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7-Ethoxyresorufin

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    7-<wbr/>Ethoxyresorufin
  • 7-<wbr/>Ethoxyresorufin
Cat No: 16122
Cayman

7-Ethoxyresorufin (7-ER) is a fluorogenic substrate for, and competitive inhibitor of, the cytochrome P450 (CYP) isoform CYP1A1 (IC50 = 0.1 µM).{26089,26092,26091} Upon enzymatic cleavage by CYP1A1, resorufin is released and its fluorescence can be us...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 7-ethoxy-3H-phenoxazin-3-one
Correlated keywords:
  • fluorometric substrates seven 7 ERs 7-ER cytochromes P450 CYP1A1 CYP inhibits inhibitions inhibitors vasodilation nNOS nitric oxides arachidonic acids metabolism ethoxy resorufin CYP1A1 enzymes substrates NOs competitive nNOS uncoupling O-ethylresorufin 7-Ethoxyphenoxazin-3-one 7-Ethoxy-3H-phenoxazin-3-one O-Ethylresorufin
Product Overview:
7-Ethoxyresorufin (7-ER) is a fluorogenic substrate for, and competitive inhibitor of, the cytochrome P450 (CYP) isoform CYP1A1 (IC50 = 0.1 µM).{26089,26092,26091} Upon enzymatic cleavage by CYP1A1, resorufin is released and its fluorescence can be used to quantify CYP1A1 activity. Resorufin displays excitation/emission maxima of 570/580 nm, respectively.{50356} 7-ER has been used in the study of arachidonic acid (Item Nos. 90010
90010.1
10006607) metabolism and the mechanisms of vasodilation.{15972,12467} 7-ER is a noncompetitive inhibitor of neuronal nitric oxide synthase (nNOS; Ki = 0.76 µM).{26088,26090}
Size 1 mg
Shipping dry ice
CAS Number 5725-91-7
Molecular Formula C14H11NO3
SMILES O=C1C=CC2=NC(C=CC(OCC)=C3)=C3OC2=C1
Molecular Weight 241,2
Formulation A solid
Purity ≥95%
Custom Code 2922.19
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

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.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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