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302953-06-6

302953-06-6 Structure

302953-06-6 Structure
IdentificationBack Directory
[Name]

SALOR-INT L135356-1EA
[CAS]

302953-06-6
[Synonyms]

DCHC
SALOR-INT L135356-1EA
DCHC >=98% (HPLC), solid
3-(2,4-Dichlorophenyl)-7-hydroxy-4H-chromen-4-one
[Molecular Formula]

C15H8Cl2O3
[MDL Number]

MFCD01848896
[MOL File]

302953-06-6.mol
[Molecular Weight]

307.13
Chemical PropertiesBack Directory
[Boiling point ]

498.5±45.0 °C(Predicted)
[density ]

1.523±0.06 g/cm3(Predicted)
[solubility ]

DMSO: >20mg/mL
[form ]

solid
[pka]

6.72±0.20(Predicted)
[color ]

yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P301+P310
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

DCHC is a SIRT1 activator but does not induce SIRT1 expression. DCHC can be used for mitochondrial damage related studies[1].
[Definition]

ChEBI: 3-(2,4-dichlorophenyl)-7-hydroxy-4H-chromen-4-one is a member of the class of 7-hydroxyisoflavones that is 3-phenyl-4H-chromen-4-one which is substituted by a hydroxy group at position 7 and chloro groups at positions 2' and 4'. It is a SIRT1 activator. It is a member of 7-hydroxyisoflavones and a dichlorobenzene.
[IC 50]

SIRT1
[References]

[1] Rasbach KA, et al. Isoflavones promote mitochondrial biogenesis. J Pharmacol Exp Ther. 2008 May;325(2):536-43. DOI:10.1124/jpet.107.134882
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