Found 2 publications.
Displayed publications from 1 to 2
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 7749)
Chen HP, Liu JK
Secondary metabolites from higher fungi
Progress in the Chemistry of Organic Natural Products 106 (2017)
1-201
Secondary metabolites of higher fungi (mushrooms) are an underexplored resource compared to plant-derived secondary metabolites. An increasing interest in mushroom natural products has been noted in recent years. This chapter gives a comprehensive overview of the secondary metabolites from higher fungi, with 765 references highlighting the isolation, structure elucidation, biological activities, chemical syntheses, and biosynthesis of pigments, nitrogen-containing compounds, and terpenoids from mushrooms. Mushroom toxins are also included in each section.In a section on pigments of higher fungi, pigments are classified into four categories, namely, those from the shikimate-chorismate, acetate-malonate, and mevalonate biosynthetic pathways, and pigments containing nitrogen, with 145 references covering the years 2010-2016.In a section on other nitrogen-containing compounds of higher fungi, compounds are categorized primarily into nitrogen heterocycles, nucleosides, non-protein amino acids, cyclic peptides, and sphingolipids, with 65 references covering the years 2010-2016. In turn, in a section describing terpenoids of higher fungi, the sesquiterpenoids and diterpenoids are thoroughly elaborated, spanning the years 2001-2016, and 2009-2016, respectively. The divergent biosynthetic pathways from farnesyl pyrophosphate to sesquiterpenoids are also described. Selected triterpenoids with novel structures and promising biological activities, including lanostanes and ergostanes, are reported from the genus Ganoderma, and the fungi Antrodia cinnamomea and Poria cocos. In addition, cucurbitanes and saponaceolides are also compiled in this section.
biosynthesis, biological activity, chemical synthesis, mushrooms, secondary metabolites, higher fungi, triterpenoids, diterpenoids, mushroom toxins, nitrogen-containing compounds, pigments, sesquiterpenoids
NCBI PubMed ID: 28762089Publication DOI: 10.1007/978-3-319-59542-9_1Journal NLM ID: 101605200Publisher: Wien: Springer
Correspondence: liujikai

mail.scuec.edu.cn
Institutions: State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China, School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan, China
The publication contains the following compound(s):
- Compound ID: 19657
|
Xyl-(1-21)-Subst
Subst = fomitoside E aglycon = SMILES C[C@]([C@]1(C)CC2)(CC[C@@H]1[C@@H](C/C=C/{25}C(C)(O)C){21}C(O)=O)C3=C2[C@]4(C)[C@](CC3)([H])C(C)(C)[C@H](OC(C)=O)CC4 |
Show graphically |
Structure type: monomer
Compound class: triterpenoid glycoside
- Compound ID: 19649
|
R-2HOSte-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E,8E)-2-amino-9-methylpentadeca-4,8-diene-1,3-diol = SMILES CCCCCC/C(C)=C/CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
Show graphically |
Structure type: monomer
Compound class: glycosphingolipid, cerebroside
- Compound ID: 18812
|
b-D-Glcp-(1-21)-Subst3Ac
Subst = fomitoside K aglycon = SMILES C[C@]([C@]1(C)CC2)(CC[C@@H]1[C@@H](CCC(C(C)C)=C){21}C(O)=O)C3=C2[C@]4(C)[C@](CC3)([H])C(C)(C){3}[C@H](O)CC4 |
Show graphically |
Structure type: monomer
C39H62O9
Trivial name: fomitoside K
Compound class: glycoside, triterpene glycoside, triterpenoid glycoside
- Compound ID: 19647
Structure type: monomer
Reference(s) to other database(s): GTC:G81533KY
- Compound ID: 19648
Structure type: monomer
Reference(s) to other database(s): GTC:G43724HA
- Compound ID: 19650
|
a-D-GlcpNAc-(1-11)-Subst
Subst = trichobrasilenol = SMILES C[C@H]1CC[C@@H]2/C(CC(C)(C)C[C@@H]21)=C({11}CO)\C |
Show graphically |
Structure type: monomer
Trivial name: brasilane A
Compound class: glycoside, terpene glycoside
- Compound ID: 19651
|
b-D-Glcp-(1-16)-Subst
Subst = 16-hydroxyisopimar-7-en-19-oic acid = SMILES C[C@]1({19}C(O)=O)CCC[C@@]2(C)[C@H]1CC=C3[C@@H]2CC[C@](C)(C{16}CO)C3 |
Show graphically |
Structure type: monomer
Compound class: terpene glycoside
- Compound ID: 19652
|
b-D-Glcp-(1-7)-Subst
Subst = diplopimarane = SMILES CC1(C)CCCC2=C1{6}C(O)={7}C(O)C3=C2CC[C@](C)(C=C){14}[C@@H]3O |
Show graphically |
Structure type: monomer
Compound class: terpene glycoside
