NP-MRD: Showing NP-Card for macrosporin (NP0034376)

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Record Information

Version

2.0

Created at

2021-06-20 18:07:24 UTC

Updated at

2021-06-30 00:04:43 UTC

NP-MRD ID

NP0034376

Secondary Accession Numbers

None

Natural Product Identification

Common Name

macrosporin

Provided By

JEOL Database JEOL Logo

Description

1,7-Dihydroxy-3-methoxy-6-methyl-9,10-dihydroanthracene-9,10-dione 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. macrosporin is found in Alternaria bataticola, Alternaria porri, Alternaria solani, Ampelomyces sp., Dichotomophthora lutea, Mentha pulegium and Stemphylium botryosum. macrosporin was first documented in 2009 (Debbab, A., et al.). Based on a literature review very few articles have been published on 1,7-dihydroxy-3-methoxy-6-methyl-9,10-dihydroanthracene-9,10-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202120073D          

 33 35  0  0  0  0            999 V2000
    1.9510   -0.4470    7.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913   -0.0599    6.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0936   -0.2305    4.8092 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2426   -0.7489    4.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3145   -0.8681    2.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.3871    2.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2439   -0.4728    2.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.0450    2.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0227    0.1652    4.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512    0.4713    1.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0601    0.9266    2.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687    0.3426    0.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0504    0.7435   -0.4834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9874    0.6276   -1.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1485    1.0582   -2.7298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8265    0.1052   -2.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7706   -0.0055   -3.8204 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2541   -0.2961   -1.6780 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1781   -0.1750   -0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203   -0.5990    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3356   -1.0565    0.0270 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566   -1.5193    6.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8522    0.1452    6.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6316   -0.2476    8.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -1.0693    4.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4060   -1.4194    1.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741    0.5700    4.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    1.1478   -0.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8419    1.8562   -3.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5297    0.2103   -3.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9726    1.4418   -2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0876   -0.3807   -4.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1524   -0.7010   -2.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 19  2  0  0  0  0
  8  7  2  0  0  0  0
 19 18  1  0  0  0  0
  5  7  1  0  0  0  0
 18 16  2  0  0  0  0
 16 14  1  0  0  0  0
  8  9  1  0  0  0  0
 14 13  2  0  0  0  0
 13 12  1  0  0  0  0
  4  5  2  0  0  0  0
 14 15  1  0  0  0  0
  8 10  1  0  0  0  0
 16 17  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 19  1  0  0  0  0
 10 11  2  0  0  0  0
 12 10  1  0  0  0  0
  5  6  1  0  0  0  0
  9  3  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  1  0  0  0  0
  2  1  1  0  0  0  0
  4 25  1  0  0  0  0
  9 27  1  0  0  0  0
 18 33  1  0  0  0  0
 13 28  1  0  0  0  0
 15 29  1  0  0  0  0
 15 30  1  0  0  0  0
 15 31  1  0  0  0  0
 17 32  1  0  0  0  0
  6 26  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
M  END

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
    1.9510   -0.4470    7.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913   -0.0599    6.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0936   -0.2305    4.8092 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2426   -0.7489    4.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3145   -0.8681    2.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.3871    2.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2439   -0.4728    2.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.0450    2.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0227    0.1652    4.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512    0.4713    1.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0601    0.9266    2.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687    0.3426    0.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0504    0.7435   -0.4834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9874    0.6276   -1.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1485    1.0582   -2.7298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8265    0.1052   -2.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7706   -0.0055   -3.8204 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2541   -0.2961   -1.6780 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1781   -0.1750   -0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203   -0.5990    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3356   -1.0565    0.0270 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566   -1.5193    6.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8522    0.1452    6.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6316   -0.2476    8.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -1.0693    4.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4060   -1.4194    1.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741    0.5700    4.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    1.1478   -0.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8419    1.8562   -3.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5297    0.2103   -3.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9726    1.4418   -2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0876   -0.3807   -4.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1524   -0.7010   -2.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 19  2  0
  8  7  2  0
 19 18  1  0
  5  7  1  0
 18 16  2  0
 16 14  1  0
  8  9  1  0
 14 13  2  0
 13 12  1  0
  4  5  2  0
 14 15  1  0
  8 10  1  0
 16 17  1  0
  7 20  1  0
 20 21  2  0
 20 19  1  0
 10 11  2  0
 12 10  1  0
  5  6  1  0
  9  3  2  0
  3  2  1  0
  3  4  1  0
  2  1  1  0
  4 25  1  0
  9 27  1  0
 18 33  1  0
 13 28  1  0
 15 29  1  0
 15 30  1  0
 15 31  1  0
 17 32  1  0
  6 26  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
M  END


  Mrv1652306202120073D          

 33 35  0  0  0  0            999 V2000
    1.9510   -0.4470    7.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913   -0.0599    6.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0936   -0.2305    4.8092 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2426   -0.7489    4.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3145   -0.8681    2.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.3871    2.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2439   -0.4728    2.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.0450    2.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0227    0.1652    4.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512    0.4713    1.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0601    0.9266    2.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687    0.3426    0.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0504    0.7435   -0.4834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9874    0.6276   -1.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1485    1.0582   -2.7298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8265    0.1052   -2.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7706   -0.0055   -3.8204 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2541   -0.2961   -1.6780 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1781   -0.1750   -0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203   -0.5990    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3356   -1.0565    0.0270 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566   -1.5193    6.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8522    0.1452    6.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6316   -0.2476    8.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -1.0693    4.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4060   -1.4194    1.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741    0.5700    4.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    1.1478   -0.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8419    1.8562   -3.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5297    0.2103   -3.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9726    1.4418   -2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0876   -0.3807   -4.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1524   -0.7010   -2.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 19  2  0  0  0  0
  8  7  2  0  0  0  0
 19 18  1  0  0  0  0
  5  7  1  0  0  0  0
 18 16  2  0  0  0  0
 16 14  1  0  0  0  0
  8  9  1  0  0  0  0
 14 13  2  0  0  0  0
 13 12  1  0  0  0  0
  4  5  2  0  0  0  0
 14 15  1  0  0  0  0
  8 10  1  0  0  0  0
 16 17  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 19  1  0  0  0  0
 10 11  2  0  0  0  0
 12 10  1  0  0  0  0
  5  6  1  0  0  0  0
  9  3  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  1  0  0  0  0
  2  1  1  0  0  0  0
  4 25  1  0  0  0  0
  9 27  1  0  0  0  0
 18 33  1  0  0  0  0
 13 28  1  0  0  0  0
 15 29  1  0  0  0  0
 15 30  1  0  0  0  0
 15 31  1  0  0  0  0
 17 32  1  0  0  0  0
  6 26  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0034376

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(OC([H])([H])[H])=C([H])C2=C1C(=O)C1=C(C([H])=C(C(O[H])=C1[H])C([H])([H])[H])C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H12O5/c1-7-3-9-10(6-12(7)17)16(20)14-11(15(9)19)4-8(21-2)5-13(14)18/h3-6,17-18H,1-2H3

> <INCHI_KEY>
FKTPLNFTYJEAAB-UHFFFAOYSA-N

> <FORMULA>
C16H12O5

> <MOLECULAR_WEIGHT>
284.267

> <EXACT_MASS>
284.068473486

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
29.12331074473809

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,7-dihydroxy-3-methoxy-6-methyl-9,10-dihydroanthracene-9,10-dione

> <ALOGPS_LOGP>
2.93

> <JCHEM_LOGP>
3.317325554999999

> <ALOGPS_LOGS>
-3.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.284588516614672

