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(Q104983396)
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4-methoxy-6-styryl-pyran-2-one
chemical compound
4-methoxy-6-(2-phenylethenyl)pyran-2-one
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No label defined
No description defined
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Statements
instance of
group of stereoisomers
0 references
subclass of
chemical compound
0 references
mass
228.078644244
dalton
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₄H₁₂O₃
0 references
canonical SMILES
O=C1OC(C=CC=2C=CC=CC2)=CC(OC)=C1
0 references
found in taxon
Alpinia blepharocalyx
2 references
stated in
A new antiplatelet diarylheptanoid from Alpinia blepharocalyx
stated in
Calyxin H, Epicalyxin H, and Blepharocalyxins A and B, Novel Diarylheptanoids from the Seeds of Alpinia blepharocalyx
Alpinia mutica
2 references
stated in
Phytochemical and cytotoxic investigations of Alpinia mutica rhizomes.
stated in
Constituents of the rhizomes of two Alpinia species of Malaysia
Alpinia rafflesiana
1 reference
stated in
Constituents of the rhizomes of two Alpinia species of Malaysia
Aniba firmula
2 references
stated in
The Chemistry of Rosewood. III. Isolation of 5,6-Dehydrokavain and 4-Methoxyparacotoin from Aniba firmula Mez
stated in
The 2-pyrones of Aniba species
Aniba permollis
1 reference
stated in
The 2-pyrones of Aniba species
Boesenbergia rotunda
2 references
stated in
Bioactive secondary metabolites from Boesenbergia pandurata of Myanmar and their preferential cytotoxicity against human pancreatic cancer PANC-1 cell line in nutrient-deprived medium.
stated in
Medicinal foodstuffs. XXXIV. Structures of new prenylchalcones and prenylflavanones with TNF-alpha and aminopeptidase N inhibitory activities from Boesenbergia rotunda
Lindera umbellata
3 references
stated in
A lignan from Lindera praecox
stated in
A chalcone derivative from the bark of Lindera umbellata
stated in
ChemInform Abstract: Two Novel Flavonoids from the Leaves of Lindera umbellata var. lancea and L. umbellata.
Piper cubeba
1 reference
stated in
Radical scavenging ability of some compounds isolated from Piper cubeba towards free radicals
Piper lolot
1 reference
stated in
Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot
Piper sarmentosum
1 reference
stated in
Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot
Piper methysticum
4 references
stated in
Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses
stated in
Melanogenesis stimulation in murine B16 melanoma cells by Kava (Piper methysticum) rhizome extract and kavalactones
stated in
A chemical and pharmacological investigation of Piper methysticum Forst
stated in
Extracts and kavalactones of Piper methysticum G. Forst (kava-kava) inhibit P-glycoprotein in vitro
Piper sanctum
1 reference
stated in
Antimycobacterial compounds from Piper sanctum
Piper auritum
1 reference
stated in
Antimycobacterial compounds from Piper sanctum
Piper majusculum
4 references
stated in
Extracts and kavalactones of Piper methysticum G. Forst (kava-kava) inhibit P-glycoprotein in vitro
stated in
Melanogenesis stimulation in murine B16 melanoma cells by Kava (Piper methysticum) rhizome extract and kavalactones
stated in
Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses
stated in
A chemical and pharmacological investigation of Piper methysticum Forst
Alpinia roxburghii
2 references
stated in
Calyxin H, Epicalyxin H, and Blepharocalyxins A and B, Novel Diarylheptanoids from the Seeds of Alpinia blepharocalyx
stated in
A new antiplatelet diarylheptanoid from Alpinia blepharocalyx
Alpinia zerumbet
4 references
stated in
Death receptor 5 promoter-enhancing compounds isolated from Catimbium speciosum and their enhancement effect on TRAIL-induced apoptosis.
stated in
HIV-1 integrase and neuraminidase inhibitors from Alpinia zerumbet.
stated in
Advanced glycation end products inhibitors from Alpinia zerumbet rhizomes
stated in
Phenolic compounds from the rhizomes of Alpinia speciosa
Etlingera elatior
1 reference
stated in
Phenolic compounds from the rhizomes of Alpinia speciosa
Identifiers
InChI
InChI=1S/C14H12O3/c1-16-13-9-12(17-14(15)10-13)8-7-11-5-3-2-4-6-11/h2-10H,1H3
0 references
InChIKey
DKKJNZYHGRUXBS-UHFFFAOYSA-N
0 references
CAS Registry Number
1952-41-6
1 reference
stated in
CAS (formerly Chemical Abstracts Service)
retrieved
25 January 2022
PubChem CID
164901
0 references
UniChem compound ID
22625220
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID70860158
1 reference
matched by identifier from
InChIKey
InChIKey
DKKJNZYHGRUXBS-UHFFFAOYSA-N
Probes And Drugs ID
PD087704
0 references
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