399019
6′-メトキシ-2′-アセトナフトン
98%
別名:
1-(6-Methoxy-2-naphthalenyl)ethanone, 2-Acetyl-6-methoxynaphthalene, NSC 105564
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この商品について
化学式:
CH3OC10H6COCH3
CAS番号:
分子量:
200.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-453-8
MDL number:
製品名
6′-メトキシ-2′-アセトナフトン, 98%
InChI key
GGWCZBGAIGGTDA-UHFFFAOYSA-N
InChI
1S/C13H12O2/c1-9(14)10-3-4-12-8-13(15-2)6-5-11(12)7-10/h3-8H,1-2H3
SMILES string
COc1ccc2cc(ccc2c1)C(C)=O
assay
98%
mp
107-109 °C (lit.)
functional group
ketone
Quality Level
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関連するカテゴリー
General description
6′-Methoxy-2′-acetonaphthone (6-methoxy-2-naphthylacetic acid ) is metabolite of nabumetone, a phototoxic nonsteroidal antiinflammatory drug.1
6′-Methoxy-2′-acetonaphthone is suitable for use in the synthesis of 6-methoxy-2-naphthylacetic acid. It may be used in the preparation of fluorogenic aldol sensors.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Skin Irrit. 2
保管分類
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
F Boscá et al.
Photochemistry and photobiology, 71(2), 173-177 (2000-02-25)
Nabumetone is a phototoxic nonsteroidal antiinflammatory drug used for the treatment of osteoarthritis. However, nabumetone is considered a prodrug with its metabolite 6-methoxy-2-naphthylacetic acid the active form. Photophysical and photochemical studies on this metabolite have been undertaken. It undergoes photodecarboxylation
M Nobilis et al.
Journal of pharmaceutical and biomedical analysis, 32(4-5), 641-656 (2003-08-06)
The disposition of the non-steroidal anti-inflammatory drug (NSAID) nabumetone after a single oral dose administration of nabumetone tablets to humans and minipigs was investigated. Nabumetone is a prodrug, which is metabolized in the organism to the principal pharmacodynamically active metabolite
B List et al.
Proceedings of the National Academy of Sciences of the United States of America, 95(26), 15351-15355 (1998-12-23)
The synthesis of novel fluorogenic retro-aldol substrates for aldolase antibody 38C2 is described. These substrates are efficiently and specifically processed by antibody aldolases but not by natural cellular enzymes. Together, the fluorogenic substrates and antibody aldolases provide reporter gene systems
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