NP-MRD: Showing NP-Card for Pleosporone (NP0007723)

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Record Information

Version

2.0

Created at

2020-12-09 04:31:36 UTC

Updated at

2021-07-15 16:58:21 UTC

NP-MRD ID

NP0007723

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Pleosporone

Provided By

NPAtlas

Description

Pleosporone 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. Pleosporone is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Pleosporone is found in Unknown-fungus endophyte MF7028. Pleosporone was first documented in 2009 (PMID: 18442914). Based on a literature review very few articles have been published on pleosporone.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119023D          

 35 37  0  0  0  0            999 V2000
    5.1378    1.1513    0.9740 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697    0.4999    0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8180   -0.7351   -0.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6026   -1.3288   -0.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6563   -2.5526   -0.9802 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4233   -0.6571   -0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4850    0.5952    0.3772 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973    1.1596    0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2469    1.3161    0.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3009    2.4701    1.1407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0593    0.7541    0.2159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0812   -0.4343   -0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1502   -1.2177   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0637   -2.3531   -1.1271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454   -1.0816   -0.7566 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7097   -2.0962    0.1405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4501   -0.0820   -0.8373 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6759   -0.7457   -0.9424 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994    0.7919    0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6951    0.0095    1.5299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461    1.5984    0.4982 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2679    2.0506    0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0894    1.4116    2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9604    0.4329    0.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -1.2806   -0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0433   -3.2048   -1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6629    2.1412    1.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2375   -1.5737   -1.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7701   -2.9779   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3341    0.5566   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4050   -0.0827   -0.8240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3947    1.4392    0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527   -0.4552    1.8027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1417    2.0611    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3033    2.4194   -0.2721 H   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
  8  2  1  0  0  0  0
 21 11  1  0  0  0  0
 13  6  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
  3 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
 15 28  1  6  0  0  0
 16 29  1  0  0  0  0
 17 30  1  6  0  0  0
 18 31  1  0  0  0  0
 19 32  1  6  0  0  0
 20 33  1  0  0  0  0
 21 34  1  0  0  0  0
 21 35  1  0  0  0  0
M  END

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
    5.1378    1.1513    0.9740 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697    0.4999    0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8180   -0.7351   -0.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6026   -1.3288   -0.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6563   -2.5526   -0.9802 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4233   -0.6571   -0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4850    0.5952    0.3772 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973    1.1596    0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2469    1.3161    0.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3009    2.4701    1.1407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0593    0.7541    0.2159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0812   -0.4343   -0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1502   -1.2177   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0637   -2.3531   -1.1271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454   -1.0816   -0.7566 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7097   -2.0962    0.1405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4501   -0.0820   -0.8373 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6759   -0.7457   -0.9424 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994    0.7919    0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6951    0.0095    1.5299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461    1.5984    0.4982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2679    2.0506    0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0894    1.4116    2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9604    0.4329    0.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -1.2806   -0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0433   -3.2048   -1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6629    2.1412    1.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2375   -1.5737   -1.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7701   -2.9779   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3341    0.5566   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4050   -0.0827   -0.8240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3947    1.4392    0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527   -0.4552    1.8027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1417    2.0611    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3033    2.4194   -0.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
  8  2  1  0
 21 11  1  0
 13  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  8 27  1  0
 15 28  1  6
 16 29  1  0
 17 30  1  6
 18 31  1  0
 19 32  1  6
 20 33  1  0
 21 34  1  0
 21 35  1  0
M  END


  Mrv1652306242119023D          

 35 37  0  0  0  0            999 V2000
    5.1378    1.1513    0.9740 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697    0.4999    0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8180   -0.7351   -0.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6026   -1.3288   -0.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6563   -2.5526   -0.9802 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4233   -0.6571   -0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4850    0.5952    0.3772 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973    1.1596    0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2469    1.3161    0.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3009    2.4701    1.1407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0593    0.7541    0.2159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0812   -0.4343   -0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1502   -1.2177   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0637   -2.3531   -1.1271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454   -1.0816   -0.7566 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7097   -2.0962    0.1405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4501   -0.0820   -0.8373 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6759   -0.7457   -0.9424 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994    0.7919    0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6951    0.0095    1.5299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461    1.5984    0.4982 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2679    2.0506    0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0894    1.4116    2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9604    0.4329    0.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -1.2806   -0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0433   -3.2048   -1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6629    2.1412    1.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2375   -1.5737   -1.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7701   -2.9779   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3341    0.5566   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4050   -0.0827   -0.8240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3947    1.4392    0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527   -0.4552    1.8027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1417    2.0611    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3033    2.4194   -0.2721 H   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
  8  2  1  0  0  0  0
 21 11  1  0  0  0  0
 13  6  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
  3 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
 15 28  1  6  0  0  0
 16 29  1  0  0  0  0
 17 30  1  6  0  0  0
 18 31  1  0  0  0  0
 19 32  1  6  0  0  0
 20 33  1  0  0  0  0
 21 34  1  0  0  0  0
 21 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007723

