Chen, C.W.; Huang, T.J.; Kuo, Y.C.; Han, C.C.; Hsu, M.H. Advanced generation of Paeonol-Phenylsufonyl derivatives as potential anti-hbv agents. RSC. Adv., 2016, 6(49), 43556-43562.
[73]
Rehman, F.; Mairaj, S. Antimicrobial studies of Allicin with Paeonol and its oxime. Int. J. Pharma Bio Sci., 2013, 4(1), 240-249.
[75]
Teruyaki, M.; Yoshiharu, H.; Ka, Y. Oxime derivative thereof, process for preparing thereof, Herbicidal composition and methods for the destruction of undesirable weeds; Asahi Chem: Ind., 1986.
[78]
Mairaj, S.; Rehman, F. Studies on the complexes of 2-hydroxy-4-mothoxy acetophenone oxime. Orient. J. Chem., 2011, 27(1), 221-225.
[86]
Kang, Y.B.; Shang, H.S.; Cheng, Y.M. Inhibition activities of paeonol to plant pathogenic fungi in vitro. Acta Phytophysiol. Sin., 2007, 34(6), 580-584.
[87]
Xia, C.G.; Chen, J.L. Toxicity of fumigation and contact of moutan extracts and paeonol to several species of stored product insects of Chinese medicinal materials. J. Zhongkai Agrotech. Coll., 1999, 12(2), 1-8.
[88]
Lai, P.H.; Tian, G.H.; Zhao, H. Synthesis and antimicrobial activity of a paeonol derivative. J. Wuhan Univ., 2010, 56(5), 523-526.
[89]
Liu, C.F. Synthesis and antimicrobial activity of a paeonol derivative: 3-hydroxy-1-(2-hydroxy-4-methoxyphenyl)-3-(2′-bromophenyl)-1-acetone. Chin. J. Pest. Sci., 2016, 18(1), 119-123.
[90]
Gao, J.; Xiang, H.Y.; Xu, T.T.; Hu, J.P.; Wu, Q. Study on the antimicrobial activity of paeonol and its Schiff base derivatives. Chem. Reagents, 2007, 29(1), 59-60.
[91]
Lin, M.; Liu, X.D.; Cao, Z.W. Synthesis and antibacterial activities of Schiff base condensed from paeonol with ethanolamine and its Ni(II), complex. Guangdong Chem. Ind., 2013, 40(2), 24-25.
[95]
Li, F.Y.; Huang, G.D.; Ruan, C.K.; Wei, H.L.; Fan, Q.Q. Design and synthesis of a NO-releasing paeonol derivative. Anhui Nongye Kexue, 2010, 38(14), 7350-7400.
[96]
Bai, Z.W.; He, L.Q.; Fang, W. Synthesis and bioactivity of NO-donating paeonol derivatives. Chem. World, 2018, 59(4), 241-245.
[101]
Pao, K.C.; Zhao, J.F.; Lee, T.S.; Huang, Y.P.; Han, C.C.; Huang, L.C.S.; Wua, K.H.; Hsu, M.H. Low-dose paeonol derivatives alleviate lipid accumulation. RSC. Adv., 2015, 5(8), 5652-5656.
[107]
Kang, J.J.; Chen, L.M.; Lin, Y.W. Synthesis and anti-oxidation activity of paeonol Schiff base derivatives. J. Fujian Med. Univ., 2011, 45(1), 26-28.
[109]
Xu, T.T. The research of antioxidant activity about paeonol derivative. Tianjin Chem. Ind., 2012, 26(4), 20-21.