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무하마드아미르Saleem ( Muhammad Aamir Saleem ),무하마드우스만Saleem ( Muhammad Usman Saleem ),KifayatUllah칸 ( Kifayat Ullah Khan ),( S. Y. Lee ) 한국정보처리학회 2012 한국정보처리학회 학술대회논문집 Vol.19 No.2
The growth in number and capacity of smart devices such as GPS enabled smart phones and PDAs present an unparalleled opportunity for diverse areas of life. In this paper we propose an approach for vehicle theft protection using GPS based trajectory anomaly detection. The detailed methodology of the proposed system is briefly described in this paper.
Chlorodifluoromethane (R22) Gas and Its Mixtures with CO2/N2/Air as an Alternative to SF6
Saleem Muhammad Zaheer,Kamran Muhammad,Amin Salman,Ullah Rahmat,Abbas Kharal Hafiz Shafqat,Nasimullah,Muhammad Fazal,Rahman Taqi ur 대한전기학회 2021 Journal of Electrical Engineering & Technology Vol.16 No.3
SF 6 has been extensively deployed in high voltage gas insulated equipment to be used as a dielectric medium since 1960 because of its excellent dielectric strength and arc interruption performance. This research proposes promising substitute of SF 6 , by investigating a refrigerant gas such as Chlorodifl uoromethane (CHClF 2 ) with a mixture of CO 2 /N 2 /Air to mitigate environmental hazards of SF 6 . R 22 has less atmospheric life and low cost as compared to SF 6 . It has less GWP (1,810) as compared to SF 6 (23,900). In this research, the AC and DC breakdown properties of R 22 mixtures along with varying ratios of CO 2 , N 2, and Air were investigated. The best alternative to SF 6 has been found to be a mixture of R 22 + N 2 which is close to 81% of SF 6 dielectric strength. The dielectric strength of diff erent optimal mixtures was found in the order of SF 6 > R 22 + N 2 > R 22 + Air > R 22 + CO 2 under AC voltage at 0.4 MPa. Moreover, the boiling point and GWP were further reduced by adding the buff er gases such as N 2, , CO 2 , and Air. R 22 also has acceptable insulation self-recoverability and liquefaction temperature. The results of this study are promising in terms of low cost and environment-friendly alternative to SF 6 .
Metabolites of Marine Algae Collected from Karachi-coasts of Arabian Sea
Muhammad Shaiq Ali,Muhammad Jahangir,Muhammad Saleem,Muhammad Kashif Pervez,Shaista Hameed,Viqar Uddin Ahmad 한국생약학회 2000 Natural Product Sciences Vol.6 No.2
The ethanolic extracts of marine green, brown and red algae collected from Karachi coasts of Arabian Sea afforded a new enol-derivative of N-acylsphingosine named as coelarthenol (1) from Coelarthrum muelleri, two new glucose-derivatives named: botryenal (2) and botryenol (3) from Botryocladia leptopoda, α-tocopherol quinone (4) from Codium iyengarii, β-sitosterol and hexadecanoic acid from Stokeyia indica. The known constituents (4, β-sitosterol & hexadecanoic acid) have not been reported so far from their corresponding sources and the structures were determined through spectroscopic methods, whereas, the structures of new constituents (1-3) were elucidated with the aid of selective HMBC experiments. The phytotoxicity of 4 was also monitored.
Muhammad Saleem,Muhammad Rafiq,Muhammad Hanif,Nasim Hasan Rama,Sung-Yum Seo,Ki-Hwan Lee 대한화학회 2012 Bulletin of the Korean Chemical Society Vol.33 No.8
A new series of 2,5-disubstituted-1,3,4-thiadiazoles 6a-i was synthesized by overnight stirring various 1,4- disubstituted thiosemicarbazides 5a-i in polyphosphoric acid followed by neutralization. The structures of newly synthesized compounds 5a-i and 6a-i were characterized by IR, 1H and 13C NMR, elemental analysis and mass spectrometric studies. All the synthesized compounds were evaluated for their urease and acetylcholine esterase inhibition activities. Thiosemicarbazides 5a-i are found to possess excellent potential for urease inhibition, more than the standard drug. Thiosemicarbazides 5a-i are more potent urease inhibitor than their cyclic analogues thiadiazoles 6a-i. Almost all of the compounds are excellent inhibitors of acetylcholine esterase. The inhibition of acetylcholine esterase of compounds 5a, 5c, 5d, 5g, 5i, 6e, 6f, 6g, and 6i is much more than that of standard drug.
