Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Upasana Issar"'
Autor:
Richa Arora, Upasana Issar
Publikováno v:
Environmental Applications of Carbon Nanomaterials-Based Devices
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f6131fe6c797495df7523697c691b37
https://doi.org/10.1002/9783527830978.ch17
https://doi.org/10.1002/9783527830978.ch17
Autor:
Richa Arora, Upasana Issar
Publikováno v:
Chitosan-Based Nanocomposite Materials ISBN: 9789811953378
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76150bb9b5874313fbcc683855389c80
https://doi.org/10.1007/978-981-19-5338-5_11
https://doi.org/10.1007/978-981-19-5338-5_11
Autor:
Upasana Issar, Richa Arora
Publikováno v:
Metal-Organic Frameworks (MOFs) as Catalysts ISBN: 9789811679582
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eb46bdc2639cba8e4236064f76be4b7
https://doi.org/10.1007/978-981-16-7959-9_9
https://doi.org/10.1007/978-981-16-7959-9_9
Autor:
Richa Arora, Upasana Issar
Publikováno v:
Metal-Organic Frameworks (MOFs) as Catalysts ISBN: 9789811679582
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::105be77c68c7b576ef10bd66db3f8ea2
https://doi.org/10.1007/978-981-16-7959-9_17
https://doi.org/10.1007/978-981-16-7959-9_17
Publikováno v:
Structural Chemistry. 30:1185-1201
Certain DNA minor groove binders, especially bis-benzimdazole containing compounds, such as Hoechst 33258 and its derivatives, act as potent topoisomerase I inhibitors. The mechanism of action of these drugs is complex and involves hindering the brea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae78657779e2a7035215039523bb6719
https://doi.org/10.1007/s11224-018-1257-3
https://doi.org/10.1007/s11224-018-1257-3
Publikováno v:
Computational and Theoretical Chemistry. 1138:57-65
The complexing abilities of para-substituted benzohydroxamates to the tin metal center of organotin(IV) ions have been investigated using DFT, since organotin(IV) compounds have been touted as promising anti-cancer agents. We have studied the coordin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04b750c563a531383473ab2174059dc8
https://doi.org/10.1016/j.comptc.2018.06.005
https://doi.org/10.1016/j.comptc.2018.06.005
Publikováno v:
Journal of Molecular Graphics and Modelling. 83:64-73
Hydroxamic acids have emerged as the most promising candidates from among the different classes of inhibitors of urease. In order to understand the mechanism of their action, we have studied in detail using quantum mechanics the active site of Helico
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66f9778aee432828367dff4ae360c3c5
https://doi.org/10.1016/j.jmgm.2018.04.018
https://doi.org/10.1016/j.jmgm.2018.04.018
Publikováno v:
Computational and Theoretical Chemistry. 1113:32-41
Drugs which are capable of targeting sequence specific DNA constitute a novel approach to chemotherapy and have been exploited in detail in recent years. In this context, the synthetic minor groove binder Hoechst 33258 has been in focus due to its ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ded24df27b218b1b5d360fa68a7a183f
https://doi.org/10.1016/j.comptc.2017.05.006
https://doi.org/10.1016/j.comptc.2017.05.006
Publikováno v:
Computational and Theoretical Chemistry. 1105:18-26
Benzohydroxamic acid (BHA), an important member of the hydroxamic acid family (R-CO-NH-OH), has been investigated in detail in the gas and aqueous phase using density functional methods. Like the other members, it displays amide/imide tautomerism. Ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::998ef730cbaf20f203ac62f4aa813455
https://doi.org/10.1016/j.comptc.2017.02.014
https://doi.org/10.1016/j.comptc.2017.02.014
Pharmacophore modeling and atom-based three-dimensional quantitative structure–activity relationship (3D-QSAR) have been developed on N-acylglycino- and hippurohydroxamic acid derivatives, which are known potential inhibitors of urease. This is fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::268222c1f4f3239bcd998bae8be9b16e