scholarly journals Pairing collectivity in medium-mass neutron-rich nuclei near drip-line

2007 ◽  
Vol 788 (1-4) ◽  
pp. 307-315 ◽  
Author(s):  
M. Matsuo ◽  
Y. Serizawa ◽  
K. Mizuyama
Keyword(s):  
1998 ◽  
Vol 07 (03) ◽  
pp. 389-403 ◽  
Author(s):  
M. Rajasekaran ◽  
Mamta Aggarwal

Neutron rich nuclei in the medium mass region with thermal excitation and rotational energies, are investigated. A macroscopic-microscopic approach to reproduce the ground state separation energy combined with statistical approach for the excited rotating nuclei yields good results. Shell effects and shape transitions due to rotation alter the boundary of the drip line considerably at low temperatures and with increasing temperature the drip line is lowered to less neutron rich nuclei.


1995 ◽  
Vol 588 (1) ◽  
pp. c171-c177 ◽  
Author(s):  
B. Blank ◽  
S. Andriamonje ◽  
T. Brohm ◽  
S. Czajkowski ◽  
E. Davi ◽  
...  

2005 ◽  
Vol 71 (6) ◽  
Author(s):  
Masayuki Matsuo ◽  
Kazuhito Mizuyama ◽  
Yasuyoshi Serizawa

Marine Drugs ◽  
2021 ◽  
Vol 19 (7) ◽  
pp. 378
Author(s):  
Van-Tuyen Le ◽  
Samuel Bertrand ◽  
Thibaut Robiou du Pont ◽  
Fabrice Fleury ◽  
Nathalie Caroff ◽  
...  

Very little is known about chemical interactions between fungi and their mollusc host within marine environments. Here, we investigated the metabolome of a Penicillium restrictum MMS417 strain isolated from the blue mussel Mytilus edulis collected on the Loire estuary, France. Following the OSMAC approach with the use of 14 culture media, the effect of salinity and of a mussel-derived medium on the metabolic expression were analysed using HPLC-UV/DAD-HRMS/MS. An untargeted metabolomics study was performed using principal component analysis (PCA), orthogonal projection to latent structure discriminant analysis (O-PLSDA) and molecular networking (MN). It highlighted some compounds belonging to sterols, macrolides and pyran-2-ones, which were specifically induced in marine conditions. In particular, a high chemical diversity of pyran-2-ones was found to be related to the presence of mussel extract in the culture medium. Mass spectrometry (MS)- and UV-guided purification resulted in the isolation of five new natural fungal pyran-2-one derivatives—5,6-dihydro-6S-hydroxymethyl-4-methoxy-2H-pyran-2-one (1), (6S, 1’R, 2’S)-LL-P880β (3), 5,6-dihydro-4-methoxy-6S-(1’S, 2’S-dihydroxy pent-3’(E)-enyl)-2H-pyran-2-one (4), 4-methoxy-6-(1’R, 2’S-dihydroxy pent-3’(E)-enyl)-2H-pyran-2-one (6) and 4-methoxy-2H-pyran-2-one (7)—together with the known (6S, 1’S, 2’S)-LL-P880β (2), (1’R, 2’S)-LL-P880γ (5), 5,6-dihydro-4-methoxy-2H-pyran-2-one (8), (6S, 1’S, 2’R)-LL-P880β (9), (6S, 1’S)-pestalotin (10), 1’R-dehydropestalotin (11) and 6-pentyl-4-methoxy-2H-pyran-2-one (12) from the mussel-derived culture medium extract. The structures of 1-12 were determined by 1D- and 2D-MMR experiments as well as high-resolution tandem MS, ECD and DP4 calculations. Some of these compounds were evaluated for their cytotoxic, antibacterial, antileishmanial and in-silico PTP1B inhibitory activities. These results illustrate the utility in using host-derived media for the discovery of new natural products.


2020 ◽  
Vol 1643 ◽  
pp. 012107
Author(s):  
L. Stuhl ◽  
M. Sasano ◽  
J. Gao ◽  
Y. Hirai ◽  
K. Yako ◽  
...  
Keyword(s):  

2020 ◽  
Vol 101 (3) ◽  
Author(s):  
N. Itagaki ◽  
A. V. Afanasjev ◽  
D. Ray
Keyword(s):  

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