Tsutomu Inokuchi - Search Results

Year	Number of Results
2004	1
2005	2
2006	1
2007	1
2009	1
2010	1
2012	2
2013	5
2014	4
2015	1
2016	1
2017	2
2019	1
2022	1

1

Structural Modifications of Nature-Inspired Indoloquinolines: A Mini Review of Their Potential Antiproliferative Activity.

Wang N, Świtalska M, Wang L, Shaban E, Hossain MI, El Sayed IET, Wietrzyk J, Inokuchi T. Wang N, et al. Among authors: inokuchi t. Molecules. 2019 Jun 5;24(11):2121. doi: 10.3390/molecules24112121. Molecules. 2019. PMID: 31195640 Free PMC article. Review.

2

5-Methyl-N-(8-(5,6,7,8-tetrahydroacridin-9-ylamino)octyl)-5H-indolo[2,3-b]quinolin-11-amine: a highly potent human cholinesterase inhibitor.

Wang L, Moraleda I, Iriepa I, Romero A, López-Muñoz F, Chioua M, Inokuchi T, Bartolini M, Marco-Contelles J. Wang L, et al. Among authors: inokuchi t. Medchemcomm. 2017 Apr 28;8(6):1307-1317. doi: 10.1039/c7md00143f. eCollection 2017 Jun 1. Medchemcomm. 2017. PMID: 30108842 Free PMC article.

3

Donepezil-like multifunctional agents: Design, synthesis, molecular modeling and biological evaluation.

Wu MY, Esteban G, Brogi S, Shionoya M, Wang L, Campiani G, Unzeta M, Inokuchi T, Butini S, Marco-Contelles J. Wu MY, et al. Among authors: inokuchi t. Eur J Med Chem. 2016 Oct 4;121:864-879. doi: 10.1016/j.ejmech.2015.10.001. Epub 2015 Oct 9. Eur J Med Chem. 2016. PMID: 26471320

4

Synthesis and In Vitro Antiproliferative Activity of 11-Substituted Neocryptolepines with a Branched ω-Aminoalkylamino Chain.

Shaban E, Świtalska M, Wang L, Wang N, Xiu F, Hayashi I, Ngoc TA, Nagae S, El-Ghlban S, Shimoda S, Gokha AAAE, Sayed IETE, Wietrzyk J, Inokuchi T. Shaban E, et al. Among authors: inokuchi t. Molecules. 2017 Nov 12;22(11):1954. doi: 10.3390/molecules22111954. Molecules. 2017. PMID: 29137152 Free PMC article.

5

Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted chromeno[2,3-b]indoles.

Peng W, Świtalska M, Wang L, Mei ZW, Edazawa Y, Pang CQ, El-Tantawy El-Sayed I, Wietrzyk J, Inokuchi T. Peng W, et al. Among authors: inokuchi t. Eur J Med Chem. 2012 Dec;58:441-51. doi: 10.1016/j.ejmech.2012.10.023. Epub 2012 Oct 24. Eur J Med Chem. 2012. PMID: 23151321

6

Synthesis and in vitro cytotoxic effect of 6-amino-substituted 11H- and 11Me-indolo[3,2-c]quinolines.

Wang N, Świtalska M, Wu MY, Imai K, Ngoc TA, Pang CQ, Wang L, Wietrzyk J, Inokuchi T. Wang N, et al. Among authors: inokuchi t. Eur J Med Chem. 2014 May 6;78:314-23. doi: 10.1016/j.ejmech.2014.03.038. Epub 2014 Mar 19. Eur J Med Chem. 2014. PMID: 24686018

7

Design, synthesis, and biological evaluation of artemisinin-indoloquinoline hybrids as potent antiproliferative agents.

Wang L, Świtalska M, Wang N, Du ZJ, Fukumoto Y, Diep NK, Kiguchi R, Nokami J, Wietrzyk J, Inokuchi T. Wang L, et al. Among authors: inokuchi t. Molecules. 2014 Nov 18;19(11):19021-35. doi: 10.3390/molecules191119021. Molecules. 2014. PMID: 25412047 Free PMC article.

8

Solvent-free microwave-assisted multi-component reaction for preparation of 2-amino-1-aryl-2-(cyclohex-1-enyl)ethanones as precursors of pseudoephedrine analogues.

Ma LJ, Inokuchi T. Ma LJ, et al. Among authors: inokuchi t. Chem Commun (Camb). 2010 Oct 7;46(37):7037-9. doi: 10.1039/c0cc00859a. Epub 2010 Aug 25. Chem Commun (Camb). 2010. PMID: 20737087

9

Synthesis and in vitro antimalarial testing of neocryptolepines: SAR study for improved activity by introduction and modifications of side chains at C2 and C11 on indolo[2,3-b]quinolines.

Mei ZW, Wang L, Lu WJ, Pang CQ, Maeda T, Peng W, Kaiser M, El Sayed I, Inokuchi T. Mei ZW, et al. Among authors: inokuchi t. J Med Chem. 2013 Feb 28;56(4):1431-42. doi: 10.1021/jm300887b. Epub 2013 Feb 15. J Med Chem. 2013. PMID: 23360309

10

Synthesis and antimalarial testing of neocryptolepine analogues: addition of ester function in SAR study of 2,11-disubstituted indolo[2,3-b]quinolines.

Lu WJ, Wicht KJ, Wang L, Imai K, Mei ZW, Kaiser M, El Sayed Iel T, Egan TJ, Inokuchi T. Lu WJ, et al. Among authors: inokuchi t. Eur J Med Chem. 2013 Jun;64:498-511. doi: 10.1016/j.ejmech.2013.03.072. Epub 2013 Apr 15. Eur J Med Chem. 2013. PMID: 23685569

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