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2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyron

Luteolin Struktur
491-70-3
CAS-Nr.
491-70-3
Bezeichnung:
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyron
Englisch Name:
Luteolin
Synonyma:
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4h-1-benzopyran-4-on;LUTEOLOL;luteoline;cyanidenon;digitoflavone;Rose extract P.E;uteoL;tgrtg;LUTEOLIN;weldlake
CBNumber:
CB7282616
Summenformel:
C15H10O6
Molgewicht:
286.24
MOL-Datei:
491-70-3.mol

2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyron Eigenschaften

Schmelzpunkt:
~330 °C(lit.)
Siedepunkt:
348.61°C (rough estimate)
Dichte
1.2981 (rough estimate)
Brechungsindex
1.4413 (estimate)
storage temp. 
2-8°C
L?slichkeit
Methanol (Slightly, Heated)
Aggregatzustand
powder
pka
6.50±0.40(Predicted)
Farbe
yellow
Wasserl?slichkeit
Soluble in aqueous alkaline solutions (1.4 mg/ml), ethanol (~5 mg/ml), dimethyl sulfoxide (7 mg/ml), 1eq. Sodium hydroxide (5 mM), dimethylformamide (~20 mg/ml), water (1 mg/ml) at 25°C and methanol.
Merck 
14,5614
BRN 
292084
InChIKey
IQPNAANSBPBGFQ-UHFFFAOYSA-N
LogP
2.40
CAS Datenbank
491-70-3(CAS DataBase Reference)
EPA chemische Informationen
Luteolin (491-70-3)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xi
R-S?tze: 36/37/38
S-S?tze: 26-36-36/37/39
WGK Germany  3
RTECS-Nr. LK9275210
HS Code  29329990
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P304+P340 BEI EINATMEN: Die Person an die frische Luft bringen und für ungehinderte Atmung sorgen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.
P405 Unter Verschluss aufbewahren.

2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyron Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-S?tze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.

Beschreibung

Luteolin is a flavone derived from Honeysuckle(Lonicera japonica Thunb). Luteolin is widely distributed in nature. It can be isolated from a variety of natural herbs, vegetables, and fruits. At present, luteolin is found mainly in honeysuckle, chrysanthemum, Schizonepeta, Ajuga, artichokes, Scutellaria, and Callicarpa nudiflora natural herbs. Dietary sources include celery, broccoli, green pepper, parsley, thyme, dandelion, perilla, chamomile tea, carrots, olive oil, peppermint, rosemary, navel oranges, and oregano. It can also be found in the seeds of the palm Aiphanes aculeata.

Chemische Eigenschaften

Yellow Needles

Physikalische Eigenschaften

Appearance: yellow needle crystal. Solubility: slightly soluble in water and soluble in alkaline solution (monohydrate). Density, 1.654 g/cm3. Melting point, 330 °C. Boiling point, 616.1 °C (760 mmHg). Flash point, 239.5 °C. Vapor pressure, 9.03E-16 mmHg (25 °C). Acidity, weak acid.

History

At present, luteolin does not have the application of the proprietary medicine, but as one of the main active ingredients of medicinal plants, there is a long history of application. In northern and southern dynasties, honeysuckle with sweet taste, nontoxic, can treat swelling, lose weight, and prolong life under long-term use. In Tang dynasty, honeysuckle was used for treatment of abdominal distension, hot toxic blood dysentery, and water dysentery. It was showed that the clinical application of honeysuckle had made significant progress.
During the Song and Yuan dynasties, honeysuckle was widely used for the treatment of diseases such as sore and ulcer. To the Ming dynasty, there were many treatises about honeysuckle. For example, it is said in Compendium of Materia Medica: honeysuckle cure all rheumatism QI and all sorts of swollen poison, ulcer,scab, and heat dissipation detoxify. The prescription has also expanded its scope of application. Up to the Qing dynasty, the application of honeysuckle can not only inherit the theory of the predecessors but also put forward some original ideas and innovation in some respects.
In recent years, through the in-depth study of pharmacological effects, it is found that luteolin has significant effects on antitumor, cardioprotection, neuroprotection,respiratory system, immune regulation, anti-inflammatory, spasmolysis, expectorant, anti-allergic, enzyme activities, antioxidant, diuretic, and other aspects.

