Unknown

Dataset Information

0

Stereocalpin B, a New Cyclic Depsipeptide from the Antarctic Lichen Ramalina terebrata.


ABSTRACT: Stereocalpin B, a new cyclic depsipeptide (1), and a new dibenzofuran derivative (3), were isolated from the Antarctic lichen, Ramalina terebrata (Ramalinaceae), along with a known cyclic depsipeptide (2). The structures of new compounds were characterized by comprehensive spectrometric analyses; high-resolution fast atom bombardment mass spectrometry (HR-FABMS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). Stereocalpin B (1) existed in a rotameric equilibrium, which was confirmed using nuclear Overhauser effect spectroscopy (NOESY)/exchange spectroscopy (EXSY) spectrum. Absolute configurations of the amino acid units in 1 were assigned using the advanced Marfey's method and subsequent NOESY analysis of the 5-hydroxy-2,4-dimethyl-3-oxo-decanoic acid residue confirmed the complete stereochemistry of 1. Compounds 1-3 exhibited moderate antimicrobial activities against E. coli, with the IC50 values ranging from 18-30 μg/mL. Compound 2 exhibited cell growth inhibition against HCT116 cell lines, with the IC50 value of 20 ± 1.20 μM, and compounds 1 and 2 also showed potent anti-inflammatory activities against lipopolysaccharide (LPS)-induced RAW264.7 macrophages with the IC50 values ranging from 5-7 μM.

SUBMITTER: Lee S 

PROVIDER: S-EPMC8880677 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Stereocalpin B, a New Cyclic Depsipeptide from the Antarctic Lichen <i>Ramalina terebrata</i>.

Lee Seulah S   Jeong Se Yun SY   Nguyen Dieu Linh DL   So Jae Eun JE   Kim Ki Hyun KH   Kim Ji Hee JH   Han Se Jong SJ   Suh Sung-Suk SS   Lee Jun Hyuck JH   Youn Ui Joung UJ  

Metabolites 20220203 2


Stereocalpin B, a new cyclic depsipeptide (<b>1</b>), and a new dibenzofuran derivative (<b>3</b>), were isolated from the Antarctic lichen, <i>Ramalina terebrata</i> (Ramalinaceae), along with a known cyclic depsipeptide (<b>2</b>). The structures of new compounds were characterized by comprehensive spectrometric analyses; high-resolution fast atom bombardment mass spectrometry (HR-FABMS) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). Stereocalpin B (<b>1</b>) existed in a rotam  ...[more]

Similar Datasets

| S-EPMC2566935 | biostudies-literature
| S-EPMC5992360 | biostudies-literature
| S-EPMC5392050 | biostudies-literature
| S-EPMC4206788 | biostudies-literature
| S-EPMC6918221 | biostudies-literature
| S-EPMC3002467 | biostudies-literature
| S-EPMC6331918 | biostudies-literature
| S-EPMC6681199 | biostudies-literature
| S-EPMC9000585 | biostudies-literature
| S-EPMC10195087 | biostudies-literature