Results 141 to 150 of about 912 (190)

A Novel Bis-Spiroketal Scaffold and Other Secondary Metabolites from the Marine-Derived Fungus <i>Talaromyces stipitatus</i> HF05001: Structural Diversity and Bioactivities. [PDF]

Mar Drugs
Yang L, Qiu Y, Liu Y, Wei X, He X, Wang Y, Yan Y, Bai K, Wang Z, Ren J.   +9 more
europepmc   +1 more source

Recent Advances in Anti-Inflammatory Compounds from Marine Microorganisms. [PDF]

Mar Drugs
Yang G, Lin M, Kaliaperumal K, Lu Y, Qi X, Jiang X, Xu X, Gao C, Liu Y, Luo X.   +9 more
europepmc   +1 more source

mGem: How many fungal secondary metabolites are produced by filamentous fungi? Conservatively, at least 1.4 million. [PDF]

mBio
Riedling OL, Rokas A.
europepmc   +1 more source

Effects of VeA Gene on the Growth, Pigment and Citrinin Synthesis of Monascus ruber M7. [PDF]

Microorganisms
Kuang L, Ma P, He X, Wang L, Xie Q, He Y, Tan H.   +6 more
europepmc   +1 more source

Isolation of <i>Monascus purpureus</i> HC-5 and Optimization of Solid-State Fermentation for High-Yield Pigment Production. [PDF]

Microorganisms
Quan W, Chen S, Li H, Tang Z, Alam MN, Liu X.   +5 more
europepmc   +1 more source

Bulbillosins A - E, azaphilones from <i>Tengochaetabulbillosa</i> sp. nov. (<i>Chaetomiaceae</i>), a root endophyte of the Chinese medicinal plant <i>Astertataricus</i>. [PDF]

IMA Fungus
Barrera-Adame DA, Marin-Felix Y, Wegener AK, Lalk M, Stadler M, Niedermeyer THJ.   +5 more
europepmc   +1 more source

Identification of natural products and synthetic analogs which inhibit microsporidia spores and prevent infection. [PDF]

J Invertebr Pathol
Huang Q, Brown LE, Pan G, Wei J, Porco JA, Chen J, Reinke AW.   +6 more
europepmc   +1 more source

Diversity and Distribution of Non-Reducing Polyketide Synthases (NR-PKSs) in Ascomycota (Fungi). [PDF]

J Fungi (Basel)
Chattopadhyay P, Banerjee G.
europepmc   +1 more source

<i>Monascus purpureus</i> Red Yeast Rice: A Review of the in vitro and in vivo Pharmacological Activities, Studies in Humans, and Case Reports. [PDF]

Clin Pharmacol
Shaleha RR, Yuliana A, Amin S, Levita J, Sumiwi SA.   +4 more
europepmc   +1 more source

Synthesis of Azaphilone-Based Chemical Libraries [PDF]

ACS Combinatorial Science, 2012
The synthesis of azaphilone scaffolds that have been further diversified by cross coupling acylation and amine addition is reported. Methodology development also led to novel modifications including C5 acetoxylation and condensations producing isoquinolin-6(7H) structures. Overall, the library synthesis afforded three azaphilone sublibraries, including
Aaron Beeler, John A Porco, Mathieu Achard   +2 more
exaly   +5 more sources