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Details

Stereochemistry ACHIRAL
Molecular Formula C22H24O9
Molecular Weight 432.4206
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,5,6,7,8,3',4'-HEPTAMETHPHOXYFLAVONE

SMILES

COC1=CC=C(C=C1OC)C2=C(OC)C(=O)C3=C(O2)C(OC)=C(OC)C(OC)=C3OC

InChI

InChIKey=SSXJHQZOHUYEGD-UHFFFAOYSA-N
InChI=1S/C22H24O9/c1-24-12-9-8-11(10-13(12)25-2)16-19(27-4)15(23)14-17(26-3)20(28-5)22(30-7)21(29-6)18(14)31-16/h8-10H,1-7H3

HIDE SMILES / InChI

Molecular Formula C22H24O9
Molecular Weight 432.4206
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Isolation and identification of polymethoxyflavones from the hybrid Citrus, hallabong.
2010-09-08
Flavonoids from the stems of Croton caudatus Geisel. var. tomentosus Hook.
2010-02-26
Simultaneous determination of five bioactive flavonoids in pericarpium Citri reticulatae from china by high-performance liquid chromatography with dual wavelength detection.
2009-08-12
Polymethoxyflavones activate Ca2+-dependent apoptotic targets in adipocytes.
2009-07-08
Monodemethylated polymethoxyflavones from sweet orange (Citrus sinensis) peel inhibit growth of human lung cancer cells by apoptosis.
2009-03
Anti-inflammatory activity of an orange peel polymethoxylated flavone, 3',4',3,5,6,7,8-heptamethoxyflavone, in the rat carrageenan/paw edema and mouse lipopolysaccharide-challenge assays.
2008-10-22
A citrus polymethoxyflavonoid, nobiletin, is a novel MEK inhibitor that exhibits antitumor metastasis in human fibrosarcoma HT-1080 cells.
2008-02-01
Validated reversed phase LC method for quantitative analysis of polymethoxyflavones in citrus peel extracts.
2008-01
Effects of various methoxyflavones on vincristine uptake and multidrug resistance to vincristine in P-gp-overexpressing K562/ADM cells.
2007-10
Efficient and scalable method in isolation of polymethoxyflavones from orange peel extract by supercritical fluid chromatography.
2007-02-01
Preparative isolation and purification of polymethoxylated flavones from Tangerine peel using high-speed counter-current chromatography.
2005-10-07
Effect of flavones on rat brain and lung matrix metalloproteinase activity measured by film in-situ zymography.
2005-04
[Chemical study of citrus plants in the search for cancer chemopreventive agents].
2005-03
Topochemical model for prediction of anti-HIV activity of HEPT analogs.
2005-01-17
Fungicidal potential of methoxylated flavones from citrus for in vitro control of Colletotrichum gloeosporioides, causal agent of anthracnose disease in tropical fruits.
2003-11
Identification of epoxybergamottin as a CYP3A4 inhibitor in grapefruit peel.
2003-02
Genetic toxicity of a standardized mixture of citrus polymethoxylated flavones.
2002-05
Immunotoxicity of a standardized citrus polymethoxylated flavone extract.
2001-11
Cancer chemopreventive activity of 3,5,6,7,8,3',4'-heptamethoxyflavone from the peel of citrus plants.
2001-02-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:21:20 GMT 2025
Edited
by admin
on Mon Mar 31 19:21:20 GMT 2025
Record UNII
288R4CAV1V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,5,6,7,8,3',4'-HEPTAMETHOXYFLAVONE
Preferred Name English
3,5,6,7,8,3',4'-HEPTAMETHPHOXYFLAVONE
Systematic Name English
3-METHOXYNOBILETIN
Common Name English
3',4',3,5,6,7,8-HEPTAMETHOXYFLAVONE
Systematic Name English
FLAVONE, 3,3',4',5,6,7,8-HEPTAMETHOXY-
Systematic Name English
4H-1-BENZOPYRAN-4-ONE, 2-(3,4-DIMETHOXYPHENYL)-3,5,6,7,8-PENTAMETHOXY-
Systematic Name English
2-(3,4-DIMETHOXYPHENYL)-3,5,6,7,8-PENTAMETHOXY-4H-1-BENZOPYRAN-4-ONE
Systematic Name English
3,3',4',5,6,7,8-HEPTAMETHOXYFLAVONE
Systematic Name English
NSC-618928
Code English
Code System Code Type Description
FDA UNII
288R4CAV1V
Created by admin on Mon Mar 31 19:21:20 GMT 2025 , Edited by admin on Mon Mar 31 19:21:20 GMT 2025
PRIMARY
CAS
1178-24-1
Created by admin on Mon Mar 31 19:21:20 GMT 2025 , Edited by admin on Mon Mar 31 19:21:20 GMT 2025
PRIMARY
PUBCHEM
150893
Created by admin on Mon Mar 31 19:21:20 GMT 2025 , Edited by admin on Mon Mar 31 19:21:20 GMT 2025
PRIMARY
EPA CompTox
DTXSID70151912
Created by admin on Mon Mar 31 19:21:20 GMT 2025 , Edited by admin on Mon Mar 31 19:21:20 GMT 2025
PRIMARY
NSC
618928
Created by admin on Mon Mar 31 19:21:20 GMT 2025 , Edited by admin on Mon Mar 31 19:21:20 GMT 2025
PRIMARY
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