(Q27106408)

(3~{S},4~{S})-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one

Yatein (English)

5 October 2016

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₂H₂₄O₇

1 reference

Yatein (English)

5 October 2016

COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4

1 reference

Yatein (English)

5 October 2016

COC1=CC(=CC(=C1OC)OC)C[C@@H]2[C@H](COC2=O)CC3=CC4=C(C=C3)OCO4

1 reference

Yatein (English)

5 October 2016

Anthriscus sylvestris

8 references

Lignan profiles of indoor-cultivated Anthriscus sylvestris

A fast and simple GC MS method for lignan profiling in Anthriscus sylvestris and biosynthetically related Plant species

Antiproliferative constituents in umbelliferae plants. III. Constituents in the root and the ground part of Anthriscus sylvestris Hoffm

Antiproliferative constituents in umbelliferae plants. IV. Constituents in the fruits of Anthriscus sylvestris Hoffm

Biosynthesis of yatein in Anthriscus sylvestris

Lignans and coumarins from the roots of Anthriscus sylvestris and their increase of caspase-3 activity in HL-60 cells.

Antiproliferative constituents in umbelliferae plants. III. Constituents in the root and the ground part of Anthriscus sylvestris Hoffm

Antiproliferative constituents in umbelliferae plants. IV. Constituents in the fruits of Anthriscus sylvestris Hoffm

Bupleurum scorzonerifolium

1 reference

Immunosuppressive flavones and lignans from Bupleurum scorzonerifolium

Macrococculus pomiferus

1 reference

Constituents of the stems of Macrococculus pomiferus and their inhibitory activities against cyclooxygenases-1 and -2.

Juniperus

1 reference

Oxygenated Diterpenes and Other Constituents from Moroccan Juniperus phoenicea and Juniperus thurifera Var. africana

Bursera simaruba

1 reference

Phenolic compounds from Bursera simaruba Sarg. bark: phytochemical investigation and quantitative analysis by tandem mass spectrometry

Chaerophyllum aureum

1 reference

Lignans, phenylpropanoids and polyacetylenes from Chaerophyllum aureum L. (Apiaceae).

Hernandia cordigera

1 reference

5'-Methoxyyatein and 5'-Methoxypodorhizol New Lignans Isolated from Hernandia cordigera Viell

Hernandia nymphaeifolia

3 references

Antineoplastic agents. 522. Hernandia peltata (Malaysia) and Hernandia nymphaeifolia (Republic of Maldives).

Anti-platelet aggregation alkaloids and lignans from Hernandia nymphaeifolia

New dimeric aporphine alkaloids and cytotoxic constituents of Hernandia nymphaeifolia

Hernandia ovigera

5 references

Constituents of the twigs of Hernandia ovigera that inhibit the transformation of JB6 murine epidermal cells.

Studies on the constituents of the seeds of Hernandia ovigerd L.. VI. Isolation and structural determination of three lignans.

Studies on the Constituents of the Seeds of Hernandia ovigera L. IX. Identification of Two Dibenzylbutyrolactone-Type Lignans and an Attempt of Conversion into Phenyltetralin-Type Lignan.

Constituents of the seeds of Hernandia ovigera with inhibitory activity against cyclooxygenase-2.

Studies on the constituents of the seeds of Hernandia ovigerd L.. VI. Isolation and structural determination of three lignans.

Condea verticillata

1 reference

Cytotoxic constituents from Hyptis verticillata

Juniperus communis

1 reference

Structure Elucidation of Germacrane Alcohols from Juniperus communis subsp. Hemisphaerica

Juniperus sabina

2 references

Acetylated lignans from Juniperus sabina

Lignans from Juniperus sabina

Juniperus thurifera

4 references

Lignans from polar extracts ofJuniperus thurifera

Lignans from Juniperus thurifera

Oxygenated diterpenes and other constituents from Moroccan Juniperus phoenicea and Juniperus thurifera var. africana.

