TY - JOUR
T1 - Ergostane-type steroids from the Cameroonian ‘white tiama’ Entandrophragma angolense
AU - Happi, Gervais Mouthé
AU - Wouamba, Steven Collins N.
AU - Ismail, Mohamed
AU - Kouam, Simeon Fogue
AU - Frese, Marcel
AU - Lenta, Bruno Ndjakou
AU - Sewald, Norbert
PY - 2020/4
Y1 - 2020/4
N2 - Two new ergostane-type steroids named tiamenones A and B (1–2) were isolated from the bark of Entandrophragma angolense (Meliaceae) along with ten known compounds identified as 20S-hydroxy-4,6,24(28)-ergostatrien-3-one (3), 3β,7α,20β-trihydroxyergosta-5,24(28)-diene (4), 3β,5α-dihydroxyergosta-7,22-diene (5), stigmasterol, β-sitosterol, β-amyrin, oleanolic acid, asperphenamate, sucrose and daucosterol. The structures of the isolated compounds have been established using NMR spectroscopic and mass spectrometric analyses. The assignment of relative and absolute configurations of compound 1 was achieved by a NOESY experiment and comparison of its NMR data with those of known compound reported in literature. Compounds 1–3, β-amyrin and asperphenamate were evaluated for their antibacterial potencies against five bacterial model strains viz. Escherichia coli DSMZ 1058, Pseudomonas agarici DSMZ 11810, Bacillus subtilis DSMZ 704, Micrococcus luteus DMSZ 1605 and Staphylococcus warneri DSMZ 20036 and their cytotoxicity on two cell lines KB3-1 and HT-29. No potencies were exhibited by the tested compounds even at the highest concentration of 0.5 mg/mL. Compounds 1–3 were found to be potential HIV-1 inhibitors based on their molecular docking analyses.
AB - Two new ergostane-type steroids named tiamenones A and B (1–2) were isolated from the bark of Entandrophragma angolense (Meliaceae) along with ten known compounds identified as 20S-hydroxy-4,6,24(28)-ergostatrien-3-one (3), 3β,7α,20β-trihydroxyergosta-5,24(28)-diene (4), 3β,5α-dihydroxyergosta-7,22-diene (5), stigmasterol, β-sitosterol, β-amyrin, oleanolic acid, asperphenamate, sucrose and daucosterol. The structures of the isolated compounds have been established using NMR spectroscopic and mass spectrometric analyses. The assignment of relative and absolute configurations of compound 1 was achieved by a NOESY experiment and comparison of its NMR data with those of known compound reported in literature. Compounds 1–3, β-amyrin and asperphenamate were evaluated for their antibacterial potencies against five bacterial model strains viz. Escherichia coli DSMZ 1058, Pseudomonas agarici DSMZ 11810, Bacillus subtilis DSMZ 704, Micrococcus luteus DMSZ 1605 and Staphylococcus warneri DSMZ 20036 and their cytotoxicity on two cell lines KB3-1 and HT-29. No potencies were exhibited by the tested compounds even at the highest concentration of 0.5 mg/mL. Compounds 1–3 were found to be potential HIV-1 inhibitors based on their molecular docking analyses.
KW - Antibacterial
KW - Cytotoxicity
KW - Entandrophragma angolense
KW - HIV-1 inhibitors
KW - Meliaceae
KW - Tiamenones A and B
U2 - 10.1016/j.steroids.2020.108584
DO - 10.1016/j.steroids.2020.108584
M3 - Article
C2 - 31982421
AN - SCOPUS:85079198680
SN - 0039-128X
VL - 156
JO - Steroids
JF - Steroids
M1 - 108584
ER -