MARC details
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04810ntm a2200373 i 4500 |
| 003 - CONTROL NUMBER IDENTIFIER |
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MY-KuUP |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
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20251125110726.0 |
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t||||fr|||| 000 0 |
| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION |
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ta |
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230410t20222022my a|||fr|||| 000 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
THE0009443 (Local) |
| Qualifying information |
Hardback |
| 040 ## - CATALOGING SOURCE |
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| Original cataloging agency |
UMP |
| Language of cataloging |
eng |
| Transcribing agency |
UMP |
| Description conventions |
rda |
| 090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN) |
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| Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) |
FSTI .M53 2022 r Thesis |
| 100 1# - MAIN ENTRY--PERSONAL NAME |
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| Personal name |
Miah Roney, |
| Relator term |
author. |
| 245 10 - TITLE STATEMENT |
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| Title |
Identification of usnic acid derivatives as new antiviral agents via virtual screening on dengue, influenza A and avian influenza A / |
| Statement of responsibility, etc. |
Miah Roney |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
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| Place of production, publication, distribution, manufacture |
Pahang : |
| Name of producer, publisher, distributor, manufacturer |
UMP, |
| Date of production, publication, distribution, manufacture, or copyright notice |
2022 |
| 264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
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| Date of production, publication, distribution, manufacture, or copyright notice |
© 2022 |
| 300 ## - PHYSICAL DESCRIPTION |
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| Extent |
318 pages : |
| Other physical details |
Illustration ; |
| Dimensions |
30 cm. + |
| Accompanying material |
1 CD-ROM |
| 336 ## - CONTENT TYPE |
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| Source |
rdacontent |
| Content type term |
text |
| 336 ## - CONTENT TYPE |
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| Source |
rdacontent |
| Content type term |
text |
| 337 ## - MEDIA TYPE |
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| Source |
rdamedia |
| Media type term |
unmediated |
| 337 ## - MEDIA TYPE |
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| Source |
rdamedia |
| Media type term |
computer |
| 338 ## - CARRIER TYPE |
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| Source |
rdacarrier |
| Carrier type term |
volume |
| 338 ## - CARRIER TYPE |
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| Source |
rdacarrier |
| Carrier type term |
computer disc |
| 347 ## - DIGITAL FILE CHARACTERISTICS |
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| Source |
rda |
| File type |
text file |
| Encoding format |
PDF |
| 500 ## - GENERAL NOTE |
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| General note |
Faculty of Industrial Sciences and Technology |
| 502 ## - DISSERTATION NOTE |
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| Dissertation note |
Thesis (Master of Science) -- Universiti Malaysia Pahang – 2022 |
| 504 ## - BIBLIOGRAPHY, ETC. NOTE |
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| Bibliography, etc. note |
Includes bibliographical references |
| 520 3# - SUMMARY, ETC. |
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| Summary, etc. |
Emerging viral infections continue to pose a significant threat to global public health in recent years. Viral diseases such as Dengue, Influenza (H1N1), and Avian Influenza have caused a significant challenge to the healthcare systems, economic growth, and development. Still now, there are no drugs available to combat the DENV and Avian Influenza A viruses. On the other hand, only two drugs have been developed against Influenza A virus based on the neuraminidase enzyme but need to annual updating because these drugs ineffective against the new subtype of Influenza A. Even though new antiviral drugs have been developed and approved annually, the cost and environmental issues remain the main challenges for scientists. The new innovative approaches involving computational technology need to be employed in drug development and discovery. Thus, the studies aimed to discover new potential antiviral lead compounds from usnic acid derivatives in-house database through virtual screening via various in silico approaches such as pharmacophore filtering, molecular docking screening, and pharmacokinetic prediction. There were three main parts covered; Part 1: Discovery of anti-DENV’s lead compound, Part 2: Discovery of anti-Influenza A’s lead compound and Part 3: Discovery of anti-avian Influenza A’s lead compound. Four hundred twenty-eight usnic acid derivatives as in-house database was generated by retrieved from the various literature sources. The use of usnic acid derivatives is due to their incredible antiviral activities. According to current research, usnic acid has strong larvicidal properties toward Aedes aegypti. The combination of ligand-based and structure-based virtual screening model was built leading by pharmacophore filtering, molecular docking screening followed by pharmacokinetic predictions including drug-likeness and CYP2D6 filtering to afford the lead compounds for each target (dengue, Influenza A and avian Influenza A). The in-house usnic acid derivatives database was screened using the selected pharmacophore models to afford one hundred sixteen compounds for novel DENV-3 NS5 protease, twenty-three compounds for Influenza A, and twenty-one compounds for Avian Influenza A inhibitors. In the next virtual screening stage, molecular docking and interaction analysis indicated that forty-one DENV compounds, four Influenza compounds, and five Avian Influenza compounds could plausibly be active against the targets. Further filtering by ADME prediction tools and drug-likeness prediction of forty-one, four and five compounds from DENV, Influenza and Avian Influenza, respectively, resulted in seven hit compounds for DENV, two hit compounds for Influenza and two compounds for Avian Influenza virus, respectively. The lead molecule, called compound-362, compound-4, and compound-5, was discovered after screening the hit compounds against DENV, Influenza, and Avian Influenza utilising the cytochrome P450 enzyme. To corroborate the durability of docked complexes and the binding conformation established during docking testing, a molecular dynamic (MD) simulation of lead compounds 362, 4 and 5 was performed. Ultimately, the lead compounds 362, 4 and 5 discovered for DENV, Influenza A and Avian Influenza A, respectively, exhibited a high pharmacophore fit value, string binding affinity, excellent pharmacokinetics, and drug-like characteristics in general. Thus, it proved that the virtual screening model employed in this study was reliable. |
| 610 20 - SUBJECT ADDED ENTRY--CORPORATE NAME |
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| Corporate name or jurisdiction name as entry element |
Faculty of Industrial Sciences and Technology |
| General subdivision |
Dissertations |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Universities and colleges |
| General subdivision |
Dissertations |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Thesis |
| General subdivision |
Dissertations |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) |
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| Source of classification or shelving scheme |
Library of Congress Classification |
| Koha item type |
Thesis |