2,4-diamino-9H-pyrimido[4,5-b]indol-5-ols: Synthesis, in vitro cytotoxic activity, and QSAR investigations

Dotzauer B, Grunert R, Bednarski PJ, Lanig H, Landwehr J, Troschütz R (2006)


Publication Status: Published

Publication Type: Journal article, Original article

Publication year: 2006

Journal

Publisher: PERGAMON-ELSEVIER SCIENCE LTD

Book Volume: 14

Pages Range: 7282-7292

Journal Issue: 21

DOI: 10.1016/j.bmc.2006.06.051

Abstract

A series of novel 2,4-diaminopyrimido[4,5-b]indol-6-ols has been synthesized and the in vitro cytotoxic activities were evaluated against four human cancer cell lines originating from solid tumors. An increase in activity was observed when a heteroaromatic ring was annulated on side g of the pyrimido[4,5-b]indole system to give compounds with activities comparable to ellipticine and cisplatin. To understand the experimental cytotoxic activities, QSAR investigations were performed, which showed a very good linearity between the experimental and predicted IC50. (c) 2006 Elsevier Ltd. All rights reserved.

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How to cite

APA:

Dotzauer, B., Grunert, R., Bednarski, P.J., Lanig, H., Landwehr, J., & Troschütz, R. (2006). 2,4-diamino-9H-pyrimido[4,5-b]indol-5-ols: Synthesis, in vitro cytotoxic activity, and QSAR investigations. Bioorganic & Medicinal Chemistry, 14(21), 7282-7292. https://doi.org/10.1016/j.bmc.2006.06.051

MLA:

Dotzauer, Bernd, et al. "2,4-diamino-9H-pyrimido[4,5-b]indol-5-ols: Synthesis, in vitro cytotoxic activity, and QSAR investigations." Bioorganic & Medicinal Chemistry 14.21 (2006): 7282-7292.

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