NP-MRD: Showing NP-Card for 8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione (NP0036700)

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Record Information

Version

2.0

Created at

2021-06-20 19:48:17 UTC

Updated at

2021-06-30 00:08:29 UTC

NP-MRD ID

NP0036700

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione

Provided By

JEOL Database JEOL Logo

Description

CHEMBL2047320 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. 8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione is found in Nigrospora sp. 8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione was first documented in 2012 (Yang, K. -L., et al.). Based on a literature review very few articles have been published on CHEMBL2047320.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121483D          

 39 41  0  0  0  0            999 V2000
    1.3563   -0.6374    5.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3938   -1.1382    4.0361 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.2345    3.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9278    1.1160    3.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7758    1.9400    2.0744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4943    3.2551    2.3406 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9026    1.4322    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1795    0.0774    0.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3559   -0.7384    1.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505   -2.1013    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0114   -2.3115    1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614   -3.7821    1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.4523    1.3660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -0.4679   -0.7958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4226   -1.6661   -1.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1740    0.4504   -1.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3296   -0.0458   -3.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2299    0.8104   -4.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.2738   -5.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    2.1670   -4.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8734    2.9970   -5.2169 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8128    2.6695   -2.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9165    1.8026   -1.7525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7456    2.3300   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4768    3.5150   -0.2109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3661   -0.2378    5.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5518   -1.4744    6.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1376    0.1124    5.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8129    1.5634    4.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120    3.7357    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7294   -4.1631    0.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9402   -4.3045    2.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3323   -3.9547    1.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5301   -1.1060   -3.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2423    0.7650   -6.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5979   -0.8030   -5.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4873    0.4402   -6.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6990    3.9037   -4.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6104    3.7249   -2.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  7  2  0  0  0  0
 16 17  2  0  0  0  0
 23 22  2  0  0  0  0
 22 20  1  0  0  0  0
 20 18  2  0  0  0  0
 18 17  1  0  0  0  0
  3  4  2  0  0  0  0
 18 19  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  2  0  0  0  0
  7 24  1  0  0  0  0
  9 10  1  0  0  0  0
 24 23  1  0  0  0  0
  3  2  1  0  0  0  0
 16 14  1  0  0  0  0
  2  1  1  0  0  0  0
 16 23  1  0  0  0  0
  5  6  1  0  0  0  0
  8  9  2  0  0  0  0
 24 25  2  0  0  0  0
  9  3  1  0  0  0  0
 20 21  1  0  0  0  0
  8  7  1  0  0  0  0
 10 11  1  0  0  0  0
 11 13  2  0  0  0  0
  4  5  1  0  0  0  0
 11 12  1  0  0  0  0
  4 29  1  0  0  0  0
 22 39  1  0  0  0  0
 17 34  1  0  0  0  0
 19 35  1  0  0  0  0
 19 36  1  0  0  0  0
 19 37  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  6 30  1  0  0  0  0
 21 38  1  0  0  0  0
 12 31  1  0  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
M  END

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    1.3563   -0.6374    5.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3938   -1.1382    4.0361 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.2345    3.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9278    1.1160    3.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7758    1.9400    2.0744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4943    3.2551    2.3406 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9026    1.4322    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1795    0.0774    0.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3559   -0.7384    1.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505   -2.1013    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0114   -2.3115    1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614   -3.7821    1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.4523    1.3660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -0.4679   -0.7958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4226   -1.6661   -1.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1740    0.4504   -1.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3296   -0.0458   -3.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2299    0.8104   -4.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.2738   -5.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    2.1670   -4.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8734    2.9970   -5.2169 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8128    2.6695   -2.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9165    1.8026   -1.7525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7456    2.3300   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4768    3.5150   -0.2109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3661   -0.2378    5.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5518   -1.4744    6.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1376    0.1124    5.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8129    1.5634    4.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120    3.7357    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7294   -4.1631    0.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9402   -4.3045    2.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3323   -3.9547    1.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5301   -1.1060   -3.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2423    0.7650   -6.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5979   -0.8030   -5.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4873    0.4402   -6.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6990    3.9037   -4.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6104    3.7249   -2.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  7  2  0
 16 17  2  0
 23 22  2  0
 22 20  1  0
 20 18  2  0
 18 17  1  0
  3  4  2  0
 18 19  1  0
  8 14  1  0
 14 15  2  0
  7 24  1  0
  9 10  1  0
 24 23  1  0
  3  2  1  0
 16 14  1  0
  2  1  1  0
 16 23  1  0
  5  6  1  0
  8  9  2  0
 24 25  2  0
  9  3  1  0
 20 21  1  0
  8  7  1  0
 10 11  1  0
 11 13  2  0
  4  5  1  0
 11 12  1  0
  4 29  1  0
 22 39  1  0
 17 34  1  0
 19 35  1  0
 19 36  1  0
 19 37  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 30  1  0
 21 38  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
M  END


