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46127

Sigma-Aldrich

7-Ethoxy-4-(trifluoromethyl)-cumarin

suitable for fluorescence, ≥98.0% (TLC)

Synonym(e):

Ethyl-4-(trifluormethyl)-umbelliferylether

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About This Item

Empirische Formel (Hill-System):
C12H9F3O3
CAS-Nummer:
115453-82-2
Molekulargewicht:
258.19
Beilstein:
8555209
MDL-Nummer:
MFCD00467588
UNSPSC-Code:
12352204
PubChem Substanz-ID:
24869840

Assay

≥98.0% (TLC)

Löslichkeit

DMF: soluble
DMSO: soluble
methanol: soluble

Fluoreszenz

λex 333 nm; λem 415 nm in methanol

Eignung

suitable for fluorescence

SMILES String

CCOc1ccc2c(OC(=O)C=C2C(F)(F)F)c1

InChI

1S/C12H9F3O3/c1-2-17-7-3-4-8-9(12(13,14)15)6-11(16)18-10(8)5-7/h3-6H,2H2,1H3

InChIKey

OLHOIERZAZMHGK-UHFFFAOYSA-N

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Sonstige Hinweise

Substrate for monitoring the activity of cytochrome P450

Ersetzt durch

Produkt-Nr.
Beschreibung
Preisangaben

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
1336926
429539/1
426319/1
386498/1
382955/1

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Maori Mitsuda et al.
Protein expression and purification, 46(2), 401-405 (2005-11-29)
Improvement of CYP2B6 expression was examined by co-expression with molecular chaperones GroES/EL. Although a CO-reduced difference spectrum was not detected in Escherichia coli transformed only by the CYP2B6-expressing vector, co-expression of GroES/EL resulted in high-level expression which reached over 2000
Thomas Van Leeuwen et al.
Pest management science, 62(5), 425-433 (2006-03-22)
Tetranychus urticae Koch has recently developed resistance to chlorfenapyr in Australia and Japan, but no attempt has yet been made to describe the biochemical mechanisms involved in chlorfenapyr resistance. In this study a laboratory-selected chlorfenapyr-resistant strain was investigated. Resistance to
Emily E Scott et al.
Chemical research in toxicology, 15(11), 1407-1413 (2002-11-20)
Until recently, all known structures of bacterial cytochromes P450 suggested that substrate access to the buried active site occurred via the F-G region, a surface loop distal to the heme cavity. However, the structure of P450 51 indicates a large
Shih-Feng Lan et al.
Toxicology in vitro : an international journal published in association with BIBRA, 24(4), 1314-1323 (2010-02-23)
In this study, we have evaluated the use of ultra-sterile alginate hydrogels encapsulated with HepG2 liver cells for applications in high throughput drug screening. We have studied the cellular viability and metabolic capacity of the encapsulated cells in two different
J Chun et al.
Drug metabolism and disposition: the biological fate of chemicals, 28(8), 905-911 (2000-07-20)
2-Phenyl-2-(1-piperidinyl)propane (PPP), an analog of phencyclidine, was tested for its ability to inactivate cytochrome P450s (P450s) 2B1 and 2B6. PPP inactivated the 7-(benzyloxy)resorufin O-dealkylation activity of liver microsomes obtained from phenobarbital-induced rats with a K(I) of 11 microM. The 7-ethoxy-4-(trifluoromethyl)coumarin
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