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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 22:48:30 UTC

Update Date

2021-09-23 22:48:31 UTC

HMDB ID

HMDB0303037

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Cyanidin 3-O-alpha-L-galactoside

Description

Cyanidin 3-o-alpha-l-galactoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Cyanidin 3-o-alpha-l-galactoside can be found in highbush blueberry, which makes cyanidin 3-o-alpha-l-galactoside a potential biomarker for the consumption of this food product.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02241220392D          

 32 35  0  0  0  0            999 V2000
   -5.5693    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1403    0.2225    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   -4.1403   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    1.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5680    1.4600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9981    0.2225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    2.2850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -2.2526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1405   -4.7275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4260   -2.6650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4260   -3.4900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7115   -3.9025    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9970   -3.4901    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9970   -2.6651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7115   -2.2525    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7114   -1.4275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825   -2.2526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2826   -3.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7116   -4.7275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1405   -3.9025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5  8  1  0  0  0  0
  7 10  2  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 13 11  2  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  2  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 20  1  0  0  0  0
 16 17  1  0  0  0  0
  2 18  1  0  0  0  0
  9 28  1  0  0  0  0
 12 19  1  0  0  0  0
 32 21  1  0  0  0  0
 22 23  1  0  0  0  0
 22 27  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 26 29  1  1  0  0  0
 25 30  1  6  0  0  0
 24 31  1  6  0  0  0
 23 32  1  6  0  0  0
M  CHG  1   7   1
M  END

HMDB0303037
     RDKit          3D
Cyanidin 3-O-alpha-L-galactoside
 53 56  0  0  0  0  0  0  0  0999 V2000
    3.3929   -1.2602   -2.0685 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6682   -2.1878   -1.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4123   -1.7695    0.3124 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1126   -1.4383    0.6092 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7884   -0.1247    0.2718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4347    0.1045    0.4616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5912    0.0869   -0.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3733   -0.2192   -1.7756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4206   -0.2400   -2.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2291   -0.5361   -4.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0076   -0.8261   -4.5158 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2824   -0.5594   -4.9319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5401   -0.2760   -4.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6067   -0.2919   -5.3693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7234    0.0209   -3.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6953    0.0462   -2.2195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8443    0.3180   -0.9721 O   0  0  0  0  0  3  0  0  0  0  0  0
   -1.8772    0.3550   -0.0543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3051    0.6914    1.3194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4655    0.8559    2.3801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9678    1.1479    3.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3264    1.2781    3.8579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8616    1.5649    5.0842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1980    1.1128    2.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5854    1.2376    2.9810 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6656    0.8285    1.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6255    0.9169    0.9367 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9555    1.8959    1.6164 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6521    0.1626    1.7817 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5095    1.0117    2.4622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4013   -0.7398    0.8082 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8958    0.0668   -0.1767 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1020   -0.5845   -2.2287 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.5159   -1.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637   -3.1101   -1.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6316   -2.6921    0.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9771   -0.0714   -0.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6080   -0.4417   -2.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8457   -0.8523   -3.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0932   -0.7918   -5.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4548   -0.5094   -6.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7193    0.2416   -2.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4066    0.7650    2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2823    1.2806    4.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8599    1.6443    5.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1922    1.1124    2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3518    0.7042    0.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2527    1.4487    0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8489    1.6849    2.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1390   -0.4818    2.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9881    0.5059    3.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2425   -1.1857    1.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6344    0.6157    0.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  2  0
  5 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 18  7  1  0
 26 19  1  0
 16  9  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  5 37  1  6
  8 38  1  0
 11 39  1  0
 12 40  1  0
 14 41  1  0
 15 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 25 46  1  0
 26 47  1  0
 27 48  1  6
 28 49  1  0
 29 50  1  1
 30 51  1  0
 31 52  1  1
 32 53  1  0
M  CHG  1  17   1
M  END


