NP-MRD: Showing NP-Card for Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside (NP0337514)

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Record Information

Version

2.0

Created at

2024-09-11 11:11:35 UTC

Updated at

2024-09-11 11:11:35 UTC

NP-MRD ID

NP0337514

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside

Description

Based on a literature review very few articles have been published on Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05262313432D          

 63 69  0  0  0  0            999 V2000
    1.0725   -2.2693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -1.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3575   -1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3575   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575    0.2056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575    1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2146   -0.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9295    0.2056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6445   -0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3580    0.2056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -5.9815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -5.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -4.7428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -3.9178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -3.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010   -3.9192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010   -4.7428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2146   -5.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2145   -3.9178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -3.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859   -3.9178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709   -3.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575   -3.9178    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
    0.3575   -3.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3575   -2.6818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575   -2.2693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709   -2.6804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859   -2.2679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -2.6804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859   -1.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    0.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2145   -1.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9294   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430   -1.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3580   -1.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430    0.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9294   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2145    0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2145    1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    1.0304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -1.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010   -1.4443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2146   -1.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9295   -1.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6445   -1.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3580   -1.4443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010    0.2056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9295   -2.2693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    1.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    2.2693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    2.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    3.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    3.9191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    4.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996    3.9191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996    4.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    5.1565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    5.9815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 25  1  0  0  0  0
  2  3  1  0  0  0  0
  2 45  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4 43  1  0  0  0  0
  5  6  1  0  0  0  0
  6 54  1  0  0  0  0
  7  8  1  0  0  0  0
  7 47  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 49  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 24  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 29  2  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 27  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 34  1  0  0  0  0
 32 33  1  0  0  0  0
 32 40  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 39  1  0  0  0  0
 36 37  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 51  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 52  1  0  0  0  0
 49 50  1  0  0  0  0
 53 54  2  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 57 60  2  0  0  0  0
 58 59  2  0  0  0  0
 59 62  1  0  0  0  0
 60 61  1  0  0  0  0
 61 62  2  0  0  0  0
 62 63  1  0  0  0  0
M  CHG  1  23   1
M  END


  Mrv2104 05262313432D          

 63 69  0  0  0  0            999 V2000
    1.0725   -2.2693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -1.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3575   -1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3575   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575    0.2056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575    1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2146   -0.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9295    0.2056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6445   -0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3580    0.2056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -5.9815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -5.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -4.7428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -3.9178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -3.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010   -3.9192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010   -4.7428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2146   -5.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0709   -2.6804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4996   -2.6804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859   -1.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    0.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2145   -1.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9294   -1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430   -1.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3580   -1.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430    0.2069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9294   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2145    0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2145    1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    1.0304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7860   -1.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010   -1.4443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2146   -1.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9295   -1.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6445   -1.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3580   -1.4443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5010    0.2056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9295   -2.2693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    1.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    1.4443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    2.2693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    2.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    3.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    3.9191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0709    4.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996    3.9191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7859    5.1565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7859    5.9815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 25  1  0  0  0  0
  2  3  1  0  0  0  0
  2 45  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4 43  1  0  0  0  0
  5  6  1  0  0  0  0
  6 54  1  0  0  0  0
  7  8  1  0  0  0  0
  7 47  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 49  1  0  0  0  0
 11 12  1  0  0  0  0
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 13 14  1  0  0  0  0
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 44 51  1  0  0  0  0
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 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 52  1  0  0  0  0
 49 50  1  0  0  0  0
 53 54  2  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 57 60  2  0  0  0  0
 58 59  2  0  0  0  0
 59 62  1  0  0  0  0
 60 61  1  0  0  0  0
 61 62  2  0  0  0  0
 62 63  1  0  0  0  0
M  CHG  1  23   1
M  END
> <DATABASE_ID>
NP0337514

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1OC(OC2=C3C=C(OC4OC(COC(=O)\C=C\C5=CC=C(O)C=C5)C(O)C(O)C4OC4OCC(O)C(O)C4O)C(=[O+]C3=CC(O)=C2)C2=CC=C(O)C(O)=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1/C41H44O22/c42-13-27-31(50)33(52)36(55)40(61-27)59-25-11-19(44)10-24-20(25)12-26(37(58-24)17-4-7-21(45)22(46)9-17)60-41-38(63-39-35(54)30(49)23(47)14-57-39)34(53)32(51)28(62-41)15-56-29(48)8-3-16-1-5-18(43)6-2-16/h1-12,23,27-28,30-36,38-42,47,49-55H,13-15H2,(H3-,43,44,45,46,48)/p+1

> <INCHI_KEY>
JSYDBTWJIIAZPU-UHFFFAOYNA-O

> <FORMULA>
C41H45O22

> <MOLECULAR_WEIGHT>
889.788

> <EXACT_MASS>
889.239699509

> <JCHEM_ACCEPTOR_COUNT>
21

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
85.84342253348541

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-{[4,5-dihydroxy-6-({[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1lambda4-chromen-1-ylium

