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About This Item
Empirical Formula (Hill Notation):
C11H11NO
CAS Number:
Molecular Weight:
173.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
≥98%
form
solid
storage temp.
−20°C
SMILES string
COc1cc(N)cc2ccccc12
InChI
1S/C11H11NO/c1-13-11-7-9(12)6-8-4-2-3-5-10(8)11/h2-7H,12H2,1H3
InChI key
SFKZPTYRENGBTJ-UHFFFAOYSA-N
Related Categories
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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S H Randell et al.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 33(7), 677-686 (1985-07-01)
Dipeptidyl peptidase II (DPP II) in normal rat lung was evaluated by the enzymes' ability to hydrolyze Lys-Ala or Lys-Pro derivatives of 4-methoxy-2-naphthylamine (MNA). For visualization of this activity, the liberated MNA was coupled with fast blue B for light
Epidermal aminopeptidase activity and metabolism as observed in an organized HaCaT cell sheet model.
I Steinsträsser et al.
Journal of pharmaceutical sciences, 86(3), 378-383 (1997-03-01)
Metabolism studies on organized HaCaT keratinocyte cell sheets are reported. Cells were grown on porous membranes to form organized cell sheets of several cell layers, which were considered as a model of viable epidermis. Metabolism was studied by reflection kinetics
S Scharpé et al.
Clinical chemistry, 34(11), 2299-2301 (1988-11-01)
A new fluorometric assay for determining dipeptidyl peptidase IV (DPP IV; EC 3.4.14.5) was developed. The synthetic substrate glycyl-L-proline-4-methoxy-2-naphthylamide (20 mmol/L), Tris buffer (50 mmol/L, pH 8.3), and serum (20 microL) are mixed and incubated. The reaction is stopped with
B Ulbricht et al.
Biological chemistry Hoppe-Seyler, 376(7), 407-414 (1995-07-01)
The cysteine proteases cathepsin B and cathepsin L are very likely involved in invasive processes of normal and malignant cells, they become relevant for a number of diseases and are possibly prognostic markers for the outcome of human lung cancer.
R Gossrau
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 29(3A Suppl), 464-480 (1981-03-01)
Aminopeptidase (AP) A, B, and M, gamma-glutamyltranspeptidase (GGT), endopeptidase I and II, membrane-associated endopeptidase I and II, dipeptidylaminopeptidase (DAP) I, II, and IV, trypsin and chymotrypsin were investigated with 4-methoxy-2-naphthylamine (MNA) substrates and ester proteinases with n-acetyl-L-methionine-1-naphthylester as substrate in
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