Glycitin

CAT: 0013-GTR19171609-02Size: 1 ml x 10 mM (in DMSO)Dry Ice: NoHazardous: No

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CAT#:0013-GTR19171609-02Size:1 ml x 10 mM (in DMSO)

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24/48H Stock Items & 2 to 6 Weeks non Stock Items.

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Description

Glycitin is a legume-derived isoflavone glycoside studied for its osteogenic properties. Research indicates it stimulates the proliferation of bone marrow stromal cells and osteoblasts in vitro while demonstrating an overall bone turnover-suppressing effect in related studies.

CAS Number

40246-10-4

Product Name Alternative

Bacterial, Inhibitor, InfluenzaVirus, Influenza Virus, inhibit, Glycitein-7-beta-O-glucoside, Glycitein-7-b-O-glucoside, Glycitein-7-β-O-glucoside, Glycitin, Glycitein 7-O-beta-glucoside, Glycitein 7-O-b-glucoside, Glycitein 7-O-β-glucoside

Field of Research

Infectious Disease & Virology

Purity

98.54% (May vary between batches)

Solubility

DMSO:55.00 mg/mL (123.21 mM) ;10% DMSO+40% PEG300+5% Tween 80+45% Saline:2.00 mg/mL (4.48 mM)

Smiles

O=C1C=2C (=CC (O[C@@H]3O[C@H] (CO) [C@@H] (O) [C@H] (O) [C@H]3O) =C (OC) C2) OC=C1C4=CC=C (O) C=C4

Molecular Formula

C22H22O10

Molecular Weight

446.40

Storage Conditions

-20°C

Notes

For research use only.

Chemical Information

Glycitin

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 7-hydroxyisoflavones 7-O-beta-D-glucoside, a hydroxyisoflavone, a methoxyisoflavone and a monosaccharide derivative.

CAS Number	40246-10-4
PubChem CID	187808
IUPAC Name	3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Molecular Formula	C22H22O10
Molecular Weight	446.4
XLogP	0.6
Topological Polar Surface Area	155
Hydrogen Bond Donor Count	5
Hydrogen Bond Acceptor Count	10
Rotatable Bond Count	5
Heavy Atom Count	32
Formal Charge	0
Complexity	690

SMILES

COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

InChI

InChI=1S/C22H22O10/c1-29-15-6-12-14(30-9-13(18(12)25)10-2-4-11(24)5-3-10)7-16(15)31-22-21(28)20(27)19(26)17(8-23)32-22/h2-7,9,17,19-24,26-28H,8H2,1H3/t17-,19-,20+,21-,22-/m1/s1

InChIKey

OZBAVEKZGSOMOJ-MIUGBVLSSA-N

Chemical Structure

2D Structure

CAS: 40246-10-4

CID: 187808

Formula: C22H22O10

MW: 446.4

Interactive 3D Structure

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View on PubChem Raw 3D data

Computed Properties

Property	Value
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 Å²
Heavy Atom Count	32
Formal Charge	0
Complexity	690
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently-Bonded Unit Count	1
Compound Is Canonicalized	Yes

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Alternative Products

Catalog	Name
HY-N0012-01	Glycitin
HY-N0012R-01	Glycitin (Standard)
BC036-005	Glycitin, >99%

Glycitin

Chemical Information

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