NP-MRD: Showing NP-Card for (3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione (NP0204496)

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Record Information

Version

2.0

Created at

2022-09-05 00:10:54 UTC

Updated at

2022-09-05 00:10:55 UTC

NP-MRD ID

NP0204496

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione

Description

(3S,4aS,12bS)-3,4a,8,12b-tetrahydroxy-3-methyl-1,2,3,4,4a,5,6,7,12,12b-decahydrotetraphene-1,7,12-trione 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. (3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione is found in Streptomyces phaeochromogenes. Based on a literature review very few articles have been published on (3S,4aS,12bS)-3,4a,8,12b-tetrahydroxy-3-methyl-1,2,3,4,4a,5,6,7,12,12b-decahydrotetraphene-1,7,12-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052202102D          

 26 29  0  0  1  0            999 V2000
    5.8256    1.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0260    0.1671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1449    0.8802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -1.3025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7651   -0.9907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246   -1.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  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
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  2 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
   -4.7567    0.7577    1.1370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5662    0.6706    0.1714 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0983    1.0016   -1.0887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5313    1.6857    0.5111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3469    1.1779    1.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8925    1.8431    2.1268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7276   -0.1094    0.7939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5953   -0.8506    1.9959 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6377    0.0385    0.2624 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9510   -0.1822   -0.9844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0330   -0.6158   -1.9989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454   -0.5629   -1.5546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6268   -0.8957   -0.0903 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3060   -2.2569    0.0472 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0800   -0.7499    0.2297 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3514   -0.0124   -1.4664 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6323   -0.2323   -2.6835 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4237    0.4023   -0.5792 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7159    0.5500   -1.0637 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9773    0.2938   -2.4241 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7084    0.9451   -0.1920 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3972    1.1844    1.1377 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1007    1.0317    1.6038 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0987    0.6358    0.7371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7214    0.4616    1.1785 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4360    0.6807    2.3987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2378   -0.2321    1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5089    1.4745    0.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3146    0.9990    2.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8820    0.4321   -1.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0570    2.4782    1.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1832    2.2681   -0.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1020   -1.6747    1.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2570   -1.5911   -2.4547 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0670    0.1416   -2.8360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9744    0.3694   -1.8270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0086   -1.3724   -2.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8449   -2.6144    0.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3178   -1.2599    1.1848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6497   -1.3124   -0.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8906    0.3871   -2.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7144    1.0597   -0.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1795    1.4930    1.8120 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8271    1.2106    2.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  6
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  1
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 10 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 15  2  1  0
 24 18  1  0
 13  7  1  0
 25  9  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  8 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 20 41  1  0
 21 42  1  0
 22 43  1  0
 23 44  1  0
M  END


  Mrv1652309052202102D          

 26 29  0  0  1  0            999 V2000
    5.8256    1.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0260    0.1671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1449    0.8802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -1.3025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7651   -0.9907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246   -1.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  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
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  2 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0204496

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]1(O)CC(=O)[C@]2(O)C3=C(CC[C@]2(O)C1)C(=O)C1=C(O)C=CC=C1C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O7/c1-17(24)7-12(21)19(26)14-10(5-6-18(19,25)8-17)15(22)13-9(16(14)23)3-2-4-11(13)20/h2-4,20,24-26H,5-8H2,1H3/t17-,18+,19+/m1/s1

> <INCHI_KEY>
GUYWBYSVTCSING-QYZOEREBSA-N

> <FORMULA>
C19H18O7

> <MOLECULAR_WEIGHT>
358.346

> <EXACT_MASS>
358.10525292

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
35.213758909919875

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4aS,12bS)-3,4a,8,12b-tetrahydroxy-3-methyl-1,2,3,4,4a,5,6,7,12,12b-decahydrotetraphene-1,7,12-trione

> <JCHEM_LOGP>
0.3596182790000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.232817614593536

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.239209713886236

> <JCHEM_PKA_STRONGEST_BASIC>
-2.899661500347734

> <JCHEM_POLAR_SURFACE_AREA>
132.13

> <JCHEM_REFRACTIVITY>
90.32659999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4aS,12bS)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      10.874   2.256   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.249   0.312   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.375   3.098   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.870   1.643   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.862  -1.267   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.870  -2.431   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.383  -2.140   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.895  -1.849   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.399  -0.394   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.350  -1.558   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.846  -3.013   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.326  -2.140   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.326   1.934   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.358   1.352   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.862   2.807   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   15                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9   13                                             
CONECT    8    7                                                            
CONECT    9    7   10   25                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14   15                                             
CONECT   14   13                                                            
CONECT   15   13    2                                                       
CONECT   16   10   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   24                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   18   25                                                  
CONECT   25   24    9   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₈O₇

Average Mass

358.3460 Da

Monoisotopic Mass

358.10525 Da

IUPAC Name

(3S,4aS,12bS)-3,4a,8,12b-tetrahydroxy-3-methyl-1,2,3,4,4a,5,6,7,12,12b-decahydrotetraphene-1,7,12-trione

Traditional Name

(3S,4aS,12bS)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione

CAS Registry Number

Not Available

SMILES

C[C@@]1(O)CC(=O)[C@]2(O)C3=C(CC[C@]2(O)C1)C(=O)C1=C(O)C=CC=C1C3=O

InChI Identifier

InChI=1S/C19H18O7/c1-17(24)7-12(21)19(26)14-10(5-6-18(19,25)8-17)15(22)13-9(16(14)23)3-2-4-11(13)20/h2-4,20,24-26H,5-8H2,1H3/t17-,18+,19+/m1/s1

InChI Key

GUYWBYSVTCSING-QYZOEREBSA-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 phaeochromogenes	LOTUS Database	35616633

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
Naphthalene
Quinone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Vinylogous acid
Tertiary alcohol
Cyclic alcohol
Ketone
Polyol
Hydrocarbon derivative
Alcohol
Organooxygen compound
Carbonyl group
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	0.36	ChemAxon
pKa (Strongest Acidic)	8.24	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	132.13 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	90.33 m³·mol⁻¹	ChemAxon
Polarizability	35.21 Å³	ChemAxon
Number of Rings	4	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

8513893

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10338434

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione (NP0204496)

MOL for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

3D MOL for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

3D SDF for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

3D-SDF for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

PDB for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

3D PDB for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

SMILES for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

INCHI for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

Structure for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)

3D Structure for NP0204496 ((3s,4as,12bs)-3,4a,8,12b-tetrahydroxy-3-methyl-2,4,5,6-tetrahydrotetraphene-1,7,12-trione)