Verwenden

Luteolin has been used:
  • to induce and elucidate the apoptotic pathway in renal cell carcinoma 786-O cells
  • as an additive in M9 minimal medium to induce nodF gene expression
  • as a reference standard to qualitatively and quantitatively analyse luteolin using reverse phase-high performance liquid chromatography with diode array detector (RP-HPLC-DAD)
  • as a reaction supplement for β-galactosidase assay
  • to elucidate the anti-inflammatory efficacy of luteolin in pseudorabies virus infected RAW264.7 cell line by measuring the anti-inflammatory mediators production and also cell viability and cytotoxicity assay

Definition

ChEBI: Luteolin is a tetrahydroxyflavone in which the four hydroxy groups are located at positions 3', 4', 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers. It has a role as an EC 2.3.1.85 (fatty acid synthase) inhibitor, an antineoplastic agent, a vascular endothelial growth factor receptor antagonist, a plant metabolite, a nephroprotective agent, an angiogenesis inhibitor, a c-Jun N-terminal kinase inhibitor, an anti-inflammatory agent, an apoptosis inducer, a radical scavenger and an immunomodulator. It is a 3'-hydroxyflavonoid and a tetrahydroxyflavone. It is a conjugate acid of a luteolin-7-olate.

Indications

Luteolin compound prescription is mainly used for relieving cough, eliminating phlegm, diminishing inflammation, treating cardiovascular diseases, and treating amyotrophic lateral sclerosis, severe acute respiratory syndrome (SARS), hepatitis, etc.

Allgemeine Beschreibung

Luteolin is a naturally occurring flavone, readily present in vegetables. It may possess many biological properties like anti-tumor activity against condition of skin papilloma. Luteolin is one of the most potent flavanoid inhibitors of soybean and reticulocyte 15-lipoxygenases, with an IC50 of 0.6 μM. Luteolin has also been found to inhibit the release of TNFα from neutrophils, and to inhibit matrix metalloproteinases.

Biologische Aktivit?t

Anti-inflammatory, antioxidant and free radical scavenger. Inhibits LPS-induced TNF- α , IL-6 and inducible nitric oxide production and blocks NF- κ B and AP-1 activation. Antiproliferative; inhibits proliferation of Lewis lung carcinoma cells in vivo .

Pharmakologie

Luteolin can selectively inhibit the fatty acid synthase activity in prostate cancer and breast cancer cells, which is related to the inhibitory effect of luteolin on tumor cell growth and apoptosis. Luteolin can significantly reduce the incidence of colon cancer and the size of tumor caused by dimethylhydrazine, which may be related to the regulation of lipid peroxidation, antioxidation, and antiproliferative effect.
The anti-inflammatory activity of luteolin is related to the inhibition of nitric oxide (NO) and other inflammatory cytokines such as tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) generation and inhibition of protein tyrosine phosphorylation and nuclear transcription factor KB (NF-KB)-mediated gene expression.
Luteolin can enhance the transfer of synapses in the hippocampus dentate gyrus, causing long-term potentiation. Moreover, in chronic hypoperfusion injury caused by vascular occlusion, luteolin can still protect synapses, causing long-term potentiation, and reduce the escape latency in the Morris water maze test in rats.
Luteolin can reduce the degree of hepatic fibrosis, hydroxyproline level in liver tissues (HYP), malondialdehyde (MDA) content, and mRNA expression of procollagen type I and inhibit hepatic stellate cell (HSC) proliferation and collagen synthesis in vitro. Luteolin can also improve the histological changes of pulmonary fibrosis induced by bleomycin, reduce the lung weight index, significantly reduce the increase in MDA and HYP, and inhibit the level of mRNA of transforming growth factor beta 1 (TGF-β1) in lung tissue. Luteolin in vitro can inhibit the proliferation of human embryonic lung fibroblast cells and promote apoptosis .

Anticancer Research

It is a flavone with yellow crystalline appearance. Dietary sources of luteolin includeoregano, celery, orange, broccoli, rosemary, green pepper, peppermint, parsley,olive oil, thyme, carrot, dandelion, chamomile tea, and perilla. It is found to obstructepithelial-mesenchymal transition (Singh et al. 2016b). It is inhibiting the cancercell proliferation, angiogenesis, and metastasis. In addition, it suppresses thepathways like PI3K/AKT, NF-κB, and X-linked inhibitor of apoptosis protein(XIAP) which enhances the cell growth and function. It also induces apoptosis andtumor suppressor p53. Hence, luteolin can be used as a potential antineoplasticagent in different cancers (Lin et al. 2008).

