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PD166793 hydrate_Molecular_structure_CAS_)
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PD166793 hydrate

Catalog No. P0047 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C17H20BrNO5S Telephone 1-800-521-8956
M. W. 430.3134 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 154459

SYNONYMS

IUPAC name
(2S)-2-[4-(4-bromophenyl)benzenesulfonamido]-3-methylbutanoic acid hydrate
IUPAC Traditional name
(2S)-2-[4-(4-bromophenyl)benzenesulfonamido]-3-methylbutanoic acid hydrate
Synonyms
(S)-2-(4′-Bromo-biphenyl-4-sulfonylamino)-3-methyl-butyric acid hydrate

DATABASE IDS

MDL Number MFCD12912437

PROPERTIES

Empirical Formula (Hill Notation) C17H18BrNO4S · xH2O
Purity ≥98% (HPLC)
Apperance solid
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature 2-8°C
German water hazard class 2

DETAILS

Description (English)
Biochem/physiol Actions
PD166793 is a broad spectrum, but class-selective, MMP inhibitor (low nM at MMP-2 & 3 and low μM at MMP-1, 7 & 9). Adding PD166793 to the high-fat diet substantially reduced the rise in blood glucose. The improvement of glucose homeostasis in PD166793-treated ZDF rats was a result of the enhancement of β-cell function. It prevents β-cell dysfunction and diabetes in female ZDF rats on a high-fat diet. It has been shown to block left ventricular remodeling and dysfunction in a rat model of heart failure. Preservation of normoglycemia and normal glucose tolerance in compound PD166793-treated animals is accompanied by preservation of the high serum insulin levels that are a consequence of the insulin resistance present in these animals. It is not reversing insulin resistance these animals. The most striking effect of the compound is on pancreatic insulin content and β-cell volume.
Description (简体中文)
Biochem/physiol Actions
PD166793 is a broad spectrum, but class-selective, MMP inhibitor (low nM at MMP-2 & 3 and low μM at MMP-1, 7 & 9). Adding PD166793 to the high-fat diet substantially reduced the rise in blood glucose. The improvement of glucose homeostasis in PD166793-treated ZDF rats was a result of the enhancement of β-cell function. It prevents β-cell dysfunction and diabetes in female ZDF rats on a high-fat diet. It has been shown to block left ventricular remodeling and dysfunction in a rat model of heart failure. Preservation of normoglycemia and normal glucose tolerance in compound PD166793-treated animals is accompanied by preservation of the high serum insulin levels that are a consequence of the insulin resistance present in these animals. It is not reversing insulin resistance these animals. The most striking effect of the compound is on pancreatic insulin content and β-cell volume.

REFERENCES