“紫锥菊素衍生物酪氨酸- dna磷酸二酯酶1抑制剂的发现、结构修饰和构效关系研究及其潜在的抗肿瘤活性”的勘误表[欧洲]。医学化学。298 (2025)118040]

IF 5.9 2区医学 Q1 CHEMISTRY, MEDICINAL

European Journal of Medicinal Chemistry Pub Date : 2025-09-19 DOI:10.1016/j.ejmech.2025.118101

Chuan-Sheng Yao, Jiaqi Zhu, Xiang Gao, Ao Chen, Yue-Wen Li, Wen-Ya Liu, Li-Shuang Guo, Yong-Chun Wu, Cui-Xian Zhang, Xi-Xin He, Lin-Kun An

{"title":"“紫锥菊素衍生物酪氨酸- dna磷酸二酯酶1抑制剂的发现、结构修饰和构效关系研究及其潜在的抗肿瘤活性”的勘误表[欧洲]。医学化学。298 (2025)118040]","authors":"Chuan-Sheng Yao, Jiaqi Zhu, Xiang Gao, Ao Chen, Yue-Wen Li, Wen-Ya Liu, Li-Shuang Guo, Yong-Chun Wu, Cui-Xian Zhang, Xi-Xin He, Lin-Kun An","doi":"10.1016/j.ejmech.2025.118101","DOIUrl":null,"url":null,"abstract":"The authors regret that the publication shows that some compounds’ structures are incorrect because of text editing reason in Tables 1–3, including compounds 9–16 in Table 1, compounds 17–18, 29–33, 35–54, 56–59 in Table 2, and compounds 62–67 in Table 3. Corrected Tables 1–3 are shown below.","PeriodicalId":314,"journal":{"name":"European Journal of Medicinal Chemistry","volume":"120 1","pages":""},"PeriodicalIF":5.9000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Corrigendum to “Discovery, structural modification and structure-activity relationship study of Echinulin derivatives as tyrosyl-DNA phosphodiesterase 1 inhibitors and their potential antitumor activity” [Eur. J. Med. Chem. 298 (2025) 118040]\",\"authors\":\"Chuan-Sheng Yao, Jiaqi Zhu, Xiang Gao, Ao Chen, Yue-Wen Li, Wen-Ya Liu, Li-Shuang Guo, Yong-Chun Wu, Cui-Xian Zhang, Xi-Xin He, Lin-Kun An\",\"doi\":\"10.1016/j.ejmech.2025.118101\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The authors regret that the publication shows that some compounds’ structures are incorrect because of text editing reason in Tables 1–3, including compounds 9–16 in Table 1, compounds 17–18, 29–33, 35–54, 56–59 in Table 2, and compounds 62–67 in Table 3. Corrected Tables 1–3 are shown below.\",\"PeriodicalId\":314,\"journal\":{\"name\":\"European Journal of Medicinal Chemistry\",\"volume\":\"120 1\",\"pages\":\"\"},\"PeriodicalIF\":5.9000,\"publicationDate\":\"2025-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Medicinal Chemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ejmech.2025.118101\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ejmech.2025.118101","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}

引用次数: 0

摘要

在表1 - 3中，由于文字编辑的原因，部分化合物的结构出现了错误，包括表1中的化合物9-16，表2中的化合物17-18、29-33、35-54、56-59，表3中的化合物62-67。更正后的表1-3如下所示。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Corrigendum to “Discovery, structural modification and structure-activity relationship study of Echinulin derivatives as tyrosyl-DNA phosphodiesterase 1 inhibitors and their potential antitumor activity” [Eur. J. Med. Chem. 298 (2025) 118040]

The authors regret that the publication shows that some compounds’ structures are incorrect because of text editing reason in Tables 1–3, including compounds 9–16 in Table 1, compounds 17–18, 29–33, 35–54, 56–59 in Table 2, and compounds 62–67 in Table 3. Corrected Tables 1–3 are shown below.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

European Journal of Medicinal Chemistry 化学-医药化学

CiteScore

11.70

自引率

9.00%

发文量

863

审稿时长

29 days

期刊介绍： The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.