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Cited by 163

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Cationic pillar[6]arene/ATP host–guest recognition: selectivity, inhibition of ATP hydrolysis, and application in multidrug resistance treatment

Open access
Yu, Guocan, Zhou, Jiong, Shen, Jie, Tang, Guping, Huang, Feihe·2016·Chemical Science
DOI 10.1039/c6sc00531d
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Abstract

The efficacy of DOX·HCl against drug resistant human breast cancer cells is enhanced in the presence of a water-soluble pillar[6]arene (WP6) due to the inhibition of ATP hydrolysis upon formation of WP6⊃ATP in cells, providing a novel strategy to overcome multidrug resistance.

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Metadata

Authors
Yu, G., Zhou, J., Shen, J., Tang, G., & Huang, F.
Venue
Chemical Science
Publisher
Royal Society of Chemistry (RSC)
Published
2016
Volume
7
Issue
7
Pages
4073-4078
ISSN
  • 2041-6520 (ISSN-L)
  • 2041-6539
DOI
10.1039/c6sc00531d
OpenAlex
W2288772177
Cited by
163
References
2
FWCI
11.14
Type
journal article
Language
en
Open access
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CoChat. (2026). Citation check: Cationic pillar[6]arene/ATP host–guest recognition: selectivity, inhibition of ATP hydrolysis, and application in multidrug resistance treatment. https://app.cochat.ai/papers/10.1039/c6sc00531d
The paper
Yu, G., Zhou, J., Shen, J., Tang, G., & Huang, F. (2016). Cationic pillar[6]arene/ATP host–guest recognition: selectivity, inhibition of ATP hydrolysis, and application in multidrug resistance treatment. Chemical Science. https://doi.org/10.1039/c6sc00531d

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.