dc.contributor.author |
Lu GL |
|
dc.contributor.author |
Tong AST |
|
dc.contributor.author |
Conole D |
|
dc.contributor.author |
Sutherland HS |
|
dc.contributor.author |
Choi PJ |
|
dc.contributor.author |
Franzblau SG |
|
dc.contributor.author |
Upton AM |
|
dc.contributor.author |
Lotlikar MU |
|
dc.contributor.author |
Cooper CB |
|
dc.contributor.author |
Denny WA |
|
dc.contributor.author |
Palmer BD |
|
dc.date.accessioned |
2020-11-12T22:26:40Z |
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dc.date.available |
2020-11-12T22:26:40Z |
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dc.date.issued |
2020-11-15 |
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dc.identifier.citation |
Bioorganic & medicinal chemistry 28(22):115784 24 Sep 2020 |
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dc.identifier.issn |
0968-0896 |
|
dc.identifier.uri |
http://hdl.handle.net/2292/53616 |
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dc.description.abstract |
© 2020 The Authors A series of 5,8-disubstituted tetrahydroisoquinolines were shown to be effective inhibitors of M. tb in culture and modest inhibitors of M. tb ATP synthase. There was a broad general trend of improved potency with higher lipophilicity. Large substituents (e.g., Bn) at the tetrahydroquinoline 5-position were well-tolerated, while N-methylpiperazine was the preferred 8-substituent. Structure-activity relationships for 7-linked side chains showed that the nature of the 7-linking group was important; –CO– and –COCH2– linkers were less effective than –CH2– or –CONH– ones. This suggests that the positioning of a terminal aromatic ring is important for target binding. Selected compounds showed much faster rates of microsomal clearance than did the clinical ATP synthase inhibitor bedaquiline, and modest inhibition of mycobacterial ATP synthase. |
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dc.relation.ispartofseries |
Bioorganic and Medicinal Chemistry |
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dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. |
|
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
|
dc.rights.uri |
https://creativecommons.org/licenses/by/4.0/ |
|
dc.subject |
0304 Medicinal And Biomolecular Chemistry |
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dc.subject |
1115 Pharmacology And Pharmaceutical Sciences |
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dc.subject |
0305 Organic Chemistry |
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dc.title |
Synthesis and structure-activity relationships for tetrahydroisoquinoline-based inhibitors of Mycobacterium tuberculosis |
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dc.type |
Journal Article |
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dc.identifier.doi |
10.1016/j.bmc.2020.115784 |
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pubs.issue |
22 |
|
pubs.volume |
28 |
|
dc.date.updated |
2020-10-08T23:12:20Z |
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dc.rights.holder |
Copyright: The authors |
en |
pubs.publication-status |
Accepted |
|
dc.rights.accessrights |
http://purl.org/eprint/accessRights/OpenAccess |
en |
pubs.subtype |
Journal Article |
|
pubs.elements-id |
817665 |
|
dc.identifier.eissn |
1464-3391 |
|