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Cat. No.: HY-182438

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SDZ 51641

SDZ 51641 is an orally active fatty acid oxidation inhibitor. By reducing fatty acid oxidation, SDZ 51641 deprives the gluconeogenesis process of required energy and cofactors, thereby lowering blood glucose levels in diabetic models. SDZ 51641 can be used in diabetes research.

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

CAS No.: 91456-99-4
Formula: C₁₄H₂₀O₂
Molecular Weight:220.31

Storage:

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

SDZ 51641 Chemical Structure

CAS No.: 91456-99-4

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Biological Activity
- Description
- In Vivo
Chemical Information
Purity & Documentation
References
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Biological Activity

Description

In Vivo

SDZ 51641 (70-100 μmol/kg; p.o.; days 1-11) reduces fatty acid oxidation and blood glucose levels without causing peripheral toxicity in 18-hour fasted normal Sprague‑Dawley rats and streptozotocin (STZ) (HY-13753)-induced diabetic rats^[1].
SDZ 51641 (700 µmol/kg; p.o.; once daily; for 28 days) reduces body weight and testicular weight, while increases liver weight, in normal Sprague Dawley rats compared with the control group^[1].

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

Animal Model:

Male Sprague‑Dawley rats treated STZ^[1]
Dosage:

70 µmol/kg
Administration:

p.o.; daily; 11 days
Result:

Inhibited hepatic fatty acid oxidation, decreased β‑hydroxybutyrate levels, reduced blood glucose production, and lowered serum glucose levels, while avoiding toxic effects on peripheral tissues such as the testes.

Chemical Information

CAS No. 91456-99-4
Molecular Weight 220.31
Formula C₁₄H₂₀O₂
SMILES

CC(C=C1)=CC=C1C2(C(C)(C)C)OCCO2
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

Handling Instructions (2659 KB)

References

[1]. Bebernitz GR, et al. Reduction in glucose levels in STZ diabetic rats by 4-(2,2-dimethyl-1-oxopropyl)benzoic acid: a prodrug approach for targeting the liver. J Med Chem. 2001;44(4):512-523. [Content Brief]

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

100 mg

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