Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C29H36O15 |
Molecular Weight | 624.5871 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 11 / 11 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1OC)[C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2
InChI
InChIKey=GUMSHIGGVOJLBP-SLRPQMTOSA-N
InChI=1S/C29H36O15/c1-11-22(32)24(34)26(36)28(41-11)40-10-20-23(33)25(35)27(37)29(44-20)42-13-7-14(30)21-15(31)9-17(43-19(21)8-13)12-4-5-16(38-2)18(6-12)39-3/h4-8,11,17,20,22-30,32-37H,9-10H2,1-3H3/t11-,17-,20+,22-,23+,24+,25-,26+,27+,28+,29+/m0/s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/23220657
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23220657
Methyl hesperidin is a flavanone-type flavonoid and a methylated derivative of hesperidin. It exhibits better bioactivities and water-solubility than hesperidin. It could improve the permeability and integrity of the capillary lining and usually found in association with vitamin C to enhance its effect.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2272558
In a preclinical study, mice were treated with dietary concentrations of 0, 1.25 or 5% for 96 weeks.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23220657
In a fluorescence titration experiment, 2.0 ml solution containing an appropriate concentration of BSA was titrated manually by successive addition of a 10(-3) mol/L solution of methyl hesperidin (to give a final concentration of 5*10(-6) mol/L to 4.76*10(-5) mol/L).
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5284419
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C052037
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100000166450
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K324U7386B
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11013-97-1
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DTXSID7020841
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SUB180597
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SUBSTANCE RECORD