5-Hydroxyflavone
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5-Hydroxyflavone
structure -
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CAS No:
491-78-1
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Formula:
C15H10O3
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Chemical Name:
5-Hydroxyflavone
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Synonyms:
4H-1-Benzopyran-4-one,5-hydroxy-2-phenyl-;Flavone,5-hydroxy-;5-Hydroxy-2-phenyl-4H-1-benzopyran-4-one;5-Hydroxyflavone;5-Hydroxy-2-phenylchromone;Primuletin;NSC 26745;5-Hydroxy-2-phenylchromen-4-one;5-Hydroxy-2-phenyl-4H-chromen-4-one
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CAS No:
Description
5-Hydroxyflavone, a flavonoid ligand, shows no cytotoxic activity against MCF-7, FaDU, MDA-MB-435S, U87, RPE-1, and HEK293 cells[1].
5-Hydroxyflavone is a member of flavones.
5-Hydroxyflavone Basic Attributes
238.24
238.24
194429
207-743-1
378AE9MHL3
26745
DTXSID90197690
29329990
Characteristics
46.5
3.16560
1.34g/cm3
156-157 °C
425ºC at 760 mmHg
165.4ºC
1.666
7.97E-08mmHg at 25°C
147.3 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]
Safety Information
3
36/37/38
26-36-36/37/39-27-37
Xi
P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
H315
Drug Information
5-Hydroxyflavone has known human metabolites that include (2S,3S,4S,5R)-3,4,5-trihydroxy-6-(4-oxo-2-phenylchromen-5-yl)oxyoxane-2-carboxylic acid.
5-hydroxyflavone
5-Hydroxyflavone Use and Manufacturing
Reactant involved in:• ;Condensation reactions for synthesis of copper(II) complexes as bioactive molecules to combat antioxidants1• ;Thermal behavior studies of vanadyl complexes with flavone derivatives in terms of insulin-mimetic agents2• ;O-methylation with di-Me carbonate3• ;DFT studies on excited-state intramolecular proton transfer4
Polyketides [PK] -> Flavonoids [PK12] -> Flavones and Flavonols [PK1211]
Computed Properties
Molecular Weight:238.24
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:238.062994177
Monoisotopic Mass:238.062994177
Topological Polar Surface Area:46.5
Heavy Atom Count:18
Complexity:355
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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