An broad-spectrum MMP inhibitor
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PD 166793

Item No. 23762

Technical Information
Formal Name
N-[(4'-bromo[1,1'-biphenyl]-4-yl)sulfonyl]-L-valine
CAS Number
199850-67-4
Molecular Formula
C17H18BrNO4S
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 50 mg/mlDMSO: 50 mg/mlDMSO:PBS (pH 7.2) (1:1): 0.5 mg/mlEthanol: 10 mg/ml
λmax
204, 272 nm
SMILES
BrC1=CC=C(C2=CC=C(S(N[C@@H](C(C)C)C(O)=O)(=O)=O)C=C2)C=C1
InChi Code
InChI=1S/C17H18BrNO4S/c1-11(2)16(17(20)21)19-24(22,23)15-9-5-13(6-10-15)12-3-7-14(18)8-4-12/h3-11,16,19H,1-2H3,(H,20,21)/t16-/m0/s1
InChi Key
GJOCABIDMCKCEG-INIZCTEOSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    PD 166793 is a broad-spectrum matrix metalloproteinase (MMP) inhibitor (IC50s = 6.1, 0.047, 0.012, 7.2, 7.9, 0.008, and 0.24 μM for MMP-1, MMP-2, MMP-3, MMP-7, MMP-9, MMP-13CD, and MMP-14CD, respectively).1 It reverses peroxynitrite-induced decreases in contraction cease time, a measure of cardiac contractility, in isolated rat ventricular myocytes when used at a concentration of 2 μM.2 In vivo, PD 166793 (2 mg/kg per day, p.o.) reduces left ventricular (LV) peak wall stress in a porcine model of congestive heart failure.3 It reduces LV dilation and preserves systolic function in a rat model of progressive heart failure.1 PD 166793 also inhibits age-associated increases in aortic gelatinase and interstitial collagenase activity and mean arterial pressure in rats.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Peterson, J.T., Hallak, H., Johnson, L., et alMatrix metalloproteinase inhibition attenuates left ventricular remodeling and dysfunction in a rat model of progressive heart failure. Circulation 103(18), 2303-2309 (2001).

    2. León, H., Baczkó, I., Sawicki, G., et alInhibition of matrix metalloproteinases prevents peroxynitrite-induced contractile dysfunction in the isolated cardiac myocyte. Br. J. Pharmacol. 153(4), 676-683 (2008).

    3. McElmurray, J.H., III, Mukherjee, R., New, R.B., et alAngiotensin-converting enzyme and matrix metalloproteinase inhibition with developing heart failure: Comparative effects on left ventricular function and geometry. J. Pharmacol. Exp. Ther. 291(2), 799-811 (1999).

    4. Wang, M., Zhang, J., Telljohann, R., et alChronic matrix metalloproteinase inhibition retards age-associated arterial proinflammation and increase in blood pressure. Hypertension 60(2), 459-466 (2012).