NP-MRD: Showing NP-Card for 4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one (NP0312617)

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Record Information

Version

2.0

Created at

2022-09-11 09:33:30 UTC

Updated at

2022-09-11 09:33:30 UTC

NP-MRD ID

NP0312617

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one

Description

4,6,10,14-Tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]Trideca-2(7),3,5,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]Heptadeca-3(8),4,6,11(16),12,14-hexaen-2-one belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety. 4,6,10,14-Tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]Trideca-2(7),3,5,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]Heptadeca-3(8),4,6,11(16),12,14-hexaen-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241512042D          

 42 48  0  0  0  0            999 V2000
    3.9256    3.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2529    3.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3301    2.5383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6573    2.0608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7345    1.2394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4535    1.6440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0605    1.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8818    1.1624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3594    0.4897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1808    0.5669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0155   -0.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1942   -0.3374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7166    0.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8971    0.4306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1434   -0.3568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2780   -0.1146    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4962    0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8771   -0.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0953   -0.1327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5238   -0.6780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3176    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0583    1.8954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6326    1.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3492    2.2498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5519    1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3892    2.0301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3336    0.9577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9528    1.5030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901    2.3118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5030    3.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
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 37 38  1  0  0  0  0
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 17 39  1  0  0  0  0
 39 40  1  0  0  0  0
  5 40  1  0  0  0  0
 40 41  2  0  0  0  0
  2 42  1  0  0  0  0
M  END

     RDKit          3D

 72 78  0  0  0  0  0  0  0  0999 V2000
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   -5.3995    2.0861    2.6052 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3215    0.4760    1.5431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3261   -0.1892    0.1750 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4669    0.2074   -0.5098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3152   -0.8448   -0.7730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5617   -0.8671   -1.4148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2609   -2.0427   -1.5802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5033   -2.0647   -2.2194 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0776   -0.9108    0.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.9106    0.9055    1.6497 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2  4  2  3
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M  END


  Mrv1533004241512042D          

 42 48  0  0  0  0            999 V2000
    3.9256    3.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6151    1.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2149    0.2626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3917    0.3183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8362    0.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5213    0.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2619    0.7089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3176    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0583    1.8954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6326    1.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8919    1.6284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3492    2.2498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5519    1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3892    2.0301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3336    0.9577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9528    1.5030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901    2.3118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5030    3.7035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 22 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 29 35  1  0  0  0  0
 35 36  1  0  0  0  0
 24 36  1  0  0  0  0
 21 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
 17 39  1  0  0  0  0
 39 40  1  0  0  0  0
  5 40  1  0  0  0  0
 40 41  2  0  0  0  0
  2 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0312617

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC12OC3=CC(O)=CC=C3C1(O)OC1=CC(O)=C(C(O)=C1C2=O)C1=CC2(C)CC(C1)C1=CC=C(O)C=C1O2

> <INCHI_IDENTIFIER>
InChI=1S/C33H30O9/c1-16(2)8-9-32-30(38)28-26(42-33(32,39)22-7-5-20(35)12-25(22)41-32)13-23(36)27(29(28)37)18-10-17-14-31(3,15-18)40-24-11-19(34)4-6-21(17)24/h4-8,11-13,15,17,34-37,39H,9-10,14H2,1-3H3

> <INCHI_KEY>
UIIUFSXWGFBRFW-UHFFFAOYSA-N

> <FORMULA>
C33H30O9

> <MOLECULAR_WEIGHT>
570.594

> <EXACT_MASS>
570.188982546

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
60.41667628460201

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one

> <ALOGPS_LOGP>
3.94

> <JCHEM_LOGP>
6.393108823666667

> <ALOGPS_LOGS>
-4.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.758440154960558

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.518568471400272

> <JCHEM_PKA_STRONGEST_BASIC>
-4.511584544502092

> <JCHEM_POLAR_SURFACE_AREA>
145.91

> <JCHEM_REFRACTIVITY>
154.15680000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.76e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one

> <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       7.328   7.163   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.072   6.271   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.216   4.738   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.960   3.847   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.104   2.314   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.447   3.069   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       7.580   2.026   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.113   2.170   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.004   0.914   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      11.537   1.058   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.362  -0.486   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.829  -0.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.938   0.626   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.408   0.804   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.868  -0.666   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       4.252  -0.214   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.793   0.278   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.637  -0.740   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.178  -0.248   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.978  -1.266   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.126   1.262   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.585   1.754   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.689   3.291   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.849   4.304   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.357   5.763   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.015   2.236   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.134   0.490   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.598   0.594   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.294   1.503   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.573   0.645   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.956   1.323   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -8.059   2.860   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -9.442   3.538   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -6.781   3.718   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -5.398   3.040   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -4.385   4.200   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       1.030   2.280   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.727   3.790   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       2.489   1.788   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.645   2.806   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       3.342   4.315   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       4.672   6.913   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   14   40                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14                                                  
CONECT   14   13    5   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   39                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   37                                                  
CONECT   22   21   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26   36                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27   22                                                       
CONECT   29   27   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   29   36                                                  
CONECT   36   35   24                                                       
CONECT   37   21   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   17   40                                                  
CONECT   40   39    5   41                                                  
CONECT   41   40                                                            
CONECT   42    2                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₃₀O₉

Average Mass

570.5940 Da

Monoisotopic Mass

570.18898 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)=CCC12OC3=CC(O)=CC=C3C1(O)OC1=CC(O)=C(C(O)=C1C2=O)C1=CC2(C)CC(C1)C1=CC=C(O)C=C1O2

InChI Identifier

InChI=1S/C33H30O9/c1-16(2)8-9-32-30(38)28-26(42-33(32,39)22-7-5-20(35)12-25(22)41-32)13-23(36)27(29(28)37)18-10-17-14-31(3,15-18)40-24-11-19(34)4-6-21(17)24/h4-8,11-13,15,17,34-37,39H,9-10,14H2,1-3H3

InChI Key

UIIUFSXWGFBRFW-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Chromones

Alternative Parents

Substituents

Chromone
Coumaran
Aryl ketone
Aryl alkyl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous acid
Hemiacetal
Ketone
Polyol
Ether
Oxacycle
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	3.94	ALOGPS
logP	6.39	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	7.52	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	145.91 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	154.16 m³·mol⁻¹	ChemAxon
Polarizability	60.42 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00008665

Chemspider ID

Not Available

KEGG Compound ID

C17870

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

157791

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one (NP0312617)

MOL for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

3D MOL for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

3D SDF for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

3D-SDF for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

PDB for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

3D PDB for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

SMILES for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

INCHI for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

Structure for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)

3D Structure for NP0312617 (4,6,10,14-tetrahydroxy-5-{5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.0²,⁷]trideca-2,4,6,10-tetraen-11-yl}-1-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one)