(Q27149840)

rel-(4aR,8aS)-3,8a-Dimethyl-5-methylene-4,4a,5,6,7,8,8a,9-octahydronaphtho[2,3-b]furan

Atractylon (English)

8 October 2016

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₅H₂₀O

1 reference

Atractylon (English)

8 October 2016

CC1=COC2=C1CC3C(=C)CCCC3(C2)C

1 reference

Atractylon (English)

8 October 2016

CC1=COC2=C1C[C@H]3C(=C)CCC[C@@]3(C2)C

1 reference

Composition of the essential oil of rootstock from Cimicifuga simplex

Atractylon (English)

8 October 2016

1 reference

Cimicifuga simplex

1 reference

Composition of the essential oil of rootstock from Cimicifuga simplex

Eugenia uniflora

2 references

Antinociceptive and hypothermic evaluation of the leaf essential oil and isolated terpenoids from Eugenia uniflora L. (Brazilian Pitanga).

Influence of fruit biotypes on the chemical composition and antifungal activity of the essential oils of eugenia uniflora leaves

Atractylodes

3 references

Determination of atractylon in Atractylodes rhizome using supercritical fluid chromatography on-line coupled with supercritical fluid extraction by the direct induction method

STUDIES ON THE CONSTITUENTS OF ATRACTYLODES. IX. STRUCTURE AND AUTOXIDATION OF ATRACTYLON

Antihepatotoxic principles of Atractylodes rhizomes

Atractylodes japonica

3 references

Atractylodis Rhizoma extract and its component, atractylon, inhibit tumor promotion in mouse skin two-stage carcinogenesis.

Clonal Propagation of Atractylodes japonica and A. ovata by Tip Tissue Culture and the Atractylon Content of Clonally Propagated Plants

Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi

Atractylodes koreana

1 reference

Variation of Essential Oil Components of Atractylodes chinensis Growing in China

Atractylodes lancea

10 references

5-Lipoxygenase and cyclooxygenase-1 inhibitory active compounds from Atractylodes lancea.

Cytotoxic activity of sesquiterpenoids from Atractylodes ovata on leukemia cell lines

A comparative study on essential oil components of wild and cultivated Atractylodes lancea and A. chinensis

Clonal Propagation of Atractylodes japonica and A. ovata by Tip Tissue Culture and the Atractylon Content of Clonally Propagated Plants

Variation of Essential Oil Components of Atractylodes chinensis Growing in China

5-Lipoxygenase and cyclooxygenase-1 inhibitory active compounds from Atractylodes lancea.

5-Lipoxygenase and cyclooxygenase-1 inhibitory active compounds from Atractylodes lancea.

Cytotoxic activity of sesquiterpenoids from Atractylodes ovata on leukemia cell lines

Atractylodis Rhizoma extract and its component, atractylon, inhibit tumor promotion in mouse skin two-stage carcinogenesis.

Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi

Prumnopitys taxifolia

1 reference

Foliage sesquiterpenes and diterpenes of Podocarpus spicatus

Prumnopitys andina

1 reference

Foliage sesquiterpenes and diterpenes of Podocarpus spicatus

Identifiers

InChI

InChI=1S/C15H20O/c1-10-5-4-6-15(3)8-14-12(7-13(10)15)11(2)9-16-14/h9,13H,1,4-8H2,2-3H3/t13-,15+/m0/s1

1 reference

Atractylon (English)

8 October 2016

2 references

Atractylon (English)

8 October 2016

ChEBI release 2020-09-01

2 references

https://commonchemistry.cas.org/detail?cas_rn=6989-21-5

Atractylone (English)

8 October 2016

6 April 2021

InChIKey

1 reference

(4aS,8aR)-3,8a-Dimethyl-5-methylene-4,4a,5,6,7,8,8a,9-octahydronaphtho[2,3-b]furan (English)

8 October 2016

2 references

matched by identifier from

Atractylon (English)

retrieved

8 October 2016

InChIKey

ChEBI ID

80796

mapping relation type

2 references

matched by identifier from

Atractylone (English)

retrieved

8 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H20O/c1-10-5-4-6-15(3)8-14-12(7-13(10)15)11(2)9-16-14/h9,13H,1,4-8H2,2-3H3/t13-,15+/m0/s1

1 reference

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

ATRACTYLON (English)

8 October 2016

1 reference

2 references

matched by identifier from

InChIKey

DSSTOX compound identifier

0 references

0 references

1 reference