Clinical Use

The natural extract containing luteolin has been used in clinical treatment of many diseases. Lamiophlomis rotata Kudo capsule is made from traditional Chinese medicine Lamiophlomis rotata Kudo, which consists of the medicinal components such as flavonoids, saponins, sterols, amino acids, and many trace elements. Among these components, luteolin content is not less than 0.80 mg/g. This capsule is mainly used for a variety of surgical incision pain, postoperative bleeding, fracture, sprain of muscles, rheumatic pain, dysmenorrhea, uterine bleeding, gingival swelling, and bleeding.

2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyron Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyron Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 607)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Bonerge(Hunan) Lifescience Co., Ltd.
+86-731-82791134 +86-17673622440
Alav.w@bonerge.com China 30 58
Hebei baicao biology science and technology co., ltd
+86-19131911055 +8617824879454
zhang@hbbocao.com China 1029 58
PNP Biotech Co. Ltd
+8618516098983
sales@pnpbiotech.com China 1001 58
Rixing Chemical CO.,LTD.
+86-852-57055271 +8613237129059
sales@rixingbiz.com China 232 58
Shaanxi Dideu Medichem Co. Ltd
18192627656
1012@dideu.com China 3003 58
Hebei Chuanghai Biotechnology Co,.LTD
+86-13131129325
sales1@chuanghaibio.com China 5889 58
Hebei Weibang Biotechnology Co., Ltd
+8617732866630
bess@weibangbio.com China 18151 58
Hebei Kingfiner Technology Development Co.Ltd
+86-15532196582 +86-15373005021
lisa@kingfinertech.com China 3010 58
Anhui Ruihan Technology Co., Ltd
+8617756083858
daisy@anhuiruihan.com China 973 58
Chongqing Zhihe Biopharmaceutical Co., Ltd.
+86-18580541567; +8618580541567
sales@zhswyy.com China 301 58

491-70-3(2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-benzopyron)Verwandte Suche:


  • 3',4',5,7-TETRAHYDROXYFLAVONE,FLACITRAN,LUTEOLOL
  • 2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-4H-1-BENZOPYRAN-4-ONE
  • 2-(3,4-DIHYDROXY-PHENYL)-5,7-DIHYDROXY-CHROMEN-4-ONE
  • 5,7,3',4'-TETRAHYDROXYFLAVONE
  • LUTEOLIN
  • LUTEOLIN-3',7-O-DIGLUCURONIDE
  • FLACITRAN
  • cyanidenon digitoflavone 3',4',5,7-Tetrahydroxyflavone 5,7,3',4'-Tetrahydroxyflavone
  • peannt shell extract
  • 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-
  • Luteolin Synonyms : 3`,4`,5,7-Tetrahydroxyflavone
  • Luteolin, >=98%(HPLC)
  • Flavopurpol
  • Daphneflavonol
  • 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-chroMen-4-one
  • YaMa Kariyasu
  • Salifazide
  • 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-benzopyran-4-one
  • RARECHEM AB DU K001
  • weldlake
  • cyanidenon1470
  • c.i.naturalyellow2
  • c.i.75590
  • 3’,4’,5,7-tetrahydroxy-flavon
  • LUTEOLIN MONOHYDRATE
  • LUTEOLIN(P)
  • Luteolin,3′,4′,5,7-Tetrahydroxyflavone
  • Luteolin ,96%
  • 5,7-dihydroxy-
  • 3’,4’,5,7-tetrahydroxyflavone Digitoflavone Cyanidenon
  • Luteolin 98.0%min
  • LUTEOLIN WITH HPLC
  • 3',4',5,7-Tetrahydroxyflavone
  • LUTEOLIN hplc
  • LUTEOLIN(SH)
  • Luteolin(PeanutShellPe)98%ByHplc
  • LUTEOLIN 98+% BY HPLC
  • 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-benzopyrone
  • Luteolin (Ingredients)
  • Luteolin 491-70-3
  • Luteolin extract powder
  • Nano-Liposomal Luteolin,Water-Soluble Luteolin
  • Luteolin - CAS 491-70-3 - Calbiochem
  • Nano Liposomal Luteolin
  • Luteloin
  • Luteolin USP/EP/BP
  • Luteolin / luteoline
  • Luteolin (Digitoflavone)
  • 4-(5,7-dihydroxy-4-oxo-1-benzopyran-2-yl)-2-hydroxyphenolate
  • uteoL
  • 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4h-1-benzopyran-4-on
  • LUTEOLOL
  • luteoline
  • digitoflavone
  • Rose extract P.E
  • cyanidenon
  • Sophora flower bud extract
  • Luteolin (6CI)
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