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Orientin

Short Description:

Common name: kaempferoside English Name: orientin

CAS No.: 28608-75-5 molecular weight: 448.377

Density: 1.8 ± 0.1 g / cm3 boiling point: 816.1 ± 65.0 ° C at 760 mmHg

Molecular formula: c21h20o11 melting point: 260-285 º C

Flash point: 289.1 ± 27.8 ° C


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Application of Orientin

Orientin is a naturally occurring bioactive flavonoid with a variety of biological characteristics, including anti-inflammatory, antioxidant, anti-tumor, heart protection and so on. Orientin is a promising neuroprotective agent, which is suitable for the treatment of neuropathic pain.

Bioactivity of Orientin

Description: orientin is a naturally occurring bioactive flavonoid with a variety of biological characteristics, including anti-inflammatory, antioxidant, anti-tumor, heart protection and so on. Orientin is a promising neuroprotective agent, which is suitable for the treatment of neuropathic pain.

Related Categories:  research field > > cancer
Signal path > > other > > other
Research field > > neurological diseases

Reference: [1]. Dhakal H, et al. Inhibitory effects of orientin in mast cell-mediated allergic inflammation. Pharmacol Rep. 2020 Jan 24.
[2]. Guo D, et al. Orientin and neuropathic pain in rats with spinal nerve ligation. 61Int Immunopharmacol. 2018 May;58:72-79.

Physicochemical Properties of Orientin

Density: 1.8 ± 0.1 g / cm3

Boiling Point: 816.1 ± 65.0 ° C at 760 mmHg

Melting Point: 260-285 º C

Molecular Formula: C21H20O11

Molecular Weight: 448.377

Flash Point: 289.1 ± 27.8 ° C

Accurate Mass: 448.100555

PSA: 201.28000

LogP: 1.58

Appearance: yellow powder

Vapor Pressure: 0.0 ± 3.1 mmHg at 25 ° C

Refractive Index: 1.767

Water Solubility: 1 M

NaOH: soluble1mg / ml, clear, yellow orange

Digitalis safety information

Safety statement (Europe): 24 / 25

Transport code of dangerous goods: nonh for all modes of transportRTECS号:DJ3009300

Literature review of Orientin

Distinction of the C-glycosylflavone isomer pairs orientin/isoorientin and vitexin/isovitexin using HPLC-MS exact mass measurement and in-source CID.

Phytochem. Anal. 16(5) , 295-301, (2005)

HPLC-MS using collision induced dissociation (CID) has been utilised for the identification of the C-glycosylflavone isomer pairs orientin/isoorientin and vitexin/isovitexin. HPLC-CID/MS analyses prod..

Antihypertensive and cardioprotective effects of the Lagenaria siceraria fruit in NG-nitro-L-arginine methyl ester (L-NAME) induced hypertensive rats.

Pharm. Biol. 50(11) , 1428-35, (2012)

Lagenaria siceraria (Molina) Standl. (Cucurbitacae) (LS) has been reported to possess cardioprotective, antihyperlipidemic, and diuretic activities.To evaluate antihypertensive and cardioprotective ef...

Development and validation of an HPTLC method for simultaneous quantitation of isoorientin, isovitexin, orientin, and vitexin in bamboo-leaf flavonoids.

J. AOAC Int. 93(5) , 1376-83, (2010)

A simple HPTLC method has been developed for the simultaneous determination of isoorientin, isovitexin, orientin, and vitexin, both pure and in commercial samples of bamboo-leaf flavonoids. The flavon...

English Alias of Orientin

(1S)-1,5-Anhydro-1-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-8-yl]-D-glucitol

2-(3,4-Dihydroxyphényl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxyméthyl)tétrahydro-2H-pyran-2-yl]-4H-chromén-4-one

Orientin 8-C-β-D-glucopyranoside

3',4',5,7-tetrahydroxyflavone-8-C-glucoside

2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]-4H-chromen-4-on

Luteolin-8-C-glucoside

3',4',5,7-tetrahydroxyflavone 8-glucoside

4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-8-β-D-glucopyranosyl-5,7-dihydroxy-

D-Glucitol, 1,5-anhydro-1-C-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-8-yl]-, (1S)-

Orientin

lutexin

2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]-4H-chromen-4-one

2-(3,4-Dihydroxyphenyl)-8-b-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one


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