Laatsch, Hartmut G.

[["dc.bibliographiccitation.firstpage","1139"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Analytical and Bioanalytical Chemistry"],["dc.bibliographiccitation.lastpage","1147"],["dc.bibliographiccitation.volume","390"],["dc.contributor.author","Fitzner, Ansgar"],["dc.contributor.author","Frauendorf, Holm"],["dc.contributor.author","Laatsch, Hartmut"],["dc.contributor.author","Diederichsen, Ulf"],["dc.date.accessioned","2018-11-07T11:18:24Z"],["dc.date.available","2018-11-07T11:18:24Z"],["dc.date.issued","2008"],["dc.description.abstract","Formation and fragmentation of recognition complexes between trioxacarcin A and various DNA sequences were examined by temperature-dependent UV and CD spectroscopy, HPLC analysis, and ESI mass spectrometry with regard to reaction conditions, intermediates, products, mechanism, and sequence specificity. Cleavage of the trioxacarcin-DNA complexes provided the natural product gutingimycin by guanine abstraction. The resulting DNA with an abasic site was further cleaved into a DNA fragment with a furanyl unit at the 3'-end and an oligonucleotide with a phosphorylated 5'-end."],["dc.identifier.doi","10.1007/s00216-007-1737-6"],["dc.identifier.isi","000252918100017"],["dc.identifier.pmid","18210096"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3482"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/55029"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.publisher.place","Heidelberg"],["dc.relation.issn","1618-2642"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Formation of gutingimycin: analytical investigation of trioxacarcin A-mediated alkylation of dsDNA"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3109"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Marine Drugs"],["dc.bibliographiccitation.lastpage","3123"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Abou-El-Wafa, Ghada S. E."],["dc.contributor.author","Shaaban, Mohamed"],["dc.contributor.author","Shaaban, Khaled Attia"],["dc.contributor.author","El-Naggar, Mohamed E. E."],["dc.contributor.author","Maier, Armin"],["dc.contributor.author","Fiebig, Heinz-Herbert"],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2018-11-07T09:20:08Z"],["dc.date.available","2018-11-07T09:20:08Z"],["dc.date.issued","2013"],["dc.description.abstract","Two new diterpenoids, pachydictyol B (1a/1b) and C (2), were isolated from the dichloromethane extract of the marine brown alga, Dictyota dichotoma, collected from the Red Sea coast of Egypt, along with the known metabolites, pachydictyol A (3a), dictyol E (4), cis-africanan-1-ol (5a), fucosterol (6), tetrahydrothiophen-1,1-dioxide and poly--hydroxybutyric acid. GC-MS analysis of the nonpolar fractions also indicated the presence of -bourbonene and nonanal, along with three hydrocarbons and five fatty acids or their simple derivatives, respectively. GC-MS analysis of the unsaponifiable algal petroleum ether extract revealed the presence of a further eight compounds, among them 2,2,6,7-tetramethyl-10-oxatricyclo[4.3.0.1(1,7)]decan-5-one (7), N-(4-bromo-n-butyl)-piperidin-2-one (8) and tert-hexadecanethiol. Structures 1-6 were assigned by 1D and 2D NMR, mass spectra (EI, CI, HREI and HRESI) and by comparison with data from related structures. The crude algal extract was potently active against the breast carcinoma tumor cell line, MCF7 (IC50 = 0.6 mu g mL(-1)); pachydictyol B (1a) and dictyol E (4) showed weak antimicrobial properties, and the other compounds were inactive. Pachydictyols B (1a) and C (2) demonstrated a weak and unselective cytotoxicity against twelve human tumor cell lines with a mean IC50 of >30.0 mu M."],["dc.description.sponsorship","German Academic Exchange Service (DAAD)"],["dc.identifier.doi","10.3390/md11093109"],["dc.identifier.isi","000328621900001"],["dc.identifier.pmid","23975221"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10028"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28807"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Mdpi Ag"],["dc.relation.issn","1660-3397"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Pachydictyols B and C: New Diterpenes from Dictyota dichotoma Hudson"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","269"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Natural Products and Bioprospecting"],["dc.bibliographiccitation.lastpage","273"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Feussi Tala, Michel"],["dc.contributor.author","Qin, Jianchun"],["dc.contributor.author","Ndongo, Joseph T."],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2019-07-09T11:44:19Z"],["dc.date.available","2019-07-09T11:44:19Z"],["dc.date.issued","2017"],["dc.description.abstract","In the 1H NMR-guided fractionation of extracts from the edible mushroom Lactarius deliciosus, two new azulene-type sesquiterpenoids, 7-isopropenyl-4-methyl-azulene-1-carboxylic acid (1) and 15-hydroxy-3,6-dihydrolactarazulene (2), together with seven known compounds were characterized. Their structures were determined on basis of spectroscopic evidence, as well as by comparing with