Lignans from Juniperus thurifera

Calocedrus formosana

1 reference

Lignans from leaves of Calocedrus formosana

Lychnophora ericoides

1 reference

Analgesic activity of the lignans from Lychnophora ericoides

West African Pepper

1 reference

Lignans of Piper clusii☆

Piper cubeba

5 references

Dibenzylbutyrolactone lignans from Piper cubeba

Potent CYP3A4 inhibitory constituents of Piper cubeba

Potent CYP3A4 inhibitory constituents of Piper cubeba

Potent CYP3A4 inhibitory constituents of Piper cubeba

Potent CYP3A4 Inhibitory Constituents of Piper cubeba

Podolepis canescens

1 reference

Pyrones and other constituents from Podolepis species

Podolepis lessonii

1 reference

Pyrones and other constituents from Podolepis species

Podolepis rugata

1 reference

Pyrones and other constituents from Podolepis species

Thuja plicata

1 reference

Totarol, totaradiol and ferruginol: three diterpenes from Thuja plicata (Cupressaceae)

Chamaecyparis obtusa

2 references

Yatein from Chamaecyparis obtusa suppresses herpes simplex virus type 1 replication in HeLa cells by interruption the immediate-early gene expression

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

Thuja occidentalis

1 reference

Bioactive constituents of Thuja occidentalis.

Eriope blanchetii

1 reference

Podophyllotoxin and other aryltetralin lignans from Eriope latifolia and Eriope blanchetii

Illigera luzonensis

1 reference

Aporphine alkaloids and cytotoxic lignans from the roots of Illigera luzonensis

Juniperus brevifolia

1 reference

Cytotoxic activity of diterpenes and extracts of Juniperus brevifolia.

Eleutherococcus divaricatus

1 reference

Inhibitory lignans against NFAT transcription factor from Acanthopanax koreanum

Austrocedrus chilensis

1 reference

Antiproliferative activity of yatein isolated from Austrocedrus chilensis against murine myeloma cells: cytological studies and chemical investigations.

Hernandia guianensis

4 references

Constituents of the seeds of Hernandia ovigera with inhibitory activity against cyclooxygenase-2.

Studies on the constituents of the seeds of Hernandia ovigerd L.. VI. Isolation and structural determination of three lignans.

Studies on the Constituents of the Seeds of Hernandia ovigera L. IX. Identification of Two Dibenzylbutyrolactone-Type Lignans and an Attempt of Conversion into Phenyltetralin-Type Lignan.

Constituents of the twigs of Hernandia ovigera that inhibit the transformation of JB6 murine epidermal cells.

Identifiers

InChI

InChI=1S/C22H24O7/c1-24-19-9-14(10-20(25-2)21(19)26-3)7-16-15(11-27-22(16)23)6-13-4-5-17-18(8-13)29-12-28-17/h4-5,8-10,15-16H,6-7,11-12H2,1-3H3/t15-,16+/m0/s1

1 reference

Yatein (English)

5 October 2016

2 references

Yatein (English)

5 October 2016

ChEBI release 2020-09-01

2 references

dihydroanhydropodorhizol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=40456-50-6

8 April 2021

1 reference

Deoxypodorhizone (English)

5 October 2016

2 references

Yatein (English)

5 October 2016

Reaxys registry number

4300660

1 reference

dihydroanhydropodorhizol (English)

5 October 2016

ChEBI ID

4553

mapping relation type

2 references

dihydroanhydropodorhizol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C22H24O7/c1-24-19-9-14(10-20(25-2)21(19)26-3)7-16-15(11-27-22(16)23)6-13-4-5-17-18(8-13)29-12-28-17/h4-5,8-10,15-16H,6-7,11-12H2,1-3H3/t15-,16+/m0/s1

1 reference

CHEMBL471067 (English)

5 October 2016

2 references

inferred from InChIKey

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

1 reference

2 references

DSSTOX compound identifier

0 references

1 reference

dihydroanhydropodorhizol (English)

5 October 2016

0 references

1 reference

dihydroanhydropodorhizol (English)