> <JCHEM_LOGP>
-0.30680000000000174

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.975606266665731

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.64741993644012

> <JCHEM_PKA_STRONGEST_BASIC>
-3.678946886908562

> <JCHEM_POLAR_SURFACE_AREA>
357.81

> <JCHEM_REFRACTIVITY>
216.40130000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-{[4,5-dihydroxy-6-({[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1lambda4-chromen-1-ylium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  O   UNK     0       2.002  -4.236   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.002  -2.696   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.667  -1.926   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.667  -0.384   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.667   0.384   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.667   1.926   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.001  -0.386   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.335   0.384   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.670  -0.386   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.002   0.384   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       3.334 -11.165   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.334  -9.623   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.002  -8.853   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.002  -7.313   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.334  -6.543   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.669  -7.316   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.669  -8.853   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.001  -9.626   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -6.000  -7.313   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.666  -6.543   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.334  -7.313   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.999  -6.543   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.667  -7.313   0.000  0.00  0.00           O+1
HETATM   24  C   UNK     0       0.667  -6.543   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.667  -5.006   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.667  -4.236   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.999  -5.003   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.334  -4.233   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.666  -5.003   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -3.334  -2.693   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.666  -1.924   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.666  -0.384   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -3.334   0.386   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -6.000  -2.693   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -7.335  -1.924   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -8.667  -2.693   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0     -10.002  -1.924   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -8.667   0.386   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -7.335  -0.384   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -6.000   0.386   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -6.000   1.926   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       2.002   1.923   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       2.002   0.386   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.334  -0.386   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.334  -1.926   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       4.669  -2.696   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       6.001  -1.926   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       7.335  -2.696   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       8.670  -1.926   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      10.002  -2.696   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       4.669   0.384   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0       7.335  -4.236   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0      -3.334   1.926   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      -1.999   2.696   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      -1.999   4.236   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -3.334   5.006   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -3.334   6.546   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -1.999   7.316   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -1.999   8.856   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      -4.666   7.316   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      -4.666   8.856   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      -3.334   9.625   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0      -3.334  11.165   0.000  0.00  0.00           O+0
CONECT    1    2   25                                                       
CONECT    2    1    3   45                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   43                                                  
CONECT    5    4    6                                                       
CONECT    6    5   54                                                       
CONECT    7    8   47                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   49                                                  
CONECT   10    9                                                            
CONECT   11   12                                                            
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   12   16   18                                                  
CONECT   18   17                                                            
CONECT   19   20                                                            
CONECT   20   19   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   14   23   25                                                  
CONECT   25    1   24   26                                                  
CONECT   26   25   27                                                       
CONECT   27   22   26   28                                                  
CONECT   28   27   29   30                                                  
CONECT   29   20   28                                                       
CONECT   30   28   31                                                       
CONECT   31   30   32   34                                                  
CONECT   32   31   33   40                                                  
CONECT   33   32                                                            
CONECT   34   31   35                                                       
CONECT   35   34   36   39                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   39                                                            
CONECT   39   35   38   40                                                  
CONECT   40   32   39   41                                                  
CONECT   41   40                                                            
CONECT   42   43                                                            
CONECT   43    4   42   44                                                  
CONECT   44   43   45   51                                                  
CONECT   45    2   44   46                                                  
CONECT   46   45   47                                                       
CONECT   47    7   46   48                                                  
CONECT   48   47   49   52                                                  
CONECT   49    9   48   50                                                  
CONECT   50   49                                                            
CONECT   51   44                                                            
CONECT   52   48                                                            
CONECT   53   54                                                            
CONECT   54    6   53   55                                                  
CONECT   55   54   56                                                       
CONECT   56   55   57                                                       
CONECT   57   56   58   60                                                  
CONECT   58   57   59                                                       
CONECT   59   58   62                                                       
CONECT   60   57   61                                                       
CONECT   61   60   62                                                       
CONECT   62   59   61   63                                                  
CONECT   63   62                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  138    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₄₅O₂₂

Average Mass

889.7880 Da

Monoisotopic Mass

889.23970 Da

IUPAC Name

3-{[4,5-dihydroxy-6-({[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1lambda4-chromen-1-ylium

Traditional Name

CAS Registry Number

Not Available

SMILES

OCC1OC(OC2=C3C=C(OC4OC(COC(=O)\C=C\C5=CC=C(O)C=C5)C(O)C(O)C4OC4OCC(O)C(O)C4O)C(=[O+]C3=CC(O)=C2)C2=CC=C(O)C(O)=C2)C(O)C(O)C1O

InChI Identifier

InChI=1/C41H44O22/c42-13-27-31(50)33(52)36(55)40(61-27)59-25-11-19(44)10-24-20(25)12-26(37(58-24)17-4-7-21(45)22(46)9-17)60-41-38(63-39-35(54)30(49)23(47)14-57-39)34(53)32(51)28(62-41)15-56-29(48)8-3-16-1-5-18(43)6-2-16/h1-12,23,27-28,30-36,38-42,47,49-55H,13-15H2,(H3-,43,44,45,46,48)/p+1

InChI Key

JSYDBTWJIIAZPU-UHFFFAOYNA-O

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	-0.31	ChemAxon
pKa (Strongest Acidic)	6.65	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	21	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	357.81 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	216.4 m³·mol⁻¹	ChemAxon
Polarizability	85.84 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00006836

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside (NP0337514)

MOL for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

3D MOL for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

3D SDF for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

3D-SDF for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

PDB for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

3D PDB for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

SMILES for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

INCHI for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

Structure for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)

3D Structure for NP0337514 (Cyanidin 3-O-[b-D-Xylopyranosyl-(1->2)-(4-hydroxy-Z-cinnamoyl)-(->6)-b-D-glucopyranoside] 5-glucoside)