3,5-Dimethylorsellinic Acid Derived Meroterpenoids from Penicillium chrysogenum MT-12, an Endophytic Fungus Isolated from Huperzia serrata. (Q47900470)

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31 March 2020

title

3,5-Dimethylorsellinic Acid Derived Meroterpenoids from Penicillium chrysogenum MT-12, an Endophytic Fungus Isolated from Huperzia serrata (English)

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31 March 2020

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Penicillium chrysogenum

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Methyl 11-hydroxy-2,6,6,11,14,19-hexamethyl-8,15,20-trioxo-7,16,18-trioxapentacyclo[12.6.1.02,12.05,10.017,21]henicosa-4,9-diene-1-carboxylate

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2,6,6,14,20-Pentamethylspiro[7,16,18,21,24-pentaoxaheptacyclo[12.8.1.13,19.01,19.02,12.05,10.017,23]tetracosa-4,9-diene-11,2'-oxirane]-8,15,22-trione

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Huperzia serrata

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methyl (1R,2S,12S,14R,16R,18R)-16-hydroxy-2,6,6,11,14,16-hexamethyl-8,15-dioxospiro[7-oxatetracyclo[12.3.1.02,12.05,10]octadeca-4,10-diene-18,2'-oxirane]-1-carboxylate

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methyl (1S,2S,12S,14R,17R,19R,21R)-2,6,6,11,14,19-hexamethyl-8,15,20-trioxo-7,16,18-trioxapentacyclo[12.6.1.02,12.05,10.017,21]henicosa-4,10-diene-1-carboxylate

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methyl (1R,2S,12S,14R,17R,19S,21R)-2,6,6,14,19-pentamethyl-11-methylidene-8,15,20-trioxo-7,16,18-trioxapentacyclo[12.6.1.02,12.05,10.017,21]henicosa-4,9-diene-1-carboxylate

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inferred from

reverse claim

(1S,2S,12S,14R,18S,21R)-2,6,6,11,14-pentamethyl-7,17,19-trioxahexacyclo[12.6.1.11,16.02,12.05,10.018,21]docosa-4,10-diene-8,15,20,22-tetrone

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5

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Ikuro Abe

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Shepo Shi

12

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author name string

Bowen Qi

1

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Xiao Liu

2

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Ting Mo

3

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Zhixiang Zhu

4

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Juan Wang

6

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31 March 2020

Xiaoping Shi

7

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Kewu Zeng

8

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Xiaohui Wang

9

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Pengfei Tu

10

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publication date

29 September 2017

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Journal of Natural Products

31 March 2020

published in

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volume

80

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page(s)

2699-2707

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issue

10

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The role of nitric oxide in inflammatory reactions

31 March 2020

cites work

1 reference

9 February 2024

https://opencitations.net/index/api/v1/citations/10.1111/J.1574-695X.2007.00329.X

An Unusual Stress Metabolite from a Hydrothermal Vent Fungus Aspergillus sp. WU 243 Induced by Cobalt.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.3390/MOLECULES21010105

Identifiers

DOI

10.1021/ACS.JNATPROD.7B00438

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31 March 2020

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