  Mrv1652306202121483D          

 39 41  0  0  0  0            999 V2000
    1.3563   -0.6374    5.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3938   -1.1382    4.0361 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.2345    3.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9278    1.1160    3.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7758    1.9400    2.0744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4943    3.2551    2.3406 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9026    1.4322    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1795    0.0774    0.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3559   -0.7384    1.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505   -2.1013    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0114   -2.3115    1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614   -3.7821    1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.4523    1.3660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -0.4679   -0.7958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4226   -1.6661   -1.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1740    0.4504   -1.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3296   -0.0458   -3.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2299    0.8104   -4.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.2738   -5.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    2.1670   -4.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8734    2.9970   -5.2169 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8128    2.6695   -2.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9165    1.8026   -1.7525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7456    2.3300   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4768    3.5150   -0.2109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3661   -0.2378    5.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5518   -1.4744    6.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1376    0.1124    5.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8129    1.5634    4.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120    3.7357    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7294   -4.1631    0.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9402   -4.3045    2.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3323   -3.9547    1.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5301   -1.1060   -3.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2423    0.7650   -6.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5979   -0.8030   -5.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4873    0.4402   -6.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6990    3.9037   -4.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6104    3.7249   -2.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  7  2  0  0  0  0
 16 17  2  0  0  0  0
 23 22  2  0  0  0  0
 22 20  1  0  0  0  0
 20 18  2  0  0  0  0
 18 17  1  0  0  0  0
  3  4  2  0  0  0  0
 18 19  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  2  0  0  0  0
  7 24  1  0  0  0  0
  9 10  1  0  0  0  0
 24 23  1  0  0  0  0
  3  2  1  0  0  0  0
 16 14  1  0  0  0  0
  2  1  1  0  0  0  0
 16 23  1  0  0  0  0
  5  6  1  0  0  0  0
  8  9  2  0  0  0  0
 24 25  2  0  0  0  0
  9  3  1  0  0  0  0
 20 21  1  0  0  0  0
  8  7  1  0  0  0  0
 10 11  1  0  0  0  0
 11 13  2  0  0  0  0
  4  5  1  0  0  0  0
 11 12  1  0  0  0  0
  4 29  1  0  0  0  0
 22 39  1  0  0  0  0
 17 34  1  0  0  0  0
 19 35  1  0  0  0  0
 19 36  1  0  0  0  0
 19 37  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  6 30  1  0  0  0  0
 21 38  1  0  0  0  0
 12 31  1  0  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0036700

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C([H])=C2C(=O)C3=C(OC(=O)C([H])([H])[H])C(OC([H])([H])[H])=C([H])C(O[H])=C3C(=O)C2=C1[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H14O7/c1-7-4-9-10(5-11(7)20)16(22)14-12(21)6-13(24-3)18(25-8(2)19)15(14)17(9)23/h4-6,20-21H,1-3H3

> <INCHI_KEY>
SLRWHAFJOXBJHC-UHFFFAOYSA-N

> <FORMULA>
C18H14O7

> <MOLECULAR_WEIGHT>
342.303

> <EXACT_MASS>
342.073952791

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
34.0504366705794

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,6-dihydroxy-2-methoxy-7-methyl-9,10-dioxo-9,10-dihydroanthracen-1-yl acetate

> <ALOGPS_LOGP>
2.67

> <JCHEM_LOGP>
2.9245865293333324

> <ALOGPS_LOGS>
-3.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.39008438555048

