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Glycitin

Glycitin structure

Glycitin 

structure
  • CAS No:

    40246-10-4

  • Formula:

    C22H22O10

  • Chemical Name:

    Glycitin

  • Synonyms:

    4H-1-Benzopyran-4-one,7-(β-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-;7-(β-D-Glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one;Glycitein 7-O-β-glucoside;Glycitein 7-O-glucoside;Glycitein-7-β-O-glucoside;Glycitin

  • Categories:

    Biochemical Engineering  >  Biosynthetic Natural Products

Description

Glycitin is a natural isoflavone isolated from legumes; promotes the proliferation of bone marrow stromal cells and osteoblasts and suppresses bone turnover.


Glycitin is a glycosyloxyisoflavone that is isoflavone substituted by a methoxy group at position 6, a hydroxy group at position 4' and a beta-D-glucopyranosyloxy group at position 7. It has a role as a plant metabolite. It is a methoxyisoflavone, a hydroxyisoflavone, a monosaccharide derivative and a 7-hydroxyisoflavones 7-O-beta-D-glucoside.

Glycitin Basic Attributes

446.4

446.40

G2S44P62XC

DTXSID80193227

29389090

Characteristics

155

0.6

White solid

1.5±0.1 g/cm3

203-204 °C

751.1±60.0°C at 760 mmHg

264.1±26.4 °C

1.675

Storeat-20

Safety Information

NONH for all modes of transport

3

24/25

Drug Information

Compounds derived from plants, primarily ISOFLAVONES that mimic or modulate endogenous estrogens, usually by binding to ESTROGEN RECEPTORS. (See all compounds classified as Phytoestrogens.)

glycitein 7-O-glucoside

Glycitin Use and Manufacturing

A metabolite of isoflavone derivatives.

Computed Properties

Molecular Weight:446.4
XLogP3:0.6
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:5
Exact Mass:446.12129689
Monoisotopic Mass:446.12129689
Topological Polar Surface Area:155
Heavy Atom Count:32
Complexity:690
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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