- Compound ID: 19653
|
b-D-Altp4Me-(1-17)-Subst
Subst = sordarin C aglycon = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@H]4C[C@@](C=O)2[C@]({13}[C@](O)=O)3C(C({19}CO)C)=C4 |
Show graphically |
Structure type: monomer
Trivial name: sordarin C
Compound class: glycoside, diterpene glycoside
- Compound ID: 19654
|
b-D-Altp4Me-(1-17)-Subst
Subst = sordarin E aglycon = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@H]4C[C@@](C=O)2[C@]({13}[C@](O)=O)3C5(C(C)C5)C4=O |
Show graphically |
Structure type: monomer
Compound class: diterpene glycoside
- Compound ID: 19655
|
b-D-Altp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
Show graphically |
Structure type: monomer
Trivial name: hydroxysordarin
Compound class: glycoside, diterpene glycoside
- Compound ID: 19656
|
b-D-Xylp-(1-1)-C-(1-14)-Subst
Subst = mutilin = SMILES C=C[C@@]1(C){11}[C@@H](O)[C@H](C)[C@]23[C@]([C@]({14}[C@H](O)C1)([C@H](C)CC2)C)(C(CC3)=O)[H] |
Show graphically |
Structure type: monomer
Compound class: glycoside
- Compound ID: 19658
|
b-D-Glcp-(1-3)-+
|
b-D-Glcp-(1-16)-Subst
Subst = hebevinoside aglycon = SMILES O{3}[C@H]1C[C@@]2(C)[C@]3([H])CC=C4C(C)(C){16}[C@@H](O)CC[C@@]4([H])[C@]3(C)CC[C@]2(C)[C@H]1[C@@H](CC/C=C({23}C(O)=O)\C)C |
Show graphically |
Structure type: monomer
Compound class: triterpenoid glycoside
Expand this publication
Collapse this publication
2. (Article ID: 8167)
Kim SE, Hwang BS, Song JG, Lee SW, Lee IK, Yun BS
New bioactive compounds from korean native mushrooms
Mycobiology 41(4) (2013)
171-176
Mushrooms are ubiquitous in nature and have high nutritional attributes. They have demonstrated diverse biological effects and therefore have been used in treatments of various diseases, including cancer, diabetes, bacterial and viral infections, and ulcer. In particular, polysaccharides, including β-glucan, are considered as the major constituents responsible for the biological activity of mushrooms. Although an overwhelming number of reports have been published on the importance of polysaccharides as immunomodulating agents, not all of the healing properties found in these mushrooms could be fully accounted for. Recently, many research groups have begun investigations on biologically active small-molecular weight compounds in wild mushrooms. In this mini-review, both structural diversity and biological activities of novel bioactive substances from Korean native mushrooms are described.
biological activity, bioactive compounds, Korean native mushrooms, structure diversity
NCBI PubMed ID: 24493936Publication DOI: 10.5941/MYCO.2013.41.4.171Journal NLM ID: 100960027Publisher: Seoul, Korea: Korean Society of Mycology
Correspondence: Yun BS < bsyun

jbnu,ac.kr>
Institutions: Division of Biotechnology and Advanced Institute of Environment and Bioscience, College of Environmental and Bioresource Sciences, Chonbuk National University, Iksan, Korea
The publication contains the following compound(s):
- Compound ID: 18812
|
b-D-Glcp-(1-21)-Subst3Ac
Subst = fomitoside K aglycon = SMILES C[C@]([C@]1(C)CC2)(CC[C@@H]1[C@@H](CCC(C(C)C)=C){21}C(O)=O)C3=C2[C@]4(C)[C@](CC3)([H])C(C)(C){3}[C@H](O)CC4 |
Show graphically |
Structure type: monomer
C39H62O9
Trivial name: fomitoside K
Compound class: glycoside, triterpene glycoside, triterpenoid glycoside
- Compound ID: 19779
|
b-D-Glcp-(1-12)-Subst
Subst = oligoporin A aglycon = SMILES C/C(=C/CC[C@@H](C)[C@H]3CC[C@@]4(C)/C/2=C/C[C@H]1C(C)(C)C(=O)CC[C@]1(C)C2=C\{12}[C@@H](O)[C@]34C){23}C(=O)O |
Show graphically |
Structure type: monomer
C36H54O9
Trivial name: oligoporin A
Compound class: glycoside, triterpene glycoside
- Compound ID: 19780
|
b-D-Glcp-(1-12)-Subst
Subst = oligoporin B aglycon = SMILES C/C(=C/CC[C@@H](C)[C@H]3CC[C@@]4(C)/C/2=C/C[C@H]1C(C)(C){3}[C@@H](O)CC[C@]1(C)C2=C\{12}[C@@H](O)[C@]34C){23}C(=O)O |
Show graphically |
Structure type: monomer
C36H56O9
Trivial name: oligoporin B
Compound class: glycoside, triterpene glycoside
- Compound ID: 19781
|
b-D-Glcp-(1-12)-Subst
Subst = oligoporin C aglycon = SMILES C/C(=C/CC[C@@H](C)[C@H]1CC[C@@]2(C)/C4=C(C{12}[C@@H](O)[C@]12C)/[C@@]3(C)CC{3}[C@H](O)C(C)(C)[C@@H]3CC4=O){23}C(=O)O |
Show graphically |
Structure type: monomer
C36H56O10
Trivial name: oligoporin C
Compound class: glycoside, triterpene glycoside
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: 1 sec