1. Cell Cycle/DNA Damage Vitamin D Related/Nuclear Receptor Metabolic Enzyme/Protease
  2. PPAR
  3. L-796449

L-796449 is a potent PPARγ agonist. L-796449 shows neuroprotective. L-796449 has the potential for the research of stroke.

For research use only. We do not sell to patients.

L-796449 Chemical Structure

L-796449 Chemical Structure

CAS No. : 194608-80-5

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Description

L-796449 is a potent PPARγ agonist. L-796449 shows neuroprotective. L-796449 has the potential for the research of stroke[1].

IC50 & Target

PPARγ[1]

In Vivo

L-796449 (1 mg/kg; i.p.) shows neuroprotective in middle cerebral artery occlusion (MCAO) in the rat brain[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 250 g adult male Fischer rats[1]
Dosage: 1 mg/kg (MCAO 10 minutes before IP injection)
Administration: I.p.
Result: Decreased MCAO-induced infarct size determined 2 and 7 days after the ischemic injury, inhibited MCAO-induced expression of iNOS and MMP-9 but did not affect COX-2 levels at the time examined; increased the expression of heme oxygenase-1 (HO-1) and inhibited NF-κB signaling.
Molecular Weight

495.03

Formula

C28H27ClO4S

CAS No.
SMILES

O=C(CC1=CC=C(C(Cl)=C1)SCCCOC2=C(C3=C(C(C4=CC=CC=C4)=CO3)C=C2)CCC)O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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L-796449
Cat. No.:
HY-123654
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