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.540839349076551

> <JCHEM_PKA_STRONGEST_BASIC>
-4.855135958921227

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
76.6172

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,7-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
    1.9510   -0.4470    7.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913   -0.0599    6.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0936   -0.2305    4.8092 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2426   -0.7489    4.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3145   -0.8681    2.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.3871    2.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2439   -0.4728    2.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.0450    2.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0227    0.1652    4.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512    0.4713    1.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0601    0.9266    2.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687    0.3426    0.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0504    0.7435   -0.4834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9874    0.6276   -1.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1485    1.0582   -2.7298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8265    0.1052   -2.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7706   -0.0055   -3.8204 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2541   -0.2961   -1.6780 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1781   -0.1750   -0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203   -0.5990    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3356   -1.0565    0.0270 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566   -1.5193    6.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8522    0.1452    6.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6316   -0.2476    8.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -1.0693    4.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4060   -1.4194    1.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741    0.5700    4.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    1.1478   -0.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8419    1.8562   -3.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5297    0.2103   -3.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9726    1.4418   -2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0876   -0.3807   -4.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1524   -0.7010   -2.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 19  2  0
  8  7  2  0
 19 18  1  0
  5  7  1  0
 18 16  2  0
 16 14  1  0
  8  9  1  0
 14 13  2  0
 13 12  1  0
  4  5  2  0
 14 15  1  0
  8 10  1  0
 16 17  1  0
  7 20  1  0
 20 21  2  0
 20 19  1  0
 10 11  2  0
 12 10  1  0
  5  6  1  0
  9  3  2  0
  3  2  1  0
  3  4  1  0
  2  1  1  0
  4 25  1  0
  9 27  1  0
 18 33  1  0
 13 28  1  0
 15 29  1  0
 15 30  1  0
 15 31  1  0
 17 32  1  0
  6 26  1  0
  1 22  1  0
  1 23  1  0
  1 24  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       1.951  -0.447   7.017  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.891  -0.060   6.150  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.094  -0.231   4.809  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.243  -0.749   4.213  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.314  -0.868   2.824  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.479  -1.387   2.323  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.244  -0.473   2.013  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.096   0.045   2.608  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.023   0.165   4.003  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.051   0.471   1.781  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.060   0.927   2.306  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.969   0.343   0.312  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.050   0.744  -0.483  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.987   0.628  -1.880  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.148   1.058  -2.730  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.827   0.105  -2.461  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.771  -0.006  -3.820  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.254  -0.296  -1.678  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.178  -0.175  -0.285  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.320  -0.599   0.545  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.336  -1.056   0.027  0.00  0.00           O+0
HETATM   22  H   UNK     0       2.157  -1.519   6.934  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.852   0.145   6.827  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.632  -0.248   8.045  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.099  -1.069   4.798  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.406  -1.419   1.341  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.874   0.570   4.471  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.945   1.148  -0.011  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.842   1.856  -3.414  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.530   0.210  -3.308  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.973   1.442  -2.119  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.088  -0.381  -4.080  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.152  -0.701  -2.137  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    3    1                                                       
CONECT    3    9    2    4                                                  
CONECT    4    5    3   25                                                  
CONECT    5    7    4    6                                                  
CONECT    6    5   26                                                       
CONECT    7    8    5   20                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3   27                                                  
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   19   13   10                                                  
CONECT   13   14   12   28                                                  
CONECT   14   16   13   15                                                  
CONECT   15   14   29   30   31                                             
CONECT   16   18   14   17                                                  
CONECT   17   16   32                                                       
CONECT   18   19   16   33                                                  
CONECT   19   12   18   20                                                  
CONECT   20    7   21   19                                                  
CONECT   21   20                                                            
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    4                                                            
CONECT   26    6                                                            
CONECT   27    9                                                            
CONECT   28   13                                                            
CONECT   29   15                                                            
CONECT   30   15                                                            
CONECT   31   15                                                            
CONECT   32   17                                                            
CONECT   33   18                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

