4-[(1S,3aR,4S,6aR)-4-(1,3-benzodioxol-5-yl)tetrahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenol (Q74410647)

4-[(3R,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol

inferred from SMILES

stereoisomer of

2 references

4-[(1R,3aS,4S,6aS)-4-(1,3-Benzodioxol-5-yl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2-methoxyphenol

1 reference

pluviatilol

2 references

4-[(3R,3aS,6R,6aS)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol

1 reference

4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol

1 reference

chemical formula

C₂₀H₂₀O₆

0 references

canonical SMILES

OC1=CC=C(C=C1OC)C2OCC3C(OCC23)C4=CC=C5OCOC5=C4

0 references

isomeric SMILES

COC1=C(C=CC(=C1)[C@@H]2[C@H]3CO[C@@H]([C@H]3CO2)C4=CC5=C(C=C4)OCO5)O

0 references

found in taxon

Ocotea usambarensis

1 reference

Analysis of the fungicidal constituents from the bark ofOcotea usambarensis Engl. (Lauraceae)

sesame

3 references

Biosynthesis of antioxidant lignans in Sesamum indicum seeds

Furanofuran lignan metabolism as a function of seed maturation in sesamum indicum: methylenedioxy bridge formation

(+)-Episesaminone, aSesamumindicumFurofuran Lignan. Isolation and Hemisynthesis

Streptomyces

1 reference

New metabolites, tetrahydrofuran lignans, produced by Streptomyces sp. IT-44

Zanthoxylum petiolare

2 references

Protolimonoid and lignans from Zanthoxylum petiolare

Protolimonoid and lignans from Zanthoxylum petiolare

Actinodaphne longifolia

1 reference

Asarum sieboldii

1 reference

Anti-inflammatory and PPAR transactivational effects of secondary metabolites from the roots of Asarum sieboldii.

Chamaecyparis obtusa

1 reference

Neurite outgrowth-promoting active constituents of the Japanese cypress (Chamaecyparis obtusa).

Daphne composita

1 reference

Dioscorea spongiosa

2 references

Antiosteoporotic activity of the water extract of Dioscorea spongiosa

The in vitro anti-osteoporotic activity of some diarylheptanoids and lignans from the rhizomes of Dioscorea spongiosa

Bracteantha acuminata

1 reference

Obliquin derivatives and other constituents from Australian Helichrysum species

Xerochrysum subundulatum

1 reference

Obliquin derivatives and other constituents from Australian Helichrysum species

Bracteantha subundulata

1 reference

Obliquin derivatives and other constituents from Australian Helichrysum species

Zanthoxylum schinifolium

1 reference

Ultrasonic nebulization extraction-heating gas flow transfer-headspace single drop microextraction of essential oil from pericarp of Zanthoxylum bungeanum Maxim

Anethum graveolens

1 reference

Constituents of Dill (Anethum graveolensL.) with Sensory Importance

Magnolia stellata

1 reference

Magnostellin A and B, novel lignans from Magnolia stellata

Aristolochia gehrtii

1 reference

Alkamides and phenethyl derivatives from Aristolochia gehrtii

Paulownia tomentosa

1 reference

(+)-Piperitol from Paulownia tomentosa

Nectandra turbacensis

1 reference

Lignans from Nectandra turbacensis

Eriosolena composita

1 reference

Actinodaphne acuminata

1 reference

Kuloa usambarensis

1 reference

Analysis of the fungicidal constituents from the bark ofOcotea usambarensis Engl. (Lauraceae)

Identifiers

InChI

InChI=1S/C20H20O6/c1-22-17-6-11(2-4-15(17)21)19-13-8-24-20(14(13)9-23-19)12-3-5-16-18(7-12)26-10-25-16/h2-7,13-14,19-21H,8-10H2,1H3/t13-,14-,19+,20+/m0/s1

0 references

2 references

ChEBI release 2019-11-01

ChEBI release 2020-09-01

PubChem CID

10247670

1 reference

ChEBI ID

141003

mapping relation type

exact match

1 reference

International Chemical Identifier

InChI

InChI=1S/C20H20O6/c1-22-17-6-11(2-4-15(17)21)19-13-8-24-20(14(13)9-23-19)12-3-5-16-18(7-12)26-10-25-16/h2-7,13-14,19-21H,8-10H2,1H3/t13-,14-,19+,20+/m0/s1

1 reference

1 reference

Natural Product Atlas ID

NPA005229

2 references