D115606
1,5-Dihydroxynaphthalene
97%
Sinónimos:
1,5-Naphthalenediol
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About This Item
Fórmula lineal:
C10H6(OH)2
Número de CAS:
Peso molecular:
160.17
Beilstein/REAXYS Number:
2044951
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
97%
form
powder
mp
259-261 °C (dec.) (lit.)
SMILES string
Oc1cccc2c(O)cccc12
InChI
1S/C10H8O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1-6,11-12H
InChI key
BOKGTLAJQHTOKE-UHFFFAOYSA-N
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1B
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Los clientes también vieron
T J Holmes et al.
Biochemical and biophysical research communications, 123(1), 156-162 (1984-08-30)
Irreversible inhibition of soybean lipoxygenase-1 (SL-1) was accomplished via a controlled potential oxidative electrolysis of 1,5-dihydroxynaphthalene (1,5-DHN) at +0.8 V vs SCE. The inactivation of SL-1 with this known inhibitor was greatly enhanced under these electrolytic conditions to which the
Shin-ya Takizawa et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 10(6), 895-903 (2011-02-08)
Photooxidation reactions of 1,5-dihydroxynaphthalene (DHN) have been carried out in the presence of cyclometalated neutral and cationic iridium (Ir) complexes 1-6 as singlet oxygen ((1)O(2)) sensitizers in order to investigate the (1)O(2) generation quantum yield and photosensitizing durability of the
S Gal et al.
Chemistry and physics of lipids, 150(2), 186-203 (2007-09-29)
Copper-induced peroxidation of liposomal palmitoyllinoleoyl-phosphatidylcholine (PLPC) is inhibited by alpha-tocopherol at micromolar concentrations. In our previous study we found that when the liposomes contain phosphatidylserine (PS), nanomolar concentrations of Toc were sufficient to inhibit peroxidation. In an attempt to gain
J Baumann et al.
Prostaglandins, 20(4), 627-639 (1980-10-01)
Until now only few data have been reported on biochemically explicable pharmacological effects of flavonoid structures. When tested against arachidonic acid metabolism many flavonoids were found to be effective against the lipoxygenase and cyclo-oxygenase pathways. Some flavonoids were predominant inhibitors
Interactions of sulfhydryl agents and soybean lipoxygenase inhibitors.
I Knippel et al.
Biochemical pharmacology, 30(12), 1677-1684 (1981-06-15)
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