Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q63396593)
Watch
English
Atractylenolide I
chemical compound
In more languages
edit
Statements
instance of
type of chemical entity
0 references
subclass of
eudesmane sesquiterpenoid
0 references
mass
230.130679816
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
(4aS,8aR)-3,8a-dimethyl-5-methylidene-4a,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-2-one
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
Atractylenolide-1
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₅H₁₈O₂
0 references
canonical SMILES
O=C1OC2=CC3(C)CCCC(=C)C3CC2=C1C
0 references
isomeric SMILES
CC1=C2C[C@H]3C(=C)CCC[C@@]3(C=C2OC1=O)C
0 references
found in taxon
Atractylodes japonica
2 references
stated in
A new polyacetylene compound from Atractylodes rhizome.
stated in
Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi
Atractylodes lancea
5 references
stated in
Phytochemical and Pharmacological Studies on Chinese Changzhu
stated in
Cytotoxic activity of sesquiterpenoids from Atractylodes ovata on leukemia cell lines
stated in
5-Lipoxygenase and cyclooxygenase-1 inhibitory active compounds from Atractylodes lancea.
stated in
A new polyacetylene compound from Atractylodes rhizome.
stated in
Anti-inflammatory and Antinociceptive Constituents of Atractylodes japonica Koidzumi
Atractylodes macrocephala
5 references
stated in
A sesquiterpene lactam from Artractylodes macrocephala
stated in
5-Lipoxygenase and cyclooxygenase-1 inhibitory active compounds from Atractylodes lancea.
stated in
Screening for the anti-inflammatory activity of fractions and compounds from Atractylodes macrocephala koidz
stated in
Inflammatory Inhibitory Activity of Sesquiterpenoids from Atractylodes macrocephala Rhizomes
stated in
The Acetylenes from Atractylodes macrocephala
Solanum lyratum
1 reference
stated in
Some sesquiterpenoids and 5α,8α-epidioxysterols fromSolanum lyratum
Chloranthus anhuiensis
1 reference
stated in
Sesquiterpenoids from Chloranthus anhuiensis with Neuroprotective Effects in PC12 Cells
Atractylodes
1 reference
stated in
Antihepatotoxic principles of Atractylodes rhizomes
Identifiers
InChI
InChI=1S/C15H18O2/c1-9-5-4-6-15(3)8-13-11(7-12(9)15)10(2)14(16)17-13/h8,12H,1,4-7H2,2-3H3/t12-,15+/m0/s1
0 references
InChIKey
ZTVSGQPHMUYCRS-SWLSCSKDSA-N
0 references
CAS Registry Number
73069-13-3
1 reference
stated in
CAS (formerly Chemical Abstracts Service)
retrieved
25 January 2022
PubChem CID
5321018
1 reference
matched by identifier from
InChIKey
InChIKey
ZTVSGQPHMUYCRS-SWLSCSKDSA-N
SureChEMBL ID
SCHEMBL1898423
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
ZTVSGQPHMUYCRS-SWLSCSKDSA-N
UniChem compound ID
96466
1 reference
stated in
UniChem
MassBank accession ID
MSBNK-Fac_Eng_Univ_Tokyo-JP002087
0 references
DSSTox substance ID
DTXSID901316467
1 reference
matched by identifier from
InChIKey
InChIKey
ZTVSGQPHMUYCRS-SWLSCSKDSA-N
Probes And Drugs ID
PD012039
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
