Euis Julaeha
Padjadjaran University
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Publication
Featured researches published by Euis Julaeha.
The Open Chemistry Journal | 2015
Lilis Siti Aisyah; Yenny Febriany Yun; Euis Julaeha; Tati Herlina; Achmad Zainuddin; Wawan Hermawan; Unang Supratman; Hideo Hayashi
Flavonoids compounds such as kaempferol (1), kaempferol-3-O- -D-glucopyranoside or astragalin (2) and kaempferol-3-O- -L-rhamnoside or afzelin (3) have been isolated from the fresh leaves of Kalanchoe tomentosa (Crassulaceae). The chemical structure of isolated compounds 1-3 were identified by spectroscopic evidences and comparison with those compound previously reported. Compounds 1-3 showed cytotoxic activity against P-388 murine leukimia cells with IC50 values of 51.8, � 100 and 3.32 μg/mL, respectively.
Acta Crystallographica Section E-structure Reports Online | 2010
Euis Julaeha; Unang Supratman; Mat Ropi Mukhtar; Khalijah Awang; Seik Weng Ng
The coumarin ring system in the title compound, C15H18O5 [IUPAC name: 8-(2,3-dihydroxy-3-methylbutyl)-7-methoxy-2H-1-benzopyran-2-one], isolated from Muraya paniculata, is planar (r.m.s. deviation 0.017 Å). In the crystal, the two hydroxy groups are involved in O—H⋯O hydrogen bonding with adjacent molecules, forming a sheet structure.
Jurnal Kimia | 2018
Tri Mayanti; Y. P. Apriantini; S. Soidah; J. Sianturi; D. Darneti; Euis Julaeha; Dadan Sumiarsa; Nurlelasari Nurlelasari; Rani Maharani
Three triterpenoid compounds, 8,14-secogammacera-7,14-dien-3,21-dione (1), 8,14-secogammacera-7en-14-hydroxy-3,21-dione (2) and 9,19-cyclolanost-24-en-3-one, 21,23 epoxy-21,22-dihydroxy (21R, 22S, 23S) (3) has been isolated from the barks and leaves of L. domesticum cv kokossan (Meliaceae). The chemical structures of compounds 1-3 were identified with spectroscopic data, including UV, IR, NMR and MS, and their spectra were compared with previously reported spectra data. Compound 1, 2 were evaluated for their antibacterial effects against Escherichia coli and Bacillus ereus. Compound 3 was evaluated for their antibacterial effects against Escherichia coli and Enterococcus feacalis. Compound 1 showed the inhibition zone values of 7.5 dan 8.0 mm at 500 and 1000 ppm against Escherichia coli, whereas for Bacillus cereus it was inactive. Compound 2 showed the inhibition zone values of 8.0 dan 10.0 mm at concentrations of 500 and 1000 ppm against Escherichia coli, whereas for Bacillus cereus it was inactive. Compound 3 showed the inhibition zone values of 3.67 mm, 3.17 mm, 2.32 mm at concentrations of 10000, 5000 and 1000 ppm respectively against Escherichia coli, whereas for Enterococcus feacalis it was inactive.
Oncology Letters | 2012
Ajeng Diantini; Anas Subarnas; Keri Lestari; Eli Halimah; Yasmiwar Susilawati; Supriyatna; Euis Julaeha; Tri H. Achmad; Eka W. Suradji; Chiho Yamazaki; Kenji Kobayashi; Hiroshi Koyama; Rizky Abdulah
Procedia Chemistry | 2015
Euis Julaeha; Yunita Permatasari; Tri Mayanti; Ajeng Diantini
Jurnal Kedokteran Maranatha | 2010
Tati Herlina; Euis Julaeha; Unang Supratman; Wahyu Widowati; Anas Subarnas; Supriyatna Sutardjo
Journal of Mathematical and Fundamental Sciences | 2018
Hadi Kuncoro; Kindi Farabi; Euis Julaeha; Unang Supratman; Yoshihito Shiono
Arena Tekstil | 2018
Tatang Wahyudi; Agus Surya Mulyawan; Doni Sugiyana; Euis Julaeha
Natural product sciences | 2017
Lilis Siti Aisyah; Yenny Febriani Yun; Tati Herlina; Euis Julaeha; Achmad Zainuddin; Ida Nurfarida; Ace Tatang Hidayat; Unang Supratman; Yoshihito Shiono
Molekul | 2017
Dewa Gede Katja; Kindi Farabi; Nurlelasari Nurlelasari; Desi Harneti; Euis Julaeha; Ace Tatang Hidayat; Tri Mayanti; Rani Maharani; Unang Supratman; Khalijah Awang