D115606
1,5-Dihydroxynaphthalene
97%
Sinônimo(s):
1,5-Naphthalenediol
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About This Item
Fórmula linear:
C10H6(OH)2
Número CAS:
Peso molecular:
160.17
Beilstein:
2044951
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
97%
forma
powder
pf
259-261 °C (dec.) (lit.)
cadeia de caracteres SMILES
Oc1cccc2c(O)cccc12
InChI
1S/C10H8O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1-6,11-12H
chave InChI
BOKGTLAJQHTOKE-UHFFFAOYSA-N
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Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1B
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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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)
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
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