NP-MRD: Showing NP-Card for 4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione (NP0280365)

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Record Information

Version

2.0

Created at

2022-09-09 06:06:50 UTC

Updated at

2022-09-09 06:06:50 UTC

NP-MRD ID

NP0280365

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione

Description

7,15-Dihydroxy-10-methoxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]Icosa-1,3(8),4,6,12,14,16(20)-heptaene-9,17-dione belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed. 4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione is found in Cladosporium cladosporioides. 7,15-Dihydroxy-10-methoxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]Icosa-1,3(8),4,6,12,14,16(20)-heptaene-9,17-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191520572D          

 26 30  0  0  0  0            999 V2000
    3.3989    3.9460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0230    3.2116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4711    2.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0952    1.7845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5433    1.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0229    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1505   -0.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5084   -0.8816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7387   -0.5845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966   -1.1025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6111    0.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8264    0.8260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0778    0.4793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8711    1.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6068    2.0230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2979    1.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2532    0.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3672    1.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8153    0.4407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6392    0.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0151    1.2167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5670    1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9429    2.6438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7431    1.8678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2950    2.5605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6709    3.2949    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  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
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  0  0  0  0
 11 17  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END

     RDKit          3D

 42 46  0  0  0  0  0  0  0  0999 V2000
   -1.0990    3.4429    1.5833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8660    2.0735    1.4881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4038    1.5590    0.3189 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5260    0.6759    0.7317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3735    1.1451    1.5680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7187   -0.6649    0.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9160   -1.3456    0.3382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9846   -0.7083    0.9024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0117   -2.6394   -0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9502   -3.3003   -0.7136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7454   -2.5955   -0.7915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6298   -1.3279   -0.3263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3746   -0.5636   -0.3845 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8687   -0.9505   -0.2435 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380   -2.2591    0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9769   -2.2519   -0.5141 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7473   -1.0831   -0.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8499   -1.0980    0.5277 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0910    0.2084   -0.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7733    1.3959   -0.3414 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1406    1.3465   -0.2372 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0348    2.5546   -0.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6595    2.5288   -0.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9642    1.3269   -0.5331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404    0.2175   -0.3350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4173    0.8944   -0.5850 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1981    3.6692    1.5830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629    4.0425    0.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7420    3.7997    2.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8716    2.4004   -0.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8662   -1.1867    0.9736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9644   -3.1714   -0.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9704   -4.3056   -1.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9071   -3.0672   -1.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0824   -3.1355   -0.4195 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6890   -2.3657    1.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9243   -2.1801   -1.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4179   -3.2093   -0.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6880    2.1942   -0.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5852    3.4811   -0.6219 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0823    3.4151   -0.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7543    1.0381   -1.6622 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 26  1  0
 26 24  1  0
 24 25  2  0
 25 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  9  2  0
  9  7  1  0
  7  8  1  0
  7  6  2  0
  6  4  1  0
  4  5  2  0
  4  3  1  0
 13 26  1  0
  6 12  1  0
 23 24  1  0
 19 25  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  6
 26 42  1  6
 15 35  1  0
 15 36  1  0
 16 37  1  0
 16 38  1  0
 21 39  1  0
 22 40  1  0
 23 41  1  0
 11 34  1  0
 10 33  1  0
  9 32  1  0
  8 31  1  0
M  END


  Mrv1533004191520572D          

 26 30  0  0  0  0            999 V2000
    3.3989    3.9460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0230    3.2116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4711    2.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0952    1.7845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5433    1.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0229    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1505   -0.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5084   -0.8816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7387   -0.5845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966   -1.1025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6111    0.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8264    0.8260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0778    0.4793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8711    1.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6068    2.0230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2979    1.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2532    0.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3672    1.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8153    0.4407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6392    0.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0151    1.2167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5670    1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9429    2.6438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7431    1.8678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2950    2.5605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6709    3.2949    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  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
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  0  0  0  0
 11 17  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0280365

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C2C3=C4C(CCC(=O)C4=C(O)C=C3)=C2C2=CC=CC(O)=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H16O5/c1-26-21-18-11-6-8-14(24)19-13(23)7-5-10(16(11)19)15(18)9-3-2-4-12(22)17(9)20(21)25/h2-4,6,8,18,21-22,24H,5,7H2,1H3

> <INCHI_KEY>
HPRHYYHXYCISPL-UHFFFAOYSA-N

> <FORMULA>
C21H16O5

> <MOLECULAR_WEIGHT>
348.354

> <EXACT_MASS>
348.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
35.6506919927278

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7,15-dihydroxy-10-methoxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]icosa-1,3,5,7,12(20),13,15-heptaene-9,17-dione

> <ALOGPS_LOGP>
3.07

> <JCHEM_LOGP>
3.6021145799999994

> <ALOGPS_LOGS>
-4.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.358725547447786

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.750944410351468

> <JCHEM_PKA_STRONGEST_BASIC>
-4.184169208808487

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
96.04359999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.10e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,15-dihydroxy-10-methoxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]icosa-1,3,5,7,12(20),13,15-heptaene-9,17-dione

> <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       6.345   7.366   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.643   5.995   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.479   4.702   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.778   3.331   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.614   2.038   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.643   0.843   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.881  -0.679   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.682  -1.646   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.246  -1.091   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.047  -2.058   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.007   0.430   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.543   1.542   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.145   0.895   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.626   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.999   3.776   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.289   2.935   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.206   1.397   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.152   2.116   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.988   0.823   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.527   0.900   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.228   2.271   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.392   3.564   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.093   4.935   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.854   3.487   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.017   4.780   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.719   6.150   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6   18                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    4   17                                                  
CONECT   17   16    6   11                                                  
CONECT   18    5   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   18   25                                                  
CONECT   25   24    3   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₆O₅

Average Mass

348.3540 Da

Monoisotopic Mass

348.09977 Da

IUPAC Name

7,15-dihydroxy-10-methoxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]icosa-1,3,5,7,12(20),13,15-heptaene-9,17-dione

Traditional Name

7,15-dihydroxy-10-methoxypentacyclo[10.7.1.0²,¹¹.0³,⁸.0¹⁶,²⁰]icosa-1,3,5,7,12(20),13,15-heptaene-9,17-dione

CAS Registry Number

Not Available

SMILES

COC1C2C3=C4C(CCC(=O)C4=C(O)C=C3)=C2C2=CC=CC(O)=C2C1=O

InChI Identifier

InChI=1S/C21H16O5/c1-26-21-18-11-6-8-14(24)19-13(23)7-5-10(16(11)19)15(18)9-3-2-4-12(22)17(9)20(21)25/h2-4,6,8,18,21-22,24H,5,7H2,1H3

InChI Key

HPRHYYHXYCISPL-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
Cladosporium cladosporioides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Not Available

Sub Class

Not Available

Direct Parent

Lignans, neolignans and related compounds

Alternative Parents

Substituents

Neolignan skeleton
Tetralin
Indene
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Vinylogous acid
Ketone
Ether
Dialkyl ether
Organooxygen compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.07	ALOGPS
logP	3.6	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	7.75	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.04 m³·mol⁻¹	ChemAxon
Polarizability	35.65 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

9928270

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione (NP0280365)

MOL for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

3D MOL for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

3D SDF for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

3D-SDF for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

PDB for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

3D PDB for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

SMILES for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

INCHI for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

Structure for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)

3D Structure for NP0280365 (4,9-dihydroxy-7-methoxy-1h,2h,6bh,7h-benzo[j]fluoranthene-3,8-dione)