Dakshina U. GanihigamaSanya SureramSasithorn SangherPoonpilas HongmaneeThammarat AreeChulabhorn MahidolSomsak RuchirawatPrasat KittakoopChulabhorn Graduate InstituteChulabhorn Research InstituteMahidol UniversityChulalongkorn UniversitySouth Carolina Commission on Higher Education2018-11-092018-11-092014-01-01European Journal of Medicinal Chemistry. Vol.89, (2014), 1-1217683254022352342-s2.0-84908405187https://repository.li.mahidol.ac.th/handle/20.500.14594/33671© 2014 Elsevier Masson SAS. All rights reserved. Various classes of natural products and synthetic compounds were tested against reference strains and clinical multidrug resistant isolates of Mycobacterium tuberculosis. Vermelhotin (19), a natural tetramic acid from fungi, was the most active toward clinical MDR TB isolates (MIC 1.5-12.5 μg/mL). Synthetic compounds (i.e. benzoxazocines, coumarins, chromenes, and pyrrolodiquinoline derivatives) were prepared by green chemistry approaches. Under microwave irradiation, a one-pot synthesis of pyrrolodiquinoline 85 was achieved by homocoupling of 1-methylquinolinium iodide; the structure of 85 was confirmed by single-crystal X-ray analysis. Compound 85 and its derivative 86 exhibited potent antitubercular activity (MIC 0.3-6.2 μg/mL) against clinical MDR TB isolates, and they displayed weak cytotoxicity toward normal cell line. The scaffold of 85 and 86 is potential for antimycobacterial activity.Mahidol UniversityChemistryPharmacology, Toxicology and PharmaceuticsArticleSCOPUS10.1016/j.ejmech.2014.10.026