Format

Send to

Choose Destination
Fitoterapia. 2019 Apr;134:422-428. doi: 10.1016/j.fitote.2019.02.018. Epub 2019 Mar 8.

Isolation of yeast Ca2+ signal transduction inhibitors from the Early Cretaceous Burmese amber.

Author information

1
Graduate School of Agriculture, Iwate University, Morioka, Iwate 020-8550, Japan.
2
RIKEN Center for Sustainable Resource Science, Wako, Saitama 351-0198, Japan.
3
Iwate Biotechnology Research Center, Kitakami, Iwate 024-0003, Japan.
4
Graduate School of Agriculture, Iwate University, Morioka, Iwate 020-8550, Japan. Electronic address: kimurak@iwate-u.ac.jp.

Abstract

Two kinds of biologically active compounds were isolated from the MeOH extract of the Early Cretaceous Burmese amber [99 million years ago (Ma)], which is older than the K-Pg boundary (65 Ma). These compounds had inhibitory activity against the hypersensitive mutant yeast strain (zds1∆ erg3∆ pdr1∆ pdr3∆) with respect to Ca2+ signal transduction. They were identified as 16,17-bisnordehydroabietic acid (1) and 16,17-bisnorcallitrisic acid (2), respectively, on the basis of spectral analyses including HREIMS, 1D, and 2D NMR. Both have faint growth restoring activities around the clear inhibition zone against the mutant yeast on the 0.31-0.16 μg/spot. This is the first report of direct structural elucidation of 1 and 2 and the biologically active compounds derived from Burmese amber.

KEYWORDS:

16,17-Bisnorcallitrisic acid; 16,17-Bisnordehydroabietic acid; Biomarker; Burmese amber; Saccharomyces cerevisiae

PMID:
30858047
DOI:
10.1016/j.fitote.2019.02.018
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center