Results 1 to 10 of about 602 (107)

Penazaphilones J–L, Three New Hydrophilic Azaphilone Pigments from Penicillium sclerotiorum cib-411 and Their Anti-Inflammatory Activity [PDF]

open access: yesMolecules, 2023
Penazaphilones J–L (1–3), three new hydrophilic azaphilone pigments, as well as six known compounds, were discovered from the filamentous fungus Penicillium sclerotiorum cib-411.
Xia Zhang   +5 more
doaj   +2 more sources

Generation of Novel Natural Products by Disrupting Azaphilone Synthesis in Penicillum sclerotiorum E23Y-1A [PDF]

open access: yesMarine Drugs
Marine-derived filamentous fungi are a rich source of structurally diverse and biologically active natural products. However, many biosynthetic gene clusters (BGCs) in fungi remain silent under standard conditions.
Wenjun Chang   +5 more
doaj   +2 more sources

A Novel Azaphilone Muyophilone A From the Endophytic Fungus Muyocopron laterale 0307-2

open access: yesFrontiers in Chemistry, 2021
Two known azaphilone derivatives, 4,6-dimethylcurvulinic acid (1) and austdiol (2), and their novel heterotrimer, muyophilone A (3), were isolated and identified from an endophytic fungus, Muyocopron laterale 0307-2.
Ke Wang, Longfei Li, Chao Yuan
exaly   +3 more sources

Nitrogen Enriched Solid-State Cultivation for the Overproduction of Azaphilone Red Pigments by Penicillium sclerotiorum SNB-CN111 [PDF]

open access: yesJournal of Fungi, 2023
Azaphilones are microbial specialized metabolites employed as yellow, orange, red or purple pigments. In particular, yellow azaphilones react spontaneously with functionalized nitrogen groups, leading to red azaphilones.
Téo Hebra   +2 more
doaj   +2 more sources

Hydroxyl Radical Formation: A Key Mechanism and Regulatory Target in Monascin Photo-Degradation [PDF]

open access: yesJournal of Fungi
Monascin, a yellow azaphilone pigment derived from Monascus fermentation, undergoes significant photo-degradation that limits its applications. This study reveals that free radical formation, particularly hydroxyl radicals (·OH) generated via H2O2 ...
Zhihan Shang   +7 more
doaj   +2 more sources

Cytotoxic Mechanism of Deep-Sea Fungus Chaetomium globosum YP-106 Metabolite Chaetomugilin O in Thyroid Cancer Cells [PDF]

open access: yesMarine Drugs
This study investigated the potential of the deep-sea-derived fungal metabolite, chlorinated azaphilone compound chaetomugilin O, in the treatment of thyroid cancer.
Yaqin Fan   +6 more
doaj   +2 more sources

A New Azaphilone, Kasanosin C, from an Endophytic Talaromyces sp. T1BF

open access: yesMolecules, 2010
The strain T1BF was isolated from the old bast tissue of Taxus yunnanensis and determined to be a member of Talaromyces. The extracts from the solid fermentation of Talaromycessp.
Ying Zeng, Pei-Ji Zhao, Liang-Qun Li
exaly   +3 more sources

Penicilazaphilone C triggers ferroptosis in triple-negative breast cancer cells via the MDM2/p53/SLC7 A11/GPX4 pathway [PDF]

open access: yesDiscover Oncology
Penicilazaphilone C (PAC) is a novel azaphilone isolated by our research team. While known for its antitumor properties, the potential of PAC to trigger ferroptosis in triple-negative breast cancer (TNBC) cells remains unexplored.
Hua-Tao Liang   +8 more
doaj   +2 more sources

Isolation and Characterization of Antimicrobial Metabolites from the Sophora tonkinensis-Associated Fungus Penicillium sp. GDGJ-N37 [PDF]

open access: yesMolecules
Chemical investigation of Penicillium sp. GDGJ-N37, a Sophora tonkinensis-associated fungus, yielded two new azaphilone derivatives, N-isoamylsclerotiorinamine (1) and 7-methoxyl-N-isoamylsclerotiorinamine (2), and four known azaphilones (3–6), together ...
Lili Huang   +9 more
doaj   +2 more sources

OSMAC-Driven Discovery of Six New Alkaloids from the Cold-Seep-Derived Fungus Talaromyces amestolkiae HDN21-0307 [PDF]

open access: yesMarine Drugs
Six new alkaloid compounds, including two rare aromatic nitrile compounds talaronitriles A–B (1–2), a novel oxime-functionalized azadiphilone analogue talarooxime A (3), a new phenylhydrazone alkaloid talarohydrazone E (4), and two new dipeptide ...
Xinsheng Huang   +8 more
doaj   +2 more sources

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