NP-MRD: Showing NP-Card for 16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde (NP0330223)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-12 15:22:16 UTC

Updated at

2022-09-12 15:22:16 UTC

NP-MRD ID

NP0330223

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde

Description

16,18-Dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]Octadeca-3,5,7,10-tetraene-18-carbaldehyde belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone. 16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde is found in Stereospermum chelonoides, Stereospermum colais and Stereospermum kunthianum. 16,18-Dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]Octadeca-3,5,7,10-tetraene-18-carbaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241502132D          

 24 28  0  0  0  0            999 V2000
   -0.2827    0.3892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0705   -0.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6944   -0.9444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3274   -1.7014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772   -1.6107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5938   -0.5358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1995   -0.0276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8323   -0.4635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5438   -0.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6011    0.7542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2014   -0.5639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9506   -0.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6243   -0.6948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5487   -1.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7995   -1.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1258   -1.3854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3423   -1.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2800   -2.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5783   -1.2493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3604   -1.0708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2153   -1.8755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8507   -2.4017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0691   -2.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2928   -2.9668    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  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
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
 19 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END

     RDKit          3D

 42 46  0  0  0  0  0  0  0  0999 V2000
   -0.1018   -2.1272   -1.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7381   -1.5583   -0.0799 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6484   -2.5952    0.9577 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3760   -3.2232    1.0999 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1841   -1.2196   -0.4296 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9204   -0.9512    0.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3414    0.5287    0.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0607    1.0406    0.0864 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0947    2.4818   -0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0276    0.6221    0.8917 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1137   -0.2293    0.3060 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0615   -0.3291    1.1621 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9607   -0.9470    2.2518 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3695    0.2454    0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960    0.1517    1.7757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6407    0.6771    1.5191 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8327    1.3011    0.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8254    1.4075   -0.6448 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5977    0.8751   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4919    0.9642   -1.3402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6472    1.5270   -2.4501 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2136    0.4025   -1.0309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8396    0.3530   -1.8554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1361    0.1207   -1.1451 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8395   -2.1658   -2.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2833   -3.1488   -1.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7504   -1.5216   -1.6849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4798   -2.8084    1.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6637   -1.9991   -1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7635   -1.6112    1.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2501   -0.9650    1.7612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1944    0.5517    0.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4984    0.9774    1.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6103    2.6302   -1.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420    2.8547   -0.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6376    3.0401    0.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2518   -0.3337    2.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4341    0.5966    2.2572 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8120    1.7095    0.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0031    1.8977   -1.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7472    0.4700   -2.9142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0146    0.3074   -1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  9  1  6
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5 24  1  0
 24 23  1  0
 23 22  2  0
 22 20  1  0
 20 21  2  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  2  0
 14 12  1  0
 12 13  2  0
 11 12  1  1
 11 10  1  0
 11  2  1  0
  2  1  1  0
  2  3  1  1
  3  4  2  0
 24  8  1  0
 11 22  1  0
 10  8  1  0
  2  5  1  0
 14 19  1  0
  9 34  1  0
  9 35  1  0
  9 36  1  0
  7 32  1  0
  7 33  1  0
  6 30  1  0
  6 31  1  0
  5 29  1  6
 24 42  1  6
 23 41  1  0
 18 40  1  0
 17 39  1  0
 16 38  1  0
 15 37  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
M  END


  Mrv1533004241502132D          

 24 28  0  0  0  0            999 V2000
   -0.2827    0.3892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0705   -0.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6944   -0.9444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3274   -1.7014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772   -1.6107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5938   -0.5358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1995   -0.0276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8323   -0.4635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5438   -0.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6011    0.7542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2014   -0.5639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9506   -0.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6243   -0.6948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5487   -1.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7995   -1.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1258   -1.3854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3423   -1.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2800   -2.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5783   -1.2493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3604   -1.0708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2153   -1.8755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8507   -2.4017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0691   -2.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2928   -2.9668    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  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
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
 19 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0330223

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCC3C1C=C1C(=O)C4=CC=CC=C4C(=O)C1(O2)C3(C)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O4/c1-18(10-21)13-7-8-19(2)14(13)9-15-16(22)11-5-3-4-6-12(11)17(23)20(15,18)24-19/h3-6,9-10,13-14H,7-8H2,1-2H3

> <INCHI_KEY>
NSNGIRMJTMEZBF-UHFFFAOYSA-N

> <FORMULA>
C20H18O4

> <MOLECULAR_WEIGHT>
322.36

> <EXACT_MASS>
322.12050906

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
33.24969229986016

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde

> <ALOGPS_LOGP>
2.92

> <JCHEM_LOGP>
2.215542298

> <ALOGPS_LOGS>
-4.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.306537439790141

> <JCHEM_POLAR_SURFACE_AREA>
60.440000000000005

> <JCHEM_REFRACTIVITY>
88.21599999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.53e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde

> <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      -0.528   0.726   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.132  -0.762   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.296  -1.763   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.611  -3.176   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.891  -3.007   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.108  -1.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.239  -0.052   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.420  -0.865   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.748  -0.129   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.855   1.408   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.976  -1.053   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.375  -0.408   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.632  -1.297   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.491  -2.830   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.092  -3.475   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.835  -2.586   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.372  -3.173   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.256  -4.709   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.946  -2.332   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.673  -1.999   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.269  -3.501   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.455  -4.483   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.996  -5.017   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.547  -5.538   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    6   20                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    2    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    8   20   21                                             
CONECT   20   19    2                                                       
CONECT   21   19    5   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₈O₄

Average Mass

322.3600 Da

Monoisotopic Mass

322.12051 Da

IUPAC Name

16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde

Traditional Name

16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC12CCC3C1C=C1C(=O)C4=CC=CC=C4C(=O)C1(O2)C3(C)C=O

InChI Identifier

InChI=1S/C20H18O4/c1-18(10-21)13-7-8-19(2)14(13)9-15-16(22)11-5-3-4-6-12(11)17(23)20(15,18)24-19/h3-6,9-10,13-14H,7-8H2,1-2H3

InChI Key

NSNGIRMJTMEZBF-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
Stereospermum chelonoides	LOTUS Database	35616633
Stereospermum colais	LOTUS Database	35616633
Stereospermum kunthianum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

9,10-anthraquinone
Anthraquinone
Naphthopyranone
Naphthopyran
Naphthalene
Tetralin
Aryl alkyl ketone
Aryl ketone
Quinone
Oxepane
Pyranone
Oxane
Pyran
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Aldehyde
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.92	ALOGPS
logP	2.22	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	60.44 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.22 m³·mol⁻¹	ChemAxon
Polarizability	33.25 Å³	ChemAxon
Number of Rings	5	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde (NP0330223)

MOL for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

3D MOL for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

3D SDF for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

3D-SDF for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

PDB for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

3D PDB for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

SMILES for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

INCHI for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

Structure for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)

3D Structure for NP0330223 (16,18-dimethyl-2,9-dioxo-17-oxapentacyclo[11.4.1.0¹,¹⁰.0³,⁸.0¹²,¹⁶]octadeca-3,5,7,10-tetraene-18-carbaldehyde)