  Mrv0541 02241220392D          

 32 35  0  0  0  0            999 V2000
   -5.5693    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1403    0.2225    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   -4.1403   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    1.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5680    1.4600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9981    0.2225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    2.2850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -2.2526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1405   -4.7275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4260   -2.6650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4260   -3.4900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7115   -3.9025    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9970   -3.4901    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9970   -2.6651    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7115   -2.2525    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7114   -1.4275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825   -2.2526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2826   -3.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7116   -4.7275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1405   -3.9025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5  8  1  0  0  0  0
  7 10  2  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 13 11  2  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  2  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 20  1  0  0  0  0
 16 17  1  0  0  0  0
  2 18  1  0  0  0  0
  9 28  1  0  0  0  0
 12 19  1  0  0  0  0
 32 21  1  0  0  0  0
 22 23  1  0  0  0  0
 22 27  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 26 29  1  1  0  0  0
 25 30  1  6  0  0  0
 24 31  1  6  0  0  0
 23 32  1  6  0  0  0
M  CHG  1   7   1
M  END
> <DATABASE_ID>
HMDB0303037

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@@H]1O[C@@H](OC2=CC3=C(C=C(O)C=C3O)[O+]=C2C2=CC(O)=C(O)C=C2)[C@@H](O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O11/c22-7-16-17(27)18(28)19(29)21(32-16)31-15-6-10-12(25)4-9(23)5-14(10)30-20(15)8-1-2-11(24)13(26)3-8/h1-6,16-19,21-22,27-29H,7H2,(H3-,23,24,25,26)/p+1/t16-,17+,18+,19-,21+/m0/s1

> <INCHI_KEY>
RKWHWFONKJEUEF-KWLWEVDOSA-O

> <FORMULA>
C21H21O11

> <MOLECULAR_WEIGHT>
449.3848

> <EXACT_MASS>
449.108386514

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
43.24903892446655

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium

> <ALOGPS_LOGP>
0.98

> <JCHEM_LOGP>
0.38699999999999934

> <ALOGPS_LOGS>
-2.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.457961070975373

