NP-MRD: Showing NP-Card for 6,7-dimethoxydihydrolindbladione (NP0004682)

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Record Information

Version

2.0

Created at

2020-12-09 02:06:28 UTC

Updated at

2021-07-15 16:49:51 UTC

NP-MRD ID

NP0004682

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,7-dimethoxydihydrolindbladione

Provided By

NPAtlas

Description

4,5-Dihydroxy-6,7-dimethoxy-3-(3-oxohexyl)-1,2-dihydronaphthalene-1,2-dione belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone). 6,7-dimethoxydihydrolindbladione is found in Lindbladia tubulina. 6,7-dimethoxydihydrolindbladione was first documented in 2003 (PMID: 12880324). Based on a literature review very few articles have been published on 4,5-dihydroxy-6,7-dimethoxy-3-(3-oxohexyl)-1,2-dihydronaphthalene-1,2-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242121113D          

 45 46  0  0  0  0            999 V2000
    6.0929    0.0743    1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5277   -0.9113    0.1291 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8361   -0.1442   -0.9698 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7439    0.6642   -0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6006    0.5512    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8704    1.5579   -1.1726 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7487    0.9160   -1.8325 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7172    0.2010   -1.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071    0.7697   -1.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7049    2.0084   -1.7440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6590    0.1985   -0.4566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -1.0110    0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6870   -1.5325    0.8050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057   -0.8784    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0400   -1.3891    1.4031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9307   -2.6321    2.0675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0212    0.3447    0.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2500    0.9881    0.1354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6638    1.8924    1.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9017    0.8539   -0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9951    2.0667   -1.1151 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2648   -1.6904    0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402   -2.7983    0.7791 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8787   -1.0799   -0.4677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0070   -1.6052   -0.5017 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9896    1.1091    0.7073 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8078   -1.5796    0.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3556   -1.5394   -0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4259   -0.8349   -1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642    1.9411   -1.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6403    2.5047   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2634    1.6527   -2.5450 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1946    0.1722   -2.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7863    2.0656   -2.7541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5819   -2.4874    1.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0304   -2.6425    2.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7916   -3.4439    1.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8564   -2.8394    2.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1340    2.7733    0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4746    1.4012    1.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8386    2.2682    1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8391    2.5912   -1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
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  6 33  1  0  0  0  0
  6 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
 10 37  1  0  0  0  0
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 19 42  1  0  0  0  0
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 19 44  1  0  0  0  0
 21 45  1  0  0  0  0
M  END

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    6.0929    0.0743    1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5277   -0.9113    0.1291 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8361   -0.1442   -0.9698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7439    0.6642   -0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6006    0.5512    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8704    1.5579   -1.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7487    0.9160   -1.8325 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.2010   -1.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071    0.7697   -1.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7049    2.0084   -1.7440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6590    0.1985   -0.4566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -1.0110    0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6870   -1.5325    0.8050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057   -0.8784    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0400   -1.3891    1.4031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9307   -2.6321    2.0675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0212    0.3447    0.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2500    0.9881    0.1354 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1402   -2.7983    0.7791 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8787   -1.0799   -0.4677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0070   -1.6052   -0.5017 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1819   -0.1007    1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9896    1.1091    0.7073 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5225    0.0126    2.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8078   -1.5796    0.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3556   -1.5394   -0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6038    0.5020   -1.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4259   -0.8349   -1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642    1.9411   -1.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6403    2.5047   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2634    1.6527   -2.5450 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1946    0.1722   -2.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7863    2.0656   -2.7541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5819   -2.4874    1.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0304   -2.6425    2.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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  3  4  1  0
  4  5  2  0
  4  6  1  0
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M  END


  Mrv1652306242121113D          

 45 46  0  0  0  0            999 V2000
    6.0929    0.0743    1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5277   -0.9113    0.1291 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8361   -0.1442   -0.9698 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7439    0.6642   -0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6006    0.5512    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8704    1.5579   -1.1726 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7487    0.9160   -1.8325 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.5071    0.7697   -1.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0070   -1.6052   -0.5017 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  4  6  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0004682

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H20O7/c1-4-5-9(19)6-7-10-14(20)13-11(16(22)15(10)21)8-12(24-2)18(25-3)17(13)23/h8,20,23H,4-7H2,1-3H3

> <INCHI_KEY>
VBCLWCRRZXKXIS-UHFFFAOYSA-N

> <FORMULA>
C18H20O7

> <MOLECULAR_WEIGHT>
348.351

> <EXACT_MASS>
348.120902984

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
35.87694591846285

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,5-dihydroxy-6,7-dimethoxy-3-(3-oxohexyl)-1,2-dihydronaphthalene-1,2-dione

