NP-MRD: Showing NP-Card for 6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate (NP0303611)

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Record Information

Version

2.0

Created at

2022-09-10 18:06:20 UTC

Updated at

2022-09-10 18:06:20 UTC

NP-MRD ID

NP0303611

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate

Description

6-(Furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]Octadeca-2(11),9-dien-17-yl 2-methylbutanoate belongs to the class of organic compounds known as anthocyanidin 5-o-6-p-coumaroyl glycosides. These are anthocyanidin 5-O-glycosides where the carbohydrate moiety is esterified at the C6 position with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring. 6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate is found in Xylocarpus moluccensis. 6-(Furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]Octadeca-2(11),9-dien-17-yl 2-methylbutanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191523032D          

 47 52  0  0  0  0            999 V2000
    3.7189    3.0653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9487    2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8157    1.9300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6378    1.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3090    1.1841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9001    1.9007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7796    0.2779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8887   -0.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0678    0.1187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0437   -0.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8094   -0.8813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4636   -1.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0935   -1.9931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6442   -2.4267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3619   -2.0198    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6378   -3.2517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3491   -3.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4067   -1.6920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1126   -0.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4673    0.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608    0.7040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0854    0.6127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8168    1.4775    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6445    0.8298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3058   -1.3068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4027   -1.3395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5803   -1.4047    0.0000 C   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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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
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  8 18  1  0  0  0  0
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 44 45  1  0  0  0  0
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 20 47  1  0  0  0  0
M  END

     RDKit          3D

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 47 91  1  0
 41 83  1  0
 41 84  1  0
 41 85  1  0
 20 70  1  0
 12 62  1  1
 16 63  1  0
 17 64  1  0
 17 65  1  0
 17 66  1  0
 18 67  1  0
 18 68  1  0
 18 69  1  0
 30 78  1  0
 34 79  1  1
 39 82  1  0
 37 81  1  0
 36 80  1  0
 28 75  1  0
 28 76  1  0
 28 77  1  0
 26 73  1  0
 26 74  1  0
 25 71  1  0
 25 72  1  0
M  END


  Mrv1533004191523032D          

 47 52  0  0  0  0            999 V2000
    3.7189    3.0653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9487    2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8157    1.9300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6378    1.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3090    1.1841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9001    1.9007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7796    0.2779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8887   -0.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0678    0.1187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0437   -0.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8094   -0.8813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4636   -1.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0935   -1.9931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6442   -2.4267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3619   -2.0198    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6378   -3.2517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3491   -3.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2437   -0.8350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4067   -1.6920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1126   -0.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4673    0.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608    0.7040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6724    1.5506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0854    0.6127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8168    1.4775    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2093    0.6023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3750    1.3061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1957    1.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3839    2.3574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7972    0.9895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6090    0.1863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5870    1.2281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2898    0.0849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6445    0.8298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4669    0.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1021    1.5495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9346    0.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5799   -0.5295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0475   -1.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8723   -1.2302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1070   -2.0211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4274   -2.4888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7726   -1.9870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7574   -0.5947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3058   -1.3068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4027   -1.3395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5803   -1.4047    0.0000 C   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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  8 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  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
 21 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 39 43  1  0  0  0  0
 38 44  1  0  0  0  0
 33 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 20 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303611

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)OC12CC3(C)C(CC(=O)OC)C1(C)C1=C(C(=O)C2(O)C3OC(=O)C(C)C)C2=CC(=O)OC(C3=COC=C3)C2(C)CC1

> <INCHI_IDENTIFIER>
InChI=1S/C36H44O11/c1-9-19(4)30(41)47-35-17-33(6)23(15-24(37)43-8)34(35,7)21-10-12-32(5)22(14-25(38)45-28(32)20-11-13-44-16-20)26(21)27(39)36(35,42)31(33)46-29(40)18(2)3/h11,13-14,16,18-19,23,28,31,42H,9-10,12,15,17H2,1-8H3