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.388329617449456

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923799280262

> <JCHEM_POLAR_SURFACE_AREA>
193.44

> <JCHEM_REFRACTIVITY>
116.25749999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0303037
     RDKit          3D
Cyanidin 3-O-alpha-L-galactoside
 53 56  0  0  0  0  0  0  0  0999 V2000
    3.3929   -1.2602   -2.0685 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6682   -2.1878   -1.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4123   -1.7695    0.3124 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1126   -1.4383    0.6092 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7884   -0.1247    0.2718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4347    0.1045    0.4616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5912    0.0869   -0.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3733   -0.2192   -1.7756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4206   -0.2400   -2.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2291   -0.5361   -4.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0076   -0.8261   -4.5158 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2824   -0.5594   -4.9319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5401   -0.2760   -4.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6067   -0.2919   -5.3693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7234    0.0209   -3.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6953    0.0462   -2.2195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8443    0.3180   -0.9721 O   0  0  0  0  0  3  0  0  0  0  0  0
   -1.8772    0.3550   -0.0543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3051    0.6914    1.3194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4655    0.8559    2.3801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9678    1.1479    3.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3264    1.2781    3.8579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8616    1.5649    5.0842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1980    1.1128    2.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5854    1.2376    2.9810 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6656    0.8285    1.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6255    0.9169    0.9367 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9555    1.8959    1.6164 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6521    0.1626    1.7817 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5095    1.0117    2.4622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4013   -0.7398    0.8082 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8958    0.0668   -0.1767 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1020   -0.5845   -2.2287 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.5159   -1.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637   -3.1101   -1.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6316   -2.6921    0.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9771   -0.0714   -0.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6080   -0.4417   -2.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8457   -0.8523   -3.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0932   -0.7918   -5.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4548   -0.5094   -6.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7193    0.2416   -2.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4066    0.7650    2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2823    1.2806    4.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8599    1.6443    5.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1922    1.1124    2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3518    0.7042    0.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2527    1.4487    0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8489    1.6849    2.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1390   -0.4818    2.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9881    0.5059    3.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2425   -1.1857    1.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6344    0.6157    0.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  2  0
  5 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 18  7  1  0
 26 19  1  0
 16  9  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  5 37  1  6
  8 38  1  0
 11 39  1  0
 12 40  1  0
 14 41  1  0
 15 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 25 46  1  0
 26 47  1  0
 27 48  1  6
 28 49  1  0
 29 50  1  1
 30 51  1  0
 31 52  1  1
 32 53  1  0
M  CHG  1  17   1
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0     -10.396   0.415   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -11.730  -0.355   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.730  -1.895   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.396  -2.665   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.062  -1.895   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.062  -0.355   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -7.729   0.415   0.000  0.00  0.00           O+1
HETATM    8  C   UNK     0      -7.729  -2.665   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.395  -1.895   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.395  -0.355   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.061   0.415   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.728   2.725   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.061   1.955   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.728  -0.355   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.394   0.415   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.394   1.955   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.060   2.725   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0     -13.063   0.415   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -3.728   4.265   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0     -10.396  -4.205   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -7.729  -8.825   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -6.395  -4.975   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -6.395  -6.515   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.061  -7.285   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.728  -6.515   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.728  -4.975   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.061  -4.205   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.061  -2.665   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -2.394  -4.205   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -2.394  -7.285   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -5.062  -8.825   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -7.729  -7.285   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   18                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6    8                                                  
CONECT    6    1    7    5                                                  
CONECT    7    6   10                                                       
CONECT    8    5    9                                                       
CONECT    9    8   10   28                                                  
CONECT   10    7    9   11                                                  
CONECT   11   10   13   14                                                  
CONECT   12   13   16   19                                                  
CONECT   13   11   12                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   12   15   17                                                  
CONECT   17   16                                                            
CONECT   18    2                                                            
CONECT   19   12                                                            
CONECT   20    4                                                            
CONECT   21   32                                                            
CONECT   22   23   27                                                       
CONECT   23   22   24   32                                                  
CONECT   24   23   25   31                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27   29                                                  
CONECT   27   22   26   28                                                  
CONECT   28    9   27                                                       
CONECT   29   26                                                            
CONECT   30   25                                                            
CONECT   31   24                                                            
CONECT   32   21   23                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

