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Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate

Cat. No. M31349
Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate Structure
Synonym:

DDC

Size Price Availability Quantity
5g USD 65  USD65 In stock
25g USD 140  USD140 In stock
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Quality Control & Documentation
Biological Activity

Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5- pyridinedicarboxylate (DDC) can be used to induce liver injury in animal models.

Chemical Information
Molecular Weight 267.32
Formula C14H21NO4
CAS Number 632-93-9
Form Solid
Solubility (25°C) DMF 30 mg/mL
DMSO 20 mg/mL
Ethanol 20 mg/mL
Storage RT, protect from light, dry, sealed
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] Ho Taek Oh, et al. J Cell Physiol. CD133-Src-TAZ signaling stimulates ductal fibrosis following DDC diet-induced liver injury

[2] Dan Qin, et al. Theranostics. Lgr5 + cell fate regulation by coordination of metabolic nuclear receptors during liver repair

[3] Li Nan, et al. Exp Mol Pathol. Mallory body (cytokeratin aggresomes) formation is prevented in vitro by p38 inhibitor

[4] Li Nan, et al. Exp Mol Pathol. The p105/50 NF-kappaB pathway is essential for Mallory body formation

[5] Yong Wu, et al. Exp Mol Pathol. The role of laminin-integrin signaling in triggering MB formation. An in vivo and in vitro study

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