NP-MRD: Showing NP-Card for methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate (NP0219306)

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Record Information

Version

2.0

Created at

2022-09-05 20:15:12 UTC

Updated at

2022-09-05 20:15:12 UTC

NP-MRD ID

NP0219306

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate

Description

Methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5H-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]Decan]-9'-ene-10'-carboxylate belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate is found in Morinda morindoides. Based on a literature review very few articles have been published on methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5H-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]Decan]-9'-ene-10'-carboxylate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052222152D          

 42 47  0  0  0  0            999 V2000
    5.8135    4.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069    3.8140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6176    3.0497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4348    2.9366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1110    2.3985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4217    1.6343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9151    0.9831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0979    1.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5913    0.4450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9020   -0.3192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7192   -0.4323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0299   -1.1966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8471   -1.3097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1577   -2.0740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5233   -1.8478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8339   -2.6121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7061   -1.7347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1995   -2.3859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3954   -0.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5782   -0.8573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7872    1.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2938    2.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8310    3.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2364    3.7665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0385    2.9656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0114    2.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9843    1.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1918    1.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9112    0.3116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4429   -0.3193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0991    0.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -0.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0064   -0.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5253   -0.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3374   -0.2683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2447    0.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7763    1.2834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4958    2.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5675    0.7975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7290    1.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9045    1.7975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2356    2.4216    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
  3  5  1  0  0  0  0
  5  6  2  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  1  0  0  0  0
 10 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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 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
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  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
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 39  2  0  0  0  0
 31 39  1  0  0  0  0
 28 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 26 42  1  0  0  0  0
M  END


  Mrv1652309052222152D          

 42 47  0  0  0  0            999 V2000
    5.8135    4.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069    3.8140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6176    3.0497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4348    2.9366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1110    2.3985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4217    1.6343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9151    0.9831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0979    1.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5913    0.4450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9020   -0.3192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7192   -0.4323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0299   -1.1966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8471   -1.3097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1577   -2.0740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5233   -1.8478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8339   -2.6121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7061   -1.7347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1995   -2.3859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3954   -0.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5782   -0.8573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7872    1.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2938    2.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8310    3.1946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2364    3.7665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0385    2.9656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0114    2.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9843    1.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1918    1.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9112    0.3116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4429   -0.3193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0991    0.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -0.6092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0064   -0.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5253   -0.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3374   -0.2683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2447    0.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7763    1.2834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4958    2.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5675    0.7975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7290    1.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9045    1.7975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2356    2.4216    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
  3  5  1  0  0  0  0
  5  6  2  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  1  0  0  0  0
 10 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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 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
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  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
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 39  2  0  0  0  0
 31 39  1  0  0  0  0
 28 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 26 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219306

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C1C1OC1C21OC(=O)C(=C1)C(O)C1=CC=C(O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O15/c1-36-13-5-9(3-4-12(13)29)17(30)10-6-27(42-24(10)35)16-15(21-22(27)40-21)11(23(34)37-2)8-38-25(16)41-26-20(33)19(32)18(31)14(7-28)39-26/h3-6,8,14-22,25-26,28-33H,7H2,1-2H3

> <INCHI_KEY>
YCKDJQYUDRMPHQ-UHFFFAOYSA-N

> <FORMULA>
C27H30O15

> <MOLECULAR_WEIGHT>
594.522

> <EXACT_MASS>
594.158470266

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
56.75350203770143

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5H-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0^{2,4}]decan]-9'-ene-10'-carboxylate

> <JCHEM_LOGP>
-1.434444747666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.194143055991404

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.903715686558568

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601979864

> <JCHEM_POLAR_SURFACE_AREA>
223.42999999999998

> <JCHEM_REFRACTIVITY>
133.51229999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0^{2,4}]decan]-9'-ene-10'-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      10.852   8.335   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.906   7.119   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.486   5.693   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      12.012   5.482   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.541   4.477   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.120   3.051   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.175   1.835   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.649   2.046   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.704   0.831   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.284  -0.596   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.809  -0.807   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.389  -2.234   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.915  -2.445   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.494  -3.871   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.443  -3.449   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.023  -4.876   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.918  -3.238   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.972  -4.454   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.338  -1.811   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.813  -1.600   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.070   3.473   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.015   4.688   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.151   5.963   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.041   7.031   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.672   5.536   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.621   3.997   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.571   2.457   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.091   2.030   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.568   0.582   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.560  -0.596   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.052   0.311   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.528  -1.137   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.012  -1.408   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.980  -0.230   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.497  -0.501   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -0.457   1.218   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.449   2.396   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.925   3.844   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.059   1.489   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.228   3.305   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.688   3.355   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       4.173   4.520   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   22                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   21                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19                                                            
CONECT   21    8   22   26                                                  
CONECT   22   21    5   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   25                                                       
CONECT   25   24   23   26                                                  
CONECT   26   25   21   27   42                                             
CONECT   27   26   28                                                       
CONECT   28   27   29   40                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   39                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   39                                                  
CONECT   37   36   38                                                       
CONECT   38   37                                                            
CONECT   39   36   31                                                       
CONECT   40   28   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   26                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5H-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0,]decan]-9'-ene-10'-carboxylic acid	Generator

Chemical Formula

C₂₇H₃₀O₁₅

Average Mass

594.5220 Da

Monoisotopic Mass

594.15847 Da

IUPAC Name

methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5H-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0^{2,4}]decan]-9'-ene-10'-carboxylate

Traditional Name

methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0^{2,4}]decan]-9'-ene-10'-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C1C1OC1C21OC(=O)C(=C1)C(O)C1=CC=C(O)C(OC)=C1

InChI Identifier

InChI=1S/C27H30O15/c1-36-13-5-9(3-4-12(13)29)17(30)10-6-27(42-24(10)35)16-15(21-22(27)40-21)11(23(34)37-2)8-38-25(16)41-26-20(33)19(32)18(31)14(7-28)39-26/h3-6,8,14-22,25-26,28-33H,7H2,1-2H3

InChI Key

YCKDJQYUDRMPHQ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Morinda morindoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
O-glycosyl compound
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
2-furanone
Dicarboxylic acid or derivatives
Benzenoid
Monosaccharide
Oxane
Vinylogous ester
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Secondary alcohol
Lactone
Carboxylic acid ester
Polyol
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Dialkyl ether
Acetal
Oxirane
Ether
Aromatic alcohol
Organic oxide
Primary alcohol
Alcohol
Hydrocarbon derivative
Carbonyl group
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	-1.4	ChemAxon
pKa (Strongest Acidic)	9.9	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	223.43 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	133.51 m³·mol⁻¹	ChemAxon
Polarizability	56.75 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

73812732

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate (NP0219306)

MOL for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

3D MOL for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

3D SDF for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

3D-SDF for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

PDB for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

3D PDB for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

SMILES for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

INCHI for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

Structure for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)

3D Structure for NP0219306 (methyl 4-[hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-5-oxo-7'-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',8'-dioxaspiro[furan-2,5'-tricyclo[4.4.0.0²,⁴]decan]-9'-ene-10'-carboxylate)