411035
6-Hydroxyflavone
98%
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About This Item
Formula empirica (notazione di Hill):
C15H10O3
Numero CAS:
Peso molecolare:
238.24
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
98%
Forma fisica
solid
Punto di fusione
234-236 °C (lit.)
Stringa SMILE
Oc1ccc2OC(=CC(=O)c2c1)c3ccccc3
InChI
1S/C15H10O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-9,16H
GPZYYYGYCRFPBU-UHFFFAOYSA-N
Informazioni sul gene
rat ... Ar(24208) , Gabra2(29706)
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Zia Ud Din et al.
Histology and histopathology, 35(10), 1197-1209 (2020-09-11)
In this study, the flavonoid, 6-hydroxyflavone was investigated for its renal protective activity in the cisplatin rat model of nephrotoxicity. Male Sprague-Dawley rats weighing 200-250 g were included in the study. 6-Hydroxyflavone was daily administered at 25 and 50 mg/kg
A novel and facile iodine (III)-mediated approach for C (5)-acetoxylation of 6-hydroxyflavone and 6-hydroxyflavanones.
Prakash O, et al.
Tetrahedron Letters, 45(49), 9065-9067 (2004)
Chien-Hung Lai et al.
Evidence-based complementary and alternative medicine : eCAM, 2014, 924560-924560 (2014-05-06)
Osteoblast differentiation plays an essential role in bone integrity. Isoflavones and some flavonoids are reported to have osteogenic activity and potentially possess the ability to treat osteoporosis. However, limited information concerning the osteogenic characteristics of hydroxyflavones is available. This study
Structure of 6-hydroxyflavone.
Seetharaman J and Rajan SS.
Acta Crystallographica Section C, Structural Chemistry, 48(9), 1714-1715 (1992)
Xing Wang et al.
PloS one, 10(3), e0116409-e0116409 (2015-03-20)
Inflammatory responses by kidney mesangial cells play a critical role in the glomerulonephritis. The anti-inflammatory potential of nineteen mono-, di- and polyhydroxylated flavones including fisetin, quercetin, morin, tricetin, gossypetin, apigenin and myricetin were investigated on rat mesangial cells with lipopolysaccharide
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