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

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.

2

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.

3

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.

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

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

6

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.

7

Donepezil + propargylamine + 8-hydroxyquinoline hybrids as new multifunctional metal-chelators, ChE and MAO inhibitors for the potential treatment of Alzheimer's disease.

Wang L, Esteban G, Ojima M, Bautista-Aguilera OM, Inokuchi T, Moraleda I, Iriepa I, Samadi A, Youdim MB, Romero A, Soriano E, Herrero R, Fernández Fernández AP, Ricardo-Martínez-Murillo, Marco-Contelles J, Unzeta M. Wang L, et al. Among authors: inokuchi t. Eur J Med Chem. 2014 Jun 10;80:543-61. doi: 10.1016/j.ejmech.2014.04.078. Epub 2014 Apr 29. Eur J Med Chem. 2014. PMID: 24813882

8

Synthesis, β-haematin inhibition, and in vitro antimalarial testing of isocryptolepine analogues: SAR study of indolo[3,2-c]quinolines with various substituents at C2, C6, and N11.

Wang N, Wicht KJ, Imai K, Wang MQ, Anh Ngoc T, Kiguchi R, Kaiser M, Egan TJ, Inokuchi T. Wang N, et al. Among authors: inokuchi t. Bioorg Med Chem. 2014 May 1;22(9):2629-42. doi: 10.1016/j.bmc.2014.03.030. Epub 2014 Mar 26. Bioorg Med Chem. 2014. PMID: 24721829

9

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

10

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

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