Inokuchi T - Search Results

1

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.

2

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.

3

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.

4

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

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

Design, synthesis, and in vitro cancer cell growth inhibition evaluation and antimalarial testing of trioxanes installed in cyclic 2-enoate substructures.

Hossain MI, Świtalska M, Peng W, Takashima M, Wang N, Kaiser M, Wietrzyk J, Dan S, Yamori T, Inokuchi T. Hossain MI, et al. Among authors: inokuchi t. Eur J Med Chem. 2013 Nov;69:294-309. doi: 10.1016/j.ejmech.2013.08.008. Epub 2013 Aug 13. Eur J Med Chem. 2013. PMID: 24056020

7

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

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

Reactivity of N-alkanoyloxy-2,2,6,6-tetramethylpiperidines (O-acylTEMPOs) towards hydride-transferring or metallic alkylating reagents; unprecedented stability and application to chemoselective transformations.

Inokuchi T, Kawafuchi H, Nokami J. Inokuchi T, et al. Chem Commun (Camb). 2005 Jan 28;(4):537-9. doi: 10.1039/b414129f. Epub 2004 Dec 6. Chem Commun (Camb). 2005. PMID: 15654395

10

Cyclopentanoids from cyclopentadiene: synthesis of (-)-methyl jasmonate and (+)-12-oxophytodienoic acid.

Nokami J, Fujii K, Mizutani Y, Omatsu R, Watanabe K, Yasuda H, Inokuchi T. Nokami J, et al. Among authors: inokuchi t. Nat Prod Commun. 2013 Jul;8(7):919-23. Nat Prod Commun. 2013. PMID: 23980424

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