References
- Khatun, S.; Singh, A.; Bader, G. N.; Sofi, F. A. J. Biomol. Struct. Dynamics 2021. DOI: https://doi.org/10.1080/07391102.2021.1997818.
- Bagdi, A. K.; Santra, S.; Monir, K.; Hajra, A. Chem. Commun. (Camb.) 2015, 51, 1555–1575. DOI: https://doi.org/10.1039/C4CC08495K.
- Tashrifi, Z.; Mohammadi-Khanaposhtani, M.; Larijani, B.; Mahdavi, M. Eur. J. Org. Chem. 2020, 2020, 269–284. DOI: https://doi.org/10.1002/ejoc.201901491.
- Kishbaugh, T. L. S. Curr. Top. Med. Chem. 2016, 16, 3274–3302. DOI: https://doi.org/10.2174/1568026616666160506145141.
- Liu, Y.; Lu, L.; Zhou, H.; Xu, F.; Ma, C.; Huang, Z.; Xu, J.; Xu, S. RSC Adv. 2019, 9, 34671–34676. DOI: https://doi.org/10.1039/C9RA06724H.
- Patil, S. M.; Mascarenhas, M.; Sharma, R.; Roopan, S. M.; Roychowdhury, A. J. Heterocyclic Chem. 2014, 51, 1509–1515. DOI: https://doi.org/10.1002/jhet.1764.
- Groselj, U.; Bezensek, J.; Meden, A.; Svete, J.; Stanovnik, B.; Oblak, M.; Anderluh, P. S.; Urleb, U. Heterocycles 2008, 75, 1355–1370. DOI: https://doi.org/10.3987/COM-07-11303
- Monir, K.; Bagdi, A. K.; Ghosh, M.; Hajra, A. Org Lett. 2014, 16, 4630–4633. DOI: https://doi.org/10.1021/ol502218u.
- Tzani, M. A.; Kallitsakis, M. G.; Symeonidis, T. S.; Lykakis, IN. ACS Omega 2018, 3, 17947–17956. DOI: https://doi.org/10.1021/acsomega.8b03047.
- Tian, X.; Song, L.; Wang, M.; Lv, Z.; Wu, J.; Yu, W.; Chang, J. Chemistry 2016, 22, 7617–7622. DOI: https://doi.org/10.1002/chem.201600849.
- Stasyuk, A. J.; Banasiewicz, M.; Cyrański, M. K.; Gryko, D. T. J. Org. Chem. 2012, 77, 5552–5558. DOI: https://doi.org/10.1021/jo300643w.
- Jaramillo, C.; Diego, J. E.; Hamdouchi, C. Synlett 2002, 2002, 1544–1546. DOI: https://doi.org/10.1055/s-2002-33539.
- Vega, J. A.; Vaquero, J. J.; Builla, J. A.; Ezquerra, J.; Hamdouchi, C. Tetrahedron 1999, 55, 2317–2326. DOI: https://doi.org/10.1016/S0040-4020(99)00012-5.
- Shaaban, S.; Wahab, B. F. Mol. Divers. 2016, 20, 233–254. DOI: https://doi.org/10.1007/s11030-015-9602-6.
- Carballares, S.; Cifuentes, M. M.; Stephenson, G. A. Tet. Lett. 2007, 48, 2041–2045. DOI: https://doi.org/10.1016/j.tetlet.2006.11.181.
- Semreen, M. H.; El-Awady, R.; Abu-Odeh, R.; Saber-Ayad, M.; AlQawasmeh, R. A.; Chouaib, S.; Voelter, W.; Al-Tel, T. H. Curr. Med. Chem. 2013, 20, 1445–1459. DOI: https://doi.org/10.2174/0929867311320110007.
- Jacquier, R. L.; Helene, L.; Georges, M. J. Heterocyclic Chem. 1973, 10, 755–762. DOI: https://doi.org/10.1002/jhet.5570100513.
- Maruyama, Y.; Anami, K.; Terasawa, M.; Goto, K.; Imayoshi, T.; Kadobe, Y.; Mizushima, Y. Arzneim Forsch 1981, 31, 1111–1118.
- Prasher, P.; Mudila, H.; Sharma, M.; Khati, B. Med. Chem. Res. 2019, 28, 417–449. DOI: https://doi.org/10.1007/s00044-019-02315-7.
- Flores, M. Y. K.; Campos-Aldrete, M. E.; Salgado-Zamora, H.; Basurto, J.-C.; Camargo, M. E. M. Med. Chem. Res. 2012, 21, 3491–3498. DOI: https://doi.org/10.1007/s00044-011-9870-3.
- Katsura, Y.; Nishino, S.; Takasugi, H. Chem. Pharm. Bull. 1991, 39, 2937–2943. DOI: https://doi.org/10.1248/cpb.39.2937.
- Murmann, W.; Carminati, G. M.; Cattaneo, R. Panminerva Med. 1974, 16, 335–346.