Saleem, Muhammad,Rafiq, Muhammad,Hanif, Muhammad,Rama, Nasim Hasan,Seo, Sung-Yum,Lee, Ki-Hwan Korean Chemical Society 2012 Bulletin of the Korean Chemical Society Vol.33 No.8
A new series of 2,5-disubstituted-1,3,4-thiadiazoles 6a-i was synthesized by overnight stirring various 1,4-disubstituted thiosemicarbazides 5a-i in polyphosphoric acid followed by neutralization. The structures of newly synthesized compounds 5a-i and 6a-i were characterized by IR, $^1H$ and $^{13}C$ NMR, elemental analysis and mass spectrometric studies. All the synthesized compounds were evaluated for their urease and acetylcholine esterase inhibition activities. Thiosemicarbazides 5a-i are found to possess excellent potential for urease inhibition, more than the standard drug. Thiosemicarbazides 5a-i are more potent urease inhibitor than their cyclic analogues thiadiazoles 6a-i. Almost all of the compounds are excellent inhibitors of acetylcholine esterase. The inhibition of acetylcholine esterase of compounds 5a, 5c, 5d, 5g, 5i, 6e, 6f, 6g, and 6i is much more than that of standard drug.
Muhammad Rizwan Maqsood,Muhammad Hanif,Muhammad Rafiq,Muhammad Saleem,Sumera Zaib,Aftab Ahmed Khan,Mazhar Iqbal,Jamshed Iqbal,Nasim Hasan Rama,서승염,Ki-Hwan Lee 대한화학회 2012 Bulletin of the Korean Chemical Society Vol.33 No.12
The target compounds 6-11a-e were synthesized by condensing 4-amino-5-aryl-3H-1,2,4-triazole-3-thiones 5a-f with various aromatic carboxylic acids in the presence of phosphorous oxychloride. The structures of newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR, elemental analysis and mass spectrometric studies. All the synthesized compounds were screened for their antibacterial activity. Almost all the tested compounds were potent against four different strains of bacteria when compared with that of reference drug ciprofloxacin. Compounds 6c, 6e, 8d, 9b, 9e, 11a and 11b showed nearly equal or lower MIC values than standard drug, against all four tested bacterial strains but rest of the compounds showed excellent antibacterial activities.
Muhammad Rafiq,Muhammad Saleem,Muhammad Hanif,Muhammad Rizwan Maqsood,Nasim Hasan Rama,Ki-Hwan Lee,서승염 대한화학회 2012 Bulletin of the Korean Chemical Society Vol.33 No.12
A series of aromatic hydrazides 3a-j were prepared by refluxing esters 2a-j with hydrazine hydrate in methanol, which were prepared by the esterification of 1a-j. Acetohydrazides 3a-j upon treatment with carbon disulfide and methanolic potassium hydroxide yielded potassium dithiocarbazate salts 4a-j, which on refluxing with hydrazine hydrate yielded substituted 4-amino-5-aryl-3H-1,2,4-triazole-3-thiones 5a-j. The target compounds 6a-j were synthesized by condensing furan-3-carboxylic acid in the presence of polyphosphoric acid under reflux. The structures of newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR, elemental analysis and mass spectrometric studies. All the synthesized compounds were screened for their urease, acetylcholine esterase inhibition, antioxidant and alkaline phosphatase inhibition activity. Almost all of the compounds 6a-j showed good to excellent activities against urease and acetylcholine esterase more than the reference drugs. Compounds 6f and 6g were more potent scavenger of free radicals than the reference n-propyl gallate. Compound 6b and 6h showed excellent activities of alkaline phosphatase as compare to the reference KH2PO4.
Rafiq, Muhammad,Saleem, Muhammad,Hanif, Muhammad,Maqsood, Muhammad Rizwan,Rama, Nasim Hasan,Lee, Ki-Hwan,Seo, Sung-Yum Korean Chemical Society 2012 Bulletin of the Korean Chemical Society Vol.33 No.12
A series of aromatic hydrazides 3a-j were prepared by refluxing esters 2a-j with hydrazine hydrate in methanol, which were prepared by the esterification of 1a-j. Acetohydrazides 3a-j upon treatment with carbon disulfide and methanolic potassium hydroxide yielded potassium dithiocarbazate salts 4a-j, which on refluxing with hydrazine hydrate yielded substituted 4-amino-5-aryl-3H-1,2,4-triazole-3-thiones 5a-j. The target compounds 6a-j were synthesized by condensing furan-3-carboxylic acid in the presence of polyphosphoric acid under reflux. The structures of newly synthesized compounds were characterized by IR, $^1H$ NMR, $^{13}C$ NMR, elemental analysis and mass spectrometric studies. All the synthesized compounds were screened for their urease, acetylcholine esterase inhibition, antioxidant and alkaline phosphatase inhibition activity. Almost all of the compounds 6a-j showed good to excellent activities against urease and acetylcholine esterase more than the reference drugs. Compounds 6f and 6g were more potent scavenger of free radicals than the reference n-propyl gallate. Compound 6b and 6h showed excellent activities of alkaline phosphatase as compare to the reference $KH_2PO_4$.