> <ALOGPS_LOGP>
2.11

> <JCHEM_LOGP>
2.2730204976666664

> <ALOGPS_LOGS>
-3.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.604572843485569

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.077892444390401

> <JCHEM_PKA_STRONGEST_BASIC>
-4.646007168814128

> <JCHEM_POLAR_SURFACE_AREA>
110.13

> <JCHEM_REFRACTIVITY>
90.96809999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.87e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5-dihydroxy-6,7-dimethoxy-3-(3-oxohexyl)naphthalene-1,2-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    6.0929    0.0743    1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5277   -0.9113    0.1291 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8361   -0.1442   -0.9698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7439    0.6642   -0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6006    0.5512    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8704    1.5579   -1.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7487    0.9160   -1.8325 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.2010   -1.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071    0.7697   -1.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7049    2.0084   -1.7440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6590    0.1985   -0.4566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -1.0110    0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6870   -1.5325    0.8050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057   -0.8784    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0400   -1.3891    1.4031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9307   -2.6321    2.0675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0212    0.3447    0.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2500    0.9881    0.1354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6638    1.8924    1.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9017    0.8539   -0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9951    2.0667   -1.1151 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2648   -1.6904    0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402   -2.7983    0.7791 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8787   -1.0799   -0.4677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0070   -1.6052   -0.5017 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1819   -0.1007    1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9896    1.1091    0.7073 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5225    0.0126    2.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8078   -1.5796    0.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3556   -1.5394   -0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6038    0.5020   -1.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4259   -0.8349   -1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642    1.9411   -1.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6403    2.5047   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2634    1.6527   -2.5450 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1946    0.1722   -2.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7863    2.0656   -2.7541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5819   -2.4874    1.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0304   -2.6425    2.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7916   -3.4439    1.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8564   -2.8394    2.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1340    2.7733    0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4746    1.4012    1.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8386    2.2682    1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8391    2.5912   -1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 20 21  1  0
 12 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 24  8  1  0
 20 11  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 13 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 19 42  1  0
 19 43  1  0
 19 44  1  0
 21 45  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       6.093   0.074   1.124  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.528  -0.911   0.129  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.836  -0.144  -0.970  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.744   0.664  -0.369  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.601   0.551   0.855  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.870   1.558  -1.173  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.749   0.916  -1.833  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.717   0.201  -1.134  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.507   0.770  -1.104  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.705   2.008  -1.744  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.659   0.199  -0.457  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.569  -1.011   0.192  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.687  -1.533   0.805  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.906  -0.878   0.791  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.040  -1.389   1.403  0.00  0.00           O+0
HETATM   16  C   UNK     0      -4.931  -2.632   2.067  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.021   0.345   0.141  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.250   0.988   0.135  0.00  0.00           O+0
HETATM   19  C   UNK     0      -5.664   1.892   1.115  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.902   0.854  -0.465  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.995   2.067  -1.115  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.265  -1.690   0.198  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.140  -2.798   0.779  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.879  -1.080  -0.468  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.007  -1.605  -0.502  0.00  0.00           O+0
HETATM   26  H   UNK     0       7.182  -0.101   1.270  0.00  0.00           H+0
HETATM   27  H   UNK     0       5.990   1.109   0.707  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.523   0.013   2.057  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.808  -1.580   0.662  0.00  0.00           H+0
HETATM   30  H   UNK     0       6.356  -1.539  -0.282  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.604   0.502  -1.448  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.426  -0.835  -1.754  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.564   1.941  -1.991  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.640   2.505  -0.623  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.263   1.653  -2.545  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.195   0.172  -2.584  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.786   2.066  -2.754  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.582  -2.487   1.306  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.030  -2.643   2.710  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.792  -3.444   1.300  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.856  -2.839   2.656  0.00  0.00           H+0
HETATM   42  H   UNK     0      -6.134   2.773   0.634  0.00  0.00           H+0
HETATM   43  H   UNK     0      -6.475   1.401   1.692  0.00  0.00           H+0
HETATM   44  H   UNK     0      -4.839   2.268   1.748  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.839   2.591  -1.165  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1    3   29   30                                             
CONECT    3    2    4   31   32                                             
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   33   34                                             
CONECT    7    6    8   35   36                                             
CONECT    8    7    9   24                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   37                                                       
CONECT   11    9   12   20                                                  
CONECT   12   11   13   22                                                  
CONECT   13   12   14   38                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15   39   40   41                                             
CONECT   17   14   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18   42   43   44                                             
CONECT   20   17   21   11                                                  
CONECT   21   20   45                                                       
CONECT   22   12   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25    8                                                  
CONECT   25   24                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    2                                                            
CONECT   30    2                                                            
CONECT   31    3                                                            
CONECT   32    3                                                            
CONECT   33    6                                                            
CONECT   34    6                                                            
CONECT   35    7                                                            
CONECT   36    7                                                            
CONECT   37   10                                                            
CONECT   38   13                                                            
CONECT   39   16                                                            
CONECT   40   16                                                            
CONECT   41   16                                                            
CONECT   42   19                                                            
CONECT   43   19                                                            
CONECT   44   19                                                            
CONECT   45   21                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   92    0
END

