21764-09-0,MFCD00016928
Catalog No.:AA006ZC9

21764-09-0 | 2-(3-Hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one

Pack Size
Purity
Availability
Price(USD)
Quantity
  
50mg
4 weeks  
$233.00   $163.00
- +
100mg
4 weeks  
$304.00   $213.00
- +
250mg
4 weeks  
$500.00   $350.00
- +
500mg
4 weeks  
$768.00   $538.00
- +
1g
4 weeks  
$1,215.00   $850.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA006ZC9
Chemical Name:
2-(3-Hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one
CAS Number:
21764-09-0
Molecular Formula:
C19H18O7
Molecular Weight:
358.3420
MDL Number:
MFCD00016928
SMILES:
COc1cc2oc(cc(=O)c2c(c1OC)OC)c1ccc(c(c1)O)OC
Properties
Computed Properties
 
Complexity:
534  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
26  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.7  

Literature

Title: Benzo[a]pyrene sensitizes MCF7 breast cancer cells to induction of G1 arrest by the natural flavonoid eupatorin-5-methyl ether, via activation of cell signaling proteins and CYP1-mediated metabolism.

Journal: Toxicology letters 20141015

Title: A simple isocratic HPLC method for the simultaneous determination of sinensetin, eupatorin, and 3'-hydroxy-5,6,7,4'-tetramethoxyflavone in Orthosiphon stamineus extracts.

Journal: Journal of acupuncture and meridian studies 20120801

Title: Flavonoids eupatorin and sinensetin present in Orthosiphon stamineus leaves inhibit inflammatory gene expression and STAT1 activation.

Journal: Planta medica 20120501

Title: Comparative CYP1A1 and CYP1B1 substrate and inhibitor profile of dietary flavonoids.

Journal: Bioorganic & medicinal chemistry 20110501

Title: HPLC and anti-inflammatory studies of the flavonoid rich chloroform extract fraction of Orthosiphon stamineus leaves.

Journal: Molecules (Basel, Switzerland) 20100621

Title: Polymethoxylated flavones induce Ca(2+)-mediated apoptosis in breast cancer cells.

Journal: Life sciences 20061223

Title: Effects of flavonoids on cell proliferation and caspase activation in a human colonic cell line HT29: an SAR study.

Journal: Journal of medicinal chemistry 20050421

Title: Determination of flavonoids from Orthosiphon stamineus in plasma using a simple HPLC method with ultraviolet detection.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20050225

Title: The total synthesis of an aurone isolated from Uvaria hamiltonii: aurones and flavones as anticancer agents.

Journal: Bioorganic & medicinal chemistry letters 20031103

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SDS
Tags:21764-09-0 Molecular Formula|21764-09-0 MDL|21764-09-0 SMILES|21764-09-0 2-(3-Hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one
Catalog No.: AA006ZC9
21764-09-0,MFCD00016928
21764-09-0 | 2-(3-Hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one
Pack Size: 50mg
Purity:
4 weeks
$233.00 $163.00
Pack Size: 100mg
Purity:
4 weeks
$304.00 $213.00
Pack Size: 250mg
Purity:
4 weeks
$500.00 $350.00
Pack Size: 500mg
Purity:
4 weeks
$768.00 $538.00
Pack Size: 1g
Purity:
4 weeks
$1,215.00 $850.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA006ZC9
Chemical Name: 2-(3-Hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one
CAS Number: 21764-09-0
Molecular Formula: C19H18O7
Molecular Weight: 358.3420
MDL Number: MFCD00016928
SMILES: COc1cc2oc(cc(=O)c2c(c1OC)OC)c1ccc(c(c1)O)OC
Properties
Complexity: 534  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 26  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.7  
Literature fold

Title: Benzo[a]pyrene sensitizes MCF7 breast cancer cells to induction of G1 arrest by the natural flavonoid eupatorin-5-methyl ether, via activation of cell signaling proteins and CYP1-mediated metabolism.

Journal: Toxicology letters20141015

Title: A simple isocratic HPLC method for the simultaneous determination of sinensetin, eupatorin, and 3'-hydroxy-5,6,7,4'-tetramethoxyflavone in Orthosiphon stamineus extracts.

Journal: Journal of acupuncture and meridian studies20120801

Title: Flavonoids eupatorin and sinensetin present in Orthosiphon stamineus leaves inhibit inflammatory gene expression and STAT1 activation.

Journal: Planta medica20120501

Title: Comparative CYP1A1 and CYP1B1 substrate and inhibitor profile of dietary flavonoids.

Journal: Bioorganic & medicinal chemistry20110501

Title: HPLC and anti-inflammatory studies of the flavonoid rich chloroform extract fraction of Orthosiphon stamineus leaves.

Journal: Molecules (Basel, Switzerland)20100621

Title: Polymethoxylated flavones induce Ca(2+)-mediated apoptosis in breast cancer cells.

Journal: Life sciences20061223

Title: Effects of flavonoids on cell proliferation and caspase activation in a human colonic cell line HT29: an SAR study.

Journal: Journal of medicinal chemistry20050421

Title: Determination of flavonoids from Orthosiphon stamineus in plasma using a simple HPLC method with ultraviolet detection.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences20050225

Title: The total synthesis of an aurone isolated from Uvaria hamiltonii: aurones and flavones as anticancer agents.

Journal: Bioorganic & medicinal chemistry letters20031103

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