RDKit          3D

33 35  0  0  0  0  0  0  0  0999 V2000
    1.9510   -0.4470    7.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913   -0.0599    6.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0936   -0.2305    4.8092 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2426   -0.7489    4.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3145   -0.8681    2.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -1.3871    2.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2439   -0.4728    2.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.0450    2.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0227    0.1652    4.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512    0.4713    1.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0601    0.9266    2.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687    0.3426    0.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0504    0.7435   -0.4834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9874    0.6276   -1.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1485    1.0582   -2.7298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8265    0.1052   -2.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7706   -0.0055   -3.8204 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2541   -0.2961   -1.6780 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1781   -0.1750   -0.2852 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203   -0.5990    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3356   -1.0565    0.0270 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566   -1.5193    6.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8522    0.1452    6.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6316   -0.2476    8.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -1.0693    4.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4060   -1.4194    1.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741    0.5700    4.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    1.1478   -0.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8419    1.8562   -3.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5297    0.2103   -3.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9726    1.4418   -2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0876   -0.3807   -4.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1524   -0.7010   -2.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 19  2  0
  8  7  2  0
 19 18  1  0
  5  7  1  0
 18 16  2  0
 16 14  1  0
  8  9  1  0
 14 13  2  0
 13 12  1  0
  4  5  2  0
 14 15  1  0
  8 10  1  0
 16 17  1  0
  7 20  1  0
 20 21  2  0
 20 19  1  0
 10 11  2  0
 12 10  1  0
  5  6  1  0
  9  3  2  0
  3  2  1  0
  3  4  1  0
  2  1  1  0
  4 25  1  0
  9 27  1  0
 18 33  1  0
 13 28  1  0
 15 29  1  0
 15 30  1  0
 15 31  1  0
 17 32  1  0
  6 26  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
M  END

View in JSmol

Synonyms

Value	Source
1,7-Dihydroxy-3-methoxy-6-methyl-9,10-anthracenedione	MeSH

Chemical Formula

C₁₆H₁₂O₅

Average Mass

284.2670 Da

Monoisotopic Mass

284.06847 Da

IUPAC Name

1,7-dihydroxy-3-methoxy-6-methyl-9,10-dihydroanthracene-9,10-dione

Traditional Name

1,7-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C(OC([H])([H])[H])=C([H])C2=C1C(=O)C1=C(C([H])=C(C(O[H])=C1[H])C([H])([H])[H])C2=O

InChI Identifier

InChI=1S/C16H12O5/c1-7-3-9-10(6-12(7)17)16(20)14-11(15(9)19)4-8(21-2)5-13(14)18/h3-6,17-18H,1-2H3

InChI Key

FKTPLNFTYJEAAB-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, 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
Alternaria bataticola	LOTUS Database	35616633
Alternaria porri	LOTUS Database	35616633
Alternaria solani	LOTUS Database	35616633
Ampelomyces sp.	-	KNApSAcK
Dactylaria lutea	LOTUS Database	35616633
Mentha pulegium	JEOL database	Debbab, A., et al, J. Nat. Prod. 72, 626 (2009)
Stemphylium botryosum	LOTUS Database	35616633

Species Where Detected

Species Name	Source	Reference
Cladosporium sp.	KNApSAcK Database	22123792
Stemphylium globuliferum	KNApSAcK Database	22123792

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
Aryl ketone
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Vinylogous acid
Ketone
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	2.93	ALOGPS
logP	3.32	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	7.54	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	76.62 m³·mol⁻¹	ChemAxon
Polarizability	29.12 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

C00034046

Chemspider ID

140602

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Debbab, A., et al. (2009). Debbab, A., et al, J. Nat. Prod. 72, 626 (2009). J. Nat. Prod..

Showing NP-Card for macrosporin (NP0034376)

MOL for NP0034376 (macrosporin)

3D MOL for NP0034376 (macrosporin)

3D SDF for NP0034376 (macrosporin)

3D-SDF for NP0034376 (macrosporin)

PDB for NP0034376 (macrosporin)

3D PDB for NP0034376 (macrosporin)

SMILES for NP0034376 (macrosporin)

INCHI for NP0034376 (macrosporin)

Structure for NP0034376 (macrosporin)

3D Structure for NP0034376 (macrosporin)