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C3=C(C(=O)C2=C([H])C(=C1[H])C([H])([H])[H])C([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])[C@]3([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O6/c1-5-2-6-10(8(16)3-5)14(20)11-7(12(6)18)4-9(17)13(19)15(11)21/h2-3,9,13,15-17,19,21H,4H2,1H3/t9-,13-,15+/m0/s1

> <INCHI_KEY>
YUSJPHSHLVVZRA-DYQSUWPFSA-N

> <FORMULA>
C15H14O6

> <MOLECULAR_WEIGHT>
290.271

> <EXACT_MASS>
290.079038171

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
28.7854599731322

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,3S)-1,2,3,8-tetrahydroxy-6-methyl-1,2,3,4,9,10-hexahydroanthracene-9,10-dione

> <ALOGPS_LOGP>
0.55

> <JCHEM_LOGP>
0.1900681433333332

> <ALOGPS_LOGS>
-1.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.868516356416627

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.32689871806044

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2241689099848996

> <JCHEM_POLAR_SURFACE_AREA>
115.06000000000002

> <JCHEM_REFRACTIVITY>
73.5578

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.84e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
pleosporone

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
    5.1378    1.1513    0.9740 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697    0.4999    0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8180   -0.7351   -0.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6026   -1.3288   -0.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6563   -2.5526   -0.9802 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4233   -0.6571   -0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4850    0.5952    0.3772 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973    1.1596    0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2469    1.3161    0.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3009    2.4701    1.1407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0593    0.7541    0.2159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0812   -0.4343   -0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1502   -1.2177   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0637   -2.3531   -1.1271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454   -1.0816   -0.7566 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7097   -2.0962    0.1405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4501   -0.0820   -0.8373 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6759   -0.7457   -0.9424 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994    0.7919    0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6951    0.0095    1.5299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461    1.5984    0.4982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2679    2.0506    0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0894    1.4116    2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9604    0.4329    0.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -1.2806   -0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0433   -3.2048   -1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6629    2.1412    1.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2375   -1.5737   -1.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7701   -2.9779   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3341    0.5566   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4050   -0.0827   -0.8240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3947    1.4392    0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527   -0.4552    1.8027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1417    2.0611    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3033    2.4194   -0.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
  8  2  1  0
 21 11  1  0
 13  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  8 27  1  0
 15 28  1  6
 16 29  1  0
 17 30  1  6
 18 31  1  0
 19 32  1  6
 20 33  1  0
 21 34  1  0
 21 35  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       5.138   1.151   0.974  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.870   0.500   0.553  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.818  -0.735  -0.026  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.603  -1.329  -0.415  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.656  -2.553  -0.980  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.423  -0.657  -0.212  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.485   0.595   0.377  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.697   1.160   0.752  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.247   1.316   0.598  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.301   2.470   1.141  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.059   0.754   0.216  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.081  -0.434  -0.339  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.150  -1.218  -0.590  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.064  -2.353  -1.127  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.345  -1.082  -0.757  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.710  -2.096   0.141  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.450  -0.082  -0.837  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.676  -0.746  -0.942  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.499   0.792   0.414  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.695   0.010   1.530  0.00  0.00           O+0
HETATM   21  C   UNK     0      -2.246   1.598   0.498  0.00  0.00           C+0
HETATM   22  H   UNK     0       5.268   2.051   0.336  0.00  0.00           H+0
HETATM   23  H   UNK     0       5.089   1.412   2.039  0.00  0.00           H+0
HETATM   24  H   UNK     0       5.960   0.433   0.741  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.726  -1.281  -0.197  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.043  -3.205  -1.341  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.663   2.141   1.206  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.237  -1.574  -1.744  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.770  -2.978  -0.279  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.334   0.557  -1.721  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.405  -0.083  -0.824  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.395   1.439   0.290  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.853  -0.455   1.803  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.142   2.061   1.510  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.303   2.419  -0.272  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3    8                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4   26                                                       
CONECT    6    4    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    2   27                                                  
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   21                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12   14    6                                                  
CONECT   14   13                                                            
CONECT   15   12   16   17   28                                             
CONECT   16   15   29                                                       
CONECT   17   15   18   19   30                                             
CONECT   18   17   31                                                       
CONECT   19   17   20   21   32                                             
CONECT   20   19   33                                                       
CONECT   21   19   11   34   35                                             
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    5                                                            
CONECT   27    8                                                            
CONECT   28   15                                                            
CONECT   29   16                                                            
CONECT   30   17                                                            
CONECT   31   18                                                            
CONECT   32   19                                                            
CONECT   33   20                                                            
CONECT   34   21                                                            
CONECT   35   21                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   74    0
END

RDKit          3D

35 37  0  0  0  0  0  0  0  0999 V2000
    5.1378    1.1513    0.9740 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697    0.4999    0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8180   -0.7351   -0.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6026   -1.3288   -0.4153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6563   -2.5526   -0.9802 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4233   -0.6571   -0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4850    0.5952    0.3772 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973    1.1596    0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2469    1.3161    0.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3009    2.4701    1.1407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0593    0.7541    0.2159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0812   -0.4343   -0.3394 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1502   -1.2177   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0637   -2.3531   -1.1271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454   -1.0816   -0.7566 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7097   -2.0962    0.1405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4501   -0.0820   -0.8373 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6759   -0.7457   -0.9424 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994    0.7919    0.4143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6951    0.0095    1.5299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2461    1.5984    0.4982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2679    2.0506    0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0894    1.4116    2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9604    0.4329    0.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -1.2806   -0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0433   -3.2048   -1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6629    2.1412    1.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2375   -1.5737   -1.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7701   -2.9779   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3341    0.5566   -1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4050   -0.0827   -0.8240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3947    1.4392    0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527   -0.4552    1.8027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1417    2.0611    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3033    2.4194   -0.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
  8  2  1  0
 21 11  1  0
 13  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  8 27  1  0
 15 28  1  6
 16 29  1  0
 17 30  1  6
 18 31  1  0
 19 32  1  6
 20 33  1  0
 21 34  1  0
 21 35  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄O₆

Average Mass

290.2710 Da

Monoisotopic Mass

290.07904 Da

IUPAC Name

(1R,2S,3S)-1,2,3,8-tetrahydroxy-6-methyl-1,2,3,4,9,10-hexahydroanthracene-9,10-dione

Traditional Name

pleosporone

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C2C(=O)C3=C(C[C@H](O)[C@H](O)[C@@H]3O)C(=O)C2=C1

InChI Identifier

InChI=1S/C15H14O6/c1-5-2-6-10(8(16)3-5)14(20)11-7(12(6)18)4-9(17)13(19)15(11)21/h2-3,9,13,15-17,19,21H,4H2,1H3/t9-,13-,15+/m0/s1

InChI Key

YUSJPHSHLVVZRA-DYQSUWPFSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Anthyllis vulneraria	KNApSAcK Database	22123792
Unknown-fungus endophyte MF7028	NPAtlas	18442914

Species Where Detected

Species Name	Source	Reference
Streptomyces lucensis MA7349	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
Quinone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Cyclitol or derivatives
Vinylogous acid
Ketone
Secondary alcohol
Polyol
Organooxygen compound
Alcohol
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

secondary alcohol (CHEBI:66765 )
phenols (CHEBI:66765 )
quinone (CHEBI:66765 )
carbotricyclic compound (CHEBI:66765 )

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	0.55	ALOGPS
logP	0.19	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	8.33	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	115.06 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	73.56 m³·mol⁻¹	ChemAxon
Polarizability	28.79 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

NPAtlas ID

NPA000257

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00047335

Chemspider ID

23342341

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42636900

PDB ID

Not Available

ChEBI ID

66765

Good Scents ID

Not Available

References

General References

Zhang C, Ondeyka JG, Zink DL, Basilio A, Vicente F, Collado J, Platas G, Huber J, Dorso K, Motyl M, Byrne K, Singh SB: Isolation, structure and antibacterial activity of pleosporone from a pleosporalean ascomycete discovered by using antisense strategy. Bioorg Med Chem. 2009 Mar 15;17(6):2162-6. doi: 10.1016/j.bmc.2008.04.018. Epub 2008 Apr 12. [PubMed:18442914 ]

Showing NP-Card for Pleosporone (NP0007723)

MOL for NP0007723 (Pleosporone)

3D MOL for NP0007723 (Pleosporone)

3D SDF for NP0007723 (Pleosporone)

3D-SDF for NP0007723 (Pleosporone)

PDB for NP0007723 (Pleosporone)

3D PDB for NP0007723 (Pleosporone)

SMILES for NP0007723 (Pleosporone)

INCHI for NP0007723 (Pleosporone)

Structure for NP0007723 (Pleosporone)

3D Structure for NP0007723 (Pleosporone)