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
2024	0

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

Flame retardance-donated lignocellulose nanofibers (LCNFs) by the Mannich reaction with (amino-1,3,5-triazinyl)phosphoramidates and their properties.

Ono F, Okihara T, Osaka N, Nagaoka N, Kameoka Y, Ishikawa A, Ooki H, Ito T, Todome D, Uemoto S, Furutani M, Inokuchi T, Okada K. Ono F, et al. Among authors: inokuchi t. RSC Adv. 2022 Jan 26;12(6):3300-3308. doi: 10.1039/d1ra08716a. eCollection 2022 Jan 24. RSC Adv. 2022. PMID: 35425348 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

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.

5

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

6

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.

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

Synthesis and in vitro testing of antimalarial activity of non-natural-type neocryptolepines: structure–activity relationship study of 2,11- and 9,11-disubstituted 6-methylindolo[2,3-b]quinolines.

Wang N, Wicht KJ, Wang L, Lu WJ, Misumi R, Wang MQ, El Gokha AA, Kaiser M, El Sayed Iel T, Egan TJ, Inokuchi T. Wang N, et al. Among authors: inokuchi t. Chem Pharm Bull (Tokyo). 2013;61(12):1282-90. doi: 10.1248/cpb.c13-00639. Chem Pharm Bull (Tokyo). 2013. PMID: 24436959

9

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

10

Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted 5H- and 6H-indolo[2,3-b]quinolines; structure-activity relationships of neocryptolepines and 6-methyl congeners.

Wang L, Switalska M, Mei ZW, Lu WJ, Takahara Y, Feng XW, El-Sayed Iel-T, Wietrzyk J, Inokuchi T. Wang L, et al. Among authors: inokuchi t. Bioorg Med Chem. 2012 Aug 1;20(15):4820-9. doi: 10.1016/j.bmc.2012.05.054. Epub 2012 Jun 12. Bioorg Med Chem. 2012. PMID: 22748378

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