COMPND    HMDB0303037
HETATM    1  O1  UNL     1       3.393  -1.260  -2.069  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.668  -2.188  -1.104  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.412  -1.770   0.312  1.00  0.00           C  
HETATM    4  O2  UNL     1       2.113  -1.438   0.609  1.00  0.00           O  
HETATM    5  C3  UNL     1       1.788  -0.125   0.272  1.00  0.00           C  
HETATM    6  O3  UNL     1       0.435   0.105   0.462  1.00  0.00           O  
HETATM    7  C4  UNL     1      -0.591   0.087  -0.415  1.00  0.00           C  
HETATM    8  C5  UNL     1      -0.373  -0.219  -1.776  1.00  0.00           C  
HETATM    9  C6  UNL     1      -1.421  -0.240  -2.678  1.00  0.00           C  
HETATM   10  C7  UNL     1      -1.229  -0.536  -4.010  1.00  0.00           C  
HETATM   11  O4  UNL     1       0.008  -0.826  -4.516  1.00  0.00           O  
HETATM   12  C8  UNL     1      -2.282  -0.559  -4.932  1.00  0.00           C  
HETATM   13  C9  UNL     1      -3.540  -0.276  -4.476  1.00  0.00           C  
HETATM   14  O5  UNL     1      -4.607  -0.292  -5.369  1.00  0.00           O  
HETATM   15  C10 UNL     1      -3.723   0.021  -3.135  1.00  0.00           C  
HETATM   16  C11 UNL     1      -2.695   0.046  -2.219  1.00  0.00           C  
HETATM   17  O6  UNL     1      -2.844   0.318  -0.972  1.00  0.00           O1+
HETATM   18  C12 UNL     1      -1.877   0.355  -0.054  1.00  0.00           C  
HETATM   19  C13 UNL     1      -2.305   0.691   1.319  1.00  0.00           C  
HETATM   20  C14 UNL     1      -1.465   0.856   2.380  1.00  0.00           C  
HETATM   21  C15 UNL     1      -1.968   1.148   3.644  1.00  0.00           C  
HETATM   22  C16 UNL     1      -3.326   1.278   3.858  1.00  0.00           C  
HETATM   23  O7  UNL     1      -3.862   1.565   5.084  1.00  0.00           O  
HETATM   24  C17 UNL     1      -4.198   1.113   2.782  1.00  0.00           C  
HETATM   25  O8  UNL     1      -5.585   1.238   2.981  1.00  0.00           O  
HETATM   26  C18 UNL     1      -3.666   0.829   1.562  1.00  0.00           C  
HETATM   27  C19 UNL     1       2.626   0.917   0.937  1.00  0.00           C  
HETATM   28  O9  UNL     1       1.955   1.896   1.616  1.00  0.00           O  
HETATM   29  C20 UNL     1       3.652   0.163   1.782  1.00  0.00           C  
HETATM   30  O10 UNL     1       4.509   1.012   2.462  1.00  0.00           O  
HETATM   31  C21 UNL     1       4.401  -0.740   0.808  1.00  0.00           C  
HETATM   32  O11 UNL     1       4.896   0.067  -0.177  1.00  0.00           O  
HETATM   33  H1  UNL     1       4.102  -0.585  -2.229  1.00  0.00           H  
HETATM   34  H2  UNL     1       4.729  -2.516  -1.259  1.00  0.00           H  
HETATM   35  H3  UNL     1       3.064  -3.110  -1.321  1.00  0.00           H  
HETATM   36  H4  UNL     1       3.632  -2.692   0.936  1.00  0.00           H  
HETATM   37  H5  UNL     1       1.977  -0.071  -0.838  1.00  0.00           H  
HETATM   38  H6  UNL     1       0.608  -0.442  -2.106  1.00  0.00           H  
HETATM   39  H7  UNL     1       0.846  -0.852  -3.987  1.00  0.00           H  
HETATM   40  H8  UNL     1      -2.093  -0.792  -5.957  1.00  0.00           H  
HETATM   41  H9  UNL     1      -4.455  -0.509  -6.328  1.00  0.00           H  
HETATM   42  H10 UNL     1      -4.719   0.242  -2.803  1.00  0.00           H  
HETATM   43  H11 UNL     1      -0.407   0.765   2.249  1.00  0.00           H  
HETATM   44  H12 UNL     1      -1.282   1.281   4.496  1.00  0.00           H  
HETATM   45  H13 UNL     1      -4.860   1.644   5.191  1.00  0.00           H  
HETATM   46  H14 UNL     1      -6.192   1.112   2.205  1.00  0.00           H  
HETATM   47  H15 UNL     1      -4.352   0.704   0.742  1.00  0.00           H  
HETATM   48  H16 UNL     1       3.253   1.449   0.138  1.00  0.00           H  
HETATM   49  H17 UNL     1       1.849   1.685   2.563  1.00  0.00           H  
HETATM   50  H18 UNL     1       3.139  -0.482   2.508  1.00  0.00           H  
HETATM   51  H19 UNL     1       4.988   0.506   3.194  1.00  0.00           H  
HETATM   52  H20 UNL     1       5.242  -1.186   1.383  1.00  0.00           H  
HETATM   53  H21 UNL     1       5.634   0.616   0.160  1.00  0.00           H  
CONECT    1    2   33
CONECT    2    3   34   35
CONECT    3    4   31   36
CONECT    4    5
CONECT    5    6   27   37
CONECT    6    7
CONECT    7    8    8   18
CONECT    8    9   38
CONECT    9   10   10   16
CONECT   10   11   12
CONECT   11   39
CONECT   12   13   13   40
CONECT   13   14   15
CONECT   14   41
CONECT   15   16   16   42
CONECT   16   17
CONECT   17   18   18
CONECT   18   19
CONECT   19   20   20   26
CONECT   20   21   43
CONECT   21   22   22   44
CONECT   22   23   24
CONECT   23   45
CONECT   24   25   26   26
CONECT   25   46
CONECT   26   47
CONECT   27   28   29   48
CONECT   28   49
CONECT   29   30   31   50
CONECT   30   51
CONECT   31   32   52
CONECT   32   53
END

