Narirutin
Aplikasyon Narirutin
Narirutin se youn nan eleman aktif izole nan Citrus unshiu, ki gen aktivite antioksidan ak anti-enflamatwa.Narirutin se yon inibitè shikimate kinaz ak efè anti tibèkiloz.
Non Narirutin
Non angle: narirutin
Alyas Chinwa: naringin-7-o-rutoside |naringin
Byoaktivite Narirutin
Deskripsyon: narirutin se youn nan engredyan yo aktif izole nan Citrus unshiu.Li gen aktivite antioksidan ak anti-enflamatwa.Narirutin se yon inibitè shikimate kinaz ak efè anti tibèkiloz.
Kategori ki gen rapò: chemen signal >> lòt >> lòt
Research Field >> enflamasyon / iminite
Referans: [1] Sahu PK, et al.Estrikti ki baze sou Dekouvèt Narirutin kòm yon inhibitor Shikimate Kinase ak pisans anti-tuberkulèr.Curr Comput Aided Drug Des.25 oktòb 2019.
[2].Funaguchi N, et al.Narirutin inibit enflamasyon Airway nan yon modèl sourit alèjik.Clin Exp Pharmacol Physiol.2007 Out;34(8):766-70.
Pwopriyete fizikochimik Narirutin
Dansite: 1.7 ± 0.1 g / cm3
Pwen bouyi: 924.3 ± 65.0 ° C nan 760 mmHg
Pwen k ap fonn: 152-190 º C
Fòmil molekilè: C27H32O14
Pwa molekilè: 580.535
Flash Point: 307.3 ± 27.8 ° C
Mass egzat: 580.179199
PSA:225.06000
LogP: 2.07
Aparans: poud blan
Presyon vapè: 0.0 ± 0.3 mmHg nan 25 ° C
Endèks refraktif: 1.708
Enfòmasyon sou Sekirite Narirutin
Deklarasyon Sekirite (Ewòp): 22-24 / 25
Kòd transpò machandiz danjere: nonh pou tout mòd transpò
Kòd Ladwàn: 29389090
Literati Narirutin
Berry ak Citrus Phenolic Compounds Inhibit Dipeptidyl Peptidase IV: Enplikasyon nan Jesyon Dyabèt.
Evid.Baze.Konpleman.Altènatif.Med.2013, 479505, (2013)
Efè sante benefisye fwi ak legim nan rejim alimantè a yo te atribiye nan kontni segondè flavonoid yo.Dipeptid
Huanglongbing modifye eleman bon jan kalite ak kontni flavonoid nan zoranj 'Valencia'.
J. Sci.Manje Agrik.96, 73-8, (2016)
Yo nan lòd yo evalye efè a nan Citrus Greening maladi, oswa Huanglongbing (HLB), sou eleman bon jan kalite ak flavonoid sa ki nan zoranj 'Valencia', fwi ki soti nan pye bwa ki pa enfekte (kontwòl), ki soti nan...
Angle alyas Narirutin
(2S)-5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl-6-O-(6-deoxy-α-L-mannopyranosyl)- β-D-glucopyranoside
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 6-O-(6-deoxy-aL-mannopyranosyl)-bD-glucopyranoside
ISONARINGIN
Isoningenin
Naringenin 7-O-rutinoside
4H-1-Benzopyran-4-yon, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2 -(4-hydroxyphenyl)-, (2S)-
Naringenin-7-rutinoside
(2S)-5-Idroksi-2-(4-idroksifenil)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R, 4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}methyl)tetrahydro-2H-pyran-2-yl]oxy}-2,3-dihydro- 4H-chromen-4-yon sèl
Narirutin
(2S)-5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 6-O-(6-deoxy-α-L-mannopyranosyl)-β -D-glucopyranoside
(2S)-5-Idroksi-2-(4-idroksifenil)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R, 4R,5R,6S)-3,4,5-trihydroxy-6-méthyltétrahydro-2H-pyran-2-yl]oxy}méthyl)tétrahydro-2H-pyran-2-yl]oxy}-2,3-dihydro- 4H-chromen-4-one
Naringenin 7-rutinoside
(S)-7-((6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl) -4H-1-benzopyran-4-one3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
naringenin-7-O-rutinoside
Apigenin-7-rutinosid
(2S)-5-Idroksi-2-(4-idroksifenil)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R, 4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}methyl)tetrahydro-2H-pyran-2-yl]oxy}-2,3-dihydro- 4H-chromen-4-on
