A fluorometric substrate for ALDH1A1 and chymotrypsin
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Resorufin Acetate

Item No. 21686

Technical Information
Formal Name
7-(acetyloxy)-3H-phenoxazin-3-one
CAS Number
1152-14-3
Synonyms
  • O-acetyl Resorufin
Molecular Formula
C14H9NO4
Formula Weight
Purity
≥98%
Emission
580 nm
Excitation
570 nm
A solid
DMF: 20 mg/mlDMF:PBS (pH 7.2); (1:7): 0.12 mg/mlDMSO: 5 mg/mlEthanol: 0.1 mg/ml
λmax
214, 246, 345, 435 nm
SMILES
O=C1C=CC2=NC(C=CC(OC(C)=O)=C3)=C3OC2=C1
InChi Code
InChI=1S/C14H9NO4/c1-8(16)18-10-3-5-12-14(7-10)19-13-6-9(17)2-4-11(13)15-12/h2-7H,1H3
InChi Key
UJWKHDKBOVPINX-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

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    Product Description

    Resorufin acetate is a fluorometric probe that acts as a substrate for cytosolic aldehyde dehydrogenase (ALDH1A1) esterase activity.1 It is also a useful substrate for chymotrypsin.2 Upon enzymatic cleavage, the resorufin anion displays red fluorescence (ex/em maxima = 570/580 nm, respectively).3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kitson, T.M., and Kitson, K.E. Studies of the esterase activity of cytosolic aldehyde dehydrogenase with resorufin acetate as substrate. Biochem J. 322(Pt. 3), 701-708 (1997).

    2. Kitson, T.M. Studies on the chymotrypsin-catalysed hydrolysis of resorufin acetate and resorufin bromoacetate. Biochim. Biophys. Acta 1385(1), 43-52 (1998).

    3. Hofmann, J., and Sernetz, M. Immobilized enzyme kinetics analyzed by flow-through microfluorimetry: Resorufin-β-D-galactopyranoside as a new fluorogenic substrate for β-galactosidase. Anal. Chim. Acta 163, 67-72 (1984).