HMDB0303037
     RDKit          3D
Cyanidin 3-O-alpha-L-galactoside
 53 56  0  0  0  0  0  0  0  0999 V2000
    3.3929   -1.2602   -2.0685 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6682   -2.1878   -1.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4123   -1.7695    0.3124 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1126   -1.4383    0.6092 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7884   -0.1247    0.2718 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4347    0.1045    0.4616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5912    0.0869   -0.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3733   -0.2192   -1.7756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4206   -0.2400   -2.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2291   -0.5361   -4.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0076   -0.8261   -4.5158 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2824   -0.5594   -4.9319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5401   -0.2760   -4.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6067   -0.2919   -5.3693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7234    0.0209   -3.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6953    0.0462   -2.2195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8443    0.3180   -0.9721 O   0  0  0  0  0  3  0  0  0  0  0  0
   -1.8772    0.3550   -0.0543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3051    0.6914    1.3194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4655    0.8559    2.3801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9678    1.1479    3.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3264    1.2781    3.8579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8616    1.5649    5.0842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1980    1.1128    2.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5854    1.2376    2.9810 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6656    0.8285    1.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6255    0.9169    0.9367 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9555    1.8959    1.6164 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6521    0.1626    1.7817 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5095    1.0117    2.4622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4013   -0.7398    0.8082 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8958    0.0668   -0.1767 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1020   -0.5845   -2.2287 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.5159   -1.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637   -3.1101   -1.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6316   -2.6921    0.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9771   -0.0714   -0.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6080   -0.4417   -2.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8457   -0.8523   -3.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0932   -0.7918   -5.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4548   -0.5094   -6.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7193    0.2416   -2.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4066    0.7650    2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2823    1.2806    4.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8599    1.6443    5.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1922    1.1124    2.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3518    0.7042    0.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2527    1.4487    0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8489    1.6849    2.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1390   -0.4818    2.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9881    0.5059    3.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2425   -1.1857    1.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6344    0.6157    0.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  2  0
  5 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 18  7  1  0
 26 19  1  0
 16  9  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  5 37  1  6
  8 38  1  0
 11 39  1  0
 12 40  1  0
 14 41  1  0
 15 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 25 46  1  0
 26 47  1  0
 27 48  1  6
 28 49  1  0
 29 50  1  1
 30 51  1  0
 31 52  1  1
 32 53  1  0
M  CHG  1  17   1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Cyanidin 3-O-a-L-galactoside	Generator
Cyanidin 3-O-α-L-galactoside	Generator

Chemical Formula

C₂₁H₂₁O₁₁

Average Molecular Weight

449.3848

Monoisotopic Molecular Weight

449.108386514

IUPAC Name

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium

Traditional Name

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium

CAS Registry Number

Not Available

SMILES

OC[C@@H]1O[C@@H](OC2=CC3=C(C=C(O)C=C3O)[O+]=C2C2=CC(O)=C(O)C=C2)[C@@H](O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C21H20O11/c22-7-16-17(27)18(28)19(29)21(32-16)31-15-6-10-12(25)4-9(23)5-14(10)30-20(15)8-1-2-11(24)13(26)3-8/h1-6,16-19,21-22,27-29H,7H2,(H3-,23,24,25,26)/p+1/t16-,17+,18+,19-,21+/m0/s1

