Icariside I hydrate Chemical Properties

Melting point:

222-224℃

Boiling point:

838.2±65.0 °C(Predicted)

Density 

1.508±0.06 g/cm3(Predicted)

storage temp. 

2-8°C(protect from light)

form 

Solid

pka

6.16±0.40(Predicted)

color 

Light yellow to green yellow

InChIKey

KKZRHUJZVYWXFJ-DUZPRZLHNA-N

SMILES

C(C1C(=CC(O)=C2C(C(O)=C(C3C=CC(OC)=CC=3)OC=12)=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CC(O)(C)C |&1:23,24,25,27,29,r|

Icariside I hydrate Usage And Synthesis

Uses

Maohuoside A, a single compound isolated from the E. koreanum that potently promotes osteogenesis. Maohuoside A enhances the osteogenesis of bone marrow-derived mesenchymal stem cells via bone morphogenetic protein (BMP) and MAPK signaling pathways[1][2].

References

[1] Ming Cai, et al. Maohuoside A Acts in a BMP-dependent Manner During Osteogenesis. Phytother Res. 2013 Aug;27(8):1179-84. DOI:10.1002/ptr.4840
[2] Lei Yang, et al. Maohuoside A Promotes Osteogenesis of Rat Mesenchymal Stem Cells via BMP and MAPK Signaling Pathways. Mol Cell Biochem. 2011 Dec;358(1-2):37-44. DOI:10.1007/s11010-011-0918-y

Icariside I hydrate(128988-55-6)Related Product Information

• (3S,4S,5S,6S)-2-(methoxycarbonyl)-6-(p-tolylthio)tetrahydro-2H-pyran-3,4,5-triyl tris(2-methylpropanoate)
• 4',5-DIHYDROXY-7-METHOXYFLAVONE
• 2-(3,4-Dihydroxyphenyl)-8-(2-O-beta-L-galactopyranosyl-beta-D-glucopyranosyl)-5,7-dihydroxy-4H-1-Benzopyran-4-one
• MOSLOFLAVONE
• PONCIRIN
• Naringenin 7-O-β-D-Glucuronide (Mixture of Diastereomers)
• Quercetin-7-O-β-D-glucopyranoside
• GARDENIN B
• Naringenin
• hydroxygenkwanin
• MEDICAGOL