> <INCHI_KEY>
RTUULIKPFWFGBC-UHFFFAOYSA-N

> <FORMULA>
C36H44O11

> <MOLECULAR_WEIGHT>
652.737

> <EXACT_MASS>
652.288362237

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
67.62594872295492

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate

> <ALOGPS_LOGP>
4.19

> <JCHEM_LOGP>
4.8224140449999995

> <ALOGPS_LOGS>
-4.35

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.032783789261742

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8887436007433904

> <JCHEM_POLAR_SURFACE_AREA>
155.64

> <JCHEM_REFRACTIVITY>
165.56229999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.91e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       6.942   5.722   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.504   5.170   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.256   3.603   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.791   3.732   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.310   2.210   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.547   3.548   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.322   0.519   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.659  -0.224   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.127   0.222   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.082  -0.864   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.511  -1.645   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.865  -2.214   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.174  -3.720   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.203  -4.530   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.542  -3.770   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -1.191  -6.070   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.518  -6.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.322  -1.559   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.626  -3.158   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.944  -1.354   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.606   0.037   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.660   1.314   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.122   2.894   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.026   1.144   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.525   2.758   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.391   1.124   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.700   2.438   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.232   2.901   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -2.583   4.400   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -3.355   1.847   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.004   0.348   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.829   2.293   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.141   0.159   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.803   1.549   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.338   1.671   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       9.524   2.892   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       9.211   0.402   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       8.549  -0.988   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.422  -2.257   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.962  -2.296   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      11.400  -3.773   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      10.131  -4.646   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.909  -3.709   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.014  -1.110   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       8.038  -2.439   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       6.352  -2.500   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.817  -2.622   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   18   24                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   12   26                                             
CONECT   11   10                                                            
CONECT   12   10   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   12    8   19   20                                             
CONECT   19   18                                                            
CONECT   20   18   21   47                                                  
CONECT   21   20   22   33                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    8   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   10   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   21   34   44                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   44                                                  
CONECT   39   38   40   43                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   39                                                       
CONECT   44   38   33   45   46                                             
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   20                                                       
MASTER        0    0    0    0    0    0    0    0   47    0  104    0
END

View in JSmol

Synonyms

Value	Source
6-(Furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0,.0,.0,]octadeca-2(11),9-dien-17-yl 2-methylbutanoic acid	Generator
6-(Furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoic acid	Generator

Chemical Formula

C₃₆H₄₄O₁₁

Average Mass

652.7370 Da

Monoisotopic Mass

652.28836 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)OC12CC3(C)C(CC(=O)OC)C1(C)C1=C(C(=O)C2(O)C3OC(=O)C(C)C)C2=CC(=O)OC(C3=COC=C3)C2(C)CC1

InChI Identifier

InChI=1S/C36H44O11/c1-9-19(4)30(41)47-35-17-33(6)23(15-24(37)43-8)34(35,7)21-10-12-32(5)22(14-25(38)45-28(32)20-11-13-44-16-20)26(21)27(39)36(35,42)31(33)46-29(40)18(2)3/h11,13-14,16,18-19,23,28,31,42H,9-10,12,15,17H2,1-8H3

InChI Key

RTUULIKPFWFGBC-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
Xylocarpus moluccensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthocyanidin 5-o-6-p-coumaroyl glycosides. These are anthocyanidin 5-O-glycosides where the carbohydrate moiety is esterified at the C6 position with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Anthocyanidin 5-O-6-p-coumaroyl glycosides

Alternative Parents

Substituents

Anthocyanidin 5-o-6-p-coumaroyl-glycoside
Anthocyanin
Anthocyanidin-3-o-glycoside
Anthocyanidin-5-o-glycoside
Flavonoid-3-o-glycoside
Hydroxyflavonoid
3'-hydroxyflavonoid
4'-hydroxyflavonoid
7-hydroxyflavonoid
Anthocyanidin
Phenolic glycoside
Coumaric acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Disaccharide
Glycosyl compound
O-glycosyl compound
1-benzopyran
Benzopyran
Pyrogallol derivative
Benzenetriol
Styrene
1-hydroxy-4-unsubstituted benzenoid
Phenol
Fatty acid ester
1-hydroxy-2-unsubstituted benzenoid
Oxane
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Heteroaromatic compound
Carboxylic acid ester
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Alcohol
Organic oxide
Carbonyl group
Organic cation
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	4.19	ALOGPS
logP	4.82	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	11.03	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	155.64 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	165.56 m³·mol⁻¹	ChemAxon
Polarizability	67.63 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

75150109

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate (NP0303611)

MOL for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

3D MOL for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

3D SDF for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

3D-SDF for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

PDB for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

3D PDB for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

SMILES for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

INCHI for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

Structure for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)

3D Structure for NP0303611 (6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-14-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadeca-2(11),9-dien-17-yl 2-methylbutanoate)