(Q104166898)

English

2,5-Dihydroxy-3-(3-methyl-2-butenyl)-6-heptenyl-benzaldehyde

chemical compound

In more languages

Statements

type of chemical entity

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biogenic alkylphenol

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302.188194692 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₁₉H₂₆O₃

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canonical SMILES

O=CC1=C(O)C(=CC(O)=C1C=CCCCCC)CC=C(C)C

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Aspergillus ruber

6 references

Antioxidants produced by Eurotium herbariorum of filamentous fungi used for the manufacture of karebushi, dried bonito (Katsuobushi).

Benzyl derivatives with in vitro binding affinity for human opioid and cannabinoid receptors from the fungus Eurotium repens

Asperinines A and B, dimeric tetrahydroanthracene derivatives from Aspergillus ruber.

Isolation and structures of two new metabolites from Aspergillus ruber.

Benzaldehyde derivatives from Eurotium rubrum, an endophytic fungus derived from the mangrove plant Hibiscus tiliaceus

Isolation and Structures of Two New Metabolites from Aspergillus ruber

Aspergillus chevalieri

1 reference

Structure of a new metabolite,dihydroauroglaucin,produced by Aspergillus chevalieri.

Aspergillus flavus

1 reference

New metabolic products of Aspergillus flavus. Part II. Asperflavin, anhydroasperflavin, and 5,7-dihydroxy-4-methylphthalide

Aspergillus glaucus

2 references

Antioxidants produced by Eurotium herbariorum of filamentous fungi used for the manufacture of karebushi, dried bonito (Katsuobushi).

New potent antioxidative hydroxyflavanones produced with Aspergillus saitoi from flavanone glycoside in citrus fruit

Talipariti tiliaceum

1 reference

Benzaldehyde derivatives from Eurotium rubrum, an endophytic fungus derived from the mangrove plant Hibiscus tiliaceus

Penicillium dierckxii

1 reference

Tetrahydroauroglaucin from Penicillium charlesii

Penicillium charlesii

1 reference

Tetrahydroauroglaucin from Penicillium charlesii

Identifiers

InChI=1S/C19H26O3/c1-4-5-6-7-8-9-16-17(13-20)19(22)15(12-18(16)21)11-10-14(2)3/h8-10,12-13,21-22H,4-7,11H2,1-3H3

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FYGPFTSGVSZKAJ-UHFFFAOYSA-N

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2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

FYGPFTSGVSZKAJ-UHFFFAOYSA-N

UniChem compound ID

1 reference

Sitelinks

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