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1.
Sci Rep ; 9(1): 2248, 2019 02 19.
Article in English | MEDLINE | ID: mdl-30783134

ABSTRACT

Seven pairs of new oxygenated aplysinopsin-type enantiomers, (+)- and (-)-oxoaplysinopsins A‒G (1‒7), two new bromotyrosine-derived alkaloids, subereamollines C and D (18 and 19), together with ten known compounds (8‒17) were isolated from the Xisha Islands sponge Fascaplysinopsis reticulata. The planar structures were determined by extensive NMR and MS spectroscopic data. Each of the optically pure enantiomers was achieved by chiral HPLC separation. The absolute configurations were assigned by the quantum chemical calculation methods. Compound 19 showed cytotoxicity against Jurkat cell lines with IC50 value of 0.88 µM. Compounds 2, 16 and 17 showed tyrosine phosphatase 1B (PTP1B) inhibition activity with IC50 value ranging from 7.67 to 26.5 µM, stronger than the positive control of acarbose and 1-deoxynojirimycin. A structural activity relationship for the aplysinopsin-type enantiomers were observed in PTP1B inhibition activity of 2 and cytotoxicity of 3 that the dextrorotary (+)-2 and (+)-3 showed stronger activity than the levorotary (-)-2 and (-)-3.


Subject(s)
Alkaloids , Aquatic Organisms/chemistry , Enzyme Inhibitors , Porifera/chemistry , Protein Tyrosine Phosphatase, Non-Receptor Type 1/antagonists & inhibitors , A549 Cells , Alkaloids/chemistry , Alkaloids/isolation & purification , Alkaloids/pharmacology , Animals , China , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/isolation & purification , Enzyme Inhibitors/pharmacology , Humans , Protein Tyrosine Phosphatase, Non-Receptor Type 1/chemistry , Tryptophan/analogs & derivatives , Tryptophan/chemistry , Tryptophan/isolation & purification , Tryptophan/pharmacology , Tyrosine/analogs & derivatives , Tyrosine/chemistry , Tyrosine/isolation & purification , Tyrosine/pharmacology
2.
Nat Prod Commun ; 12(1): 19-20, 2017 Jan.
Article in English | MEDLINE | ID: mdl-30549815

ABSTRACT

A new imidazole sulfate (1) and three known compounds (2-4) were isolated from the sponge Dercitus (Halinastra)japonensis. The structure of compound I was elucidated by spectroscopic means. Compound 2 was confirmed to show anti-HIV activity, whereas compounds 1, 3 and 4 were inactive.


Subject(s)
Anti-HIV Agents/pharmacology , Imidazoles/chemistry , Porifera/chemistry , Animals , Cell Line , HIV/drug effects , Humans , Imidazoles/analysis , Imidazoles/pharmacology , Molecular Structure , Spectrometry, Mass, Electrospray Ionization
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