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Resorufin benzyl ether *CAS 87687-02-3*

This fluorogenic resorufin ether is widely used for monitoring P450 activities in cell extracts and solutions. Cytochrome P450 oxidase (CYP450) is a large number of evolutionary related oxidative enzymes important in animal, plant, and bacterial physiology. Most cytochromes P450 (CYPs) have about 500 amino acids and a heme group at the active site.

Calculators

Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of Resorufin benzyl ether *CAS 87687-02-3* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM329.696 µL1.648 mL3.297 mL16.485 mL32.97 mL
5 mM65.939 µL329.696 µL659.391 µL3.297 mL6.594 mL
10 mM32.97 µL164.848 µL329.696 µL1.648 mL3.297 mL

Molarity calculator

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Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yield
Resorufin ethyl ether *CAS 5725-91-7*5715846500010.751
Resorufin methyl ether *CAS 5725-89-3*5715846500010.751
Resorufin pentyl ether *CAS 87687-03-4*5715846500010.751

Citations

View all 1 citations: Citation Explorer
Pancreatic progenitor-derived hepatocytes are viable and functional in a 3D high density bioreactor culture system
Authors: Richter, M and Fairhall, EA and Hoffmann, SA and Tröbs, S and Knöspel, F and Probert, PME and Oakley, F and Stroux, A and Wright, MC and Zeilinger, K
Journal: Toxicology Research (2016): 278--290

References

View all 57 references: Citation Explorer
Methoxy-resorufin ether as an electrochemically active biological probe for cytochrome P450 O-demethylation
Authors: Jenkins AT, Dash HA, Boundy S, Halliwell CM, ffrench-Constant RH.
Journal: Bioelectrochemistry (2006): 67
Comparison of cytochrome P450 inhibition assays for drug discovery using human liver microsomes with LC-MS, rhCYP450 isozymes with fluorescence, and double cocktail with LC-MS
Authors: Di L, Kerns EH, Li SQ, Carter GT.
Journal: Int J Pharm. (2006)
Ginkgo biloba does not alter clearance of flurbiprofen, a cytochrome P450-2C9 substrate
Authors: Greenblatt DJ, von Moltke LL, Luo Y, Perloff ES, Horan KA, Bruce A, Reynolds RC, Harmatz JS, Avula B, Khan IA, Goldman P.
Journal: J Clin Pharmacol (2006): 214
Structure of microsomal cytochrome P450 2B4 complexed with the antifungal drug bifonazole: insight into P450 conformational plasticity and membrane interaction
Authors: Zhao Y, White MA, Muralidhara BK, Sun L, Halpert JR, Stout CD.
Journal: J Biol Chem (2006): 5973
Cytochrome P450 (CYP) inhibition screening: comparison of three tests
Authors: Turpeinen M, Korhonen LE, Tolonen A, Uusitalo J, Juvonen R, Raunio H, Pelkonen O.
Journal: Eur J Pharm Sci (2006): 130
Page updated on December 17, 2024

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Physical properties

Molecular weight

303.31

Solvent

DMSO

Spectral properties

Absorbance (nm)

570

Extinction coefficient (cm -1 M -1)

650001

Excitation (nm)

571

Emission (nm)

584

Quantum yield

0.751

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12352200

CAS

87687-02-3
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