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1.

001-es BibID:BIBFORM080474
Első szerző:Ariantari, Ni P.
Cím:Expanding the chemical diversity of an endophytic fungus Bulgaria inquinans, an ascomycete associated with mistletoe, through an OSMAC approach / Ni P. Ariantari, Georgios Daletos, Attila Mándi, Tibor Kurtán, Werner E. G. Müller, Wenhan Lin, Elena Ancheeva, Peter Proksch
Dátum:2019
ISSN:2046-2069 2046-2069
Megjegyzések:An endophytic fungus Bulgaria inquinans (isolate MSp3-1), isolated from mistletoe (Viscum album), was subjected to fermentation on solid Czapek medium. Chromatographic workup of the crude EtOAc extract yielded five new natural products (1?5). Subsequent application of the "One Strain, Many Compounds" (OSMAC) strategy on this strain by the addition of a mixture of salts (MgSO4, NaNO3 and NaCl) to solid Czapek medium induced the accumulation of nine additional new secondary metabolites (6?13, 16), with most of them (8, 10?12) not detectable in cultures lacking the salt mixture. The structures of the new compounds were established on the basis of the 1D/2D NMR and HRESIMS data. The TDDFT-ECD method was applied to determine the absolute configurations of the new compounds 1, 4 and 6 as well as of the previously reported bulgarialactone B (14), for which the absolute configuration was unknown so far. The modified Mosher's method was performed to assign the absolute configurations of 12 and 13. TDDFT-ECD analysis also allowed determining the absolute configuration of (+)-epicocconone, which had an enantiomeric absolute configuration in the tricyclic moiety compared to that of bulgarialactone B (14). All the isolated metabolites were evaluated for their cytotoxic activity. Compound 2 was found to possess strong cytotoxic activity against the murine lymphoma cell line L5178Y with an IC50 value of 1.8 mM, while the remaining metabolites were shown to be inactive.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:RSC Advances. - 9 : 43 (2019), p. 25119-25132. -
További szerzők:Daletos, Georgios Mándi Attila (1981-) (vegyész, német szakfordító) Kurtán Tibor (1973-) (vegyész, angol szakfordító) Müller, Werner E. G. Lin, Wen Han Ancheeva, Elena Proksch, Peter
Pályázati támogatás:NKFI K120181
Egyéb
NKFI PD121020
Egyéb
GINOP-2.3.2-15-2016-00008
GINOP
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2.

001-es BibID:BIBFORM069592
Első szerző:Elnaggar, Mohamed S.
Cím:Hydroquinone derivatives from the marine-derived fungus Gliomastix sp. / Mohamed S. Elnaggar, Weaam Ebrahim, Attila Mandi, Tibor Kurtan, Werner E. G. Müller, Rainer Kalscheuer, Abdelnasser Singab, Wenhan Lin, Zhen Liu, Peter Proksch
Dátum:2017
ISSN:2046-2069
Megjegyzések:Eight new hydroquinone derivatives, gliomastins A-D (1-4), 9-O-methylgliomastin C (5), acremonin A 1-O-?-D-glucopyranoside (6), gliomastin E 1-O-?-D-glucopyranoside (7), and 6'-O-acetyl-isohomoarbutin (8), together with seven known analogues were isolated from the marine-derived fungus Gliomastix sp. Their structures were elucidated by extensive spectroscopic analysis including 1D and 2D NMR measurements aided by DFT NMR calculations as well as MS data. TDDFT-ECD and OR calculations were performed to determine the absolute configurations of 1 and the aglycones of 6 and 7. Compound 1 features a novel skeleton, biogenetically derived from a Diels?Alder reaction between derivatives of 11 and 13. Compound 2 represents a rare sulfur-containing alkaloid derived from the known hydroquinone 13. Compounds 1, 10 and 12 showed strong cytotoxicity against the L5178Y mouse lymphoma cell line with IC50 values of 1.8, 1.0 and 1.1 ?M, respectively. Compound 3 exhibited moderate antitubercular activity against Mycobacterium tuberculosis with a MIC value of 12.5 ?M.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:RSC Advances. - 7 : 49 (2017), p. 30640-30649. -
További szerzők:Ebrahim, Weaam Mándi Attila (1981-) (vegyész, német szakfordító) Kurtán Tibor (1973-) (vegyész, angol szakfordító) Müller, Werner E. G. Kalscheuer, Rainer Singab, Abdelnasser Lin, Wen Han Liu, Zhen Proksch, Peter
Pályázati támogatás:NKFI K120181
Egyéb
NKFI PD121020
Egyéb
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3.

