Design, Synthesis and Molecular Modeling Study of Some Thiazolidinone Derivatives as NS5B Polymerase inhibitors / (Titelsatznr. 59351)

[ MARC ]
000 -LEADER
fixed length control field 02116nam a22002417a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 180912s2018 ua a|||g bm|| 00| 0 eng d
040 ## - CATALOGING SOURCE
Transcribing agency SOUL
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Edition number 21
Classification number 615.1
Item number R D
100 1# - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 4566
Personal name Ragab, Esraa Zakaria Mohammed
245 10 - TITLE STATEMENT
Title Design, Synthesis and Molecular Modeling Study of Some Thiazolidinone Derivatives as NS5B Polymerase inhibitors /
Statement of responsibility, etc. Esraa Zakaria Mohammed Ragab ; Supervised by Farghaly Abd-El Hamed Omar, Ghaneya Sayed Hassan, Hanan Hanna Georgey.
246 01 - VARYING FORM OF TITLE
Title proper/short title تصميم وتشييد ودراسة النمذجة الجزيئية لبعض مشتقات الثيازوليدينون كمثبطات لإنزيم البوليمريز
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Cairo University,
Date of publication, distribution, etc. 2018.
300 ## - PHYSICAL DESCRIPTION
Extent 182p. :
Other physical details ill. ;
Dimensions 26 cm.
Accompanying material +CD.
500 ## - GENERAL NOTE
General note Thesis (M.Sc.) – Cairo University. Faculty of Pharmacy. Department of Pharmaceutical Chemistry.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references.
520 ## - SUMMARY, ETC.
Summary, etc. ) Hepatitis C virus (HCV) infection is a major global health challenge; it is estimated that more than 80 million people are chronically infected worldwide, 3–4 million new infections and 350 000 deaths occurring each year because of HCV-related complications.
This thesis deals with the design and synthesis of some thiazolidinone derivatives to be evaluated as HCV-NS5B polymerase allosteric inhibitors. In addition, the anti-HCV activity was carried out for the new derivatives using a highly permissive subclone of the human hepatoma cell line Huh-7.5. Molecular docking studies were carried out to predict the possible binding mode of the newly synthesized compounds with HCV-NS5B polymerase to study their interaction with the enzyme key amino acids in a trial to explain their observed activity. Furthermore, key molecular characteristics were calculated to assess their drug-likeness potentia
546 ## - LANGUAGE NOTE
Language note Text in English, abstracts in English and Arabic.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 3833
Topical term or geographic name as entry element Chemistry, Pharmaceutical
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 4568
Personal name Georgey, Hanan Hanna
Relator term Supervisor
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 4569
Personal name Hassan, Ghaneya Sayed
Relator term Supervisor
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Theses
Item part Faculty of Pharmacy كلية الصيدلة
Exemplare
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Collection code Permanent location Current location Shelving location Date acquired Full call number Barcode Date last seen Copy number Price effective from Koha item type
          Default 6october 6october 1208 2018-12-17 615.1 R D SOULE208TH0800 2021-08-25 1 2018-12-17 Theses
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