molecules Article 11-Keto-α-Boswellic Acid, a Novel Triterpenoid from Boswellia spp. with Chemotaxonomic Potential and Antitumor Activity against Triple-Negative Breast Cancer Cells Michael Schmiech 1 , Judith Ulrich 1, Sophia Johanna Lang 1, Berthold Büchele 1, Christian Paetz 2 , Alexis St-Gelais 3 , Tatiana Syrovets 1,*,† and Thomas Simmet 1,*,† 1 Institute of Pharmacology of Natural Products and Clinical Pharmacology, Ulm University, 89081 Ulm, Germany;
[email protected] (M.S.);
[email protected] (J.U.);
[email protected] (S.J.L.);
[email protected] (B.B.) 2 Max Planck Institute for Chemical Ecology, 07745 Jena, Germany;
[email protected] 3 Laboratoire PhytoChemia, Chicoutimi, QC G7J 1H4, Canada;
[email protected] * Correspondence:
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[email protected] (T.S.); Tel.: +49-731-500-65604 (T.S.); +49-731-500-65600 (T.S.) † These authors contributed equally to this work. Abstract: Boswellic acids, and particularly 11-keto-boswellic acids, triterpenoids derived from the genus Boswellia (Burseraceae), are known for their anti-inflammatory and potential antitumor efficacy. Although boswellic acids generally occur as α-isomers (oleanane type) and β-isomers (ursane type), 11-keto-boswellic acid (KBA) was found only as the β-isomer, β-KBA. Here, the existence and natural occurrence of the respective α-isomer, 11-keto-α-boswellic acid (α-KBA), is demonstrated for the first time. Initially, α-KBA was synthesized and characterized by high-resolution mass spectrometry Citation: Schmiech, M.; Ulrich, J.; (HR-MS) and nuclear magnetic resonance (NMR) spectroscopy, and a highly selective, sensitive, Lang, S.J.; Büchele, B.; Paetz, C.; and accurate high-performance liquid chromatography coupled with tandem mass spectrometry St-Gelais, A.; Syrovets, T.; Simmet, T.