Isovitexin
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Isovitexin
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CAS No:
38953-85-4
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Formula:
C21H20O10
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Chemical Name:
Isovitexin
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Synonyms:
4H-1-Benzopyran-4-one,6-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-;Homovitexin;Flavone,6-β-D-glucopyranosyl-4′,5,7-trihydroxy-;6-β-D-Glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Isovitexin;Isovitexin (C-6 isomer);Saponaretin;6-C-Glucosylapigenin;6-C-β-D-Glucopyranosylapigenin;Apigenin 6-C-β-D-glucoside;Apigenin 6-C-β-glucopyranoside;Isoavroside;Apigenin-6-C-glucoside;Avroside;Apigenin-6-C-β-D-glucopyranoside;3681-94-5;29702-25-8;36025-68-0;61383-34-4
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CAS No:
Description
Isovitexin is a flavonoid isolated from rice hulls of Oryza sativa, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB.
Isovitexin is a C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. It has a role as an EC 3.2.1.20 (alpha-glucosidase) inhibitor and a metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It derives from an apigenin. It is a conjugate acid of an isovitexin-7-olate.
Characteristics
177
1.28
1.7±0.1 g/cm3
257-258 °C
807.0±65.0 °C at 760 mmHg
287.1±27.8 °C
1.743
-20°C
Safety Information
NONH for all modes of transport
3
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
H315
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 4 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Isovitexin Use and Manufacturing
Isovitexin can be used to study biochemicals found in plants and nutrition. Isovitexin has been used in a study to assess collagenase inhibitors from Viola yedoensis. Isovitexin has also been used in a study to investigate the inhibitory activity of Gentiana lutea extracts on the enzyme myeloperoxidase (MPO), as well as the antioxidant activity of these extracts and their correlation with the total polyphenol content.
Computed Properties
Molecular Weight:432.4
XLogP3:0.2
Hydrogen Bond Donor Count:7
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:3
Exact Mass:432.10564683
Monoisotopic Mass:432.10564683
Topological Polar Surface Area:177
Heavy Atom Count:31
Complexity:690
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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