Identification

PhytoHub ID
PHUB002719
Name
Rosmarinic acid-4-glucuronide
Systematic Name
Rosmarinic acid-4-glucuronide
Synonyms
Not Available
CAS Number
Not Available
Average Mass
536.442
Monoisotopic Mass
536.116605453
Chemical Formula
C24H24O14
IUPAC Name
(2S,3S,4S,5R,6S)-6-{4-[(1E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-en-1-yl]-2-hydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid
InChI Key
HPDJIRRRFHPVHR-IYRYNMHPSA-N
InChI Identifier
InChI=1S/C24H24O14/c25-12-4-1-11(8-13(12)26)9-16(22(32)33)36-17(28)6-3-10-2-5-15(14(27)7-10)37-24-20(31)18(29)19(30)21(38-24)23(34)35/h1-8,16,18-21,24-27,29-31H,9H2,(H,32,33)(H,34,35)/b6-3+/t16-,18-,19-,20+,21-,24+/m0/s1
SMILES
O[C@@H]1[C@@H](O)[C@H](OC2=C(O)C=C(\C=C\C(=O)O[C@@H](CC3=CC(O)=C(O)C=C3)C(O)=O)C=C2)O[C@@H]([C@H]1O)C(O)=O
Structure

Calculated Properties

Solubility (ALOGPS)
4.88e-01 g/l
LogS (ALOGPS)
-3.04
LogP (ALOGPS)
2.01
Hydrogen Acceptors
13
Hydrogen Donors
8
Rotatable Bond Count
10
Polar Surface Area
240.73999999999995
Refractivity
122.96189999999997
Polarizability
49.94671341481627
Formal Charge
0
Physiological Charge
-2
pKa (strongest basic)
-3.731998669956291
pKa (strongest acidic)
2.7865916315444847
Number of Rings
3
Rule of Five
No
Bioavailability
No
Ghose Filter
No
Veber's Rule
No
MDDR-like Rule
Yes

Taxonomy as Metabolite

Family
(Poly)phenol metabolites
Class
Phenolic acid metabolites
Sub-class
Cinnamic acids

Spectra from Phytohub

Spectrum TypeInstrument TypeIon ModeCollision Energy LevelViewPeaks

Food Sources

No food source information available

Food Sources of its Food Phytochemical(s)

No food source information available of its precursor(s)

Role as Biomarker of intake

No roles as Biomarker of intake found

Metabolism

No metabolism information available

Inter-Individual Variations in Metabolism

No data on inter-individual variations available

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