Nurlelasari
Padjadjaran University
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Publication
Featured researches published by Nurlelasari.
Makara Journal of Science | 2017
Ace Tatang Hidayat; Kindi Farabi; Desi Harneti; Rani Maharani; Nurlelasari Nurlelasari; Unang Supratman; Yoshihito Shiono
800x600 Two mixture s of flavanoid compounds ( 1 and 2 ), a mixture of catechin ( 1a ) and epicatechin ( 1b ) , and a mixture of gallocatechin ( 2a ) and epigallocatechin ( 2b ) , were isolated from the active fraction of the stem bark of Aglaia elliptica methanol extract. The chemical structure of the compounds w as identified with spectroscopic data , including UV, IR, NMR ( 1 H, 13 C, DEPT 135°, HMQC, HMBC, 1 H- 1 H COSY) , and MS, and additionally compared with previously reported spectral data. All compounds were evaluated for their cytotoxic effects against P-388 murine leukemia cells. Compound 2 showed cytotoxicity against the P-388 murine leukemia cell , with an IC 50 value of 7.79 µg/mL, but compound 1 wa s found not to be active ( more than 100 µg/mL ) . Normal 0 false false false EN-ID X-NONE X-NONE
Chiang Mai University journal of natural sciences | 2017
Kindi Farabi; Desi Harneti; Nurlelasari Nurlelasari; Rani Maharani; Ace Tatang Hidayat; Unang Supratman; Khalijah Awang; Yoshihito Shiono
The study aimed to find a potential anticancer agent by isolating and identifying the chemical structure of compounds from Aglaia argentea and testing their cytotoxic effects against P-388 murine leukimia cells. Five steroids – stigmast-5-en-3β-ol (β-sitosterol) (1), stigmast-5-en-3β-ol-3β-oleate (β-sitosterol oleate) (2), stigmast-5-en-3β-ol-3-O-(6′-O-oleoyl)-β-D-glucopyranoside (sitoindoside II) (3), stigmast-5-en-3β-ol-3-O-β-D-glucopyranoside (β-sitosterol glucoside) (4), stigmast-5,22-dien-3β-ol-3-O-β-D-glucopyranoside (stigmasterol glucoside) (5) – were isolated from the bark of Aglaia argentea. The chemical structures of 1-5 were identified with spectroscopic data, including IR, NMR (1H, 13C, DEPT 135°, HMQC, HMBC, 1H-1H COSY) and HRTOFMS, as well as by comparing with previously reported spectral data. All compounds were evaluated for their cytotoxic effects against P-388 murine leukemia cells. Compounds 1-5 showed cytotoxicity against P-388 murine leukemia cell with IC50 values of 12.45 ± 0.050, 85.25 ± 0.050, >100, 52.27 ± 0.031 and 62.52 ± 0.076 μg/mL, respectively.
International Journal of Chemistry | 2016
Dewa Gede Katja; Kindi Farabi; Vidia Afina Nuraini; Nurlelasari Nurlelasari; Ace Tatang Hidayat; Tri Mayanti; Desi Harneti; Unang Supratman
Jurnal Kimia VALENSI | 2018
Ace Tatang Hidayat; Kindi Farabi; Ida Nur Farida; Kansy Haikal; Nurlelasari Nurlelasari; Desi Harneti Putri Huspa; Rani Maharani; Unang Supratman; Yoshihito Shiono
Indonesian Journal of Chemistry | 2018
Ace Tatang Hidayat; Kindi Farabi; Desi Harneti; Nurlelasari Nurlelasari; Rani Maharani; Ida Nurfarida; Unang Supratman; Yoshihito Shiono
Current Bioactive Compounds | 2018
Rani Maharani; Dadan Sumiarsa; Achmad Zainuddin; Nuruzzahra Ammatillah; Ace Tatang Hidayat; Unang Supratman; Desi Harneti; Nurlelasari Nurlelasari
Molekul | 2017
Ace Tatang Hidayat; Kindi Farabi; Desi Harneti; Nurlelasari Nurlelasari; Rani Maharani; Tri Mayanti; 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
Jurnal Kimia VALENSI | 2017
Supriatno Supriatno; Ace Tatang Hidayat; Kindi Farabi; Fajar Fauzi Abdullah; Nurlelasari Nurlelasari; Tati Herlina; Unang Supratman; Khadijah Awang
Jurnal Kimia | 2017
Nurlelasari Nurlelasari; Fajar Fauzi Abdullah; Nadya Thufaila; Rani Maharani; Desi Harnet; Ace Tatang Hidayat; Unang Supratman