FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2808263278> ?p ?o ?g. }

• W2808263278 endingPage "1438" @default.
• W2808263278 startingPage "1438" @default.
• W2808263278 abstract "first_page settings Order Article Reprints Font Type: Arial Georgia Verdana Font Size: Aa Aa Aa Line Spacing:    Column Width:    Background: Open AccessCorrection Correction: Sun, Y.; et al. Design, Synthesis, and Evaluation of Novel 2-Hydroxypyrrolobenzodiazepine-5,11-dione Analogues as Potent Angiotensin Converting Enzyme (ACE) Inhibitors. Molecules 2017, 22, 1739 by Ying Sun 1,†, Yujun Bai 1,†, Xirui He 1, Yajun Bai 1,2, Pei Liu 1, Zefeng Zhao 1, Xufei Chen 1 and Xiaohui Zheng 1,* 1 Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University, Xi’an 710069, China 2 Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry 0026 Materials Science, Northwest University, Xi’an 710127, China * Author to whom correspondence should be addressed. † These authors contributed equally to this paper. Molecules 2018, 23(6), 1438; https://doi.org/10.3390/molecules23061438 Received: 29 May 2018 / Revised: 30 May 2018 / Accepted: 31 May 2018 / Published: 13 June 2018 Download Download PDF Download PDF with Cover Download XML Download Epub Versions Notes The author wishes to make the following corrections to this paper [1]. Due to our oversight, the title of article [1] was same as that of article [2]. Because our research ideas and methods were different from those of article [2], we did not list it as a reference study in the article [1]. We would like to offer our sincere apologies to all of the authors of the article [2], who were Addla Dinesh, Jallapally Anvesh, Kanwal Abhinav, Sridhar Balasubramanian, Banerjee Sanjay K., and Kantevari Srinivas.The corrections include: (1) replacing the title “Design, Synthesis, and Evaluation of Novel 2-Hydroxypyrrolobenzodiazepine-5,11-dione Analogues as Potent Angiotensin Converting Enzyme (ACE) Inhibitors” with “Design, Synthesis, and Evaluation of Novel Phenolic acid/Dipeptide/Borneol Hybrids as Potent Angiotensin Converting Enzyme (ACE) Inhibitors with Anti-hypertension Activity”; and (2) replacing “2-hydroxypyrrolobenzodiazepine-5,11-dione analogues” with “phenolic acid/dipeptide/borneol hybrids” in the abstract.The authors would like to apologize for any inconvenience caused to the readers by these changes. Conflicts of InterestThe authors declare no conflict of interest.ReferencesSun, Y.; Bai, Y.; He, X.; Bai, Y.; Liu, P.; Zhao, Z.; Chen, X.; Zheng, X. Design, Synthesis and Evaluation of Novel 2-Hydroxypyrrolobenzodiazepine-5,11-dione Analogues as Potent Angiotensin Converting Enzyme (ACE) Inhibitors. Molecules 2017, 22, 1739. [Google Scholar] [CrossRef] [PubMed]Addla, D.; Jallapally, A.; Kanwal, A.; Sridhar, B.; Banerjee, S.K.; Kantevari, S. Design, synthesis and evaluation of novel 2-hydroxypyrrolobenzodiazepine-5,11-dione analogues as potent angiotensin converting enzyme (ACE) inhibitors. Bioorg. Med. Chem. 2013, 21, 4485–4493. [Google Scholar] [CrossRef] [PubMed] © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Share and Cite MDPI and ACS Style Sun, Y.; Bai, Y.; He, X.; Bai, Y.; Liu, P.; Zhao, Z.; Chen, X.; Zheng, X. Correction: Sun, Y.; et al. Design, Synthesis, and Evaluation of Novel 2-Hydroxypyrrolobenzodiazepine-5,11-dione Analogues as Potent Angiotensin Converting Enzyme (ACE) Inhibitors. Molecules 2017, 22, 1739. Molecules 2018, 23, 1438. https://doi.org/10.3390/molecules23061438 AMA Style Sun Y, Bai Y, He X, Bai Y, Liu P, Zhao Z, Chen X, Zheng X. Correction: Sun, Y.; et al. Design, Synthesis, and Evaluation of Novel 2-Hydroxypyrrolobenzodiazepine-5,11-dione Analogues as Potent Angiotensin Converting Enzyme (ACE) Inhibitors. Molecules 2017, 22, 1739. Molecules. 2018; 23(6):1438. https://doi.org/10.3390/molecules23061438 Chicago/Turabian Style Sun, Ying, Yujun Bai, Xirui He, Yajun Bai, Pei Liu, Zefeng Zhao, Xufei Chen, and Xiaohui Zheng. 2018. Correction: Sun, Y.; et al. Design, Synthesis, and Evaluation of Novel 2-Hydroxypyrrolobenzodiazepine-5,11-dione Analogues as Potent Angiotensin Converting Enzyme (ACE) Inhibitors. Molecules 2017, 22, 1739 Molecules 23, no. 6: 1438. https://doi.org/10.3390/molecules23061438 Find Other Styles Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here. Article Metrics No No Article Access Statistics For more information on the journal statistics, click here. Multiple requests from the same IP address are counted as one view." @default.
