dc.contributor.author | Isaksson, Johan | |
dc.contributor.author | Rylandsholm, Fredrik G. | |
dc.contributor.author | Bouř, Petr | |
dc.contributor.author | Svendsen, John Sigurd Mjøen | |
dc.contributor.author | Brichtová, Eva | |
dc.contributor.author | Choi, Sng Un | |
dc.contributor.author | Lee, Sang‑Ho | |
dc.contributor.author | Jung, Young-Sik | |
dc.contributor.author | No, Zae Sung | |
dc.contributor.author | Aasen, Arne Jørgen | |
dc.contributor.author | Dekebo, Aman | |
dc.contributor.author | Dinku, Worku | |
dc.date.accessioned | 2022-01-17T08:49:27Z | |
dc.date.available | 2022-01-17T08:49:27Z | |
dc.date.issued | 2020-03-17 | |
dc.description.abstract | Myrrh, a resin derived from the damaged bark of Commiphora genus, has traditionally been used for treatment of
various human diseases, such as amenorrhea, ache, tumors, fever, and stomach pains. In spite of this widespread use
of the myrrh in Ethiopia, the pharmacological activity and chemical composition have not been studied in detail. A
new tricyclic triterpene acid (3S,4S,14S,7E,17E,21Z)-3,30-dihydroxypodioda-7,17,21-trien-4-carboxylic acid (commafric
A) has been isolated from a crude methanolic extract of Commiphora africana (A. Rich.) Engl. resin along with the
known pentacyclic triterpene α-amyrin. The structure of commafric A was characterized using diferent spectroscopic
techniques such as 1D and 2D NMR, IR, and VCD combined with computations. The anti-proliferative activity of both
isolated compounds was evaluated using SRB based colorimetric cellular assay against four human cancer cell lines.
Etoposide was used as a positive control. Commafric A showed signifcant anti-proliferative efects against non-small
cell lung cancer (A549) with IC<sub>50</sub> values of 4.52 μg/ml. The pentacyclic triterpene α-amyrin showed a weak antiproliferative activity against A2780 (ovarian cancer), MIA-PaCa-2 (pancreatic cancer), and SNU638 (stomach cancer)
cell lines tested with IC50 values ranging 9.28 to 28.22 μg/ml. Commafric A possessed anti-proliferative activity against
non-small cell lung cancer (A549), which suggests that commafric A has potential to be further optimized being a
lead compound in the search for new drugs against cancer diseases. | en_US |
dc.identifier.citation | Dinku, Isaksson, Rylandsholm, Bouř, Svendsen. Anti-proliferative activity of a novel tricyclic triterpenoid acid from Commiphora africana resin against four human cancer cell lines. Applied Biological Chemistry. 2020;63(1):16-27 | en_US |
dc.identifier.cristinID | FRIDAID 1889961 | |
dc.identifier.doi | 10.1186/s13765-020-00499-w | |
dc.identifier.issn | 2468-0834 | |
dc.identifier.issn | 2468-0842 | |
dc.identifier.uri | https://hdl.handle.net/10037/23695 | |
dc.language.iso | eng | en_US |
dc.publisher | Springer | en_US |
dc.relation.ispartof | Rylandsholm, F.G. (2024). Structural characterisation and drug-lipid interaction by NMR spectroscopy. (Doctoral thesis). <a href=https://hdl.handle.net/10037/33752>https://hdl.handle.net/10037/33752</a> | |
dc.relation.journal | Applied Biological Chemistry | |
dc.relation.projectID | info:eu-repo/grantAgreement/RCN/BIOTEK2021/269425/Norway/DL: Digital discovery of antimicrobial molecules from marine Arctic resources with reduced risk of triggering resistance// | en_US |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2020 The Author(s) | en_US |
dc.title | Anti-proliferative activity of a novel tricyclic triterpenoid acid from Commiphora africana resin against four human cancer cell lines | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |