NP-MRD: Showing NP-Card for Corynether A (NP0008307)

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Record Information

Version

2.0

Created at

2020-12-09 05:55:52 UTC

Updated at

2021-07-15 17:00:03 UTC

NP-MRD ID

NP0008307

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Corynether A

Provided By

NPAtlas

Description

Corynether A is found in Corynespora. Corynether A was first documented in 2009 (PMID: 19230943). Based on a literature review very few articles have been published on Corynether A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106093D          

 35 36  0  0  0  0            999 V2000
   -2.1157    1.7044    1.6551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3310    0.5403    0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4009   -0.2938    1.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6638   -1.3460    0.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7323   -2.1822    0.5311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -1.5867   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8557   -0.7696   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0586   -0.9434   -2.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5762    0.3020   -0.3878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5163    1.1068   -0.7138 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8225    0.8239   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    0.9322   -1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9065    0.6657   -1.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145    0.7813   -3.1504 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5371    0.2768   -0.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8303    0.1651    0.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281   -0.2575    1.6307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4566    0.4378    0.4576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8718    0.2902    1.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9134    1.3309    2.5097 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2863   -0.8292    2.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3024    2.3089    1.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    2.3337    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8947    1.4007    2.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9971   -0.1078    1.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9892   -2.9791   -0.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1177   -2.4147   -1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1745   -1.6845   -3.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0229    1.2417   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    1.6406   -3.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5968    0.0666   -0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1010    0.5862    2.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8647   -0.7679    2.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942   -1.0079    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4084   -1.7655    1.9527 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  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
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 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
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 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
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 19 21  1  0  0  0  0
  9  2  1  0  0  0  0
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  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
  6 27  1  0  0  0  0
  8 28  1  0  0  0  0
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 17 32  1  0  0  0  0
 17 33  1  0  0  0  0
 17 34  1  0  0  0  0
 21 35  1  0  0  0  0
M  END

     RDKit          3D

 35 36  0  0  0  0  0  0  0  0999 V2000
   -2.1157    1.7044    1.6551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3310    0.5403    0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4009   -0.2938    1.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6638   -1.3460    0.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7323   -2.1822    0.5311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -1.5867   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8557   -0.7696   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0586   -0.9434   -2.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5762    0.3020   -0.3878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5163    1.1068   -0.7138 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8225    0.8239   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    0.9322   -1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9065    0.6657   -1.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145    0.7813   -3.1504 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5371    0.2768   -0.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8303    0.1651    0.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281   -0.2575    1.6307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4566    0.4378    0.4576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8718    0.2902    1.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9134    1.3309    2.5097 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2863   -0.8292    2.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3024    2.3089    1.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    2.3337    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8947    1.4007    2.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9971   -0.1078    1.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9892   -2.9791   -0.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1177   -2.4147   -1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1745   -1.6845   -3.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0229    1.2417   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    1.6406   -3.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5968    0.0666   -0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1010    0.5862    2.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2942   -1.0079    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4084   -1.7655    1.9527 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  1  0
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  9 10  1  0
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 19 21  1  0
  9  2  1  0
 18 11  1  0
  1 22  1  0
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  1 24  1  0
  3 25  1  0
  5 26  1  0
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  8 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 17 32  1  0
 17 33  1  0
 17 34  1  0
 21 35  1  0
M  END


  Mrv1652306242106093D          

 35 36  0  0  0  0            999 V2000
   -2.1157    1.7044    1.6551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3310    0.5403    0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4009   -0.2938    1.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6638   -1.3460    0.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7323   -2.1822    0.5311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -1.5867   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8557   -0.7696   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0586   -0.9434   -2.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5762    0.3020   -0.3878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5163    1.1068   -0.7138 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8225    0.8239   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    0.9322   -1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9065    0.6657   -1.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145    0.7813   -3.1504 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5371    0.2768   -0.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8303    0.1651    0.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281   -0.2575    1.6307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4566    0.4378    0.4576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8718    0.2902    1.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9134    1.3309    2.5097 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2863   -0.8292    2.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3024    2.3089    1.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    2.3337    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8947    1.4007    2.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9971   -0.1078    1.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9892   -2.9791   -0.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1177   -2.4147   -1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1745   -1.6845   -3.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0229    1.2417   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    1.6406   -3.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5968    0.0666   -0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1010    0.5862    2.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8647   -0.7679    2.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942   -1.0079    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4084   -1.7655    1.9527 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  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
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 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
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 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  9  2  1  0  0  0  0
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  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
  6 27  1  0  0  0  0
  8 28  1  0  0  0  0
 12 29  1  0  0  0  0
 14 30  1  0  0  0  0
 15 31  1  0  0  0  0
 17 32  1  0  0  0  0
 17 33  1  0  0  0  0
 17 34  1  0  0  0  0
 21 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0008307

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C(C([H])=C(O[H])C([H])=C1OC1=C(O[H])C([H])=C(O[H])C([H])=C1C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O6/c1-7-3-10(17)6-12(13(7)15(19)20)21-14-8(2)4-9(16)5-11(14)18/h3-6,16-18H,1-2H3,(H,19,20)

> <INCHI_KEY>
ZXWOXXVHOUPFOK-UHFFFAOYSA-N

> <FORMULA>
C15H14O6

> <MOLECULAR_WEIGHT>
290.271

> <EXACT_MASS>
290.079038171

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
28.355563855908603

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2,4-dihydroxy-6-methylphenoxy)-4-hydroxy-6-methylbenzoic acid

> <ALOGPS_LOGP>
2.55

> <JCHEM_LOGP>
3.2472627206666664

> <ALOGPS_LOGS>
-3.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.531218523455616

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.799994341800557

> <JCHEM_PKA_STRONGEST_BASIC>
-3.766436118795465

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
75.58009999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.26e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2,4-dihydroxy-6-methylphenoxy)-4-hydroxy-6-methylbenzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 35 36  0  0  0  0  0  0  0  0999 V2000
   -2.1157    1.7044    1.6551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3310    0.5403    0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4009   -0.2938    1.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6638   -1.3460    0.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7323   -2.1822    0.5311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -1.5867   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8557   -0.7696   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0586   -0.9434   -2.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5762    0.3020   -0.3878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5163    1.1068   -0.7138 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8225    0.8239   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    0.9322   -1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9065    0.6657   -1.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145    0.7813   -3.1504 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5371    0.2768   -0.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8303    0.1651    0.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281   -0.2575    1.6307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4566    0.4378    0.4576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8718    0.2902    1.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9134    1.3309    2.5097 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2863   -0.8292    2.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3024    2.3089    1.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    2.3337    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8947    1.4007    2.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9971   -0.1078    1.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9892   -2.9791   -0.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1177   -2.4147   -1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1745   -1.6845   -3.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0229    1.2417   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    1.6406   -3.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5968    0.0666   -0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1010    0.5862    2.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8647   -0.7679    2.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942   -1.0079    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4084   -1.7655    1.9527 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  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
  9  2  1  0
 18 11  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  6 27  1  0
  8 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 17 32  1  0
 17 33  1  0
 17 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      -2.116   1.704   1.655  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.331   0.540   0.737  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.401  -0.294   1.058  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.664  -1.346   0.214  0.00  0.00           C+0
HETATM    5  O   UNK     0      -4.732  -2.182   0.531  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.911  -1.587  -0.914  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.856  -0.770  -1.236  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.059  -0.943  -2.342  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.576   0.302  -0.388  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.516   1.107  -0.714  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.823   0.824  -0.689  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.569   0.932  -1.889  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.906   0.666  -1.954  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.615   0.781  -3.150  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.537   0.277  -0.795  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.830   0.165   0.384  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.528  -0.258   1.631  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.457   0.438   0.458  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.872   0.290   1.765  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.913   1.331   2.510  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.286  -0.829   2.282  0.00  0.00           O+0
HETATM   22  H   UNK     0      -1.302   2.309   1.181  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.049   2.334   1.588  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.895   1.401   2.680  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.997  -0.108   1.946  0.00  0.00           H+0
HETATM   26  H   UNK     0      -4.989  -2.979  -0.042  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.118  -2.415  -1.580  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.175  -1.685  -3.017  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.023   1.242  -2.769  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.062   1.641  -3.438  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.597   0.067  -0.853  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.101   0.586   2.074  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.865  -0.768   2.333  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.294  -1.008   1.307  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.408  -1.766   1.953  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3    9                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4   26                                                       
CONECT    6    4    7   27                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7   28                                                       
CONECT    9    7   10    2                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   29                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13   30                                                       
CONECT   15   13   16   31                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   32   33   34                                             
CONECT   18   16   19   11                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   35                                                       
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    5                                                            
CONECT   27    6                                                            
CONECT   28    8                                                            
CONECT   29   12                                                            
CONECT   30   14                                                            
CONECT   31   15                                                            
CONECT   32   17                                                            
CONECT   33   17                                                            
CONECT   34   17                                                            
CONECT   35   21                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   72    0
END

RDKit          3D

35 36  0  0  0  0  0  0  0  0999 V2000
   -2.1157    1.7044    1.6551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3310    0.5403    0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4009   -0.2938    1.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6638   -1.3460    0.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7323   -2.1822    0.5311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -1.5867   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8557   -0.7696   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0586   -0.9434   -2.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5762    0.3020   -0.3878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5163    1.1068   -0.7138 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8225    0.8239   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    0.9322   -1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9065    0.6657   -1.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145    0.7813   -3.1504 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5371    0.2768   -0.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8303    0.1651    0.3836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281   -0.2575    1.6307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4566    0.4378    0.4576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8718    0.2902    1.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9134    1.3309    2.5097 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2863   -0.8292    2.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3024    2.3089    1.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    2.3337    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8947    1.4007    2.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9971   -0.1078    1.9462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9892   -2.9791   -0.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1177   -2.4147   -1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1745   -1.6845   -3.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0229    1.2417   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    1.6406   -3.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5968    0.0666   -0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1010    0.5862    2.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8647   -0.7679    2.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942   -1.0079    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4084   -1.7655    1.9527 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  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
  9  2  1  0
 18 11  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  6 27  1  0
  8 28  1  0
 12 29  1  0
 14 30  1  0
 15 31  1  0
 17 32  1  0
 17 33  1  0
 17 34  1  0
 21 35  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
2-(2,4-Dihydroxy-6-methylphenoxy)-4-hydroxy-6-methylbenzoate	Generator

Chemical Formula

C₁₅H₁₄O₆

Average Mass

290.2710 Da

Monoisotopic Mass

290.07904 Da

IUPAC Name

2-(2,4-dihydroxy-6-methylphenoxy)-4-hydroxy-6-methylbenzoic acid

Traditional Name

2-(2,4-dihydroxy-6-methylphenoxy)-4-hydroxy-6-methylbenzoic acid

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=CC(O)=C1OC1=C(C(O)=O)C(C)=CC(O)=C1

InChI Identifier

InChI=1S/C15H14O6/c1-7-3-10(17)6-12(13(7)15(19)20)21-14-8(2)4-9(16)5-11(14)18/h3-6,16-18H,1-2H3,(H,19,20)

InChI Key

ZXWOXXVHOUPFOK-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
Corynespora	NPAtlas	19230943

Species Where Detected

Species Name	Source	Reference
Corynespora cassiicola	KNApSAcK Database	22123792

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Diphenylethers

Direct Parent

Diphenylethers

Alternative Parents

Substituents

Diphenylether
Diaryl ether
Hydroxybenzoic acid
Benzoic acid or derivatives
Benzoic acid
Phenoxy compound
Benzoyl
M-cresol
Phenol ether
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Toluene
Ether
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.55	ALOGPS
logP	3.25	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	3.8	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	75.58 m³·mol⁻¹	ChemAxon
Polarizability	28.36 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

NPA010612

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00048364

Chemspider ID

78434864

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42611551

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chomcheon P, Wiyakrutta S, Sriubolmas N, Ngamrojanavanich N, Kengtong S, Mahidol C, Ruchirawat S, Kittakoop P: Aromatase inhibitory, radical scavenging, and antioxidant activities of depsidones and diaryl ethers from the endophytic fungus Corynespora cassiicola L36. Phytochemistry. 2009 Feb;70(3):407-13. doi: 10.1016/j.phytochem.2009.01.007. Epub 2009 Feb 21. [PubMed:19230943 ]

Showing NP-Card for Corynether A (NP0008307)

MOL for NP0008307 (Corynether A)

3D MOL for NP0008307 (Corynether A)

3D SDF for NP0008307 (Corynether A)

3D-SDF for NP0008307 (Corynether A)

PDB for NP0008307 (Corynether A)

3D PDB for NP0008307 (Corynether A)

SMILES for NP0008307 (Corynether A)

INCHI for NP0008307 (Corynether A)

Structure for NP0008307 (Corynether A)

3D Structure for NP0008307 (Corynether A)