• W2808263278 created "2018-06-21" @default.
• W2808263278 creator A5008279507 @default.
• W2808263278 creator A5011289163 @default.
• W2808263278 creator A5011751665 @default.
• W2808263278 creator A5013847274 @default.
• W2808263278 creator A5058135877 @default.
• W2808263278 creator A5059210458 @default.
• W2808263278 creator A5059756548 @default.
• W2808263278 creator A5090246613 @default.
• W2808263278 date "2018-06-13" @default.
• W2808263278 modified "2023-10-16" @default.
• W2808263278 title "Correction: Sun, Y.; et al. Design, Synthesis, and Evaluation of Novel 2-Hydroxypyrrolobenzodiazepine-5,11-dione Analogues as Potent Angiotensin Converting Enzyme (ACE) Inhibitors. Molecules 2017, 22, 1739" @default.
• W2808263278 cites W1985864815 @default.
• W2808263278 cites W2765591637 @default.
• W2808263278 doi "https://doi.org/10.3390/molecules23061438" @default.
• W2808263278 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6099559" @default.
• W2808263278 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29899290" @default.
• W2808263278 hasPublicationYear "2018" @default.
• W2808263278 type Work @default.
• W2808263278 sameAs 2808263278 @default.
• W2808263278 citedByCount "0" @default.
• W2808263278 crossrefType "journal-article" @default.
• W2808263278 hasAuthorship W2808263278A5008279507 @default.
• W2808263278 hasAuthorship W2808263278A5011289163 @default.
• W2808263278 hasAuthorship W2808263278A5011751665 @default.
• W2808263278 hasAuthorship W2808263278A5013847274 @default.
• W2808263278 hasAuthorship W2808263278A5058135877 @default.
• W2808263278 hasAuthorship W2808263278A5059210458 @default.
• W2808263278 hasAuthorship W2808263278A5059756548 @default.
• W2808263278 hasAuthorship W2808263278A5090246613 @default.
• W2808263278 hasBestOaLocation W28082632781 @default.
• W2808263278 hasConcept C136764020 @default.
• W2808263278 hasConcept C138885662 @default.
• W2808263278 hasConcept C161191863 @default.
• W2808263278 hasConcept C17744445 @default.
• W2808263278 hasConcept C185592680 @default.
• W2808263278 hasConcept C191935318 @default.
• W2808263278 hasConcept C199539241 @default.
• W2808263278 hasConcept C23123220 @default.
• W2808263278 hasConcept C27206212 @default.
• W2808263278 hasConcept C2780154274 @default.
• W2808263278 hasConcept C41008148 @default.
• W2808263278 hasConcept C521751864 @default.
• W2808263278 hasConcept C71240020 @default.
• W2808263278 hasConcept C8797682 @default.
• W2808263278 hasConceptScore W2808263278C136764020 @default.
• W2808263278 hasConceptScore W2808263278C138885662 @default.
• W2808263278 hasConceptScore W2808263278C161191863 @default.
• W2808263278 hasConceptScore W2808263278C17744445 @default.
• W2808263278 hasConceptScore W2808263278C185592680 @default.
• W2808263278 hasConceptScore W2808263278C191935318 @default.
• W2808263278 hasConceptScore W2808263278C199539241 @default.
• W2808263278 hasConceptScore W2808263278C23123220 @default.
• W2808263278 hasConceptScore W2808263278C27206212 @default.
• W2808263278 hasConceptScore W2808263278C2780154274 @default.
• W2808263278 hasConceptScore W2808263278C41008148 @default.
• W2808263278 hasConceptScore W2808263278C521751864 @default.
• W2808263278 hasConceptScore W2808263278C71240020 @default.
• W2808263278 hasConceptScore W2808263278C8797682 @default.
• W2808263278 hasIssue "6" @default.
• W2808263278 hasLocation W28082632781 @default.
• W2808263278 hasLocation W28082632782 @default.
• W2808263278 hasLocation W28082632783 @default.
• W2808263278 hasLocation W28082632784 @default.
• W2808263278 hasOpenAccess W2808263278 @default.
• W2808263278 hasPrimaryLocation W28082632781 @default.
• W2808263278 hasRelatedWork W1788528807 @default.
• W2808263278 hasRelatedWork W188567224 @default.
• W2808263278 hasRelatedWork W2100879664 @default.
• W2808263278 hasRelatedWork W2101966962 @default.
• W2808263278 hasRelatedWork W2115485936 @default.
• W2808263278 hasRelatedWork W2153015554 @default.
• W2808263278 hasRelatedWork W2164837174 @default.
• W2808263278 hasRelatedWork W2335663899 @default.
• W2808263278 hasRelatedWork W2361533086 @default.
• W2808263278 hasRelatedWork W2748952813 @default.
• W2808263278 hasVolume "23" @default.
• W2808263278 isParatext "false" @default.
• W2808263278 isRetracted "false" @default.
• W2808263278 magId "2808263278" @default.
• W2808263278 workType "article" @default.