NP-MRD: Showing NP-Card for Lecanorin F (NP0013696)

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Record Information

Version

2.0

Created at

2021-01-05 22:59:11 UTC

Updated at

2024-09-03 04:22:17 UTC

NP-MRD ID

NP0013696

Natural Product DOI

https://doi.org/10.57994/2807

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Lecanorin F

Provided By

NPAtlas

Description

Lecanorin F is found in Setophoma sp. Lecanorin F was first documented in 2015 (PMID: 25586883). Based on a literature review very few articles have been published on Lecanorin F.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119493D          

 37 38  0  0  0  0            999 V2000
   -4.5294   -2.4089   -0.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7292   -1.1811   -0.1159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3541    0.0393   -0.1556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6185    1.1712    0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2793    2.3893    0.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2486    1.0779    0.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4574    2.2905    0.5963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6132   -0.1413    0.3897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2599   -0.1955    0.6615 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7233   -0.1457   -0.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2559   -0.0429   -1.4903 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1581   -0.1990   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0275   -0.1383   -1.1388 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4652   -0.0191   -2.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1328   -0.3554    1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7355   -0.3093    1.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9575   -0.3751    2.2883 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9493   -2.2472    0.1702 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 37 38  0  0  0  0  0  0  0  0999 V2000
   -4.5294   -2.4089   -0.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7292   -1.1811   -0.1159 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6185    1.1712    0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2486    1.0779    0.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3384   -0.3429    0.4609 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306242119493D          

 37 38  0  0  0  0            999 V2000
   -4.5294   -2.4089   -0.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7292   -1.1811   -0.1159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3541    0.0393   -0.1556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6185    1.1712    0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2793    2.3893    0.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2486    1.0779    0.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4574    2.2905    0.5963 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2559   -0.0429   -1.4903 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7355   -0.3093    1.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3680   -1.2705    0.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0013696

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(=C(C(=O)OC2=C([H])C(=C([H])C(O[H])=C2C([H])([H])[H])C([H])([H])[H])C(O[H])=C1[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H16O5/c1-8-4-12(18)10(3)14(5-8)21-16(20)15-9(2)6-11(17)7-13(15)19/h4-7,17-19H,1-3H3

> <INCHI_KEY>
CCEOVCDVGADDPO-UHFFFAOYSA-N

> <FORMULA>
C16H16O5

> <MOLECULAR_WEIGHT>
288.299

> <EXACT_MASS>
288.099773615

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
30.22214998519816

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-2,5-dimethylphenyl 2,4-dihydroxy-6-methylbenzoate

> <ALOGPS_LOGP>
3.10

> <JCHEM_LOGP>
4.914249431666668

> <ALOGPS_LOGS>
-3.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.568893436868063

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.601204635042704

> <JCHEM_PKA_STRONGEST_BASIC>
-4.006415913642319

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
78.9272

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.34e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-2,5-dimethylphenyl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 37 38  0  0  0  0  0  0  0  0999 V2000
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   -4.2793    2.3893    0.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1581   -0.1990   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0275   -0.1383   -1.1388 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4652   -0.0191   -2.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4043   -0.1846   -0.9794 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9749   -0.2938    0.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3384   -0.3429    0.4609 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1328   -0.3554    1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7355   -0.3093    1.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9575   -0.3751    2.2883 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3680   -1.2705    0.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9543   -3.3268   -0.1021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8076   -2.3972   -1.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4571   -2.3050    0.2337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4089    0.0757   -0.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8039    3.2631    0.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0785    2.9827    1.2361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5338    2.1242    1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3202    2.8579   -0.3609 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9253   -0.9459   -2.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9334    0.9200   -2.7001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3356    0.0194   -3.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0501   -0.1344   -1.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8121    0.5578    0.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5331   -0.4433    2.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0085   -0.3661    2.4757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9493   -2.2472    0.1702 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
  6  8  1  0
  8  9  1  0
  9 10  1  0
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 16 18  1  0
 18 19  2  0
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  8 21  2  0
 21  2  1  0
 19 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
 14 30  1  0
 14 31  1  0
 14 32  1  0
 15 33  1  0
 17 34  1  0
 18 35  1  0
 20 36  1  0
 21 37  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      -4.529  -2.409  -0.367  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.729  -1.181  -0.116  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.354   0.039  -0.156  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.619   1.171   0.075  0.00  0.00           C+0
HETATM    5  O   UNK     0      -4.279   2.389   0.028  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.249   1.078   0.348  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.457   2.291   0.596  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.613  -0.141   0.390  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.260  -0.196   0.662  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.723  -0.146  -0.302  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.256  -0.043  -1.490  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.158  -0.199  -0.069  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.027  -0.138  -1.139  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.465  -0.019  -2.509  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.404  -0.185  -0.979  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.975  -0.294   0.260  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.338  -0.343   0.461  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.133  -0.355   1.333  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.736  -0.309   1.181  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.958  -0.375   2.288  0.00  0.00           O+0
HETATM   21  C   UNK     0      -2.368  -1.270   0.155  0.00  0.00           C+0
HETATM   22  H   UNK     0      -3.954  -3.327  -0.102  0.00  0.00           H+0
HETATM   23  H   UNK     0      -4.808  -2.397  -1.450  0.00  0.00           H+0
HETATM   24  H   UNK     0      -5.457  -2.305   0.234  0.00  0.00           H+0
HETATM   25  H   UNK     0      -5.409   0.076  -0.368  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.804   3.263   0.187  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.079   2.983   1.236  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.534   2.124   1.145  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.320   2.858  -0.361  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.925  -0.946  -2.762  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.933   0.920  -2.700  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.336   0.019  -3.244  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.050  -0.134  -1.840  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.812   0.558   0.598  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.533  -0.443   2.348  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.008  -0.366   2.476  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.949  -2.247   0.170  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3   21                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4   26                                                       
CONECT    6    4    7    8                                                  
CONECT    7    6   27   28   29                                             
CONECT    8    6    9   21                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   19                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13   30   31   32                                             
CONECT   15   13   16   33                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   34                                                       
CONECT   18   16   19   35                                                  
CONECT   19   18   20   12                                                  
CONECT   20   19   36                                                       
CONECT   21    8    2   37                                                  
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    5                                                            
CONECT   27    7                                                            
CONECT   28    7                                                            
CONECT   29    7                                                            
CONECT   30   14                                                            
CONECT   31   14                                                            
CONECT   32   14                                                            
CONECT   33   15                                                            
CONECT   34   17                                                            
CONECT   35   18                                                            
CONECT   36   20                                                            
CONECT   37   21                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   76    0
END

RDKit          3D

37 38  0  0  0  0  0  0  0  0999 V2000
   -4.5294   -2.4089   -0.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7292   -1.1811   -0.1159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3541    0.0393   -0.1556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6185    1.1712    0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2793    2.3893    0.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2486    1.0779    0.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4574    2.2905    0.5963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6132   -0.1413    0.3897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2599   -0.1955    0.6615 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7233   -0.1457   -0.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2559   -0.0429   -1.4903 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1581   -0.1990   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0275   -0.1383   -1.1388 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4652   -0.0191   -2.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4043   -0.1846   -0.9794 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9749   -0.2938    0.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3384   -0.3429    0.4609 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1328   -0.3554    1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7355   -0.3093    1.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9575   -0.3751    2.2883 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3680   -1.2705    0.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9543   -3.3268   -0.1021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8076   -2.3972   -1.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4571   -2.3050    0.2337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4089    0.0757   -0.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8039    3.2631    0.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0785    2.9827    1.2361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5338    2.1242    1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3202    2.8579   -0.3609 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9253   -0.9459   -2.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9334    0.9200   -2.7001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3356    0.0194   -3.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0501   -0.1344   -1.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8121    0.5578    0.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5331   -0.4433    2.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0085   -0.3661    2.4757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9493   -2.2472    0.1702 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
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
  8 21  2  0
 21  2  1  0
 19 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  5 26  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
 14 30  1  0
 14 31  1  0
 14 32  1  0
 15 33  1  0
 17 34  1  0
 18 35  1  0
 20 36  1  0
 21 37  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-Hydroxy-2,5-dimethylphenyl 2,4-dihydroxy-6-methylbenzoic acid	Generator

Chemical Formula

C₁₆H₁₆O₅

Average Mass

288.2990 Da

Monoisotopic Mass

288.09977 Da

IUPAC Name

3-hydroxy-2,5-dimethylphenyl 2,4-dihydroxy-6-methylbenzoate

Traditional Name

3-hydroxy-2,5-dimethylphenyl 2,4-dihydroxy-6-methylbenzoate

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C(C)C(OC(=O)C2=C(O)C=C(O)C=C2C)=C1

InChI Identifier

InChI=1S/C16H16O5/c1-8-4-12(18)10(3)14(5-8)21-16(20)15-9(2)6-11(17)7-13(15)19/h4-7,17-19H,1-3H3

InChI Key

CCEOVCDVGADDPO-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
FAILED_TO_DETECT NMR	NMR Spectrum (1D, 500 MHz, CD3OD, experimental)	livia.soman@unifesp.br	Unifesp - Universidade Federal de São Paulo	Lívia Soman	2024-06-11	View Spectrum

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
Moorena sp.		Not Available
Setophoma sp.	NPAtlas	25586883

Chemical Taxonomy

Classification

Not classified

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	3.1	ALOGPS
logP	4.91	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	8.6	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	78.93 m³·mol⁻¹	ChemAxon
Polarizability	30.22 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

NPA016142

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435914

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587577

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

de Medeiros LS, Abreu LM, Nielsen A, Ingmer H, Larsen TO, Nielsen KF, Rodrigues-Filho E: Dereplication-guided isolation of depsides thielavins S-T and lecanorins D-F from the endophytic fungus Setophoma sp. Phytochemistry. 2015 Mar;111:154-62. doi: 10.1016/j.phytochem.2014.12.020. Epub 2015 Jan 10. [PubMed:25586883 ]
DOI: 10.1016/j.phytochem.2014.12.020
PMID: 25586883

Showing NP-Card for Lecanorin F (NP0013696)

MOL for NP0013696 (Lecanorin F)

3D MOL for NP0013696 (Lecanorin F)

3D SDF for NP0013696 (Lecanorin F)

3D-SDF for NP0013696 (Lecanorin F)

PDB for NP0013696 (Lecanorin F)

3D PDB for NP0013696 (Lecanorin F)

SMILES for NP0013696 (Lecanorin F)

INCHI for NP0013696 (Lecanorin F)

Structure for NP0013696 (Lecanorin F)

3D Structure for NP0013696 (Lecanorin F)