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1دورية أكاديمية
المؤلفون: Ferrando, I., Berrino, E., Federici, B., Gagliolo, S., Sguerso, D.
مصطلحات موضوعية: article, Verlagsveröffentlichung
وصف الملف: electronic
العلاقة: ISPRS - International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences -- http://www.isprs.org/publications/archives.aspxTest -- 2194-9034; https://doi.org/10.5194/isprs-archives-XLVIII-4-W1-2022-143-2022Test; https://noa.gwlb.de/receive/cop_mods_00062166Test; https://noa.gwlb.de/servlets/MCRFileNodeServlet/cop_derivate_00061494/isprs-archives-XLVIII-4-W1-2022-143-2022.pdfTest; https://www.int-arch-photogramm-remote-sens-spatial-inf-sci.net/XLVIII-4-W1-2022/143/2022/isprs-archives-XLVIII-4-W1-2022-143-2022.pdfTest
الإتاحة: https://doi.org/10.5194/isprs-archives-XLVIII-4-W1-2022-143-2022Test
https://noa.gwlb.de/receive/cop_mods_00062166Test
https://noa.gwlb.de/servlets/MCRFileNodeServlet/cop_derivate_00061494/isprs-archives-XLVIII-4-W1-2022-143-2022.pdfTest
https://www.int-arch-photogramm-remote-sens-spatial-inf-sci.net/XLVIII-4-W1-2022/143/2022/isprs-archives-XLVIII-4-W1-2022-143-2022.pdfTest -
2دورية أكاديمية
المؤلفون: Berrino E., Angeli A., Zhdanov D.D., Kiryukhina A.P., Milaneschi A., Bozdag M., Carradori S., Selleri S., Bartolucci G., Peat T.S., Ferraroni M., Supuran C.T., Carta F., De Luca A.
المصدر: Journal of Medicinal Chemistry
مصطلحات موضوعية: 1 [4 [4 [[(2,2 dioxidobenzo[e][1,2]oxathiin 6 yl)oxy]methyl] 1h 1,2,3 triazol 1 yl] 5 (hydroxymethyl)tetrahydrofuran 2 yl] 5 methylpyrimidine 2,4(1h,3h)dione, 1 [5 (hydroxymethyl) 4 [4 [3 [(2 oxo 2h chromen 6 yl)oxy]propyl] 1h 1,2,3 triazol 1 yl]tetrahydrofuran 2 yl] 5 methylpyrimidine 2,4(1h,3h)dione, 1 [5 (hydroxymethyl) 4 [4 [3 [(2 oxo 2h chromen 7 yl)oxy]propyl] 1h 1,2,3 triazol 1 yl]tetrahydrofuran 2 yl] 5 methylpyrimidine 2,4(1h,3h)dione, 1 [5 (hydroxymethyl) 4 [4 [4 [(2 oxo 2h chromen 4 yl)oxy]butyl] 1h 1,2,3 triazol 1 yl]tetrahydrofuran 2 yl] 5 methylpyrimidine 2,4(1h,3h)dione, 1 [5 (hydroxymethyl) 4 [4 [4 [(2 oxo 2h chromen 7 yl)oxy]butyl] 1h 1,2,3 triazol 1 yl]tetrahydrofuran 2 yl] 5 methylpyrimidine 2,4(1h,3h)dione, 1 [5 (hydroxymethyl) 4 [4 [[(2 oxo 2h chromen 6 yl)oxy]methyl] 1h 1,2,3 triazol 1 yl]tetrahydrofuran 2 yl] 5 methylpyrimidine 2,4(1h,3h)dione, 1 [5 (hydroxymethyl) 4 [4 [[(2 oxo 2h chromen 7 yl)oxy]methyl] 1h 1,2,3 triazol 1 yl]tetrahydrofuran 2 yl] 5 methylpyrimidine 2,4(1h,3h)dione, 1,2,3 triazole derivative, 3 [3 [4 [[[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]selanyl]phenyl]thioureido]benzenesulfonamide, 3 [3 [[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]ureido]benzenesulfonamide, 3 [[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl] 2 oxo 2,3 dihydrobenzo[d]oxazole 5 sulfonamide, 4 [2 [bis[[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]amino]ethyl]benzenesulfonamide, 4 [3 [4 [[[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]selanyl]phenyl]thioureido]benzenesulfonamide, 4 [3 [[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]ureido]benzenesulfonamide, 4 [bis[[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]amino]benzenesulfonamide, 4 [[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methoxy]benzenesulfonamide, 4 [[[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]amino]benzenesulfonamide, 4 [[[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl]thio]benzenesulfonamide, acetazolamide, carbonate dehydratase inhibitor, carbonate dehydratase IX, carbonate dehydratase XII, n [[1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl] 4 sulfamoylbenzamide, telomerase inhibitor, unclassified drug, zidovudine, [1 [2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl] 1h 1,2,3 triazol 4 yl]methyl 4 sulfamoylbenzoate, [1 [[2 (hydroxymethyl) 5 (5 methyl 2,4 dioxo 3,4 dihydropyrimidin 1(2h)yl)tetrahydrofuran 3 yl]methyl] 1h 1,2,3 triazol 4 yl]methyl 4 chloro 3 sulfamoylbenzoate, antineoplastic activity, Article
العلاقة: https://doi.org/10.1021/acs.jmedchem.0c00636Test; https://repository.rudn.ru/recordsTest/article/record/64540/
الإتاحة: https://doi.org/10.1021/acs.jmedchem.0c00636Test
https://repository.rudn.ru/recordsTest/article/record/64540/