NP-MRD: Showing NP-Card for 4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate (NP0193717)

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Record Information

Version

2.0

Created at

2022-09-04 11:15:12 UTC

Updated at

2022-09-04 11:15:12 UTC

NP-MRD ID

NP0193717

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate

Description

4,5-Dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. 4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate is found in Premna microphylla and Verbascum thapsus. 4,5-Dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241505572D          

 48 53  0  0  0  0            999 V2000
   -2.5371    4.1346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8550    4.5988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1120    4.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    4.7044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3130    4.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3740    3.5231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1170    3.1645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7990    3.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5420    3.2701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    3.7343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6030    2.4474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3460    2.0888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4070    1.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7249    0.8019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7859   -0.0209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4874   -0.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6791   -1.5964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4666   -3.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6628   -2.5069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0741   -4.9108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0903   -4.0003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2982   -4.2310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2911   -1.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4684   -1.3174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4531    2.6586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0280    2.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9670    3.3757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3081    3.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0511    3.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7331    2.9533    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
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 16 33  1  0  0  0  0
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  6 46  1  0  0  0  0
 46 47  2  0  0  0  0
  3 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

 88 93  0  0  0  0  0  0  0  0999 V2000
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    6.9254    1.6355   -0.5366 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3330    0.4678    0.8740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3572    1.0944    0.1682 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.2528    1.6289    1.0988 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.8274    3.7901    0.2746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4528    4.4364    1.4267 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.9560   -0.2196   -2.0505 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6115   -3.3400    4.2021 C   0  0  0  0  0  0  0  0  0  0  0  0
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 44 85  1  6
 45 86  1  0
 46 87  1  0
 48 88  1  0
M  END


  Mrv1533004241505572D          

 48 53  0  0  0  0            999 V2000
   -2.5371    4.1346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8550    4.5988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1120    4.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4300    4.7044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3130    4.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3740    3.5231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1170    3.1645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7990    3.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5420    3.2701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    3.7343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6030    2.4474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3460    2.0888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4070    1.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7249    0.8019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7859   -0.0209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4874   -0.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2795   -0.2244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8753   -0.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6791   -1.5964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8870   -1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6907   -2.6284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2866   -3.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0786   -2.9683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6745   -3.5389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4666   -3.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6628   -2.5069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4782   -4.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0741   -4.9108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6861   -4.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4899   -5.3722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0903   -4.0003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2982   -4.2310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2911   -1.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4684   -1.3174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4430   -2.1420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162   -2.5324    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6509   -1.2060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561   -0.5538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1500    0.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8320    1.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5750    1.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7710    2.1944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4531    2.6586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0280    2.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9670    3.3757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3081    3.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0511    3.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7331    2.9533    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  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
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 22 31  1  0  0  0  0
 31 32  1  0  0  0  0
 20 33  1  0  0  0  0
 16 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 15 38  1  0  0  0  0
 34 38  1  0  0  0  0
 13 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 12 44  1  0  0  0  0
 44 45  1  0  0  0  0
  6 46  1  0  0  0  0
 46 47  2  0  0  0  0
  3 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193717

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=CC(=O)OC2C(OC3C4OC4(CO)C4C3C=COC4OC3OC(CO)C(O)C(O)C3O)OC(C)C(O)C2O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H40O17/c1-12-20(36)23(39)26(45-18(35)6-4-13-3-5-16(41-2)15(34)9-13)30(43-12)46-25-14-7-8-42-28(19(14)31(11-33)27(25)48-31)47-29-24(40)22(38)21(37)17(10-32)44-29/h3-9,12,14,17,19-30,32-34,36-40H,10-11H2,1-2H3

> <INCHI_KEY>
LUCUVVSDSLWPMZ-UHFFFAOYSA-N

> <FORMULA>
C31H40O17

> <MOLECULAR_WEIGHT>
684.644

> <EXACT_MASS>
684.226549828

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
67.66431087738243

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
-0.26

> <JCHEM_LOGP>
-1.5830751580000002

> <ALOGPS_LOGS>
-2.33

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.093869660338022

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.820622485478362

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601929344

> <JCHEM_POLAR_SURFACE_AREA>
256.04999999999995

> <JCHEM_REFRACTIVITY>
156.07290000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.23e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -4.736   7.718   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.463   8.584   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.076   7.915   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.803   8.781   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.584   8.112   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.698   6.576   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.085   5.907   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.358   6.774   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.745   6.104   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.018   6.971   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       4.859   4.568   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.246   3.899   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.360   2.363   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.087   1.497   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.200  -0.039   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.510  -0.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.988  -0.419   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.101  -1.484   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.734  -2.980   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.256  -3.411   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.889  -4.906   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.002  -5.971   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.480  -5.541   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.592  -6.606   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.071  -6.175   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.437  -4.680   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.226  -8.102   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.338  -9.167   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.747  -8.532   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.381 -10.028   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.635  -7.467   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       6.157  -7.898   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.143  -2.345   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.608  -2.459   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.560  -3.998   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.204  -4.727   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       3.082  -2.251   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.025  -1.034   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.747   1.694   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       9.020   2.560   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.407   1.891   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.906   4.096   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      10.179   4.963   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       7.519   4.766   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       7.405   6.301   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -0.575   5.710   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -1.962   6.379   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -3.235   5.513   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   47                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   46                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   44                                                  
CONECT   13   12   14   39                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   38                                                  
CONECT   16   15   17   33                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   33                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   22   32                                                  
CONECT   32   31                                                            
CONECT   33   20   16   34                                                  
CONECT   34   33   35   37   38                                             
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38                                                       
CONECT   38   37   15   34                                                  
CONECT   39   13   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   12   45                                                  
CONECT   45   44                                                            
CONECT   46    6   47                                                       
CONECT   47   46    3   48                                                  
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  106    0
END

View in JSmol

Synonyms

Value	Source
4,5-Dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0,]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoic acid	Generator
4,5-Dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₃₁H₄₀O₁₇

Average Mass

684.6440 Da

Monoisotopic Mass

684.22655 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=CC(=O)OC2C(OC3C4OC4(CO)C4C3C=COC4OC3OC(CO)C(O)C(O)C3O)OC(C)C(O)C2O)C=C1O

InChI Identifier

InChI=1S/C31H40O17/c1-12-20(36)23(39)26(45-18(35)6-4-13-3-5-16(41-2)15(34)9-13)30(43-12)46-25-14-7-8-42-28(19(14)31(11-33)27(25)48-31)47-29-24(40)22(38)21(37)17(10-32)44-29/h3-9,12,14,17,19-30,32-34,36-40H,10-11H2,1-2H3

InChI Key

LUCUVVSDSLWPMZ-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
Premna microphylla	LOTUS Database	35616633
Verbascum thapsus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Coumaric acid or derivatives
Cinnamic acid ester
Glycosyl compound
O-glycosyl compound
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Fatty acid ester
Phenol
Monocyclic benzene moiety
Fatty acyl
Monosaccharide
Benzenoid
Oxane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Polyol
Acetal
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Primary alcohol
Carbonyl group
Alcohol
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	-0.26	ALOGPS
logP	-1.6	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	9.82	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	256.05 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	156.07 m³·mol⁻¹	ChemAxon
Polarizability	67.66 Å³	ChemAxon
Number of Rings	6	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate (NP0193717)

MOL for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

3D MOL for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

3D SDF for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

PDB for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

3D PDB for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

SMILES for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

INCHI for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

Structure for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)

3D Structure for NP0193717 (4,5-dihydroxy-2-{[2-(hydroxymethyl)-10-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate)