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Sulindac

Cat. No. M3461
Sulindac Structure
Size Price Availability Quantity
25mg USD 30  USD30 In stock
50mg USD 40  USD40 In stock
100mg USD 50  USD50 In stock
500mg USD 100  USD100 In stock
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Quality Control & Documentation
Biological Activity

Sulindac (Clinoril) is a non-steroidal anti-inflammatory compound of the arylalkanoic acid class. Like other NSAIDs, it is useful in the treatment of acute or chronic inflammatory conditions. Sulindac is a prodrug, derived from sulfinylindene that is converted in the body to an active NSAID. More specifically, the agent is converted by liver enzymes to a sulfide which is excreted in the bile and then reabsorbed from the intestine. This is thought to help maintain constant blood levels with reduced gastrointestinal side effects.

Chemical Information
Molecular Weight 356.41
Formula C20H17FO3S
CAS Number 38194-50-2
Form Solid
Solubility (25°C) DMSO 70 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] Carol A Burke, et al. Eflornithine plus Sulindac for Prevention of Progression in Familial Adenomatous Polyposis

[2] Jin Won Sung, et al. Population Pharmacokinetics of Sulindac and Genetic Polymorphisms of FMO3 and AOX1 in Women with Preterm Labor

[3] N M Davies, et al. Clinical pharmacokinetics of sulindac. A dynamic old drug

[4] D E Duggan. Sulindac: therapeutic implications of the prodrug/pharmacophore equilibrium

[5] E A Fagan, et al. Sulindac hepatotoxicity

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