(Q103815905)

English

Fargesin

group of stereoisomers with the chemical formula C₂₁H₂₂O₆

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Statements

instance of

group of stereoisomers

0 references

subclass of

chemical compound

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mass

370.141638424 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₁H₂₂O₆

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canonical SMILES

O(C1=CC=C(C=C1OC)C2OCC3C(OCC23)C4=CC=C5OCOC5=C4)C

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found in taxon

Leucophyllum

1 reference

stated in

Calmodulin inhibitors from Leucophyllum ambiguum.

Aristolochia albida

2 references

stated in

Lignans and diterpenes of three Aristolochia species

stated in

Aristolactams and Alkamides of Aristolochia gigantea.

Virola elongata

1 reference

stated in

Lignoids and arylalkanones from fruits of Virola elongata

Virola michelii

1 reference

stated in

Lignans from kernels of Virola michelii Heckel

Artemisia argentea

1 reference

stated in

Furfuran lignans and a flavone from Artemisia gorgonum Webb and their in vitro activity against Plasmodium falciparum

Stauranthus

1 reference

stated in

Allelochemicals from Stauranthus perforatus, a Rutaceous tree of the Yucatan Peninsula, Mexico.

Pandanus

1 reference

stated in

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Artemisia arborescens

2 references

stated in

A sesquiterpene lactone from Artemisia arborescens

stated in

Furfuran lignans and a flavone from Artemisia gorgonum Webb and their in vitro activity against Plasmodium falciparum

Aristolochia cymbifera

1 reference

stated in

Aristolactams and Alkamides of Aristolochia gigantea.

Artemisia absinthium

1 reference

stated in

Furfuran lignans and a flavone from Artemisia gorgonum Webb and their in vitro activity against Plasmodium falciparum

Aristolochia galeata

1 reference

stated in

Aristolactams and Alkamides of Aristolochia gigantea.

Aristolochia ringens

1 reference

stated in

Aristolactams and Alkamides of Aristolochia gigantea.

Aristolochia labiata

1 reference

stated in

Aristolactams and Alkamides of Aristolochia gigantea.

Zanthoxylum armatum

5 references

stated in

Quantitative and structural analysis of amides and lignans in Zanthoxylum armatum by UPLC-DAD-ESI-QTOF-MS/MS

stated in

Antinociceptive and anti-inflammatory activities of ethyl acetate fraction from Zanthoxylum armatum in mice

stated in

Simultaneous quantification and identification of flavonoids, lignans, coumarin and amides in leaves of Zanthoxylum armatum using UPLC-DAD-ESI-QTOF-MS/MS.

stated in

7,9′-Epoxylignan and other constituents of Zanthoxylum culantrillo

stated in

Bioactive Constituents of Zanthoxylum rhetsa Bark and Its Cytotoxic Potential against B16-F10 Melanoma Cancer and Normal Human Dermal Fibroblast (HDF) Cell Lines.

Magnolia kobus

2 references

stated in

Furofuran lignans from the bark of Magnolia kobus

stated in

Lignans from the Bark ofMagnolia kobus

Magnolia biondii

1 reference

stated in

Suppression of inducible nitric oxide synthase expression by furfuran lignans from flower buds of Magnolia fargesii in BV-2 microglial cells

Andaliman

7 references

stated in

A new amide from zanthoxylum armatum

stated in

7,9′-Epoxylignan and other constituents of Zanthoxylum culantrillo

stated in

Bioactive Lignans from Zanthoxylum alatum Roxb. stem bark with cytotoxic potential

stated in

Bioactive Constituents of Zanthoxylum rhetsa Bark and Its Cytotoxic Potential against B16-F10 Melanoma Cancer and Normal Human Dermal Fibroblast (HDF) Cell Lines.

stated in

Quantitative and structural analysis of amides and lignans in Zanthoxylum armatum by UPLC-DAD-ESI-QTOF-MS/MS

stated in

Antinociceptive and anti-inflammatory activities of ethyl acetate fraction from Zanthoxylum armatum in mice

stated in

Simultaneous quantification and identification of flavonoids, lignans, coumarin and amides in leaves of Zanthoxylum armatum using UPLC-DAD-ESI-QTOF-MS/MS.

Zanthoxylum alatum

1 reference

stated in

Bioactive Lignans from Zanthoxylum alatum Roxb. stem bark with cytotoxic potential

Identifiers

InChI

InChI=1S/C21H22O6/c1-22-16-5-3-12(7-18(16)23-2)20-14-9-25-21(15(14)10-24-20)13-4-6-17-19(8-13)27-11-26-17/h3-8,14-15,20-21H,9-11H2,1-2H3

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InChIKey

AWOGQCSIVCQXBT-UHFFFAOYSA-N

0 references

2 references

26 December 2021

matched by identifier from

InChIKey

AWOGQCSIVCQXBT-UHFFFAOYSA-N

ChEBI ID

175764

mapping relation type

exact match

2 references

stated in

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI

InChI=1S/C21H22O6/c1-22-16-5-3-12(7-18(16)23-2)20-14-9-25-21(15(14)10-24-20)13-4-6-17-19(8-13)27-11-26-17/h3-8,14-15,20-21H,9-11H2,1-2H3

1 reference

Human Metabolome Database ID

HMDB0038236

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

AWOGQCSIVCQXBT-UHFFFAOYSA-N

Probes And Drugs ID

PD087600

0 references

(Q103815905)

Fargesin

Statements

Identifiers

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