Isolation and Identification of Phytocompounds from Maytenus dhofarensis and Their Biological Potentials

Author:

Al-Rubaiai Fatma1,Al-Shariqi Zakiya Zahran1,Al-Shabibi Khalsa S.1,Husband John1ORCID,Al-Hattali Asmaa M.1,Goettert Marcia2,Laufer Stefan23ORCID,Baqi Younis1ORCID,Hassan Syed Imran1ORCID,Fatope Majekodunmi O.1ORCID

Affiliation:

1. Department of Chemistry, College of Science, Sultan Qaboos University, Al Khod, P.O. Box 36, Muscat 123, Oman

2. Department of Pharmaceutical and Medicinal Chemistry, Institute of Pharmacy, Eberhard Karls Universität Tübingen, D-72076 Tübingen, Germany

3. Tübingen Center for Academic Drug Discovery (TüCAD2), D-72076 Tübingen, Germany

Abstract

Maytenus dhofarensis Sebsebe (Celestraceae) is a naturally growing shrub in Oman. It is not a reputed medicinal plant in Oman, but it is regionally endemic and causes shivering attacks on goats that graze on it. The chemical investigation of the hexane and chloroform extracts of the fruits and stems of M. dhofarensis afforded dihydro-β-agarofuran-type sesquiterpene pyridine alkaloid (1), lupanyl myristoate (2) and lignanolactone (3). Compounds (1–3) are new isolates from M. dhofarensis. The structures of these compounds were assigned through comprehensive IR, NMR, and ESI-MS analyses, and the relative configurations of compounds 1 and 3 were deduced from density function theory (DFT) calculations and NMR experiments. Compound 1 was assayed against the kinase enzyme and showed no inhibition activity for p38 alpha and delta at a 10 µM test concentration. Compound 3 inhibited the 2,2′-diphenyl-1-picrylhydrazyl radical (DPPH) by 69.5%, compared to 70.9% and 78.0% for gallic acid and butylated hydroxyanisole, respectively, which were used as positive controls.

Funder

TRC

His Majesty’s Strategic Research Trust Fund

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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