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.537986645845164

> <JCHEM_PKA_STRONGEST_BASIC>
-4.930991047661738

> <JCHEM_POLAR_SURFACE_AREA>
110.13

> <JCHEM_REFRACTIVITY>
87.7496

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.42e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6-dihydroxy-2-methoxy-7-methyl-9,10-dioxoanthracen-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    1.3563   -0.6374    5.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3938   -1.1382    4.0361 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.2345    3.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9278    1.1160    3.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7758    1.9400    2.0744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4943    3.2551    2.3406 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9026    1.4322    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1795    0.0774    0.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3559   -0.7384    1.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505   -2.1013    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0114   -2.3115    1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614   -3.7821    1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.4523    1.3660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -0.4679   -0.7958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4226   -1.6661   -1.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1740    0.4504   -1.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3296   -0.0458   -3.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2299    0.8104   -4.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.2738   -5.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    2.1670   -4.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8734    2.9970   -5.2169 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8128    2.6695   -2.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9165    1.8026   -1.7525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7456    2.3300   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4768    3.5150   -0.2109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3661   -0.2378    5.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5518   -1.4744    6.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1376    0.1124    5.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8129    1.5634    4.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120    3.7357    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7294   -4.1631    0.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9402   -4.3045    2.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3323   -3.9547    1.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5301   -1.1060   -3.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2423    0.7650   -6.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5979   -0.8030   -5.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4873    0.4402   -6.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6990    3.9037   -4.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6104    3.7249   -2.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  7  2  0
 16 17  2  0
 23 22  2  0
 22 20  1  0
 20 18  2  0
 18 17  1  0
  3  4  2  0
 18 19  1  0
  8 14  1  0
 14 15  2  0
  7 24  1  0
  9 10  1  0
 24 23  1  0
  3  2  1  0
 16 14  1  0
  2  1  1  0
 16 23  1  0
  5  6  1  0
  8  9  2  0
 24 25  2  0
  9  3  1  0
 20 21  1  0
  8  7  1  0
 10 11  1  0
 11 13  2  0
  4  5  1  0
 11 12  1  0
  4 29  1  0
 22 39  1  0
 17 34  1  0
 19 35  1  0
 19 36  1  0
 19 37  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 30  1  0
 21 38  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       1.356  -0.637   5.367  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.394  -1.138   4.036  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.221  -0.235   3.021  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.928   1.116   3.190  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.776   1.940   2.074  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.494   3.255   2.341  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.903   1.432   0.771  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.180   0.077   0.582  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.356  -0.738   1.715  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.651  -2.101   1.584  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.011  -2.312   1.404  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.261  -3.782   1.257  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.885  -1.452   1.366  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.275  -0.468  -0.796  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.423  -1.666  -1.006  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.174   0.450  -1.949  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.330  -0.046  -3.251  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.230   0.810  -4.358  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.399   0.274  -5.750  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.971   2.167  -4.137  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.873   2.997  -5.217  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.813   2.670  -2.848  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.917   1.803  -1.753  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.746   2.330  -0.390  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.477   3.515  -0.211  0.00  0.00           O+0
HETATM   26  H   UNK     0       0.366  -0.238   5.609  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.552  -1.474   6.044  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.138   0.112   5.530  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.813   1.563   4.172  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.412   3.736   1.485  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.729  -4.163   0.382  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.940  -4.305   2.162  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.332  -3.955   1.117  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.530  -1.106  -3.403  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.242   0.765  -6.246  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.598  -0.803  -5.744  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.487   0.440  -6.333  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.699   3.904  -4.914  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.610   3.725  -2.684  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    3    1                                                       
CONECT    3    4    2    9                                                  
CONECT    4    3    5   29                                                  
CONECT    5    7    6    4                                                  
CONECT    6    5   30                                                       
CONECT    7    5   24    8                                                  
CONECT    8   14    9    7                                                  
CONECT    9   10    8    3                                                  
CONECT   10    9   11                                                       
CONECT   11   10   13   12                                                  
CONECT   12   11   31   32   33                                             
CONECT   13   11                                                            
CONECT   14    8   15   16                                                  
CONECT   15   14                                                            
CONECT   16   17   14   23                                                  
CONECT   17   16   18   34                                                  
CONECT   18   20   17   19                                                  
CONECT   19   18   35   36   37                                             
CONECT   20   22   18   21                                                  
CONECT   21   20   38                                                       
CONECT   22   23   20   39                                                  
CONECT   23   22   24   16                                                  
CONECT   24    7   23   25                                                  
CONECT   25   24                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    4                                                            
CONECT   30    6                                                            
CONECT   31   12                                                            
CONECT   32   12                                                            
CONECT   33   12                                                            
CONECT   34   17                                                            
CONECT   35   19                                                            
CONECT   36   19                                                            
CONECT   37   19                                                            
CONECT   38   21                                                            
CONECT   39   22                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