literature data. Amongst the known metabolites, the 13C NMR assignment of 15-hydroxy-6,7-dihydrolactarazulene (3) is reported here for the first time. Moreover, 7-acetyl-4-methylazulene-1-carbaldehyde (5) displayed a moderate antibacterial activity against Staphylococcus aureus. Digital image of L. deliciosus. Retrieved March 17, 2017 from https://upload.wikimedia.org/wikipedia/commons/e/e3/Lactarius_deliciosus_1_(1).jpg ."],["dc.identifier.doi","10.1007/s13659-017-0130-1"],["dc.identifier.pmid","28493207"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/14715"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/58992"],["dc.notes.intern","Merged from goescholar"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","New Azulene-Type Sesquiterpenoids from the Fruiting Bodies of Lactarius deliciosus"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1373"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","World Journal of Microbiology and Biotechnology"],["dc.bibliographiccitation.lastpage","1380"],["dc.bibliographiccitation.volume","27"],["dc.contributor.author","Ruanpanun, Pornthip"],["dc.contributor.author","Laatsch, Hartmut"],["dc.contributor.author","Tangchitsomkid, Nuchanart"],["dc.contributor.author","Lumyong, Saisamorn"],["dc.date.accessioned","2018-11-07T08:55:55Z"],["dc.date.available","2018-11-07T08:55:55Z"],["dc.date.issued","2011"],["dc.description.abstract","An isolate of the actinomycete, Streptomyces sp. CMU-MH021 produced secondary metabolites that inhibited egg hatch and increased juvenile mortality of the root-knot nematode Meloidogyne incognita in vitro. 16S rDNA gene sequencing showed that the isolate sequence was 99% identical to Streptomyces roseoverticillatus. The culture filtrates form different culture media were tested for nematocidal activity. The maximal activity against M. incognita was obtained by using modified basal (MB) medium. The nematicidal assay-directed fractionation of the culture broth delivered fervenulin (1) and isocoumarin (2). Fervenulin, a low molecular weight compound, shows a broad range of biological activities. However, nematicidal activity of fervenulin was not previously reported. The nematicidal activity of fervenulin (1) was assessed using the broth microdilution technique. The lowest minimum inhibitory concentrations (MICs) of the compound against egg hatch of M. incognita was 30 mu g/ml and juvenile mortality of M. incognita increasing was observed at 120 mu g/ml. Moreover, at the concentration of 250 mu g/ml fervenulin (1) showed killing effect on second-stage nematode juveniles of M. incognita up to 100% after incubation for 96 h. Isocoumarin (2), another bioactive compound produced by Streptomyces sp. CMU-MH021, showed weak nematicidal activity with M. incognita."],["dc.description.sponsorship","Royal Golden Jubilee Ph. D. Program [PHD/0064/2549]"],["dc.identifier.doi","10.1007/s11274-010-0588-z"],["dc.identifier.isi","000290320900012"],["dc.identifier.pmid","21841897"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/6819"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/23023"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0959-3993"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Nematicidal activity of fervenulin isolated from a nematicidal actinomycete, Streptomyces sp. CMU-MH021, on Meloidogyne incognita"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","35"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Marine Drugs"],["dc.bibliographiccitation.volume","19"],["dc.contributor.author","Shaaban, Mohamed"],["dc.contributor.author","Abou-El-Wafa, Ghada S. E."],["dc.contributor.author","Golz, Christopher"],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2021-04-14T08:29:39Z"],["dc.date.available","2021-04-14T08:29:39Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.3390/md19010035"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82956"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.publisher","MDPI"],["dc.relation.eissn","1660-3397"],["dc.rights","https://creativecommons.org/licenses/by/4.0/"],["dc.title","New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","226"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Acta Pharmaceutica Sinica B"],["dc.bibliographiccitation.lastpage","235"],["dc.bibliographiccitation.volume","1"],["dc.contributor.author","Bansal, Punit"],["dc.contributor.author","Paul, Piya"],["dc.contributor.author","Nayak, Pawan G."],["dc.contributor.author","Pannakal, Steve T."],["dc.contributor.author","Zou, Jian-hua"],["dc.contributor.author","Laatsch, Hartmut"],["dc.contributor.author","Priyadarsini, K.I."],["dc.contributor.author","Unnikrishnan, M.K."],["dc.date.accessioned","2019-07-09T11:40:46Z"],["dc.date.available","2019-07-09T11:40:46Z"],["dc.date.issued","2011"],["dc.description.abstract","Six phenolic compounds namely, quercetin-3-O-rutinoside (1), 3-O-caffeoylquinic acid (2), luteolin-7-O-glucoside (3), apigenin-7-O-rutinoside (4), apigenin-7-O-β-d-glucopyranoside (5) and quercetin (6) were isolated from the whole plant of Pilea microphylla using conventional