NP-MRD: Showing NP-Card for 1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid (NP0222273)

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Record Information

Version

2.0

Created at

2022-09-06 00:04:11 UTC

Updated at

2022-09-06 00:04:11 UTC

NP-MRD ID

NP0222273

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid

Description

1,2,8-Trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-1,2,3,4-tetrahydroanthracene-2-carboxylic acid belongs to the class of organic compounds known as anthracenecarboxylic acids. These are organic compounds containing a carboxylic acid group attached to an anthracene ring system. 1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid is found in Streptomyces rishiriensis. 1,2,8-Trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-1,2,3,4-tetrahydroanthracene-2-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171519452D          

 27 29  0  0  0  0            999 V2000
    2.6397    1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9218    0.8017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7343    0.6585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3915    0.1697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6737   -0.6055    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
    1.6131   -0.6055    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
    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
    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
    2.1434   -3.7125    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
    0.7145   -2.8875    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
    0.6044   -1.6212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -0.9504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3791   -0.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1673   -0.9792    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 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
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  8 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
   -5.0374    0.2648   -0.3353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5806    0.5473    0.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5594    2.0560    0.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6666    0.2185   -1.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2328    0.4322   -0.8679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5240   -0.3188    0.1965 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0592   -0.0556    1.4512 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8885    0.2162    0.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3458    1.2914   -0.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6818    1.6922   -0.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1390    2.7879   -0.9562 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2464    3.4483   -1.7853 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4602    3.2215   -0.8286 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3314    2.5582   -0.0047 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8703    1.4536    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5638    1.0306    0.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0944   -0.0770    1.2605 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7911   -0.4543    1.0950 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3103   -1.6346    1.8252 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7804   -1.9499    2.9462 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2557   -2.4326    1.1885 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8972   -3.7534    0.7656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3717   -1.7748   -0.0139 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5291   -2.0245   -1.0859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6180   -2.5381   -0.2546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5703   -2.5345    0.5633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712   -3.2857   -1.4002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6998    0.9253    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0839    0.4668   -1.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2656   -0.8072   -0.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3970    0.0239    0.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5526    2.5521   -0.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4966    2.3724    0.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6671    2.3414    0.9229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9686   -0.7613   -1.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9674    0.9436   -1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1564    1.5254   -0.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573    0.3533   -1.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3896   -0.8283    1.9225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7073    1.8343   -1.0767 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5682    4.2442   -2.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7379    4.0963   -1.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3301    2.9134    0.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5557    0.9144    1.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7679   -0.6294    1.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5552   -2.6265    1.9277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1539   -4.5708    0.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6326   -4.0069    1.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3625   -3.5862   -0.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901   -1.9336   -1.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2433   -4.1413   -1.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8 18  2  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 11  2  0
 11 12  1  0
 11 10  1  0
 10  9  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  6
 23 25  1  0
 25 27  1  0
 25 26  2  0
 23  6  1  0
  9  8  1  0
 10 16  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  7 39  1  0
 17 45  1  0
 15 44  1  0
 14 43  1  0
 13 42  1  0
 12 41  1  0
  9 40  1  0
 21 46  1  1
 22 47  1  0
 22 48  1  0
 22 49  1  0
 24 50  1  0
 27 51  1  0
M  END


  Mrv1533004171519452D          

 27 29  0  0  0  0            999 V2000
    2.6397    1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9218    0.8017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7343    0.6585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3915    0.1697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6737   -0.6055    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
    1.6131   -0.6055    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
    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
    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
    2.1434   -3.7125    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
    0.7145   -2.8875    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
    0.6044   -1.6212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -0.9504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3791   -0.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1673   -0.9792    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 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
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  8 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0222273

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC1(O)C2=C(C=C3C=CC=C(O)C3=C2)C(=O)C(C)C1(O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O6/c1-11(2)7-8-20(26)16-10-14-13(5-4-6-17(14)22)9-15(16)18(23)12(3)21(20,27)19(24)25/h4-6,9-12,22,26-27H,7-8H2,1-3H3,(H,24,25)

> <INCHI_KEY>
QUASHMJEJFFXLB-UHFFFAOYSA-N

> <FORMULA>
C21H24O6

> <MOLECULAR_WEIGHT>
372.417

> <EXACT_MASS>
372.157288493

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
39.19926447434228

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-1,2,3,4-tetrahydroanthracene-2-carboxylic acid

> <ALOGPS_LOGP>
2.25

> <JCHEM_LOGP>
3.045601114666667

> <ALOGPS_LOGS>
-3.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.42517737241072

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.664963292749859

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8814044829766

> <JCHEM_POLAR_SURFACE_AREA>
115.06000000000002

> <JCHEM_REFRACTIVITY>
99.09249999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.66e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3H-anthracene-2-carboxylic acid

> <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       4.927   2.944   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.454   1.497   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.971   1.229   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.464   0.317   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.991  -1.130   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.011  -1.130   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.128  -3.026   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.851  -1.774   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.574  -0.414   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.312  -1.828   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   23                                             
CONECT    7    6                                                            
CONECT    8    6    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17    8   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    6   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
1,2,8-Trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-1,2,3,4-tetrahydroanthracene-2-carboxylate	Generator

Chemical Formula

C₂₁H₂₄O₆

Average Mass

372.4170 Da

Monoisotopic Mass

372.15729 Da

IUPAC Name

1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-1,2,3,4-tetrahydroanthracene-2-carboxylic acid

Traditional Name

1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3H-anthracene-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(C)CCC1(O)C2=C(C=C3C=CC=C(O)C3=C2)C(=O)C(C)C1(O)C(O)=O

InChI Identifier

InChI=1S/C21H24O6/c1-11(2)7-8-20(26)16-10-14-13(5-4-6-17(14)22)9-15(16)18(23)12(3)21(20,27)19(24)25/h4-6,9-12,22,26-27H,7-8H2,1-3H3,(H,24,25)

InChI Key

QUASHMJEJFFXLB-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
Streptomyces rishiriensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenecarboxylic acids. These are organic compounds containing a carboxylic acid group attached to an anthracene ring system.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Anthracenecarboxylic acids and derivatives

Direct Parent

Anthracenecarboxylic acids

Alternative Parents

Substituents

Anthracene carboxylic acid
2-naphthalenecarboxylic acid
2-naphthalenecarboxylic acid or derivatives
1-naphthol
Tetralin
Aryl ketone
Aryl alkyl ketone
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alpha-hydroxy acid
Hydroxy acid
Tertiary alcohol
1,2-diol
Ketone
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Carboxylic acid
Alcohol
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen 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	2.25	ALOGPS
logP	3.05	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	3.66	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	115.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	99.09 m³·mol⁻¹	ChemAxon
Polarizability	39.2 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

85080637

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid (NP0222273)

MOL for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

3D MOL for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

3D SDF for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

3D-SDF for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

PDB for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

3D PDB for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

SMILES for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

INCHI for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

Structure for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)

3D Structure for NP0222273 (1,2,8-trihydroxy-3-methyl-1-(3-methylbutyl)-4-oxo-3h-anthracene-2-carboxylic acid)