RDKit          3D

39 41  0  0  0  0  0  0  0  0999 V2000
    1.3563   -0.6374    5.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3938   -1.1382    4.0361 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.2345    3.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9278    1.1160    3.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7758    1.9400    2.0744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4943    3.2551    2.3406 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9026    1.4322    0.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1795    0.0774    0.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3559   -0.7384    1.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505   -2.1013    1.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0114   -2.3115    1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614   -3.7821    1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.4523    1.3660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -0.4679   -0.7958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4226   -1.6661   -1.0058 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1740    0.4504   -1.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3296   -0.0458   -3.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2299    0.8104   -4.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.2738   -5.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    2.1670   -4.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8734    2.9970   -5.2169 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8128    2.6695   -2.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9165    1.8026   -1.7525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7456    2.3300   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4768    3.5150   -0.2109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3661   -0.2378    5.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5518   -1.4744    6.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1376    0.1124    5.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8129    1.5634    4.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120    3.7357    1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7294   -4.1631    0.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9402   -4.3045    2.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3323   -3.9547    1.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5301   -1.1060   -3.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2423    0.7650   -6.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5979   -0.8030   -5.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4873    0.4402   -6.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6990    3.9037   -4.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6104    3.7249   -2.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  7  2  0
 16 17  2  0
 23 22  2  0
 22 20  1  0
 20 18  2  0
 18 17  1  0
  3  4  2  0
 18 19  1  0
  8 14  1  0
 14 15  2  0
  7 24  1  0
  9 10  1  0
 24 23  1  0
  3  2  1  0
 16 14  1  0
  2  1  1  0
 16 23  1  0
  5  6  1  0
  8  9  2  0
 24 25  2  0
  9  3  1  0
 20 21  1  0
  8  7  1  0
 10 11  1  0
 11 13  2  0
  4  5  1  0
 11 12  1  0
  4 29  1  0
 22 39  1  0
 17 34  1  0
 19 35  1  0
 19 36  1  0
 19 37  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 30  1  0
 21 38  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₄O₇

Average Mass

342.3030 Da

Monoisotopic Mass

342.07395 Da

IUPAC Name

4,6-dihydroxy-2-methoxy-7-methyl-9,10-dioxo-9,10-dihydroanthracen-1-yl acetate

Traditional Name

4,6-dihydroxy-2-methoxy-7-methyl-9,10-dioxoanthracen-1-yl acetate

CAS Registry Number

Not Available

SMILES

[H]OC1=C(C([H])=C2C(=O)C3=C(OC(=O)C([H])([H])[H])C(OC([H])([H])[H])=C([H])C(O[H])=C3C(=O)C2=C1[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C18H14O7/c1-7-4-9-10(5-11(7)20)16(22)14-12(21)6-13(24-3)18(25-8(2)19)15(14)17(9)23/h4-6,20-21H,1-3H3

InChI Key

SLRWHAFJOXBJHC-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Nigrospora sp.	JEOL database	Yang, K. -L., et al, J. Nat. Prod. 75, 935 (2012)

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
Anisole
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Vinylogous acid
Carboxylic acid ester
Ketone
Ether
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organooxygen 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	2.67	ALOGPS
logP	2.92	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	7.54	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	87.75 m³·mol⁻¹	ChemAxon
Polarizability	34.05 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

28530615

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

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METLIN ID

Not Available

PubChem Compound

59052029

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yang, K. -L., et al. (2012). Yang, K. -L., et al, J. Nat. Prod. 75, 935 (2012). J. Nat. Prod..

Showing NP-Card for 8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione (NP0036700)

MOL for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

3D MOL for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

3D SDF for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

3D-SDF for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

PDB for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

3D PDB for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

SMILES for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

INCHI for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

Structure for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)

3D Structure for NP0036700 (8-acetoxy-3,5-dihydroxy-7-methoxy-2-methylanthracene-9,10-dione)