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4443-09-8,MFCD00016946
Catalog No.:AA00DFMR

4443-09-8 | 5,7,8-Trihydroxy-2-phenyl-4H-chromen-4-one

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1mg
≥95%
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$89.00   $62.00
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5mg
≥95%
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$386.00   $270.00
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10mg
≥95%
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$682.00   $477.00
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50mg
95% (HPLC)
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$3,361.00   $2,353.00
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100mg
95% (HPLC)
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$5,770.00   $4,039.00
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500mg
95% (HPLC)
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$18,493.00   $12,945.00
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1000mg
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$29,555.00   $20,689.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00DFMR
Chemical Name:
5,7,8-Trihydroxy-2-phenyl-4H-chromen-4-one
CAS Number:
4443-09-8
Molecular Formula:
C15H10O5
Molecular Weight:
270.2369
MDL Number:
MFCD00016946
SMILES:
Oc1cc(O)c2c(c1O)oc(cc2=O)c1ccccc1
NSC Number:
128304
Properties
Computed Properties
 
Complexity:
413  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
1  
XLogP3:
2.7  

Downstream Synthesis Route

[1]Yamashita,Yasunobu;Biard,Alan;Hanaya,Kengo;Shoji,Mitsuru;Sugai,Takeshi[Bioscience,BiotechnologyandBiochemistry,2017,vol.81,#7,p.1279-1284]

[2]Pillon[BulletindelaSocieteChimiquedeFrance,1954,p.9,21]Raoetal.[Proceedings-IndianAcademyofSciences,SectionA,1947,#25,p.427,430]

[3]CurrentPatentAssignee:JingLinlin;MaHuiping;FanPengcheng;FanXiaofei;HeLei;JiaZhengping-CN104926768,2018,B

[1]ChemischeBerichte,1939,vol.72,p.1914,1916

[2]ActaPhytochimica,1930,vol.5,p.103,110    ChemischesZentralblatt,1931,vol.102,p.1760

[1]Phytochemistry,1980,vol.19,p.741-746

[1]ChemischeBerichte,1939,vol.72,p.1914,1916

[1]JournalofAgriculturalandFoodChemistry,2003,vol.51,p.389-393

Literature

Title: Relationships between structures of hydroxyflavones and their antioxidative effects.

Journal: Bioorganic & medicinal chemistry letters 20100915

Title: New inhibitors for expression of IgE receptor on human mast cell.

Journal: Bioorganic & medicinal chemistry letters 20100401

Title: Suppressive effects of T-412, a flavone on interleukin-4 production in T cells.

Journal: Biological & pharmaceutical bulletin 20091101

Title: Empirically predicted 13C NMR chemical shifts for 8-hydroxyflavone starting from 7,8,4'-trihydroxyflavone and from 7,8-dihydroxyflavone.

Journal: Magnetic resonance in chemistry : MRC 20080701

Title: Differential apoptotic effect of wogonin and nor-wogonin via stimulation of ROS production in human leukemia cells.

Journal: Journal of cellular biochemistry 20080401

Title: Wogonin but not Nor-wogonin inhibits lipopolysaccharide and lipoteichoic acid-induced iNOS gene expression and NO production in macrophages.

Journal: International immunopharmacology 20070801

Title: The antioxidative effect of icariin in human erythrocytes against free-radical-induced haemolysis.

Journal: The Journal of pharmacy and pharmacology 20041201

Title: Insect antifeedant activity of flavones and chromones against Spodoptera litura.

Journal: Journal of agricultural and food chemistry 20030115

Title: Inhibition of VHR dual-specificity protein tyrosine phosphatase activity by flavonoids isolated from Scutellaria baicalensis: structure-activity relationships.

Journal: Planta medica 20021201

Title: Choi HJ, et al. Inhibitory Effects of Norwogonin, Oroxylin A, and Mosloflavone on Enterovirus 71. Biomol Ther (Seoul). 2016 Sep 1;24(5):552-8.

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SDS
Tags:4443-09-8 Molecular Formula|4443-09-8 MDL|4443-09-8 SMILES|4443-09-8 5,7,8-Trihydroxy-2-phenyl-4H-chromen-4-one