001-es BibID:BIBFORM067037
Első szerző:Liu, Yang
Cím:Daldinone derivatives from the mangrove-derived endophytic fungus Annulohypoxylon sp. / Yang Liu, Fabian Stuhldreier, Tibor Kurtán, Attila Mándi, Sathishkumar Arumugam, Wenhan Lin, Björn Stork, Sebastian Wesselborg, Horst Weber, Birgit Henrich, Georgios Daletos, Peter Proksch
Dátum:2017
ISSN:2046-2069
Megjegyzések:Two new benzo[j]fluoranthene metabolites, daldinones H, J (1 and 3), and the likewise undescribed artefact, daldinone I (2), along with six known compounds (4-9) were isolated from the endophytic fungus Annulohypoxylon sp. that was obtained from the Mangrove plant Rhizophora racemosa collected in Cameroon. The structures of the new compounds were elucidated by 1D and 2D NMR as well as by HRESIMS and ECD spectra analysis. Co-cultivation of this fungus with the actinomycetes Streptomyces lividans or with Streptomyces coelicolor resulted in an up to 38-fold increase of 1-hydroxy-8-methoxynaphthalene (9), while no significant induction was detected when the fungus was co-cultivated either with Bacillus subtilis or with Bacillus cereus. Compound 2 exhibited strong to moderate cytotoxicity against Ramos and Jurkat J16 cells with IC50 values of 6.6 and 14.1 ?M, respectively. Mechanistic studies indicated that compound 2 induces apoptotic cell death caused by induction of intrinsic apoptosis. Moreover, 2 potently blocks autophagy, a potential pro-survival pathway for cancer cells. Feeding experiments with 1,8-dihydroxynaphthalene (DHN) led to an enhanced accumulation of daldinone B (6), which supported the proposed biogenetic pathway.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:RSC Advances. - 7 : 9 (2017), p. 5381-5393. -
További szerzők:Stuhldreier, Fabian Kurtán Tibor (1973-) (vegyész, angol szakfordító) Mándi Attila (1981-) (vegyész, német szakfordító) Arumugam, Sathishkumar Lin, Wen Han Stork, Björn Wesselborg, Sebastian Weber, Horst Henrich, Birgit Daletos, Georgios Proksch, Peter
Pályázati támogatás:K105871
OTKA
NIIFI 10038
Egyéb
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4.

001-es BibID:BIBFORM088420
Első szerző:Mándi Attila (vegyész, német szakfordító)
Cím:TDDFT-ECD and DFT-NMR studies of thaigranatins A-E and granatumin L isolated from Xylocarpus granatum / Attila Mándi, Jun Wu, Tibor Kurtán
Dátum:2020
ISSN:2046-2069 2046-2069
Megjegyzések:TDDFT-ECD calcns. were utilized to explain the mirror image or different ECD spectra of previously reported homochiral natural products thaigranatins A-E and granatumin L, the simple comparison of which would result in a wrong stereochem. conclusion. The configurational assignment was confirmed independently and geometrical parameters of the chromophores governing the ECD spectra were identified in the structurally related natural products by analyzing the ECD spectra and geometries of the low-energy computed conformers obtained by different methods. Different conformations of the furan-2-yl-?-lactone subunit were found responsible for the mirror image ECD spectra of the homochiral thaigranatins C-E. Two DFT 13C NMR chem. shift calcn. methods and DP4+ anal. were performed on the C-6 epimers of thaigranatin D, which together with the ECD calcn., could det. the abs. configuration of C-6 as (R).
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:RSC Advances. - 10 : 53 (2020), p. 32216-32224. -
További szerzők:Wu, Jun Kurtán Tibor (1973-) (vegyész, angol szakfordító)
Pályázati támogatás:GINOP-2.3.2-15-2016-00008
GINOP
NKFI K120181
Egyéb
ÚNKP-19-4
Egyéb
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5.

001-es BibID:BIBFORM076659
Első szerző:Moussa, Mariam
Cím:Co-culture of the fungus Fusarium tricinctum with Streptomyces lividans induces production of cryptic naphthoquinone dimers / Mariam Moussa, Weaam Ebrahim, Michele Bonus, Holger Gohlke, Attila Mandi, Tibor Kurtan, Rudolf Hartmann, Rainer Kalscheuer, Wenhan Lin, Zhen Liu, Peter Proksch
Dátum:2019
ISSN:2046-2069 2046-2069
Megjegyzések:Co-cultivation of the endophytic fungus Fusarium tricinctum with Streptomyces lividans on solid rice medium led to the production of four new naphthoquinone dimers, fusatricinones A-D (1-4), and a new lateropyrone derivative, dihydrolateropyrone (5), that were not detected in axenic fungal controls. In addition, four known cryptic compounds, zearalenone (7), (_)-citreoisocoumarin (8), macrocarpon C (9) and 7-hydroxy-2-(2-hydroxypropyl)-5-methylchromone (10), that were likewise undetectable in extracts from fungal controls, were obtained from the co-culture extracts. The known antibiotically active compound lateropyrone (6), the depsipeptides enniatins B (11), B1 (12) and A1 (13), and the lipopeptide fusaristatin A (14), that were present in axenic fungal controls and in co-culture extracts, were upregulated in the latter. The structures of the new compounds were elucidated by 1D and 2D NMR spectra as well as by HRESIMS data. The relative and absolute configuration of dihydrolateropyrone (5) was elucidated by TDDFT-ECD calculations.
Tárgyszavak:Természettudományok Földtudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:RSC Advances. - 9 : 3 (2019), p. 1491-1500. -
További szerzők:Ebrahim, Weaam Bonus, Michele Gohlke, Holger Mándi Attila (1981-) (vegyész, német szakfordító) Kurtán Tibor (1973-) (vegyész, angol szakfordító) Hartmann, Rudolf Kalscheuer, Rainer Lin, Wen Han Liu, Zhen Proksch, Peter
Pályázati támogatás:NKFI K120181
Egyéb
NKFI PD121020
Egyéb
Internet cím:Szerző által megadott URL
DOI
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6.

