| scholarly article | Q13442814 |
| P356 | DOI | 10.1021/OL101817G |
| P953 | full work available at URL | https://pubs.acs.org/doi/pdf/10.1021/ol101817g |
| P698 | PubMed publication ID | 20812740 |
| P2093 | author name string | Ke-Qin Zhang | |
| Yan-Li Wang | |||
| Xue-Mei Niu | |||
| Xiao-Wei Huang | |||
| Yan-Sheng Chu | |||
| Wen-Zheng Pan | |||
| Ji-Peng Guo | |||
| P2860 | cites work | Topics in Current Chemistry | Q2443282 |
| Isolation of notoamide E, a key precursor in the biosynthesis of prenylated indole alkaloids in a marine-derived fungus, Aspergillus sp | Q24656685 | ||
| Agricultural and Biological Chemistry | Q27709610 | ||
| The genus Eurotium - members of indigenous fungal community in hypersaline waters of salterns | Q33228581 | ||
| Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600. | Q33692567 | ||
| Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp. | Q34134311 | ||
| Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells | Q34162613 | ||
| Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim report | Q34177666 | ||
| Total synthesis and biosynthesis of the paraherquamides: an intriguing story of the biological Diels-Alder construction | Q34667626 | ||
| Nematodetoxic aurovertin-type metabolites from a root-knot nematode parasitic fungus Pochonia chlamydosporia | Q38433213 | ||
| Notoamides F-K, prenylated indole alkaloids isolated from a marine-derived Aspergillus sp. | Q46216319 | ||
| A Concise Total Synthesis of the Notoamides C and D | Q59710707 | ||
| A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B | Q59710712 | ||
| Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp | Q59710735 | ||
| The structures of five new didehydropeptides related to neoechinulin, isolated from Aspergillus amstelodami | Q78431852 | ||
| Reverse versus Normal Prenyl Transferases in Paraherquamide Biosynthesis Exhibit Distinct Facial Selectivities | Q88521534 | ||
| Dipodazine, a diketopiperazine from Penicillium dipodomyis | Q104154935 | ||
| P433 | issue | 19 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Talathermophilin A | Q77561143 |
| Talaromyces thermophilus | Q80855462 | ||
| Thermomyces thermophilus | Q104095688 | ||
| Talathermophilin B | Q105312833 | ||
| P304 | page(s) | 4356-4359 | |
| P577 | publication date | 2010-09-02 | |
| 2010-10-01 | |||
| P1433 | published in | Organic Letters | Q2396276 |
| P1476 | title | Isolation of putative biosynthetic intermediates of prenylated indole alkaloids from a thermophilic fungus Talaromyces thermophilus | |
| Isolation of Putative Biosynthetic Intermediates of Prenylated Indole Alkaloids from a Thermophilic Fungus Talaromyces thermophilus | |||
| P478 | volume | 12 |
| Q27009360 | Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids |
| Q43020791 | Identification and biosynthesis of new acyloins from the thermophilic bacterium Thermosporothrix hazakensis SK20-1(T). |
| Q26771662 | Metabolites from nematophagous fungi and nematicidal natural products from fungi as an alternative for biological control. Part I: metabolites from nematophagous ascomycetes |
| Q55494251 | Novel Natural Products from Extremophilic Fungi. |
| Q34151580 | Phylogeny and nomenclature of the genus Talaromyces and taxa accommodated in Penicillium subgenus Biverticillium |
| Q58221078 | Simple indole alkaloids and those with a non-rearranged monoterpenoid unit |
| Q48246908 | Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi |
| Q36568390 | The Bioactive Secondary Metabolites from Talaromyces species |
| Q38700003 | Thermophilic molds: Biology and applications. |
| Q51577238 | Two new compounds, deacetylisowortmins A and B, isolated from an endophytic Fungus, Talaromyces wortmannii LGT-4. |
| Q48001758 | Uncovering the repertoire of fungal secondary metabolites: From Fleming's laboratory to the International Space Station |
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