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Identification of potential drug target from Plasmodium Falciparum and their novel inhibitors through molecular docking approach

Thesis Info

Author

Ata Ullah

Supervisor

Pervez Anwar

Department

Department of Bioinformatics and Biotechnology

Program

MS

Institute

International Islamic University

Institute Type

Public

City

Islamabad

Province

Islamabad

Country

Pakistan

Thesis Completing Year

2016

Thesis Completion Status

Completed

Page

viii, 57

Subject

Bioinformatics & Biotechnology

Language

English

Other

MS 616.01 ATI

Added

2021-02-17 19:49:13

Modified

2023-01-23 23:21:10

ARI ID

1676723835445

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بے قراروں سے پیار کرتا ہوں

بے قراروں سے پیار کرتا ہوں
غم کے ماروں سے پیار کرتا ہوں

تخت والوں سے کیا مجھے نسبت
خاکساروں سے پیار کرتا ہوں

بانٹ لیتا ہوں درد یاروں کے
اپنے یاروں سے پیار کرتا ہوں

جھیل کر نفرتیں ہزاروں کی
میں ہزاروں سے پیار کرتا ہوں

سارے کب مجھ سے پیار کرتے ہیں
میں تو ساروں سے پیار کرتا ہوں

میرا تائبؔ یہی سہارا ہیں
بے سہاروں سے پیار کرتا ہوں

علم مختلف الحدیث پر امام شافعی کے تفکرات کا تحقیقی مطالعہ

After the era of Prophet Muhammad (S.A.W), there were dissimilarities in interpretations of contradictive revelations by Muhammad (S.A.W) thereby questioning their authentication while being considered a basic source of extracting the Sharia acts. In this context, Imam Shāfʿī studies all the dissimilarities and contradictions and devised finest principles which performed very positive role in rationalizing the conflicting Ahadiths. He was first to discuss these matters in an innovative manner. It is therefore, essential for investigator to refer to Shāfʿīs principles to rationalize any Hadith lying under contradiction. Imam Shāfʿī stated that Hadith is not itself contradicting but its apparent meaning leads the investigator into misconception. Consequently, he has stated three methods to remove this conflict. First is the combination (جمع) which recommends working on both Ahadiths at the same time rather than leaving either of them. Second is the abrogation (تنسیخ) which requires extensive knowledge of Quran and History before inferring the final decision of Muhammad (S.A.W) and scholars widely recommend Imam Shāfiʿī in recognizing abrogated Ahadiths. Third is preference (ترجيح) which is based upon peripheral attributes.

Phytochemical and Pharmacological Investigations of Quercus Incana

The present study was aimed to extract, fractionate, isolate and standardize the chemical constituents from the plant, Quercus incana, in order to find out their phytochemical and pharmacological mode of action, so as to discover a new source for potentially active constituents used for the benefits of mankind. Quercus incana, which is a large evergreen tree belongs to family Fagaceae. The Fagaceae is a large plant family found in Asia, North America and Europe. Quercus incana has been used in different ailments such as diarrhea, neurosis, pyrexia, dysentery, pain, inflammation and burns healing in conventional medicines. It is also employed to treat gonorrhea and used as an astringent, diuretic, and various nervous disorders all over the world including Pakistan. In the present research work, the plant Quercus incana was explored for its chemical constituents using chromatographic and spectroscopic techniques for potentially new and therapeutically active agents. The bark portion was selected for isolation, on the basis of preliminary pharmacological activities and its common use by the local people and Hakims and Tabibs in different ailments. Some activities were performed on fruit extract also. Crude extract of bark and fruit of Quercus incana and the new compound isolated from bark were screened for various in-vitro and in-vivo biological activities like antibacterial, anti oxidant, analgesic, anti-inflammatory etc, inorder to give scientific background to various ethnomedicinal applications of the plant which will lead to safe, therapeutic, effective and economical way of treatment of different diseases and to examine and analyze the chemical composition of the plant. For the isolation of pure secondary metabolites, the ethyl acetate fraction (obtained from crude methanolic extract of the bark) was subjected to column chromatography. The structures of purified compounds were elucidated by using various sophisticated spectroscopic techniques i.e, 1H-NMR, 13C-NMR, COSY, NOESY, DEPT, HSQC, HMBC, UV, IR and EI-MS. The plant was found to be a new source of six compounds such as, betulinic acid, 9-octadecanoic acid methyl ester(z-form), gallic acid, gallic ester, b-sitosterol glucoside, and quercitin. Three known compounds like β-sitosterol, ursolic acid, and lupeol were also isolated. Quercuschin, which was a completely new compound was discovered for the first time from this plant source. Results of in-vivo biological studies reveal that the plant possesses very good property of producing peripheral and central analgesia. The data obtained from different experiments supports the use of the plant in relieving fever, and treating inflammatory conditions. The different in-vitro activities of new compound were conclusive of the fact that the plant is a good natural antioxidant and can be used to treat various bacterial and fungal infections. The isolation work done on the plant (bark) of Quercus incana yielded 10 compounds. In these 10 compounds, 7 were reported for first time from this plant species : THESE WERE , betulinic acid, 9-octadecenoic acid methyl ester(z-form), gallic acid, gallic ester, b-sitosterol glucoside,quercitin , and one compound NAMELY Quercuschin: was absolutely new and was never reported before from any source AND was discovered for the first time from this plant source. 3 compounds were KNOWN compounds: NAMELY β-sitosterol, ursolic acid, and lupeol, Findings of this research project, especially the biological activities of chemical constituents of the plant, strongly support the folkloric uses of the plant and its applications in traditional treatment. The isolated compounds strengthen these activities. However, further comprehensive research work on the crude extract as well as on isolated compounds is needed to explore and identify lead compounds of clinical effectiveness for the development of new drugs in order to strengthen the field of drug discovery.