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8-isopentenylnaringenin
chemical compound
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No label defined
No description defined
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Statements
instance of
type of chemical entity
0 references
subclass of
8C-substituted flavanone
0 references
mass
340.13107374
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₂₀H₂₀O₅
0 references
canonical SMILES
O=C1C2=C(O)C=C(O)C(=C2OC(C3=CC=C(O)C=C3)C1)CC=C(C)C
0 references
found in taxon
Ashitaba
2 references
stated in
Chalcones and other compounds from the exudates of Angelica keiskei and their cancer chemopreventive effects
stated in
Chalcones and other compounds from the exudates of Angelica keiskei and their cancer chemopreventive effects
Brosimum acutifolium
1 reference
stated in
Flavonoids from Brosimum acutifolium
Erythrina variegata
1 reference
stated in
Isoflavonoids and a cinnamyl phenol from root extracts of Erythrina variegata
Lespedeza cyrtobotrya
1 reference
stated in
Melanin synthesis inhibitors from Lespedeza cyrtobotrya
breadfruit
1 reference
stated in
Prenylated flavonoids from the heartwood of Artocarpus communis with inhibitory activity on lipopolysaccharide-induced nitric oxide production
Sophora alopecuroides
4 references
stated in
Chemical constituents isolated from the Mongolian medicinal plant Sophora alopecuroides L. and their inhibitory effects on LPS-induced nitric oxide production in RAW 264.7 macrophages
stated in
Studies on the constituents of Sophora species. XXII. Constituents of the root of Sophora moorcroftiana BENTH. ex BAKER.(1).
stated in
Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens
stated in
Studies on the constituents of sophora species. XIII. Constituents of the aerial parts of Sophora tomentosa L
Cullen corylifolia
1 reference
stated in
Osteoblasts proliferation and differentiation stimulating activities of the main components of Fructus Psoraleae corylifoliae
Cullen corylifolium
1 reference
stated in
Osteoblasts proliferation and differentiation stimulating activities of the main components of Fructus Psoraleae corylifoliae
liquorice
1 reference
stated in
Field Survey of Glycyrrhiza Plants in Central Asia (2)1). Characterization of Phenolics and Their Variation in the Leaves of Glycyrrhiza Plants Collected in Kazakhstan
Propolis
1 reference
stated in
Chemical constituents of propolis from Myanmar and their preferential cytotoxicity against a human pancreatic cancer cell line
Macaranga bicolor
1 reference
stated in
Prenylated flavonoids of the leaves of Macaranga conifera with inhibitory activity against cyclooxygenase-2.
Glycyrrhiza inflata
1 reference
stated in
Field Survey of Glycyrrhiza Plants in Central Asia (2)1). Characterization of Phenolics and Their Variation in the Leaves of Glycyrrhiza Plants Collected in Kazakhstan
Humulus
1 reference
stated in
Pharmacognostic and pharmacological profile of Humulus lupulus L.
Marshallia grandiflora
1 reference
stated in
New prenylflavanoids from marshallia grandiflora
Helichrysum tenuifolium
1 reference
stated in
Weitere phloroglucin-derivate aus Helichrysum-arten
Sophora tomentosa
2 references
stated in
Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens
stated in
Studies on the constituents of Sophora species. XXII. Constituents of the root of Sophora moorcroftiana BENTH. ex BAKER.(1).
Sophora moorcroftiana
2 references
stated in
Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens
stated in
Studies on the constituents of sophora species. XIII. Constituents of the aerial parts of Sophora tomentosa L
Sophora flavescens
2 references
stated in
Studies on the constituents of Sophora species. XXII. Constituents of the root of Sophora moorcroftiana BENTH. ex BAKER.(1).
stated in
Studies on the constituents of sophora species. XIII. Constituents of the aerial parts of Sophora tomentosa L
Helichrysum athrixiifolium
1 reference
stated in
Weitere phloroglucin-derivate aus Helichrysum-arten
Megaselia flavescens
1 reference
stated in
Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens
Maclura tricuspidata
1 reference
stated in
Benzylated and prenylated flavonoids from the root barks of Cudrania tricuspidata with pancreatic lipase inhibitory activity
Maclura cochinchinensis
1 reference
stated in
Benzophenones and xanthones with isoprenoid groups from Cudrania cochinchinensis
has characteristic
bitterness
1 reference
stated in
BitterDB
Identifiers
InChI
InChI=1S/C20H20O5/c1-11(2)3-8-14-15(22)9-16(23)19-17(24)10-18(25-20(14)19)12-4-6-13(21)7-5-12/h3-7,9,18,21-23H,8,10H2,1-2H3
0 references
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
0 references
CAS Registry Number
68682-02-0
1 reference
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
stated in
CAS Common Chemistry
retrieved
10 April 2021
reference URL
https://commonchemistry.cas.org/detail?cas_rn=68682-02-0
PubChem CID
509245
2 references
stated in
PubChem
retrieved
26 December 2021
inferred from
InChIKey
matched by identifier from
InChIKey
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
ChEBI ID
188606
mapping relation type
exact match
2 references
stated in
ChEBI release 2022-06-13
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C20H20O5/c1-11(2)3-8-14-15(22)9-16(23)19-17(24)10-18(25-20(14)19)12-4-6-13(21)7-5-12/h3-7,9,18,21-23H,8,10H2,1-2H3
SureChEMBL ID
SCHEMBL147316
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
UniChem compound ID
261910
1 reference
stated in
UniChem
MassBank accession ID
MSBNK-RIKEN-PR309036
1 reference
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN-PR310766
1 reference
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN-PR310767
1 reference
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
MSBNK-RIKEN-PR310772
1 reference
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
stated in
MassBank/MassBank-data: release version 2022.06 to wikidata
retrieved
4 September 2022
based on heuristic
InChIKey match
DSSTox substance ID
DTXSID00333502
1 reference
matched by identifier from
InChIKey
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
DSSTOX compound identifier
DTXCID70284592
0 references
Human Metabolome Database ID
HMDB0247465
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
LPEPZZAVFJPLNZ-UHFFFAOYSA-N
Probes And Drugs ID
PD077436
0 references
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