InChI Key

RKWHWFONKJEUEF-KWLWEVDOSA-O

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-3-O-glycosides

Alternative Parents

Substituents

Flavonoid-3-o-glycoside
4'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavone
Hydroxyflavonoid
Coumaric acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hexose monosaccharide
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Chromone
Glycosyl compound
O-glycosyl compound
1-benzopyran
Benzopyran
Styrene
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Phenol
Fatty acid ester
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Pyran
Benzenoid
Oxane
Fatty acyl
Monosaccharide
Enoate ester
Heteroaromatic compound
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Secondary alcohol
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Acetal
Organooxygen compound
Carbonyl group
Alcohol
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Highbush blueberry (FooDB: FOOD00191)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	0.98	ALOGPS
logP	0.39	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	6.39	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	193.44 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	116.26 m³·mol⁻¹	ChemAxon
Polarizability	43.25 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	203.035	32859911
AllCCS	[M+H-H2O]+	200.611	32859911
AllCCS	[M+Na]+	205.9	32859911
AllCCS	[M+NH4]+	205.263	32859911
AllCCS	[M-H]-	200.781	32859911
AllCCS	[M+Na-2H]-	201.11	32859911
AllCCS	[M+HCOO]-	201.625	32859911
DeepCCS	[M+H]+	198.428	30932474
DeepCCS	[M-H]-	196.033	30932474
DeepCCS	[M-2H]-	229.229	30932474
DeepCCS	[M+Na]+	204.341	30932474

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Cyanidin 3-O-alpha-L-galactoside,3TMS,isomer #50	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4022.3	Semi standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,3TMS,isomer #50	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4080.1	Standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,3TMS,isomer #50	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	5216.6	Standard polar	33892256
Cyanidin 3-O-alpha-L-galactoside,4TMS,isomer #64	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	3857.1	Semi standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,4TMS,isomer #64	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4041.8	Standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,4TMS,isomer #64	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4942.5	Standard polar	33892256
Cyanidin 3-O-alpha-L-galactoside,4TMS,isomer #66	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	3957.3	Semi standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,4TMS,isomer #66	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4062.7	Standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,4TMS,isomer #66	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4874.7	Standard polar	33892256
Cyanidin 3-O-alpha-L-galactoside,5TMS,isomer #55	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	3864.7	Semi standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,5TMS,isomer #55	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4009.8	Standard non polar	33892256
Cyanidin 3-O-alpha-L-galactoside,5TMS,isomer #55	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1O	4680.7	Standard polar	33892256

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-O-alpha-L-galactoside 10V, Positive-QTOF	splash10-0udi-0100900000-66702edb3ac17b9bcd2f	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-O-alpha-L-galactoside 20V, Positive-QTOF	splash10-0002-1300900000-733c7273cc2b516ea7fd	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-O-alpha-L-galactoside 40V, Positive-QTOF	splash10-01ot-6910000000-5dad4cb81406b2f0a241	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-O-alpha-L-galactoside 10V, Negative-QTOF	splash10-0002-2300900000-5d1238580ea9280c8190	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-O-alpha-L-galactoside 20V, Negative-QTOF	splash10-0002-6800900000-f91084c3d800ee4ef894	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-O-alpha-L-galactoside 40V, Negative-QTOF	splash10-0596-9300000000-1ee778ebb732d2be0d87	2016-08-03	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB007414

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

92448832

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for Cyanidin 3-O-alpha-L-galactoside (HMDB0303037)

MOL for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

3D MOL for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

3D SDF for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

3D-SDF for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

PDB for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

3D PDB for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

SMILES for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

INCHI for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

Structure for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

3D Structure for HMDB0303037 (Cyanidin 3-O-alpha-L-galactoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

MS/MS Spectra