Anti-inflammatory potential of ethanol extract of rungia pectinata : (Record no. 105224)

MARC details
000 -LEADER
fixed length control field 03691ntm a2200349 i 4500
003 - CONTROL NUMBER IDENTIFIER
control field MY-KuUP
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260715122719.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
fixed length control field t|||||r|||| 000 0
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field ta
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 260715t20252025my a|||fr|||| 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0010738 (Local)
Qualifying information Hardback
040 ## - CATALOGING SOURCE
Original cataloging agency UMPSA
Language of cataloging eng
Transcribing agency UMPSA
Description conventions rda
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) FTKKP .Z854 2025 r Bc.
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Muhammad Zulfadhli Bin Khairul Arifin, , ,
Relator term author.
245 10 - TITLE STATEMENT
Title Anti-inflammatory potential of ethanol extract of rungia pectinata :
Remainder of title in silico investigation /
Statement of responsibility, etc. Muhammad Zulfadhli Bin Khairul Arifin
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Kuantan, Pahang :
Name of producer, publisher, distributor, manufacturer UMPSA,
Date of production, publication, distribution, manufacture, or copyright notice 2025
264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice © 2025
300 ## - PHYSICAL DESCRIPTION
Extent ix, 49 pages :
Other physical details illustrations ;
336 ## - CONTENT TYPE
Source rdacontent
Content type term text
337 ## - MEDIA TYPE
Source rdamedia
Media type term unmediated
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term volume
347 ## - DIGITAL FILE CHARACTERISTICS
Source rda
File type text file
Encoding format PDF
500 ## - GENERAL NOTE
General note Faculty of Chemical and Process Engineering Technology
502 ## - DISSERTATION NOTE
Dissertation note Final Year Report (Bachelor of Manufacturing Engineering Technology (Pharmaceuticals) with Hons ) -- Universiti Malaysia Pahang Al-Sultan Abdullah - 2025
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Include bibliographical reference
520 3# - SUMMARY, ETC.
Summary, etc. Inflammation is a complex biological response that plays a crucial role in protecting the body against harm but can lead to chronic diseases if prolonged. Existing anti-inflammatory drugs often have limitations, such as side effects and long-term health risks, highlighting the need for new therapeutic agents. The Rungia pectinata plant, which is used in traditional medicine, has been studied and proven to have anti-inflammatory potential. This study aimed to identify bioactive compounds in the ethanol extract of Rungia pectinata, evaluate their interactions with target inflammatory proteins through silico methods, and predict their ADMET (Absorption, Distribution, Metabolism, Excretion, and Toxicity) properties. The methodology included Soxhlet extraction of Rungia pectinata using ethanol as a solvent, followed by compound identification through LC-QTOF-MS analysis. Computational techniques, including molecular docking using CB Dock and structural modeling with ChemDraw and ChemSketch, were employed to assess the binding affinity of the identified compounds to the selected target proteins. ADMET properties were predicted using SwissADME and ProTox-II tools to ensure the safety and efficacy of the bioactive molecules. A total of 47 compounds were identified in the extract. Among these, compounds; 2-octenal (C9), Juvabione (C19), and C13:2n-8,10 (C21), exhibited strong interactions with NF-κB proteins. Docking studies revealed that C19 formed multiple hydrogen bonds with protein 3DO7 and 1NFI, achieving the lowest binding energy, which indicates a robust interaction. ADMET predictions further supported the drug-likeness and safety of these compounds, suggesting favorable absorption and minimal toxicity. These findings elucidate the molecular mechanisms underlying the anti-inflammatory potential of Rungia pectinata and align with its traditional use as a natural remedy. The in-silico investigation confirms that the ethanol extract of Rungia pectinata contains bioactive compounds with significant anti-inflammatory potential. The combined molecular docking and ADMET analyses highlight compounds 2-octenal, Juvabione, and C13:2n-8,10 as promising candidates for further preclinical evaluation, supporting the development of novel, plant-based anti-inflammatory therapies.
610 20 - SUBJECT ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Faculty of Chemical and Process Engineering Technology
General subdivision Dissertations
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Universities and colleges
General subdivision Dissertations
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Theses
General subdivision Dissertations
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier https://umpir.ump.edu.my/id/eprint/47625
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type Final Year Report
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
  Not lost Library of Congress Classification     UMPLIB GAMBANG UMPLIB GAMBANG 15/07/2026   FTKKP .Z854 2025 r Bc. T000004332 15/07/2026 15/07/2026 Final Year Report

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