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Phloracetophenone

Cat. No. M19949
Phloracetophenone Structure
Synonym:

2,4,6-trihydroxyacetophenone

Size Price Availability Quantity
100mg USD 50  USD50 In stock
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Quality Control & Documentation
Biological Activity

Phloracetophenone, or 2,4,6-trihydroxyacetophenone (THA), the aglycone component of phloracetophenone glucoside, is a naturally occurring compound obtained from the rhizome of Curcuma comosa (Family Zingiberaceae).

Chemical Information
Molecular Weight 168.15
Formula C8H8O4
CAS Number 480-66-0
Form Solid
Solubility (25°C) DMSO 33 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Richard M LoPachin, et al. Chem Res Toxicol. Enolate-Forming Compounds as a Novel Approach to Cytoprotection

[2] Rahul S Khupse, et al. J Nat Prod. Total synthesis of xanthohumol

[3] Lukmanee Tradtrantip, et al. Am J Physiol Gastrointest Liver Physiol. Phloracetophenone-induced choleresis in rats is mediated through Mrp2

[4] Pawinee Piyachaturawat, et al. Toxicol Lett. Evaluation of the acute and subacute toxicity of a choleretic phloracetophenone in experimental animals

[5] P Piyachaturawat, et al. Eur J Pharmacol. Choleretic activity of phloracetophenone in rats: structure-function studies using acetophenone analogues

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Keywords: Phloracetophenone, 2,4,6-trihydroxyacetophenone supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators


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