NP-MRD: Showing NP-Card for 5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde (NP0157169)

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Record Information

Version

2.0

Created at

2022-09-02 14:29:38 UTC

Updated at

2022-09-02 14:29:38 UTC

NP-MRD ID

NP0157169

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde

Description

5,7-Dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-1,3-dihydro-2-benzofuran-4-carbaldehyde belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. 5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde is found in Xylaria polymorpha. Based on a literature review very few articles have been published on 5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-1,3-dihydro-2-benzofuran-4-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022216292D          

 31 32  0  0  0  0            999 V2000
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4609   -9.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9089  -10.4951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2814   -9.9682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.6170   -9.2145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4240   -9.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6789   -8.2584    0.0000 C   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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  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
 20 21  2  0  0  0  0
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 63 64  0  0  0  0  0  0  0  0999 V2000
    8.4083    2.5481   -0.9975 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0095    1.2196   -0.6529 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4448    0.7001    0.6304 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9459    0.4899    0.5985 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5327   -0.5009   -0.4382 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0461   -0.7195   -0.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5344   -1.2202    0.8330 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8394   -0.6372    0.5190 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0777   -0.5330   -0.5666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3250   -0.9452   -0.4945 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9099   -1.4620    0.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3032   -1.8868    0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3659   -0.9803    0.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6027   -1.5771    0.0678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7602   -2.9457    0.0832 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7161   -0.8303   -0.2495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9768   -1.4942   -0.5478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0110   -2.7490   -0.5047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6387    0.5711   -0.2859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4344    1.1692    0.0003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3355    0.3899    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1298    0.9708    0.6069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5922    2.6145   -0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6543    3.4406    0.0868 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8884    2.8442   -0.4743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6303    1.6223   -0.5585 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.2106    1.6056   -1.8042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5744    1.7062   -1.7155 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3120    2.4658   -1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7314    3.2848   -0.2538 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8531    2.9054   -1.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1055    1.2909   -0.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8369    0.5270   -1.5107 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9660   -0.2218    0.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6506    1.4673    1.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6823    0.0882    1.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4362    1.4654    0.4679 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8956   -0.1247   -1.4385 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0256   -1.4680   -0.2182 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5014    0.1878   -0.8319 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8271   -1.4946   -1.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7256   -0.4281    1.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720   -2.1210    1.1720 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8239   -2.2460    0.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7709   -1.7863    1.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4493    0.5893    1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5035    0.0596   -0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4458   -1.0162    1.4468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4906   -0.1493   -1.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3030   -2.4002    0.9739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6491   -0.8226    1.6386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3457   -2.7455   -0.0652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5810   -2.4246    1.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0962   -3.6463    0.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8977   -1.0135   -0.8055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9871    1.9649    0.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3906    1.6185    0.2800 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0775    0.9291   -1.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8741    2.7049   -1.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0056    1.6943   -2.7425 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 18 57  1  0
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 29 60  1  1
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 31 62  1  0
 31 63  1  0
 25 59  1  0
M  END


  Mrv1652309022216292D          

 31 32  0  0  0  0            999 V2000
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   14.2894   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   15.7184   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.5749   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4609   -9.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9089  -10.4951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2814   -9.9682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.6170   -9.2145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4240   -9.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6789   -8.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  4  0  0  0
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M  END
> <DATABASE_ID>
NP0157169

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCC=CC(=O)CCC1=C(O)C(C=O)=C2C(OC)OC(=O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O7/c1-3-4-5-6-7-8-9-10-11-12-16(26)13-14-17-21(27)18(15-25)19-20(22(17)28)23(29)31-24(19)30-2/h11-12,15,24,27-28H,3-10,13-14H2,1-2H3

> <INCHI_KEY>
YRXWGGJQBXWLGR-UHFFFAOYSA-N

> <FORMULA>
C24H32O7

> <MOLECULAR_WEIGHT>
432.513

> <EXACT_MASS>
432.21480337

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
48.245311080876306

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-1,3-dihydro-2-benzofuran-4-carbaldehyde

> <ALOGPS_LOGP>
4.74

> <JCHEM_LOGP>
7.323644143333334

> <ALOGPS_LOGS>
-4.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.16136811471187

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.912996701850768

> <JCHEM_PKA_STRONGEST_BASIC>
-4.158039504709092

> <JCHEM_POLAR_SURFACE_AREA>
110.13

> <JCHEM_REFRACTIVITY>
119.55369999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.14e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3H-2-benzofuran-4-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.337 -13.860   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.670 -14.630   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.004 -13.860   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.338 -14.630   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      21.339 -12.320   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      22.673 -14.630   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.006 -13.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      25.340 -14.630   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.674 -13.860   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      26.674 -12.320   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      28.007 -14.630   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.341 -13.860   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      29.341 -12.320   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      28.007 -16.170   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      26.674 -16.940   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.340 -16.170   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      24.006 -16.940   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      26.994 -18.446   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      25.963 -19.591   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      28.525 -18.607   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      29.152 -17.200   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      30.658 -16.880   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      31.134 -15.416   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   24                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   29                                                  
CONECT   23   22   24   26                                                  
CONECT   24   23   16   25                                                  
CONECT   25   24                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   22   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₇

Average Mass

432.5130 Da

Monoisotopic Mass

432.21480 Da

IUPAC Name

5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-1,3-dihydro-2-benzofuran-4-carbaldehyde

Traditional Name

5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3H-2-benzofuran-4-carbaldehyde

CAS Registry Number

Not Available

SMILES

CCCCCCCCCC=CC(=O)CCC1=C(O)C(C=O)=C2C(OC)OC(=O)C2=C1O

InChI Identifier

InChI=1S/C24H32O7/c1-3-4-5-6-7-8-9-10-11-12-16(26)13-14-17-21(27)18(15-25)19-20(22(17)28)23(29)31-24(19)30-2/h11-12,15,24,27-28H,3-10,13-14H2,1-2H3

InChI Key

YRXWGGJQBXWLGR-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Xylaria polymorpha	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Hydroxybenzoic acid derivatives

Alternative Parents

Substituents

Dihydroxybenzoic acid
Isobenzofuranone
Phthalide
Benzofuranone
Isocoumaran
Aryl-aldehyde
Vinylogous acid
Alpha,beta-unsaturated ketone
Enone
Acryloyl-group
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	4.74	ALOGPS
logP	7.32	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	6.91	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	119.55 m³·mol⁻¹	ChemAxon
Polarizability	48.25 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162814517

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde (NP0157169)

MOL for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

3D MOL for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

3D SDF for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

3D-SDF for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

PDB for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

3D PDB for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

SMILES for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

INCHI for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

Structure for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)

3D Structure for NP0157169 (5,7-dihydroxy-3-methoxy-1-oxo-6-(3-oxotetradec-4-en-1-yl)-3h-2-benzofuran-4-carbaldehyde)