RDKit          3D

45 46  0  0  0  0  0  0  0  0999 V2000
    6.0929    0.0743    1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5277   -0.9113    0.1291 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8361   -0.1442   -0.9698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7439    0.6642   -0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6006    0.5512    0.8545 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8704    1.5579   -1.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7487    0.9160   -1.8325 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.2010   -1.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071    0.7697   -1.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7049    2.0084   -1.7440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6590    0.1985   -0.4566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -1.0110    0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6870   -1.5325    0.8050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057   -0.8784    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0400   -1.3891    1.4031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9307   -2.6321    2.0675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0212    0.3447    0.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2500    0.9881    0.1354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6638    1.8924    1.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9017    0.8539   -0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9951    2.0667   -1.1151 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2648   -1.6904    0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402   -2.7983    0.7791 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8787   -1.0799   -0.4677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0070   -1.6052   -0.5017 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1819   -0.1007    1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9896    1.1091    0.7073 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5225    0.0126    2.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8078   -1.5796    0.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3556   -1.5394   -0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6038    0.5020   -1.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4259   -0.8349   -1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642    1.9411   -1.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6403    2.5047   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2634    1.6527   -2.5450 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1946    0.1722   -2.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7863    2.0656   -2.7541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5819   -2.4874    1.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0304   -2.6425    2.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7916   -3.4439    1.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8564   -2.8394    2.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1340    2.7733    0.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4746    1.4012    1.6919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8386    2.2682    1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8391    2.5912   -1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 20 21  1  0
 12 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 24  8  1  0
 20 11  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 10 37  1  0
 13 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 19 42  1  0
 19 43  1  0
 19 44  1  0
 21 45  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₈H₂₀O₇

Average Mass

348.3510 Da

Monoisotopic Mass

348.12090 Da

IUPAC Name

4,5-dihydroxy-6,7-dimethoxy-3-(3-oxohexyl)-1,2-dihydronaphthalene-1,2-dione

Traditional Name

4,5-dihydroxy-6,7-dimethoxy-3-(3-oxohexyl)naphthalene-1,2-dione

CAS Registry Number

Not Available

SMILES

CCCC(=O)CCC1=C(O)C2=C(O)C(OC)=C(OC)C=C2C(=O)C1=O

InChI Identifier

InChI=1S/C18H20O7/c1-4-5-9(19)6-7-10-14(20)13-11(16(22)15(10)21)8-12(24-2)18(25-3)17(13)23/h8,20,23H,4-7H2,1-3H3

InChI Key

VBCLWCRRZXKXIS-UHFFFAOYSA-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
Lindbladia tubulina	NPAtlas	12880324

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone).

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Naphthoquinone
1-naphthol
Anisole
Aryl ketone
Phenol ether
Quinone
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Vinylogous acid
Ketone
Cyclic ketone
Ether
Enol
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
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	2.11	ALOGPS
logP	2.27	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	5.08	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	90.97 m³·mol⁻¹	ChemAxon
Polarizability	35.88 Å³	ChemAxon
Number of Rings	2	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

NPA002786

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9166850

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10991655

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Misono Y, Ishikawa Y, Yamamoto Y, Hayashi M, Komiyama K, Ishibashi M: Dihydrolindbladiones, three new naphthoquinone pigments from a myxomycete Lindbladia tubulina. J Nat Prod. 2003 Jul;66(7):999-1001. doi: 10.1021/np030089x. [PubMed:12880324 ]

Showing NP-Card for 6,7-dimethoxydihydrolindbladione (NP0004682)

MOL for NP0004682 (6,7-dimethoxydihydrolindbladione)

3D MOL for NP0004682 (6,7-dimethoxydihydrolindbladione)

3D SDF for NP0004682 (6,7-dimethoxydihydrolindbladione)

3D-SDF for NP0004682 (6,7-dimethoxydihydrolindbladione)

PDB for NP0004682 (6,7-dimethoxydihydrolindbladione)

3D PDB for NP0004682 (6,7-dimethoxydihydrolindbladione)

SMILES for NP0004682 (6,7-dimethoxydihydrolindbladione)

INCHI for NP0004682 (6,7-dimethoxydihydrolindbladione)

Structure for NP0004682 (6,7-dimethoxydihydrolindbladione)

3D Structure for NP0004682 (6,7-dimethoxydihydrolindbladione)