Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011)

Yi Min Liu; Wei Chun HuangFu; Han Li Huang; Wei Cheng Wu; Yi Lin Chen; Yun Yen; Hsiang Ling Huang; Chih Ying Nien; Mei Jung Lai; Shiow Lin Pan; Jing Ping Liou

doi:10.1016/j.ejmech.2020.112633

Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011)

Yi Min Liu, Wei Chun HuangFu, Han Li Huang, Wei Cheng Wu, Yi Lin Chen, Yun Yen, Hsiang Ling Huang, Chih Ying Nien, Mei Jung Lai, Shiow Lin Pan, Jing Ping Liou

Research output: Contribution to journal › Comment/debate › peer-review

2 Citations (Scopus)

Abstract

The authors regret that the information of concentration unit of the Table 2 and 3 and the name of synthesized compound 10e in 4.1.1.5 was incorrect. The correct version should be: The concentration unit of the Table 2 and 3 is μM. The name of synthesized compound 10e is 4-(((3-Chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)amino)methyl)-N-(pyridin-4-yl)benzamide (10e) in 4.1.1.5. The authors would like to apologise for any inconvenience caused.

Original language	English
Article number	112633
Journal	European Journal of Medicinal Chemistry
Volume	202
DOIs	https://doi.org/10.1016/j.ejmech.2020.112633
Publication status	Published - Sept 15 2020

ASJC Scopus subject areas

Pharmacology
Drug Discovery
Organic Chemistry

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Liu, Y. M., HuangFu, W. C., Huang, H. L., Wu, W. C., Chen, Y. L., Yen, Y., Huang, H. L., Nien, C. Y., Lai, M. J., Pan, S. L., & Liou, J. P. (2020). Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011). European Journal of Medicinal Chemistry, 202, Article 112633. https://doi.org/10.1016/j.ejmech.2020.112633

Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011). / Liu, Yi Min ; HuangFu, Wei Chun; Huang, Han Li et al.
In: European Journal of Medicinal Chemistry, Vol. 202, 112633, 15.09.2020.

Research output: Contribution to journal › Comment/debate › peer-review

Liu, YM , HuangFu, WC, Huang, HL, Wu, WC, Chen, YL, Yen, Y, Huang, HL, Nien, CY, Lai, MJ , Pan, SL & Liou, JP 2020, 'Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011)', European Journal of Medicinal Chemistry, vol. 202, 112633. https://doi.org/10.1016/j.ejmech.2020.112633

Liu YM , HuangFu WC, Huang HL, Wu WC, Chen YL, Yen Y et al. Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011). European Journal of Medicinal Chemistry. 2020 Sept 15;202:112633. doi: 10.1016/j.ejmech.2020.112633

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title = "Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011)",

abstract = "The authors regret that the information of concentration unit of the Table 2 and 3 and the name of synthesized compound 10e in 4.1.1.5 was incorrect. The correct version should be: The concentration unit of the Table 2 and 3 is μM. The name of synthesized compound 10e is 4-(((3-Chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)amino)methyl)-N-(pyridin-4-yl)benzamide (10e) in 4.1.1.5. The authors would like to apologise for any inconvenience caused.",

author = "Liu, {Yi Min} and HuangFu, {Wei Chun} and Huang, {Han Li} and Wu, {Wei Cheng} and Chen, {Yi Lin} and Yun Yen and Huang, {Hsiang Ling} and Nien, {Chih Ying} and Lai, {Mei Jung} and Pan, {Shiow Lin} and Liou, {Jing Ping}",

note = "Publisher Copyright: {\textcopyright} 2020 Elsevier Masson SAS",

year = "2020",

month = sep,

day = "15",

doi = "10.1016/j.ejmech.2020.112633",

language = "English",

volume = "202",

journal = "European Journal of Medicinal Chemistry",

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TY - JOUR

T1 - Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011)

AU - Liu, Yi Min

AU - HuangFu, Wei Chun

AU - Huang, Han Li

AU - Wu, Wei Cheng

AU - Chen, Yi Lin

AU - Yen, Yun

AU - Huang, Hsiang Ling

AU - Nien, Chih Ying

AU - Lai, Mei Jung

AU - Pan, Shiow Lin

AU - Liou, Jing Ping

PY - 2020/9/15

Y1 - 2020/9/15

N2 - The authors regret that the information of concentration unit of the Table 2 and 3 and the name of synthesized compound 10e in 4.1.1.5 was incorrect. The correct version should be: The concentration unit of the Table 2 and 3 is μM. The name of synthesized compound 10e is 4-(((3-Chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)amino)methyl)-N-(pyridin-4-yl)benzamide (10e) in 4.1.1.5. The authors would like to apologise for any inconvenience caused.

AB - The authors regret that the information of concentration unit of the Table 2 and 3 and the name of synthesized compound 10e in 4.1.1.5 was incorrect. The correct version should be: The concentration unit of the Table 2 and 3 is μM. The name of synthesized compound 10e is 4-(((3-Chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)amino)methyl)-N-(pyridin-4-yl)benzamide (10e) in 4.1.1.5. The authors would like to apologise for any inconvenience caused.

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DO - 10.1016/j.ejmech.2020.112633

M3 - Comment/debate

C2 - 32688164

AN - SCOPUS:85088017535

SN - 0223-5234

VL - 202

JO - European Journal of Medicinal Chemistry

JF - European Journal of Medicinal Chemistry

M1 - 112633

ER -

Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011)

Abstract

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