NP-MRD: Showing NP-Card for (2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid (NP0242283)

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Record Information

Version

1.0

Created at

2022-09-07 02:34:29 UTC

Updated at

2022-09-07 02:34:29 UTC

NP-MRD ID

NP0242283

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid

Description

(2S)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)hexanoic acid belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. Based on a literature review very few articles have been published on (2S)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)hexanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072204342D          

 29 31  0  0  1  0            999 V2000
    3.1599   -4.6480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599   -6.0770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -6.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -6.0770    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0474   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -4.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -6.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -7.5059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -6.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -6.0770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1099   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -6.7914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3474   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599   -7.5059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599   -8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3474   -9.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599  -10.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -9.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1099   -8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -9.6493    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 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
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  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
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
   -4.6372    1.6209   -1.8548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0998    2.1657   -0.5852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2219    3.3375   -0.3508 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4117    1.2745    0.3993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3911   -0.1174   -0.1248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6787   -1.1241    0.7119 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2424   -1.1066    2.0979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5011   -0.8377    3.0502 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5652   -1.3884    2.2800 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2286   -1.1228    0.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5666   -2.1011    1.4066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2586   -3.0202    2.1533 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7898   -2.1883    1.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5604   -1.3197    0.7205 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9413   -0.3577   -0.0600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4550   -0.2531   -0.1168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0674    0.6806   -0.8883 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7951    0.5412   -0.8183 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3014    1.4343   -1.5445 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2737    0.4434   -0.7676 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0756    1.3022   -1.4920 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587    2.2659   -2.2739 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4580    1.2166   -1.4494 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0697    0.2572   -0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4666    0.1659   -0.6240 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2625   -0.5973    0.0500 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8718   -0.5154    0.0108 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0172   -1.4073    0.7633 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5717   -2.2888    1.4789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2122    2.3894   -2.3977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8455    1.2563   -2.5340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3188    0.7873   -1.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0988    1.3047    1.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5078    1.7371    0.7502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4762   -0.4830   -0.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1092   -0.1190   -1.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0108   -2.1821    0.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0516   -1.0079    3.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1824   -3.2499    2.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2894   -2.9459    2.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8608    1.3896   -1.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0164    2.9096   -2.8159 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0886    1.8958   -2.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9642    0.7065    0.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7274   -1.3483    0.6598 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  9  1  0
  7  8  2  0
  6 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 28  1  0
 28 29  2  0
 28 27  1  0
 27 26  2  0
 26 24  1  0
 24 25  1  0
 24 23  2  0
 23 21  1  0
 21 22  1  0
 21 20  2  0
 20 18  1  0
 18 19  2  0
 18 15  1  0
 15 16  2  0
 16 17  1  0
 16 10  1  0
 15 14  1  0
 20 27  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  6
  9 38  1  0
 12 39  1  0
 13 40  1  0
 26 45  1  0
 25 44  1  0
 23 43  1  0
 22 42  1  0
 17 41  1  0
M  END


  Mrv1652309072204342D          

 29 31  0  0  1  0            999 V2000
    3.1599   -4.6480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599   -6.0770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -6.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -6.0770    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0474   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -4.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -6.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -7.5059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -6.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -6.0770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1099   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -6.7914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3474   -8.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599   -7.5059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599   -8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3474   -9.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599  -10.3638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224   -9.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1099   -8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -9.6493    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 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
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  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
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0242283

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)CC[C@H](C(O)=O)C1=C(O)C=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O9/c1-7(21)2-3-9(20(28)29)14-13(24)6-11-16(18(14)26)19(27)15-10(17(11)25)4-8(22)5-12(15)23/h4-6,9,22-24,26H,2-3H2,1H3,(H,28,29)/t9-/m0/s1

> <INCHI_KEY>
HTBJCSXYMPBHJQ-VIFPVBQESA-N

> <FORMULA>
C20H16O9

> <MOLECULAR_WEIGHT>
400.339

> <EXACT_MASS>
400.079432095

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
38.149753565265314

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)hexanoic acid

> <JCHEM_LOGP>
3.083700443333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.935106146227724

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.9521481259801323

> <JCHEM_PKA_STRONGEST_BASIC>
-5.359795659045406

> <JCHEM_POLAR_SURFACE_AREA>
169.42999999999998

> <JCHEM_REFRACTIVITY>
99.37519999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       5.898  -8.676   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.898 -11.344   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.208 -10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.978 -11.344   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.518 -11.344   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.288 -10.010   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.518  -8.676   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      12.828 -10.010   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.288 -12.677   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.518 -14.011   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.978 -14.011   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      11.288 -15.345   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.828 -15.345   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.598 -14.011   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.828 -12.677   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.598 -11.344   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      15.138 -14.011   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      15.908 -12.677   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      15.908 -15.345   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      17.448 -15.345   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      18.218 -14.011   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      18.218 -16.678   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.448 -18.012   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      18.218 -19.346   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      15.908 -18.012   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.138 -16.678   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.598 -16.678   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      12.828 -18.012   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   10                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    6   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   28                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   10   17                                                  
CONECT   17   16                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   27                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   20   28                                                  
CONECT   28   27   14   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
(2S)-5-oxo-2-(1,3,6,8-Tetrahydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)hexanoate	Generator

Chemical Formula

C₂₀H₁₆O₉

Average Mass

400.3390 Da

Monoisotopic Mass

400.07943 Da

IUPAC Name

(2S)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)hexanoic acid

Traditional Name

(2S)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid

CAS Registry Number

Not Available

SMILES

CC(=O)CC[C@H](C(O)=O)C1=C(O)C=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1O

InChI Identifier

InChI=1S/C20H16O9/c1-7(21)2-3-9(20(28)29)14-13(24)6-11-16(18(14)26)19(27)15-10(17(11)25)4-8(22)5-12(15)23/h4-6,9,22-24,26H,2-3H2,1H3,(H,28,29)/t9-/m0/s1

InChI Key

HTBJCSXYMPBHJQ-VIFPVBQESA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Hydroxyanthraquinones

Alternative Parents

Substituents

Hydroxyanthraquinone
Medium-chain fatty acid
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Hydroxy fatty acid
1-hydroxy-4-unsubstituted benzenoid
Fatty acyl
Fatty acid
Vinylogous acid
Ketone
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
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	3.08	ChemAxon
pKa (Strongest Acidic)	2.95	ChemAxon
pKa (Strongest Basic)	-5.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	169.43 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	99.38 m³·mol⁻¹	ChemAxon
Polarizability	38.15 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

162844449

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid (NP0242283)

MOL for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

3D MOL for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

3D SDF for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

3D-SDF for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

PDB for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

3D PDB for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

SMILES for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

INCHI for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

Structure for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)

3D Structure for NP0242283 ((2s)-5-oxo-2-(1,3,6,8-tetrahydroxy-9,10-dioxoanthracen-2-yl)hexanoic acid)