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Farrerol

CAS No.:
24211-30-1
Catalog Number:
AG00BC9V
Molecular Formula:
C17H16O5
Molecular Weight:
300.3059
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
98%(HPLC)powder
In Stock USA
United States
$53
- +
5mg
98%(HPLC)powder
In Stock USA
United States
$112
- +
25mg
98%(HPLC)powder
In Stock USA
United States
$396
- +
Product Description
Catalog Number:
AG00BC9V
Chemical Name:
Farrerol
CAS Number:
24211-30-1
Molecular Formula:
C17H16O5
Molecular Weight:
300.3059
MDL Number:
MFCD00017315
IUPAC Name:
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one
InChI:
InChI=1S/C17H16O5/c1-8-15(20)9(2)17-14(16(8)21)12(19)7-13(22-17)10-3-5-11(18)6-4-10/h3-6,13,18,20-21H,7H2,1-2H3
InChI Key:
DYHOLQACRGJEHX-UHFFFAOYSA-N
SMILES:
Oc1ccc(cc1)C1CC(=O)c2c(O1)c(C)c(c(c2O)C)O
EC Number:
246-080-2
Properties
Complexity:
417  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
300.1g/mol
Formal Charge:
0
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
300.31g/mol
Monoisotopic Mass:
300.1g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
87A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1  
Literature
Title Journal
Drug interaction study of flavonoids toward CYP3A4 and their quantitative structure activity relationship (QSAR) analysis for predicting potential effects. Toxicology letters 20180915
The antioxidative potential of farrerol occurs via the activation of Nrf2 mediated HO-1 signaling in RAW 264.7 cells. Chemico-biological interactions 20150905
Far infrared-assisted extraction followed by MEKC for the simultaneous determination of flavones and phenolic acids in the leaves of Rhododendron mucronulatum Turcz. Journal of separation science 20120201
Phenolic compounds from the aerial parts of Diplomorpha canescens. Chemical & pharmaceutical bulletin 20120101
Different effects of farrerol on an OVA-induced allergic asthma and LPS-induced acute lung injury. PloS one 20120101
Mechanism and conformational studies of farrerol binding to bovine serum albumin by spectroscopic methods. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20111101
Molecular spectroscopic studies of farrerol interaction with calf thymus DNA. Journal of agricultural and food chemistry 20110824
Characterization of the interaction between farrerol and bovine serum albumin by fluorescence and circular dichroism. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110801
Involvement of estrogen receptor-β in farrerol inhibition of rat thoracic aorta vascular smooth muscle cell proliferation. Acta pharmacologica Sinica 20110401
Subinhibitory concentrations of farrerol reduce α-toxin expression in Staphylococcus aureus. FEMS microbiology letters 20110201
Synthesis and biological activity of flavanone derivatives. Bioorganic & medicinal chemistry letters 20100915
[Dihydroflavones in Rhododendron concinnum]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20100301
Quick and sensitive determination of flavonoids by capillary electrophoresis-potential gradient detection. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20090901
Flavonoids from Bauhinia glauca subsp. pernervosa. Chemical & pharmaceutical bulletin 20090601
Binding analysis of farrerol to lysozyme by spectroscopic methods. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20071001
Flavonoids possess neuroprotective effects on cultured pheochromocytoma PC12 cells: a comparison of different flavonoids in activating estrogenic effect and in preventing beta-amyloid-induced cell death. Journal of agricultural and food chemistry 20070321
Antifungal flavonoids from Hildegardia barteri. Journal of natural products 20051201
Flavanone glycosides from Miconia trailii. Journal of natural products 20030101
Aloin, cinnamic acid and sophorcarpidine are potent inhibitors of tyrosinase. Chinese medical journal 20021201
Determination of active ingredients of Rhododendron dauricum L. by capillary electrophoresis with electrochemical detection. Journal of chromatography. A 20020111
Properties