40246-10-4

40246-10-4 structure

Name: Glycitin
Chemical Name: 3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
CAS Number: 40246-10-4
Molecular Formula: C₂₂H₂₂O₁₀
Molecular Weight: 446.404
Catalog: Biochemical Natural product
Create Date: 2018-02-26 08:00:00
Modify Date: 2026-06-30 09:34:59
Glycitin is a natural isoflavone isolated from legumes; promotes the proliferation of bone marrow stromal cells and osteoblasts and suppresses bone turnover.

Name	3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Synonyms	Glycitein-7-O-beta-D-glucopyranoside GLYCITIN Glycitin(SH) 4H-1-Benzopyran-4-one 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-Glycitein Glycitein 7-O-β-glucoside 7-(b-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4- on Glycitein 7-O-\|A-glucoside 3-(4-Hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 3-(4-Hydroxyphenyl)-6-methoxy-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one Glycitein 7-glucoside Glycitein 7-O-glucoside 7,4'-DIHYDROXY-6-METHOXYISOFLAVONE-7-D-GLUCOSIDE Glycitin //BP MFCD00800711 Glycitein 7-O-β-glucoside Glycitein7-O-D-glukopyranoside Glycitin, (HPLC) Daidzin/Glycitin 4H-1-Benzopyran-4-one, 7-(.beta.-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy Glycitin, from Soybean 3-(4-hydroxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 4'-Hydroxy-6-methoxy-7-(β-D-glucopyranosyloxy)isoflavone Glycitin from Glycinemax (L.) merr Glycitein 7-O-β-glucoside, 4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy BIDD:ER0468 4',7-Dihydroxy-6-methoxyisoflavone-7-D-glucoside 3-(4-Hydroxyphenyl)-6-methoxy-7-(β-D-glucopyranosyloxy)-4H-1-benzopyran-4-one Glycitein-7-.beta.-O-glucoside 3-(4-Hydroxyphenyl)-6-methoxy-4-oxo-4H-chromen-7-yl β-D-glucopyranoside 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-Glycitein Glycitein-7-O-Glucopyranoside 4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy 7-(-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one GLYCITEIN 7-O-GLUCOSIDE 3-(4-Hydroxyphenyl)-6-methoxy-4-oxo-4H-chromen-7-yl b-D-glucopyranoside Glycitin 7-glucoside Glycitin, froM GlycineMax (L.) Merr Glycitein-7-\|A-O-glucoside Glycitein 7-O-β-D-glucoside 4H-1-Benzopyran-4-one Glycitein-7-b-O-Glucopyranoside Glycitin, >= Glycitein-7-O-β-D-glucopyranoside Glycitein-7-β-O-glucoside Glycitin (15 mg) Glycitin,4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-, Glycitein 7-O-β-glucoside

Description	Glycitin is a natural isoflavone isolated from legumes; promotes the proliferation of bone marrow stromal cells and osteoblasts and suppresses bone turnover.
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Others Natural Products >> Flavonoids
References	[1]. Uesugi T, et al. Comparative study on reduction of bone loss and lipid metabolism abnormality in ovariectomized rats by soy isoflavones, daidzin, genistin, and glycitin. Biol Pharm Bull. 2001 Apr;24(4):368-72. [2]. Li XH, et al. Effect of daidzin, genistin, and glycitin on osteogenic and adipogenic differentiation of bone marrow stromal cells and adipocytic transdifferentiation of osteoblasts. Acta Pharmacol Sin. 2005 Sep;26(9):1081-6.

Density	1.5±0.1 g/cm3
Boiling Point	751.1±60.0 °C at 760 mmHg
Melting Point	210ºC
Molecular Formula	C₂₂H₂₂O₁₀
Molecular Weight	446.404
Flash Point	264.1±26.4 °C
Exact Mass	446.121307
PSA	159.05000
LogP	0.16
Vapour Pressure	0.0±2.6 mmHg at 25°C
Index of Refraction	1.675
Storage condition	Store at -20

Hazard Codes	Xi
Safety Phrases	24/25
RIDADR	NONH for all modes of transport
WGK Germany	3.0

40957-83-3

50-99-7

~6%

1237605-01-4

40246-10-4

Literature: Shimoda, Kei; Hamada, Hiroki Molecules, 2010 , vol. 15, # 8 p. 5153 - 5161

7298-22-8

40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

182284-73-7

~68%

40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

58115-20-1

40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

40957-83-3

40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

1105697-69-5

~94%

40246-10-4

Literature: Al-Maharik, Nawaf; Botting, Nigel P. European Journal of Organic Chemistry, 2008 , # 33 p. 5622 - 5629

58115-19-8

40246-10-4

Literature: Nogradi, Mihaly; Szoellosy, Aron Liebigs Annales, 1996 , # 10 p. 1651 - 1652

Precursor 6
1105697-69-5 40957-83-3 50-99-7 7298-22-8
58115-19-8 58115-20-1
DownStream 1
40957-83-3

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