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Design, synthesis and biological activity of semisynthetic phenolic acid analogues // GP //Dr. Amal Ali // T.A. Sara El. Sayed (2018 - 2019) (Record no. 24942)

MARC details
000 -LEADER
fixed length control field 02214nam a22002537a 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20190908095547.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 190721b ||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Transcribing agency MSA
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 547
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Mena Samy Moris 150205
245 ## - TITLE STATEMENT
Title Design, synthesis and biological activity of semisynthetic phenolic acid analogues // GP //Dr. Amal Ali // T.A. Sara El. Sayed (2018 - 2019)
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Giza:
Name of publisher, distributor, etc. MSA,
Date of publication, distribution, etc. 2019
300 ## - PHYSICAL DESCRIPTION
Extent 55 P.
440 ## - SERIES STATEMENT/ADDED ENTRY--TITLE
Title PharmaciesDISTINGUISHED PROJECTS 2019
500 ## - GENERAL NOTE
General note Pharmacy - Organic Chemistry
520 ## - SUMMARY, ETC.
Summary, etc. Ferulic acid (4- hydroxy-3-methoxycinnamic acid) is derived from natural source,<br/>consequently it has low Toxicity. It is one of the most abundant phenolic acids in plants.<br/>Ferulic acid has shown anticancer activity in various types of cancers. Large amounts of<br/>hydrogen peroxide are produced and secreted by tumour cells, which are responsible for<br/>spreading and invasion of the tumour. Anti-cancer activity of Ferulic Acid is related to its<br/>antioxidant property by inhibition of oxidative enzyme, enhancement of cytoprotective<br/>enzymes and acting as free radical scavenger. Ferulic acid structure has phenolic ring which<br/>act as free radical scavenger by its hydrogen donating ability. The presence of p-hydroxyl<br/>groups in aromatic ring, meta methoxy group and conjugated double bond are essential for<br/>activity. The aim of the project is to design and synthetize ferulic acid derivatives with<br/>potential anticancer activity. The amide derivatives of ferulic acid were synthetized by the<br/>reaction between ferulic acid and the different amines using DCC and THF. Purification of<br/>the compounds was done using column chromatography which is conducted by the<br/>pharmacognosy department and characterization was done using IR spectroscopy and proton<br/>NMR. Compounds were screened for anticancer activity against caco cell lines where they<br/>showed a significant anticancer activity
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element semisynthetic phenolic
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Bassant Khaled Ragheb 151623
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Eman Mohamed Abdel Hady 154547
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Mohamed Ismail Saeid 151275
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://qrgo.page.link/wBiUJ">https://qrgo.page.link/wBiUJ</a>
Public note FULL TEXT PRESS HERE
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Distinguished Graduation Projects
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Shelving location Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
    Dewey Decimal Classification     Centeral Library Centeral Library Soft Copy located on library Cataloge 21.07.2019   GP32PH2019 - OCHEM 82023 21.07.2019 21.07.2019 Distinguished Graduation Projects