- Hendriks, C. M. M.; Nurnberg, P.; Bolm, C. Synthesis 2015, 47, 1190–1194. DOI: https://doi.org/10.1055/s-0034-1380109
- Das, D.; Bhutia, Z. T.; Panjikar, P. C.; Chatterjee, A.; Banerjee, M. J. Heterocyclic Chem. 2020, 57, 4099–4107. DOI: https://doi.org/10.1002/jhet.4106.
- Mohan, D. C.; Donthiri, R. R.; Rao, S. N.; Adimurthy, S. Adv. Synth. Catal. 2013, 355, 2217–2221. DOI: https://doi.org/10.1002/adsc.201300456.
- Bagdi, A. K.; Rahman, M.; Santra, S.; Majee, A.; Hajra, A. Adv. Synth. Catal. 2013, 355, 1741–1747. DOI: https://doi.org/10.1002/adsc.201300298.
- Zhang, Y.; Xia, M.; Jin, K.; Wang, S.; Wei, H.; Fan, C.; Wu, Y.; Li, X.; Li, X.; Li, G.; et al. Mol. Cancer 2018, 17, 45. DOI: https://doi.org/10.1186/s12943-018-0796-y.
- Jiao, Q.; Bi, L.; Ren, Y.; Song, S.; Wang, Q.; Wang, Y.-S. Mol. Cancer 2018, 17, 36. DOI: https://doi.org/10.1186/s12943-018-0801-5.
- Awazu, Y.; Mizutani, A.; Nagase, Y.; Tsuchiya, S.; Nakamura, K.; Kakoi, Y.; Kitahara, O.; Takeuchi, T.; Yamasaki, S.; Miyamoto, N.; et al. Cancer Sci. 2013, 104, 486–494. DOI: https://doi.org/10.1111/cas.12101.
- Matsumoto, S.; Miyamoto, N.; Hirayama, T.; Oki, H.; Okada, K.; Tawada, M.; Iwata, H.; Nakamura, K.; Yamasaki, S.; Miki, H.; et al. Bioorg. Med. Chem. 2013, 21, 7686–7698. DOI: https://doi.org/10.1016/j.bmc.2013.10.028.
- Takeda, K.; Shimozono, R.; Noguchi, T.; Umeda, T.; Morimoto, Y.; Naguro, I.; Tobiume, K.; Saitoh, M.; Matsuzawa, A.; Ichijo, H. J. Biol. Chem. 2007, 282, 7522–7531. DOI: https://doi.org/10.1074/jbc.M607177200.
- Hayakawa, R.; Hayakawa, T.; Takeda, K.; Ichijo, H. Proc. Jpn Acad. Ser. B Phys. Biol. Sci. 2012, 88, 434–453. DOI: https://doi.org/10.2183/pjab.88.434.
- Ogier, J. M.; Nayagam, B. A.; Lockhart, P. J. J. Mol. Med. 2020, 98, 335–348. DOI: https://doi.org/10.1007/s00109-020-01878-y.
- Terao, Y.; Suzuki, H.; Yoshikawa, M.; Yashiro, H.; Takekawa, S.; Fujitani, Y.; Okada, K.; Inoue, Y.; Yamamoto, Y.; Nakagawa, H.; et al. Bioorg. Med. Chem. Lett. 2012, 22, 7326–7329. DOI: https://doi.org/10.1016/j.bmcl.2012.10.084.
- Dankner, M.; Rose, A. A. N.; Rajkumar, S.; Siegel, P. M.; Watson, I. R. Oncogene 2018, 37, 3183–3199. DOI: https://doi.org/10.1038/s41388-018-0171-x.
- Holderfield, M.; Deuker, M. M.; McCormick, F.; McMahon, M. Nat. Rev. Cancer 2014, 14, 455–467. DOI: https://doi.org/10.1038/nrc3760.
- Agianian, B.; Gavathiotis, E. J. Med. Chem. 2018, 61, 5775–5793. DOI: https://doi.org/10.1021/acs.jmedchem.7b01306.
- Smith, A.; Ni, Z.-J.; Poon, D.; Huang, Z.; Chen, Z.; Zhang, Q.; Tandeske, L.; Merritt, H.; Shoemaker, K.; Chan, J.; et al. Bioorg. Med. Chem. Lett. 2017, 27, 5221–5224. DOI: https://doi.org/10.1016/j.bmcl.2017.10.047.
- Martin, R. J. Vet. J. 1997, 154, 11–34. DOI: https://doi.org/10.1016/S1090-0233(05)80005-X.
- Bagheri, H.; Simiand, E.; Montastruc, J.-L.; Magnaval, J.-F. Ann. Pharmacother. 2004, 38, 383–388. DOI: https://doi.org/10.1345/aph.1D325.
- Zhou, S.; Chen, G.; Huang, G. Chem. Biol. Drug Des. 2019, 93, 503–510. DOI: https://doi.org/10.1111/cbdd.13441.