سائنس اور تہذیب و تمدن کے فروغ میں اسلام کا کردار

Islam is a complete code of life. It has complete instructions regarding all aspects of life. There is no moment in human life when the wisdom of Islam has not benefited humanity. Likewise there is no such area in the world where Islam has not put the light of guidance. Allah Almighty has systematically administered this world system.  Allah created the universe and set it disciplined, then created man and gave him every kind of physical, rational, logical and argumintive ability, so that humans can know the secrets of the universe by thinking and understanding it. The journey of research and discovery, which started long ago, is still continues today after passing through different stages of research. This journey of research resulted in evolution of philosophy, civilization, promotion of new scientific innovations and discoveries. The research and discovery resulted in the secrets of heaven and earth.  Today, man stands at the stage of science and technology, about which the human being in the older days even could not imagine of it. In this entire evolutionary journey, the religion of Islam is the only religion that not only stood firmly with humans, but guided him at every step during this evolutionary journey. In this context, the Quranic teachings are comprehensive matter. Allamah Sayyuti says "There is no knowledge and problem that is not discussed in the Qur'an. So Islam invites human to research in the system of the universe and presents the system of universe for its authenticity.

Synthesis and Characterization of Potentially Biologically Active Compunds Derived from Fibric Acids.

The present study deals with the synthesis of fibric acids derivatives. The thesis has been divided into three parts (1) Synthesis of fibric acids derivatives (2) Biological screening (3) In silicio studies. In the first part of thesis two fibric acids (2a & 2b) were synthesized from two phenols (1a & 1b) followed by their conversion into corresponding esters (3a & 3b) and carbohydrazides (4a & 4b). Cyclization of these carbohydrazides was carried out to synthesize 1,3,4-oxadiazoles (5a & 5b). In next step N-substituted-2-bromoacetamides (7a- 7y) were prepared by using various anilines (6a-6y). Two main series of compounds 8-30 and 31-50 were synthesized successfully by reacting 5-(2-aryloxypropan-2-yl)-1.3.4- oxadiazol-2-thiols (5a & 5b) with N-substituted-2-bromoacetamides (7a-7y). Characterization of the compounds was carried out through spectroscopic analysis. N N O CH3 CH3 O X SH (5a-5b) 5a X=Cl 5b X=Br (Scheme 1) xiv Br N H O R1 R2 (7a-7y) 7a Cyclohexylamine 7j R1 = 3CH3 R2=5CH3 7s R1 = H R2=2Br 7b R1 = H R2=H 7k R1 = H R2=4C2H5 7t R1 = H R2=3Br 7c R1 = H R2=2CH3 7l R1 =2C2H5 R2=6CH3 7u R1 = H R2=4Br 7d R1 = H R2=3CH3 7m R1 = H R2=2OCH3 7v R1 = H R2=2Cl 7e R1 = H R2=4CH3 7n R1 = H R2=3OCH3 7w R1 = H R2=4F 7f R1 = 2CH3 R2=3CH3 70 R1 = H R2=4OCH3 7x R1 = H R2=4NO2 7g R1 = 2CH3 R2=4CH3 7p R1 = H R2=2OC2H5 7y R1 = H R2=2NH2 7h R1 = 2CH3 R2=6CH3 7q R1 = H R2=4OC2H5 7i R1 = 3CH3 R2=4CH3 7r R1 = 2OCH3 R2=5Cl (Scheme 2) N N O CH3 CH3 O Cl S N O H R1 R2 (8-30) 8 Cyclohexylamine 16 R1 = 3CH3 R2=4CH3 24 R1 = 2OCH3 R2=5Cl 9 R1 = H R2=H 17 R1 = 3CH3 R2=5CH3 25 R1 = H R2=2Br 10 R1 = H R2=2CH3 18 R1 = H R2=4C2H5 26 R1 = H R2=4Br 11 R1 = H R2=3CH3 19 R1 =2C2H5 R2=6CH3 27 R1 = H R2=2Cl 12 R1 = H R2=4CH3 20 R1 = H R2=2OCH3 28 R1 = H R2=4F xv 13 R1 = 2CH3 R2=3CH3 21 R1 = H R2=4OCH3 29 R1 = H R2=4NO2 14 R1 = 2CH3 R2=4CH3 22 R1 = H R2=2OC2H5 30 R1 = H R2=2NH2 15 R1 = 2CH3 R2=6CH3 23 R1 = H R2=4OC2H5 (Scheme 3) N N O CH3 CH3 O Br S N O H R1 R2 (31-50) 31 Cyclohexylamine 38 R1 = 2CH3 R2=6CH3 45 R1 = H R2=2OC2H5 32 R1 = H R2=H 39 R1 = 3CH3 R2=4CH3 46 R1 = H R2=4OC2H5 33 R1 = H R2=2CH3 40 R1 = 3CH3 R2=5CH3 47 R1 = 2OCH3 R2=5Cl 34 R1 = H R2=3CH3 41 R1 = H R2=4C2H5 48 R1 = H R2=2Br 35 R1 = H R2=4CH3 42 R1 =2C2H5 R2=6CH3 49 R1 = H R2=3Br 36 R1 = 2CH3 R2=3CH3 43 R1 = H R2=3OCH3 50 R1 = H R2=4Br 37 R1 = 2CH3 R2=4CH3 44 R1 = H R2=4OCH3 (Scheme 4) After the successful completion of synthetic portion and their characterization fibric acids derivatives were evaluated for their biological activities. For this purpose, protocols of anti-thrombotic (in vitro and in vivo) and anti-inflammatory activity (in vitro and in vivo) were followed. The anti-thrombotic activity (in vitro and in vivo) was performed to evaluate the FXa inhibition potential of newly synthesized compounds. In vitro, compounds 17, 27 and 36 showed higher % age of clot lysis than standard drug streptokinase; however the xvi remaining compounds showed moderate to good activities. In vivo, for compounds 9, 12, 13, 16, 17, 24, 27, 32, 36, 39, 41, and 48 enhanced clotting times (even better than standard drug heparin) were observed. Anti-inflammatory activity was performed to evaluate the COX-2 enzyme inhibition potential of fibric acids derivatives. In vitro, these compounds showed moderate to good activity while in vivo compounds 8, 9, 11, 12, 16, 17, 24, 34 and 48 showed results even better than standard drug diclofenic sodium. Compounds 14, 15, 19, 21, 31, 38 and 42 results were comparable to that of standard drug while remaining compounds exhibited moderate activity. In the last part of research work in silico studies were performed for selected compounds. For anti-thrombotic activity compounds 9-17 were docked against FXa protein. Except the compound 5a, all others showed higher docking score than the control ligand. In case of anti-inflammatory activity molecular docking of compounds 5a, 5b and 8-50 was carried out against COX-2 protein. All the compounds except 5a, 5b, 13 and 25 showed higher docking score than standard. Density functional theory (DFT) computed molecular properties of compounds 9-17 were also calculated by computational methodology. Results of biological activities showed good commitment with in silico study results. In future these compounds might be evaluated at molecular level.