FeTPPS

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FeTPPS

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Cat No: 17187

Biochemicals - More Biochemicals

Peroxynitrite (Item No. 81565) is a highly reactive nitrogen species formed from the reaction of nitric oxide (NO) and superoxide.{28295} FeTPPS is a ferric porphyrin complex that causes the decomposition of peroxynitrite by catalytic isomerization to ...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

Fe(III)5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato chloride

Correlated keywords:

98312-37-9 biochemical oxidative injury intracellular signaling nitric oxide 5,10,15,20-Tetrakis(4-sulfonatophenyl)porphyrinato Iron (III) chloride peroxynitrite decomposition catalyst ferric porphyrin complex decomposition decompose catalytic isomerization nitrate in vitro vivo reactive nitrogen species cytoprotection stress cellular damage

Product Overview:
Peroxynitrite (Item No. 81565) is a highly reactive nitrogen species formed from the reaction of nitric oxide (NO) and superoxide.{28295} FeTPPS is a ferric porphyrin complex that causes the decomposition of peroxynitrite by catalytic isomerization to produce nitrate both in vitro and in vivo.{28292} The conversion of this reactive nitrogen species to nitrate results in cytoprotection (EC50 = 5 µM).{28292,28290} FeTPPS does not complex with NO and does not alter superoxide directly. It is commonly used to elucidate the roles of peroxynitrite in oxidative stress, cell damage, and intracellular signaling.{28294,28291,28293}

Size	50 mg
Shipping	dry ice
CAS Number	90384-82-0
Molecular Formula	C₄₄H₂₄ClFeN₄O₁₂S₄ • 4H
SMILES	[Cl-][Fe+3]123[N-]4C5=CC=C4C(C6=CC=C(S([O-])(=O)=O)C=C6)=C(C=C7)[N]1=C7C(C8=CC=C(S([O-])(=O)=O)C=C8)=C(C=C9)[N-]2C9=C(C%10=CC=C(S([O-])(=O)=O)C=C%10)C%11=[N]3C(C=C%11)=C5C%12=CC=C(S([O-])(=O)=O)C=C%12.[H+].[H+].[H+].[H+]
Molecular Weight	1024,3
Formulation	A crystalline solid
Purity	≥95%
Custom Code	2903.99
UNSPSC code	12352100

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MSDS

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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