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855-97-0,MFCD00017558
Catalog No.:AA003IBJ
855-97-0 | 2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4H-chromen-4-one
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100mg
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2 weeks  
$228.00   $160.00
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  • Technical Information
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Technical Information
Catalog Number:
AA003IBJ
Chemical Name:
2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4H-chromen-4-one
CAS Number:
855-97-0
Molecular Formula:
C19H18O6
Molecular Weight:
342.3426
MDL Number:
MFCD00017558
IUPAC Name:
2-(3,4-dimethoxyphenyl)-5,7-dimethoxychromen-4-one
InChI:
InChI=1S/C19H18O6/c1-21-12-8-17(24-4)19-13(20)10-15(25-18(19)9-12)11-5-6-14(22-2)16(7-11)23-3/h5-10H,1-4H3
InChI Key:
CLXVBVLQKLQNRQ-UHFFFAOYSA-N
SMILES:
COc1cc(OC)c2c(c1)oc(cc2=O)c1ccc(c(c1)OC)OC
Properties
Computed Properties
 
Complexity:
504  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
342.11g/mol
Formal Charge:
0
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
342.347g/mol
Monoisotopic Mass:
342.11g/mol
Rotatable Bond Count:
5  
Topological Polar Surface Area:
63.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1  

Synonyms
 
3',4',5,7-tetramethoxyflavone 
3',4',5,7-tetramethyl-luteolin 
Luteolin tetramethylether 
CLXVBVLQKLQNRQ-UHFFFAOYSA-N 
MFCD00017558 
2-(3,4-dimethoxyphenyl)-5,7-dimethoxychromen-4-one 
Luteolin 5,7,3',4'-tetramethyl ether 
4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,7-dimethoxy- 
3',4',5,7-Tetramethyl-luteolin 
AC1LCIPX 
3,4,5,7-tetramethoxyflavone 
CHEMBL327340 
5,7,3',4'-tetramethylluteolin 
SCHEMBL1421511 
CTK5F5306 
5,7,3',4'-tetramethoxyflavone 
DTXSID80234705 
2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4H-1-benzopyran-4-one 
ZINC1081533 
Flavone, 3',4',5,7-tetramethoxy 
LMPK12111074 
AKOS015851531 
MCULE-4084661390 
855-97-0 
VN10045 
ZB015976 
TR-026737 
FT-0614125 
ST50309218 
A841374 
C-20386 
2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-chromen-4-one 
2-(3,4-Dimethoxy-phenyl)-5,7-dimethoxy-chromen-4-one 
2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-1-benzopyran-4-one 
3',4',5,7-Tetramethoxyflavone 
2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4H-chromen-4-one # 
4H-1-Benzopyran-4-one,2-(3,4-dimethoxyphenyl)-5,7-dimethoxy- 
Anisopirol 
C19H18O6 
CID631170 
Flavone, 3',4',5,7-tetramethoxy- 
C19-H18-O6 
C103111 
Luteolin tetramethyl ether 
2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4H-chromen-4-one 
Tetramethoxyluteolin 
5,7,3',4'-Tetramethylluteolin 
Tetramethylluteolin 
Literature

Title: The O-methylation of chrysin markedly improves its intestinal anti-inflammatory properties: Structure-activity relationships of flavones.

Journal: Biochemical pharmacology 20131215

Title: Identification of 5,7,3',4'-tetramethoxyflavone metabolites in rat urine by the isotope-labeling method and ultrahigh-performance liquid chromatography-electrospray ionization-mass spectrometry.

Journal: Journal of agricultural and food chemistry 20120822

Title: Relationship between the structures of flavonoids and their NF-κB-dependent transcriptional activities.

Journal: Bioorganic & medicinal chemistry letters 20111015

Title: Structural requirements of flavonoids for the adipogenesis of 3T3-L1 cells.

Journal: Bioorganic & medicinal chemistry 20110501

Title: Xanthine oxidase inhibitory activities and crystal structures of methoxyflavones from Kaempferia parviflora rhizome.

Journal: Biological & pharmaceutical bulletin 20110101

Title: Chemical constituents from tiger's betel, Piper porphyrophyllum N.E.Br. (Fam. Piperaceae).

Journal: Natural product research 20100301

Title: Simultaneous identification and quantitation of 11 flavonoid constituents in Kaempferia parviflora by gas chromatography.

Journal: Journal of chromatography. A 20070302

Title: Quantitative structure activity relationship studies on the flavonoid mediated inhibition of multidrug resistance proteins 1 and 2.

Journal: Biochemical pharmacology 20050215

Title: Bioactive flavonoids from Kaempferia parviflora.

Journal: Fitoterapia 20040101

Title: Structural requirements of flavonoids for nitric oxide production inhibitory activity and mechanism of action.

Journal: Bioorganic & medicinal chemistry 20030501

Title: Reversal of P-glycoprotein-mediated multidrug resistance by 5,6,7,3',4'-pentamethoxyflavone (Sinensetin).

Journal: Biochemical and biophysical research communications 20020726

Title: Flavonolignan and flavone inhibitors of a Staphylococcus aureus multidrug resistance pump: structure-activity relationships.

Journal: Journal of medicinal chemistry 20010118

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