(Q27138303)

inferred from SMILES

mass

248.141245±0 dalton

1 reference

Atractylenolide III (English)

3,8aalpha-Dimethyl-5-methylene-9aalpha-hydroxy-4abeta,5,6,7,8,8a,9,9a-octahydronaphtho[2,3-b]furan-2(4H)-one

7 October 2016

stereoisomer of

2 references

inferred from InChIKey

(4aS,8aS,9aS)-9a-hydroxy-3,8a-dimethyl-5-methylidene-4,4a,6,7,8,9-hexahydrobenzo[f][1]benzofuran-2-one

inferred from InChI

2 references

inferred from InChIKey

inferred from InChI

chemical formula

C₁₅H₂₀O₃

1 reference

Atractylenolide III (English)

7 October 2016

canonical SMILES

CC1=C2CC3C(=C)CCCC3(CC2(OC1=O)O)C

1 reference

Atractylenolide III (English)

7 October 2016

isomeric SMILES

CC1=C2C[C@H]3C(=C)CCC[C@@]3(C[C@@]2(OC1=O)O)C

1 reference

Two New Triterpenoids from the Roots of Codonopsis pilosula.

Atractylenolide III (English)

7 October 2016

1 reference

Codonopsis subglobosa

1 reference

Two New Triterpenoids from the Roots of Codonopsis pilosula.

Codonopsis pilosula

2 references

Separation and determination of 8beta-hydroxyasterolid and perlolyrine in Codonopsis pilosula by reversed-phase high- performance liquid chromatography

Two New Triterpenoids from the Roots of Codonopsis pilosula.

Atractylodes lancea

9 references

Chemical constituents of Atractylodes chinensis (DC.) Koidz.

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

Cytotoxic activity of sesquiterpenoids from Atractylodes ovata on leukemia cell lines

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

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

Three types of sesquiterpenes from rhizomes of Atractylodes lancea

Cytotoxic activity of sesquiterpenoids from Atractylodes ovata on leukemia cell lines

Antibacterial activity of phytochemicals isolated from Atractylodes japonica against methicillin-resistant Staphylococcus aureus

Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi

Lindera aggregata

1 reference

Sesquiterpene lactones from the root tubers of Lindera aggregata.

Chloranthus tianmushanensis

1 reference

Complex sesquiterpenoids with tyrosinase inhibitory activity from the leaves of Chloranthus tianmushanensis

Tetradium glabrifolium

1 reference

The heartwood constituents of Tetradium glabrifolium

Atractylodes

2 references

Analysis of natural medicines by micellar electrokinetic chromatography (MEKC) (II)--determination of atractylenolide III in Atractylodis Rhizoma

Antihepatotoxic principles of Atractylodes rhizomes

Atractylodes macrocephala

4 references

A sesquiterpene lactam from Artractylodes macrocephala

Sesquiterpenoids from Atractylodes macrocephala act as farnesoid X receptor and progesterone receptor modulators

Study on chemical fingerprinting of crude and processed Atractylodes macrocephala from different locations in Zhejiang province by reversed-phase high-performance liquid chromatography coupled with hierarchical cluster analysis

Inflammatory Inhibitory Activity of Sesquiterpenoids from Atractylodes macrocephala Rhizomes

Trattinnickia aspera

1 reference

Triterpenes and a sesquiterpene lactone in the resin of Trattinnickia aspera (Burseraceae)

Atractylodes japonica

2 references

Antibacterial activity of phytochemicals isolated from Atractylodes japonica against methicillin-resistant Staphylococcus aureus

Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi

Chloranthus henryi

1 reference

Bioactive terpenes from the roots of Chloranthus henryi

Chloranthus anhuiensis

1 reference

Sesquiterpenoids from Chloranthus anhuiensis with Neuroprotective Effects in PC12 Cells

Identifiers

InChI

InChI=1S/C15H20O3/c1-9-5-4-6-14(3)8-15(17)12(7-11(9)14)10(2)13(16)18-15/h11,17H,1,4-8H2,2-3H3/t11-,14+,15-/m0/s1

1 reference

Atractylenolide III (English)

7 October 2016

2 references

Atractylenolide III (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

73030-71-4

1 reference

https://commonchemistry.cas.org/detail?cas_rn=73030-71-4

10 April 2021

1 reference

Atractylenolide III (English)

7 October 2016

2 references

Atractylenolide III (English)

7 October 2016

ChEBI ID

69958

mapping relation type

2 references

Atractylenolide III (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H20O3/c1-9-5-4-6-14(3)8-15(17)12(7-11(9)14)10(2)13(16)18-15/h11,17H,1,4-8H2,2-3H3/t11-,14+,15-/m0/s1

1 reference

ATRACTYLENOLIDE III (English)

7 October 2016

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP002089

1 reference

MassBank accession ID

0 references

MSBNK-Univ_Toyama-TY000099

0 references

SPLASH

splash10-0002-0090000000-c2595ba0868271e59524

0 references

HSDB ID

8108

1 reference

Hazardous Substances Data Bank

28 October 2019

Atractylenolide III (English)

10 May 2021

2 references

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