001-es BibID:BIBFORM080667
Első szerző:Tran-Cong, Nam Michael
Cím:Induction of cryptic metabolites of the endophytic fungus Trichocladium sp. through OSMAC and co-cultivation / Nam Michael Tran-Cong, Attila Mándi, Tibor Kurtán, Werner E. G. Müller, Rainer Kalscheuer, Wenhan Lin, Zhen Liu, Peter Proksch
Dátum:2019
ISSN:2046-2069 2046-2069
Megjegyzések:The endophytic fungus Trichocladium sp. isolated from roots of Houttuynia cordata was cultured on solid rice medium, yielding a new amidepsine derivative (1) and a new reduced spiro azaphilone derivative (3) together with eight known compounds (4-11). Co-cultivation of Trichocladium sp. with Bacillus subtilis resulted in induction of a further new compound (2) and a 10-fold increase of 11 compared to the axenic fungal culture. Moreover, when the fungus was cultivated on peas instead of rice, a new sesquiterpene derivative (13) and two known compounds (12 and 14) were obtained. Addition of 2% tryptophan to rice medium led to the isolation of a new bismacrolactone (15). The structures of the new compounds were elucidated by HRESIMS, 1D and 2D NMR as well as by comparison with the literature. A combination of TDDFT-ECD, TDDFT-SOR, DFT-VCD and DFT-NMR calculations were applied to determine the absolute and relative configurations of 13 and 15. Compounds 7, 11 and 15 exhibited strong cytotoxicity against the L5178Y mouse lymphoma cell line with IC50 values of 0.3, 0.5 and 0.2 mM, respectively.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:RSC Advances. - 9 : 47 (2019), p. 27279-27288. -
További szerzők:Mándi Attila (1981-) (vegyész, német szakfordító) Kurtán Tibor (1973-) (vegyész, angol szakfordító) Müller, Werner E. G. Kalscheuer, Rainer Lin, Wen Han Liu, Zhen Proksch, Peter
Pályázati támogatás:GINOP-2.3.2-15-2016-00008
GINOP
NKFI K120181
Egyéb
NKFI PD121020
Egyéb
Internet cím:Szerző által megadott URL
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7.

001-es BibID:BIBFORM058850
Első szerző:Zhang, Peng
Cím:Structure, absolute configuration, and conformational study of resorcylic acid derivatives and related congeners from the fungus Penicillium brocae / Peng Zhang, Ling-Hong Meng, Attila Mandi, Xiao-Ming Li, Tibor Kurtan, Bin-Gui Wang
Dátum:2015
ISSN:2046-2069
Megjegyzések:In addition to three known resorcylic acid derivatives of the (14 R) series (1-3), six new compounds including one new resorcylic acid derivative (13-hydroxydihydroresorcylide, 4) and five new loop-opened resorcylic acid-related congeners including brocapyrone A (5) and brocaketones A?D (6?9), were isolated and identified from the culture extract of a marine mangrove-derived endophytic fungus Penicillium brocae MA-192. Conformational analysis and TDDFT-ECD calculations of 1, 3, and 4 were carried out to confirm the (14 R) absolute configuration and identify the solution conformers and factors that govern the correlation between stereochemistry and signs of the characteristic ECD bands. The single crystal X-ray of 3 and 5 allowed applying the solid-state TDDFT-ECD approach for 3 to compare the structures of solution and solid-state conformers and correlate the n-?* ECD transition of 5 with the helicity and absolute configuration of the dihydroisocoumarin moiety. All compounds were evaluated for antioxidant activity against DPPH and ABTS radicals.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Royal Society of Chemistry Advances. - 5 : 50 (2015), p. 39870-39877. -
További szerzők:Meng, Ling-Hong Mándi Attila (1981-) (vegyész, német szakfordító) Li, Xiao-Ming Kurtán Tibor (1973-) (vegyész, angol szakfordító) Wang, Bin-Gui
Pályázati támogatás:K105871
OTKA
NIIFI 10038
Egyéb
Internet cím:Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
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