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العنوان
Molecular Modeling and Synthesis of New 5, 7 Dihalo-8-Hydroxy Quinoline Derivatives Having Potential Antimicrobial Activity.\
الناشر
Ain Shams university.
المؤلف
Zain El Abedeen ,Noha Mohamed Mostafa.
هيئة الاعداد
مشرف / Dalal A. Abou El Ella
مشرف / Hoda Hanem Fahmy Said
مشرف / Mohamed Abdel Hamid Ismail,
باحث / Noha Mohamed Mostafa Zain El Abedeen
الموضوع
Antimicrobial Activity. Molecular Modeling. Quinoline Derivatives. New 5, 7 Dihalo.
تاريخ النشر
2011
عدد الصفحات
p.:126
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
العلوم الصيدلية
تاريخ الإجازة
1/1/2011
مكان الإجازة
جامعة عين شمس - كلية الطب - Pharmaceutical Chemistry
الفهرس
Only 14 pages are availabe for public view

from 160

from 160

Abstract

This thesis contains the following sections:
1-Introduction:
It contains a survey covering different antibacterial and antifungal drugs, quinoline biological uses, chemistry of quinolines and a brief introduction about the ligand base pharmacophore modeling.
2-Research Objectives:
It includes the design of 5,7 diiodo-8- hydroxyquinoline quinoline dervatives as antibacterial and antifungal agents.
3-Theoritical Discussion of experimental work :
It includes different methods of preparation that are reported in literature which were used for the preparation of the intermediate and final compounds.
4- Microbiological evaluation:
22 newely synthesized compounds were evaluated as antibacterial and antifungal agents against two bacterial and two fungal strains.

5-Molecular Modeling:
This part discusses the ligand base pharmacophore modeling to obtain a qualitative common feature hypothesis for antifungal agents and the fit values of the newly synthesized compounds.
6-Experimental:
It contains methods used in preparation of compounds and the different conditions of each reaction. The structures of these compounds were confirmed by microanalytical and spectral data.
This thesis comprises the synthesis of the following reported intermediates:
1- 1-(5,7-diiodoquinolin-8-yloxy)propan-2-one (IX).
2- Ethyl 2-(5,7-diiodoquinolin-8-yloxy)acetate (XV).
3- 2-(5,7-diiodoquinolin-8-yloxy)acetohydrazide (XVIII).
Furthermore, the study involves the synthesis of the following new targeted compounds:
1- Ethyl 2-(5,7-diiodoquinolin-8-yloxy) propanoate (IIa).
2- Ethyl 3-(5,7-diiodoquinolin-8-yloxy) propanoate (IIb).
3- 2-(5,7-diiodoquinolin-8-yloxy ) propanoic acid (IIIa).
4- 3-(5,7-diiodoquinolin-8-yloxy ) propanoic acid (IIIb).
5- 2-(5,7-diiodoquinolin-8-yloxy) propanehydrazide (IV).
6-2-(5,7-diiodoquinolin-8-yloxy)-1-(3,5-dimethyl-1H-pyrazol-1-yl)propan-1-one (V).
7- 1-(2-(5,7-diiodoquinolin-8-yloxy)propanoyl)-3-methyl-1H-pyrazol-5(4H)-one (VI).
8- 2-(5,7-diiodoquinolin-8-yloxy)-N-(1,3-dioxoisoindolin-2-yl)propanamide (VII).
9- 2-(5,7-diiodoquinolin-8-yloxy)-N-(2,5-dioxopyrrolidin-1-yl)propanamide (VIII).
10- 6-((5,7-diiodoquinolin-8-yloxy)methyl)-4-(4-fluorophenyl ) -1,2-dihydro-2-oxopyridine-3-carbonitrile (Xa).
11- 6-((5,7-diiodoquinolin-8-yloxy)methyl)-4-(4-methoxy pheny)-1,2-dihydro-2-oxopyridine-3-carbonitrile (Xb).
12- 6-((5,7-diiodoquinolin-8-yloxy)methyl)-1,2-dihydro-2-imino-4-(3,4,5-trimethoxyphenyl)pyridine-3-carbonitrile (XI).
13- 1-(5,7-diiodoquinolin-8-yloxy)-4-phenylbut-3-en-2-one (XIIa).
14- 1-(5,7-diiodoquinolin-8-yloxy)-4-(4-fluorophenyl)but-3-en-2-one (XIIb).
15-1-(5,7-diiodoquinolin-8-yloxy)-4-p-tolylbut-3-en-2-one (XIIc).
16- 8-((4,5-dihydro-5-phenyl-1H-pyrazol-3-yl)methoxy)-5,7-diiodoquinoline (XIV).
17- 8-((4,5-dihydro-1,5-diphenyl-1H-pyrazol-3-yl)methoxy)-5,7-diiodoquinoline (XIII).
18-1- (2- (5,7- diiodoquinolin -8- yloxy) acetyl) thiosemicarbazide
19-2-(5,7-diiodoquinolin-8-yloxy) -N- (2-hydroxyethyl )acetamide
20- 2- (5,7- diiodoquinolin -8- yloxy)-N,N-bis(2-hydroxyethyl)acetamide.
21- 2-(5,7-diiodoquinolin-8-yloxy) -N’-(D-glucose) acetohydrazide (XIXa).
22- 2-(5,7-diiodoquinolin-8-yloxy) -N’- (D-xylose) acetohydrazide (XIXb).
23- 2-(5,7-diiodoquinolin-8-yloxy) -N’- (D-arabinose) acetohydrazide (XIXc).
24-2-(5,7-diiodoquinolin-8-yloxy) -N’- (D-mannose) acetohydrazide (XIXd).
25-2-(5,7-diiodoquinolin-8-yloxy)-N’- (D-galactose) acetohydrazide (XIXe).
26- (1,2,3,4,5-penta-O-acetyl-D-gluco) -(5,7-diiodoquinolin-8-yl)]acetohydrazide (XXa).
27- (1,2,3,4-tetra-O-acetyl-D-xylo) -(5,7-diiodoquinolin-8-yl)]acetohydrazide (XXb).
28- (1,2,3,4-tetra-O-acetyl-D-arbino) -(5,7-diiodoquinolin-8-yl)]acetohydrazide (XXc).
29- N’-(1-((diethylamino)methyl)-2-oxoindolin-3-ylidene)-2-(5,7-diiodoquinolin-8-yloxy)acetohydrazide
30- N’-(1- (morpholino methyl)-2-oxoindolin-3-ylidene)acetohydrazide
7-Final Conclusion.
8-References:
This thesis includes 178 reference covering the time period from 1851 till 2011.