Publikasi Scopus 2023 per tanggal 30 Maret 2023 (184 artikel)

Eff A.R.Y., Huri H.Z., Radji M., Mun’im A., Suyatna F.D., Eden Y.
57190757160;34976838600;23107540200;57491481000;58114514000;58114701500;
Angiotensin converting enzyme (ACE) inhibitors activity from purified compounds Fructus Phaleria macrocarpa (Scheff) Boerl
2023
BMC Complementary Medicine and Therapies
23
1
56
Departement of Pharmacy, Faculty of Health Sciences Universitas Esa Unggul, Jakarta, Indonesia; Department of Clinical Pharmacy & Pharmacy Practice, Faculty of Pharmacy Universiti Malaya, Kuala Lumpur, Malaysia; Faculty of Pharmacy Universitas Indonesia, Jakarta, Indonesia; Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia
Eff, A.R.Y., Departement of Pharmacy, Faculty of Health Sciences Universitas Esa Unggul, Jakarta, Indonesia; Huri, H.Z., Department of Clinical Pharmacy & Pharmacy Practice, Faculty of Pharmacy Universiti Malaya, Kuala Lumpur, Malaysia; Radji, M., Departement of Pharmacy, Faculty of Health Sciences Universitas Esa Unggul, Jakarta, Indonesia; Mun’im, A., Faculty of Pharmacy Universitas Indonesia, Jakarta, Indonesia; Suyatna, F.D., Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia; Eden, Y., Departement of Pharmacy, Faculty of Health Sciences Universitas Esa Unggul, Jakarta, Indonesia
Background: Mahkota Dewa [Phaleria macrocarpa (Scheff) Boerl.] fruit in vitro and in- vivo can decrease and prevent elevation of the blood pressure, lower plasma glucose levels, possess an antioxidant effect, and recover liver and kidney damage in rats. This study aimed to determine the structure and inhibitory activity of angiotensin-converting enzyme inhibitors (ACE) from the Mahkota Dewa fruit. Methods: The fruit powder was macerated using methanol and then partitioned by hexane, ethyl acetate, n-butanol, and water. The fractions were chromatographed on the column chromatography and incorporated with TLC and recrystallization to give pure compounds. The structures of isolated compounds were determined by UV-Visible, FT-IR, MS, proton (1H-NMR), carbon (13C-NMR), and 2D-NMR techniques encompassing HMQC and HMBC spectra. The compounds were evaluated for their ACE inhibitory activity, and the strongest compound was determined by the kinetics enzyme inhibition. Results: Based on the spectral data, the isolated compounds were determined as 6,4-dihydroxy-4-methoxybenzophenone–2-O-β-D-glucopyranoside (1), 4,4′-dihydroxy-6-methoxybenzophenone-2-O-β-D-glucopyranoside (2) and mangiferin (3). IC50 values of the isolated compounds 1, 2 and 3 were 0.055, 0.07, and 0.025 mM, respectively. Conclusion: The three compounds have ACE inhibitor and mangiferin demonstrated the best ACE inhibitory activity with competitive inhibition on ACE with the type of inhibition kinetics is competitive inhibition. © 2023, The Author(s).
4,4′-dihydroxy-6-methoxybenzophenone-2-O-β-D-glucopyranoside; 6,4-dihydroxy-4-methoxybenzophenone–2-O-β-D-glucopyranoside; ACE inhibitor; Mangiferin; Phaleria macrocarpa
4,4 dihydroxy 6 methoxybenzophenone 2 O beta D glucopyranoside; 6,4 dihydroxy 4 methoxybenzophenone 2 O beta D glucopyranoside; acetic acid ethyl ester; antioxidant; butanol; captopril; dipeptidyl carboxypeptidase; hexane; hippuric acid; mangiferin; plant extract; unclassified drug; water; dipeptidyl carboxypeptidase; dipeptidyl carboxypeptidase inhibitor; animal experiment; animal model; antioxidant assay; Article; blood pressure; carbon nuclear magnetic resonance; chemical structure; column chromatography; competitive inhibition; crystallization; enzyme activity; enzyme inhibition; Fourier transform infrared spectroscopy; glucose blood level; heteronuclear multiple bond correlation; heteronuclear multiple quantum coherence; IC50; kidney injury; kinetics; mass spectrometry; nonhuman; nucl
We would like to acknowledge Ministry of Education and Research Indonesia (Kemenristek Dikti) and Education fund management agency (LPDP Indonesia) for the support under the World Class Professor.
BioMed Central Ltd
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