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Imanixil

Cat. No. M30580
Imanixil Structure
Synonym:

HOE-402(free base)

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Biological Activity

Imanixil (HOE-402 free base) is an inducer of the LDL receptor (LDLR). Imanixil (HOE-402 free base) is also a potent cholesterol-lowering compound, which inhibits very low density-lipoprotein (VLDL) production, and consequently attenuates atherosclerosis development.

Chemical Information
Molecular Weight 394.35
Formula C17H17F3N6O2
CAS Number 75689-93-9
Form Solid
Solubility (25°C) DMSO 62.5 mg/mL (ultrasonic)
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] Viviane Doggwiler, et al. J Control Release. Efficient colonic drug delivery in domestic pigs employing a tablet formulation with dual control concept

[2] Viviane Doggwiler, et al. Int J Pharm. Tablet formulation with dual control concept for efficient colonic drug delivery

[3] Maria De Mieri, et al. Bioorg Med Chem. Anti-trypanosomal cadinanes synthesized by transannular cyclization of the natural sesquiterpene lactone nobilin

[4] Myriam Sohn, et al. J Biomed Opt. Film thickness frequency distribution of different vehicles determines sunscreen efficacy

[5] Michael Lanz, et al. Drug Dev Ind Pharm. Chewability testing in the development of a chewable tablet for hyperphosphatemia

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