NP-MRD: Showing NP-Card for 5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one (NP0320929)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 22:51:06 UTC

Updated at

2022-09-11 22:51:07 UTC

NP-MRD ID

NP0320929

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one

Description

5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one is found in Catha edulis, Epilobium parviflorum, Hypericum aucheri and Vitis vinifera.

Structure

MOL 3D MOL SDF PDB SMILES InChI

Dihydromyricetin 3-O-rhamnoside
  Mrv1652309281722402D          

 33 36  0  0  0  0            999 V2000
   -0.2597   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -2.4749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2597    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9743   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6888    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4032   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1177    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4032   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6888   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6888   -2.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9743   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2597   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2597   -2.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125    1.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836    1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980   -2.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -4.9499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 19 27  1  0  0  0  0
  4 28  1  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
 30 32  1  0  0  0  0
  2 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -4.0337   -0.2511   -1.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1578   -0.4809   -0.3627 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1216    0.1543    0.2755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8890   -0.4873    0.1249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9338    0.3676    0.5973 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0555    0.7355   -0.3153 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0898    2.2009   -0.6519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0361    2.6022   -1.3639 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8559    3.1979   -0.1664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453    4.5285   -0.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7647    4.9209   -0.3284 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4916    5.4222    0.4623 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7806    5.0230    0.7803 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6877    5.9673    1.2429 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960    3.6969    0.6186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1629    2.7966    0.1566 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3918    1.4514   -0.0361 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3833    0.5243    0.3012 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9931   -0.8122    0.0584 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2636   -0.9931    0.5990 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9589   -2.1515    0.4630 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2344   -2.3488    0.9993 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3931   -3.1952   -0.2360 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0632   -4.3963   -0.4015 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1226   -3.0371   -0.7860 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5531   -4.0882   -1.4898 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476   -1.8396   -0.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9017   -1.8100    0.8647 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3898   -1.5921    2.1455 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2867   -2.3753    1.0276 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8534   -2.0626    2.2617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2318   -1.9525   -0.0635 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9822   -2.6645   -1.2429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9627   -0.5954   -2.3843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9170    0.8169   -2.1045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1828   -0.7987   -2.3046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0987    0.0105   -0.0400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6736   -0.7188   -0.9357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0934    0.2283   -1.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0004    5.8961   -0.2107 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2230    6.4723    0.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6253    5.6679    1.4724 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0920    3.3440    0.8552 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2310    0.5475    1.4285 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7514   -0.1908    1.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6333   -1.5663    1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9828   -4.4808    0.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0639   -4.9538   -1.5955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683   -1.7122   -1.0509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2422   -2.5592    0.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1873   -2.4695    2.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2085   -3.4835    0.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2808   -1.5110    2.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2559   -2.2295    0.2615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7760   -2.7650   -1.7998 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 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  2  0
 15 13  1  0
 13 14  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
  9  7  1  0
  7  8  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  2  0
  4 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32  2  1  0
  7  6  1  0
 27 19  1  0
  9 16  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  1
  4 38  1  6
  6 39  1  6
 18 44  1  1
 15 43  1  0
 14 42  1  0
 12 41  1  0
 11 40  1  0
 20 45  1  0
 22 46  1  0
 24 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  6
 29 51  1  0
 30 52  1  1
 31 53  1  0
 32 54  1  1
 33 55  1  0
M  END

Dihydromyricetin 3-O-rhamnoside
  Mrv1652309281722402D          

 33 36  0  0  0  0            999 V2000
   -0.2597   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -2.4749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4546   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2597    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9743   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6888    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4032   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1177    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4032   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6888   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6888   -2.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9743   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2597   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2597   -2.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3125    1.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836    1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980   -2.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8836   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1691   -4.9499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 19 27  1  0  0  0  0
  4 28  1  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
 30 32  1  0  0  0  0
  2 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320929

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C(O)=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O12/c1-6-14(26)17(29)18(30)21(31-6)33-20-16(28)13-9(23)4-8(22)5-12(13)32-19(20)7-2-10(24)15(27)11(25)3-7/h2-6,14,17-27,29-30H,1H3

> <INCHI_KEY>
QMGYCEQXKDMHDB-UHFFFAOYSA-N

> <FORMULA>
C21H22O12

> <MOLECULAR_WEIGHT>
466.3922

> <EXACT_MASS>
466.111126168

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
43.440550322711545

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
0.80

> <JCHEM_LOGP>
0.7888932673333328

> <ALOGPS_LOGS>
-1.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.753559218647172

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.720757334608036

> <JCHEM_PKA_STRONGEST_BASIC>
-3.612182875000423

> <JCHEM_POLAR_SURFACE_AREA>
206.59999999999997

> <JCHEM_REFRACTIVITY>
107.45939999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.91e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-SEP-17   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Dihydromyricetin 3-O-rhamnoside                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-SEP-17         0                                  
HETATM    1  C   UNK     0      -0.485  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.849  -6.930   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.849  -5.390   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.182  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.182  -3.080   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.849  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.849  -0.770   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.485   0.000   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.819  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.152   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.486  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.820   0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -4.486  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.152  -3.080   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.152  -4.620   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.819  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.485  -3.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.485  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.182   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.516  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.850   0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.183  -0.770   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.850   1.540   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.183   2.310   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.516   2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.516   3.850   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.182   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.516  -5.390   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.850  -4.620   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.516  -6.930   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.850  -7.700   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.182  -7.700   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.182  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   28                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    9   17                                                  
CONECT   17   16    6   18                                                  
CONECT   18   17                                                            
CONECT   19    7   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   19                                                       
CONECT   28    4   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    2   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₂O₁₂

Average Mass

466.3922 Da

Monoisotopic Mass

466.11113 Da

IUPAC Name

5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C(O)=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C21H22O12/c1-6-14(26)17(29)18(30)21(31-6)33-20-16(28)13-9(23)4-8(22)5-12(13)32-19(20)7-2-10(24)15(27)11(25)3-7/h2-6,14,17-27,29-30H,1H3

InChI Key

QMGYCEQXKDMHDB-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Catha edulis	LOTUS Database	35616633
Epilobium parviflorum	LOTUS Database	35616633
Hypericum aucheri	LOTUS Database	35616633
Vitis vinifera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta amino acids and derivatives. These are amino acids having a (-NH2) group attached to the beta carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Beta amino acids and derivatives

Alternative Parents

Substituents

Beta amino acid or derivatives
Medium-chain fatty acid
Amino fatty acid
Fatty acid
Fatty acyl
Amino acid
Carboxylic acid
Monocarboxylic acid or derivatives
Organopnictogen compound
Primary amine
Organooxygen compound
Organonitrogen compound
Amine
Primary aliphatic amine
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

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	0.8	ALOGPS
logP	0.79	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	7.72	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	206.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	107.46 m³·mol⁻¹	ChemAxon
Polarizability	43.44 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB021841

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

3754658

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one (NP0320929)

MOL for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

3D MOL for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

3D SDF for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

3D-SDF for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

PDB for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

3D PDB for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

SMILES for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

INCHI for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

Structure for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)

3D Structure for NP0320929 (5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one)