open-silica gel column chromatography and preparative HPLC. Further, these compounds were characterized by 1D, 2D NMR techniques and high-resolution LC–MS. Compounds 1–3 and 6 exhibited significant antioxidant potential in scavenging free radicals such as DPPH, ABTS and SOD with IC50 of 3.3–20.4 μmol/L. The same compounds also prevented lipid peroxidation with IC50 of 10.4–32.2 μmol/L. The compounds also significantly prevented the Fenton reagent-induced calf thymus DNA damage. Pre-treatment with compounds 1–3 and 6 in V79 cells attenuated radiation-induced formation of reactive oxygen species, lipid peroxidation, cytotoxicity and DNA damage, correlating the antioxidant activity of polyphenols with their radioprotective effects. Compounds 1, 3 and 6 significantly inhibited lipid peroxidation, presumably due to 3′,4′-catechol ortho-dihydroxy moiety in the B-ring, which has a strong affinity for phospholipid membranes. Oxidation of flavonoids, with catechol structure on B-ring, yields a fairly stable ortho-semiquinone radical by facilitating electron delocalization, which is involved in antioxidant mechanism. Hence, the flavonoid structure, number and location of hydroxyl groups together determine the antioxidant and radioprotection mechanism."],["dc.identifier.doi","10.1016/j.apsb.2011.10.006"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/11296"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/58245"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.rights","CC BY-NC-ND 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by-nc-nd/3.0"],["dc.title","Phenolic compounds isolated from Pilea microphylla prevent radiation-induced cellular DNA damage"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","561"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Parasitology Research"],["dc.bibliographiccitation.lastpage","566"],["dc.bibliographiccitation.volume","108"],["dc.contributor.author","Matasyoh, Josphat C."],["dc.contributor.author","Dittrich, Birger"],["dc.contributor.author","Schueffler, Anja"],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2018-11-07T08:58:52Z"],["dc.date.available","2018-11-07T08:58:52Z"],["dc.date.issued","2011"],["dc.description.abstract","In a screening for natural products with mosquito larvicidal activities, the endophytic fungus Podospora sp. isolated from the plant Laggera alata (Asteraceae) was conspicuous. Two xanthones, sterigmatocystin (1) and secosterigmatocystin (2), and an anthraquinone derivative (3) 13-hydroxyversicolorin B were isolated after fermentation on M(2) medium. These compounds were characterised using spectroscopic and X-ray analysis and examined against third instar larvae of Anopheles gambiae. The results demonstrated that compound 1 was the most potent one with LC(50) and LC(90) values of 13.3 and 73.5 ppm, respectively. Over 95% mortality was observed at a concentration 100 ppm after 24 h. These results compared farvourably with the commercial larvicide pylarvexA (R) that showed 100% mortality at the same concentration. Compound 3 was less potent and had an LC(50) of 294.5 ppm and over 95% mortality was achieved at a concentration of 1,000 ppm. Secosterigmatocystin (2) revealed relatively weak activity and therefore LC values were not determined."],["dc.description.sponsorship","Alexander von Humboldt Foundation (Germany)"],["dc.identifier.doi","10.1007/s00436-010-2098-1"],["dc.identifier.isi","000287520500009"],["dc.identifier.pmid","20922412"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/6627"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/23749"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0932-0113"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Larvicidal activity of metabolites from the endophytic Podospora sp against the malaria vector Anopheles gambiae"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","7641"],["dc.bibliographiccitation.issue","69"],["dc.bibliographiccitation.journal","Chemical Communications"],["dc.bibliographiccitation.lastpage","7643"],["dc.bibliographiccitation.volume","49"],["dc.contributor.author","Kenla, Timothee J. Nwemeguela"],["dc.contributor.author","Tatong, Michel D. Kongue"],["dc.contributor.author","Talontsi, Ferdinand Mouafo"],["dc.contributor.author","Dittrich, Birger"],["dc.contributor.author","Frauendorf, Holm"],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2018-11-07T09:29:42Z"],["dc.date.available","2018-11-07T09:29:42Z"],["dc.date.issued","2013"],["dc.description.abstract","Si-enterobactin (2a), a hexacoordinated complex of the siderophore enterobactin (2b) with silicon as the central atom, was isolated from an endophytic Streptomyces sp. occurring in Piper guinensis roots. The structure and absolute configuration were determined from NMR and MS data, and by X-ray diffraction. The orientation of the molecule along the pseudo-3-fold axis shows that the coordination environment of the silicon atom complexed with three bidentate ligands is Delta. We assume that 2a or related complexes may be involved in the transport of silicon in plants, diatoms, or other silicon-dependent organisms."],["dc.identifier.doi","10.1039/c3cc44437f"],["dc.identifier.isi","000322594900022"],["dc.identifier.pmid","23872808"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10196"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/31108"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Royal Soc Chemistry"],["dc.relation.issn","1364-548X"],["dc.relation.issn","1359-7345"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Si-enterobactin from the endophytic Streptomyces sp KT-S1-B5-a potential silicon transporter in Nature?"