NP-MRD: Showing NP-Card for 13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione (NP0318221)

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Record Information

Version

2.0

Created at

2022-09-11 18:35:21 UTC

Updated at

2022-09-11 18:35:21 UTC

NP-MRD ID

NP0318221

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione

Description

13-Hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]Heptadeca-3,5,7,12-tetraene-11,15-dione belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals. 13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione is found in Uvaria afzelii. 13-Hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]Heptadeca-3,5,7,12-tetraene-11,15-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171514402D          

 24 27  0  0  0  0            999 V2000
    0.0658   -0.3381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7376   -0.8170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467   -1.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0882   -0.0727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9121   -0.0159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1246    0.8131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5517    1.4067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9495    0.9935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5315    0.3676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0022   -0.1993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4723   -0.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1816   -1.2608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0188   -1.0311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6442   -1.5691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4229   -1.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5761   -0.4858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9506    0.0522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1720   -0.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0359   -1.4370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8162   -1.7049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9331   -2.2556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2014   -1.5047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8438   -2.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6225    0.6083    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  9 18  1  0  0  0  0
 13 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
  4 24  1  0  0  0  0
M  END

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
   -3.8807    0.6809   -0.0841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6103    0.4113    0.7178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8836    0.6312    2.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1332   -0.9696    0.4700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5067   -1.8995    1.1554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -1.2060   -0.6379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8455   -2.6693   -0.6868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7657   -0.8109   -1.9742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0697   -0.3798   -0.3644 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7941   -0.9105    0.7304 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1876   -0.7378    0.8112 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9325   -1.1371    1.8965 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3077   -0.9493    1.9392 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9563   -0.3509    0.8787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1728    0.0446   -0.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8288   -0.1421   -0.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0292    0.2851   -1.4082 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8285    1.7789   -1.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6259    2.0645   -0.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4030    3.2185   -0.0231 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3566    1.0242   -0.1346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5409    1.3721    0.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8488    2.7371    0.5249 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8284   -0.4049   -1.5117 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3923   -0.2698   -0.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5664    1.3359    0.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6095    1.2754   -0.9930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8958    0.2436    2.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7694    1.6981    2.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1247    0.0207    2.7481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9642   -3.1536    0.3241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6068   -3.1593   -1.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1696   -2.8894   -1.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1897   -1.3156   -2.7918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8169   -1.1427   -2.0706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6405    0.2848   -2.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4186   -1.6055    2.7245 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8852   -1.2655    2.7946 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0214   -0.1763    0.8500 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6990    0.5153   -1.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5940    0.0807   -2.3440 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5927    2.2113   -2.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7165    2.2612   -0.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9300    3.3699   -0.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 22  1  0
 22 23  1  0
 22 21  2  0
 21 19  1  0
 19 20  2  0
 19 18  1  0
 18 17  1  0
 17 24  1  0
 24  9  1  0
  9 10  1  1
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  9  6  1  0
  6  7  1  0
  6  8  1  0
  6  4  1  0
  4  5  2  0
  4  2  1  0
  9 21  1  0
 16 11  1  0
 16 17  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
 23 44  1  0
 18 42  1  0
 18 43  1  0
 17 41  1  6
 12 37  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  8 36  1  0
M  END


  Mrv1533004171514402D          

 24 27  0  0  0  0            999 V2000
    0.0658   -0.3381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7376   -0.8170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467   -1.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0882   -0.0727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9121   -0.0159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1246    0.8131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5517    1.4067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9495    0.9935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5315    0.3676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0022   -0.1993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4723   -0.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1816   -1.2608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0188   -1.0311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6442   -1.5691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4229   -1.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5761   -0.4858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9506    0.0522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1720   -0.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0359   -1.4370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8162   -1.7049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9331   -2.2556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2014   -1.5047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8438   -2.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6225    0.6083    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  9 18  1  0  0  0  0
 13 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
  4 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0318221

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C(O)=C2C(=O)CC3OC2(OC2=CC=CC=C32)C(C)(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H20O5/c1-17(2)15(21)14-11(20)9-13-10-7-5-6-8-12(10)23-19(14,24-13)18(3,4)16(17)22/h5-8,13,21H,9H2,1-4H3

> <INCHI_KEY>
XZEWTFGHFZJQDU-UHFFFAOYSA-N

> <FORMULA>
C19H20O5

> <MOLECULAR_WEIGHT>
328.364

> <EXACT_MASS>
328.131073744

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
33.67473532180976

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione

> <ALOGPS_LOGP>
2.63

> <JCHEM_LOGP>
3.880132867333333

> <ALOGPS_LOGS>
-3.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.981346174768413

> <JCHEM_PKA_STRONGEST_BASIC>
-4.335142727411427

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
87.1626

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.54e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       0.123  -0.631   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.377  -1.525   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.274  -2.600   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.031  -0.136   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.569  -0.030   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.966   1.518   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.896   2.626   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.506   1.855   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.592   0.686   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.604  -0.372   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.615  -1.313   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.939  -2.354   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.502  -1.925   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.669  -2.929   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.123  -2.420   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.409  -0.907   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.241   0.097   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.788  -0.411   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.800  -2.682   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.257  -3.183   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.608  -4.210   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.243  -2.809   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.575  -4.197   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       1.162   1.136   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   22                                             
CONECT    3    2                                                            
CONECT    4    2    5   24                                                  
CONECT    5    4    6   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10    5   12   19                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    9   13                                                  
CONECT   19   11   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19    2   23                                                  
CONECT   23   22                                                            
CONECT   24    4                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀O₅

Average Mass

328.3640 Da

Monoisotopic Mass

328.13107 Da

IUPAC Name

13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione

Traditional Name

13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione

CAS Registry Number

Not Available

SMILES

CC1(C)C(O)=C2C(=O)CC3OC2(OC2=CC=CC=C32)C(C)(C)C1=O

InChI Identifier

InChI=1S/C19H20O5/c1-17(2)15(21)14-11(20)9-13-10-7-5-6-8-12(10)23-19(14,24-13)18(3,4)16(17)22/h5-8,13,21H,9H2,1-4H3

InChI Key

XZEWTFGHFZJQDU-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
Uvaria afzelii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Ketals

Alternative Parents

Substituents

Ketal
Cyclohexenone
Benzenoid
Oxane
Vinylogous acid
Cyclic ketone
Ketone
Oxacycle
Organoheterocyclic compound
Enol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aldehyde
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	2.63	ALOGPS
logP	3.88	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	8.98	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	87.16 m³·mol⁻¹	ChemAxon
Polarizability	33.67 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

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

21638394

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione (NP0318221)

MOL for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

3D MOL for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

3D SDF for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

3D-SDF for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

PDB for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

3D PDB for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

SMILES for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

INCHI for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

Structure for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)

3D Structure for NP0318221 (13-hydroxy-14,14,16,16-tetramethyl-2,17-dioxatetracyclo[7.7.1.0¹,¹².0³,⁸]heptadeca-3,5,7,12-tetraene-11,15-dione)