NP-MRD: Showing NP-Card for 3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one (NP0152999)

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Record Information

Version

2.0

Created at

2022-09-02 09:35:09 UTC

Updated at

2022-09-02 09:35:09 UTC

NP-MRD ID

NP0152999

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one

Description

Deacetylvismione H belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. 3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one is found in Psorospermum tenuifolium and Vismia baccifera. Deacetylvismione H is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251503552D          

 25 27  0  0  0  0            999 V2000
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5282   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9979   -3.2502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  2  0  0  0  0
  6 24  1  0  0  0  0
  2 25  1  0  0  0  0
M  END

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -6.0762   -0.8842   -1.5317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0700   -0.3127   -0.5122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0758    0.5882   -1.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2319   -0.5992    0.7225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4927   -0.2517    1.9131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3615    0.5103    1.7649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1719    0.0331    1.1714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0405   -1.2468    0.7164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8627   -1.7411    0.1219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7944   -3.0132   -0.3077 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2088   -0.8747   -0.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4060   -1.3079   -0.5851 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563   -2.5858   -1.0441 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4379   -0.4215   -0.6901 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3211    0.8881   -0.2313 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1375    1.3029    0.3424 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0717    0.4188    0.4601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0983    0.8825    1.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4936    1.7725   -0.3914 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7943    1.0852   -0.0526 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9257    2.0300   -0.4004 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7854    0.8259    1.3172 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9963   -0.1727   -0.8727 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7271   -0.7716   -1.2959 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7196   -1.6214   -2.2134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4785   -1.2298   -2.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8192   -0.1190   -1.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5756   -1.7622   -1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1633    0.1050   -1.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5034    1.0816   -2.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8729    1.4817   -0.4729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1387   -1.2625    0.9492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1874    0.3054    2.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2852   -1.1905    2.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8798   -1.9173    0.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2619   -3.6677   -0.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2739   -3.0675   -1.4521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0840    2.3301    0.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1661    1.9087    1.3928 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5796    2.1781   -1.4315 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4014    2.6403    0.2868 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7917    1.9412    0.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2074    1.8546   -1.4674 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5534    3.0841   -0.3602 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527    1.6686    1.8000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6431   -0.0014   -1.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5398   -0.8944   -0.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 24  1  0
 24 25  2  0
 24 23  1  0
 23 20  1  0
 20 21  1  0
 20 22  1  1
 20 19  1  0
 19 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18  7  1  0
 17 11  1  0
 15 14  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  8 35  1  0
 10 36  1  0
 13 37  1  0
 23 46  1  0
 23 47  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  0
 19 40  1  0
 19 41  1  0
 16 38  1  0
 18 39  1  0
M  END


  Mrv1533004251503552D          

 25 27  0  0  0  0            999 V2000
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5282   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9979   -3.2502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  2  0  0  0  0
  6 24  1  0  0  0  0
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0152999

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCOC1=CC(O)=C2C(O)=C3C(=O)CC(C)(O)CC3=CC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O5/c1-11(2)4-5-25-14-7-12-6-13-9-20(3,24)10-16(22)18(13)19(23)17(12)15(21)8-14/h4,6-8,21,23-24H,5,9-10H2,1-3H3

> <INCHI_KEY>
PAHWTMPJUWLVGJ-UHFFFAOYSA-N

> <FORMULA>
C20H22O5

> <MOLECULAR_WEIGHT>
342.391

> <EXACT_MASS>
342.146723808

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
37.48056883651054

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-1,2,3,4-tetrahydroanthracen-1-one

> <ALOGPS_LOGP>
2.99

> <JCHEM_LOGP>
3.566811207

> <ALOGPS_LOGS>
-4.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.981249844815697

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.811324928765174

> <JCHEM_PKA_STRONGEST_BASIC>
-2.931920983531249

> <JCHEM_POLAR_SURFACE_AREA>
86.99

> <JCHEM_REFRACTIVITY>
96.47379999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.77e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.186  -4.353   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.196  -6.067   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   24                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   23                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   21                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21                                                       
CONECT   21   20   13   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   10   24                                                  
CONECT   24   23    6                                                       
CONECT   25    2                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂O₅

Average Mass

342.3910 Da

Monoisotopic Mass

342.14672 Da

IUPAC Name

3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-1,2,3,4-tetrahydroanthracen-1-one

Traditional Name

3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCOC1=CC(O)=C2C(O)=C3C(=O)CC(C)(O)CC3=CC2=C1

InChI Identifier

InChI=1S/C20H22O5/c1-11(2)4-5-25-14-7-12-6-13-9-20(3,24)10-16(22)18(13)19(23)17(12)15(21)8-14/h4,6-8,21,23-24H,5,9-10H2,1-3H3

InChI Key

PAHWTMPJUWLVGJ-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
Psorospermum tenuifolium	LOTUS Database	35616633
Vismia baccifera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Not Available

Direct Parent

Anthracenes

Alternative Parents

Substituents

Anthracene
1-naphthol
Tetralin
Aryl alkyl ketone
Aryl ketone
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Vinylogous acid
Tertiary alcohol
Ketone
Ether
Polyol
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen compound
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	2.99	ALOGPS
logP	3.57	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	7.81	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	96.47 m³·mol⁻¹	ChemAxon
Polarizability	37.48 Å³	ChemAxon
Number of Rings	3	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

13940837

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one (NP0152999)

MOL for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

3D MOL for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

3D SDF for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

3D-SDF for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

PDB for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

3D PDB for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

SMILES for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

INCHI for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

Structure for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)

3D Structure for NP0152999 (3,8,9-trihydroxy-3-methyl-6-[(3-methylbut-2-en-1-yl)oxy]-2,4-dihydroanthracen-1-one)