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","1824"],["dc.bibliographiccitation.journal","Frontiers in Microbiology"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Islam, Mohammad Tofazzal"],["dc.contributor.author","Laatsch, Hartmut G."],["dc.contributor.author","Tiedemann, Andreas von"],["dc.date.accessioned","2018-11-07T10:05:42Z"],["dc.date.available","2018-11-07T10:05:42Z"],["dc.date.issued","2016"],["dc.description.abstract","The release of zoospores from sporangia and motility of the released zoospores are critical in the disease cycle of the Peronosporomycetes that cause devastating diseases in plants, fishes, animals and humans. Disruption of any of these asexual life stages eliminates the possibility of pathogenesis. In the course of screening novel bioactive secondary metabolites, we found that extracts of some strains of marine Streptomyces spp. rapidly impaired motility and caused subsequent lysis of zoospores of the grapevine downy mildew pathogen Plasmopara viticola at 10 mu g/ml. We tested a number of secondary metabolites previously isolated from these strains and found that macrotetrolide antibiotics such as nonactin, monactin, dinactin and trinactin, and nactic acids such as (+)-nonactic acid, (+)-homonactic acid, nonactic acid methyl ester, homonactic acid methyl ester, bonactin and feigrisolide C impaired motility and caused subsequent lysis of P. viticola zoospores in a dose-and time-dependent manners with dinactin being the most active compound (MIC 0.3 mu g/ml). A cation channel-forming compound, gramicidin, and a carrier of monovalent cations, nigericin also showed similar biological activities. Among all 12 compounds tested, gramicidin most potently arrested the motility of zoospores at concentrations starting from 0.1 mu g/ml. All macrotetrolide antibiotics also displayed similar motility impairing activities against P. viticola, Phytophthora capsici, and Aphanomyces cochlioides zoospores indicating non-specific biological effects of these compounds toward peronosporomyctes. Furthermore, macrotetrolide antibiotics and gramicidin also markedly suppressed the release of zoospores from sporangia of P viticola in a dose-dependent manner. As macrotetrolide antibiotics and gramicidin are known as enhancers of mitochondrial ATPase activity, inhibition of zoosporogenesis and motility of zoospores by these compounds are likely linked with hydrolysis of ATP through enhanced ATPase activity in mitochondria. This is the first report on motility inhibitory and lytic activities of macrotetrolide antibiotics and nactic acids against the zoospores of peronosporomycete phytopathogens."],["dc.description.sponsorship","Alexander von Humboldt Foundation; World Bank [2071]"],["dc.identifier.doi","10.3389/fmicb.2016.01824"],["dc.identifier.isi","000388755900001"],["dc.identifier.pmid","27917156"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/14056"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/38951"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","1664-302X"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0/"],["dc.title","Inhibitory Effects of Macrotetrolides from Streptomyces spp. On Zoosporogenesis and Motility of Peronosporomycete Zoospores Are Likely Linked with Enhanced ATPase Activity in Mitochondria"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5409"],["dc.bibliographiccitation.issue","19"],["dc.bibliographiccitation.journal","Organic Letters"],["dc.bibliographiccitation.lastpage","5409"],["dc.bibliographiccitation.volume","13"],["dc.contributor.author","Abdalla, Muna Ali"],["dc.contributor.author","Yadav, Prem P."],["dc.contributor.author","Dittrich, Birger"],["dc.contributor.author","Schüffler, Anja"],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2019-07-09T11:54:37Z"],["dc.date.available","2019-07-09T11:54:37Z"],["dc.date.issued","2011"],["dc.description.abstract","Page 2158. In Figure 3, in structure one the oxygen bridge is missing, and in the other structures the H atom of the hydroxyl group is missing. A corrected figure is provided."],["dc.identifier.doi","10.1021/ol202247e"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/9464"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60695"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation.issn","1523-7052"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Additions and corrections ent -Homoabyssomicins A and B, Two New Spirotetronate Metabolites from Streptomyces sp. Ank 210"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]