NP-MRD: Showing NP-Card for Roseobacticide H (NP0010336)

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Record Information

Version

2.0

Created at

2021-01-05 19:53:16 UTC

Updated at

2021-07-15 17:05:48 UTC

NP-MRD ID

NP0010336

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Roseobacticide H

Provided By

NPAtlas

Description

Roseobacticide H is found in Phaeobacter gallaeciensis. Based on a literature review very few articles have been published on Roseobacticide H.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107373D          

 40 43  0  0  0  0            999 V2000
   -3.1594   -0.7401   -3.1768 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3284   -0.4736   -2.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0334   -0.4523   -2.4255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333   -0.1457   -1.3239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9332   -0.0343   -1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6109    0.7125   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1438    1.4693   -0.6417 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.5696    0.4929   -0.3747 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5394   -0.7639    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7290   -1.4789    0.3628 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9472   -0.9341   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1466   -1.6038    0.1420 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9775    0.3183   -0.5738 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7902    1.0121   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1536    0.9054    1.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1492    0.7996    1.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.6569    0.2256    0.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9406    0.3504    1.0459 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8474    1.3370    0.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5689    1.2180   -0.1612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5732   -0.5541   -1.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8905    2.0105   -1.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9027    1.1792    1.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2272    0.3211    1.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4596   -2.1296   -0.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7378   -1.9037    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2646    2.3215    0.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9349    2.0926   -0.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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   -2.3284   -0.4736   -2.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4333   -0.1457   -1.3239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9332   -0.0343   -1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6109    0.7125   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5696    0.4929   -0.3747 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5394   -0.7639    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7290   -1.4789    0.3628 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9472   -0.9341   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2646    2.3215    0.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9349    2.0926   -0.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
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M  END


  Mrv1652306242107373D          

 40 43  0  0  0  0            999 V2000
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   -2.3284   -0.4736   -2.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0334   -0.4523   -2.4255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333   -0.1457   -1.3239 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1438    1.4693   -0.6417 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.5696    0.4929   -0.3747 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5394   -0.7639    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7290   -1.4789    0.3628 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9472   -0.9341   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9775    0.3183   -0.5738 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7902    1.0121   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1536    0.9054    1.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1492    0.7996    1.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
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 14  8  1  0  0  0  0
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 26 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010336

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(SC2=C([H])C([H])=C([H])C3=C(C(=O)OC3=C2[H])C2=C([H])C([H])=C(O[H])C([H])=C2[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H14O4S/c22-14-6-4-13(5-7-14)20-18-3-1-2-17(12-19(18)25-21(20)24)26-16-10-8-15(23)9-11-16/h1-12,22-23H

> <INCHI_KEY>
DFIZEAKYMXSEJA-UHFFFAOYSA-N

> <FORMULA>
C21H14O4S

> <MOLECULAR_WEIGHT>
362.4

> <EXACT_MASS>
362.061280105

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
39.04914130160671

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(4-hydroxyphenyl)-7-[(4-hydroxyphenyl)sulfanyl]-2H-cyclohepta[b]furan-2-one

> <ALOGPS_LOGP>
5.32

> <JCHEM_LOGP>
4.067236392999999

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.407757471727793

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.723853337008434

> <JCHEM_PKA_STRONGEST_BASIC>
-5.968642185048393

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
106.608

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.89e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(4-hydroxyphenyl)-7-[(4-hydroxyphenyl)sulfanyl]cyclohepta[b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 40 43  0  0  0  0  0  0  0  0999 V2000
   -3.1594   -0.7401   -3.1768 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3284   -0.4736   -2.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0334   -0.4523   -2.4255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333   -0.1457   -1.3239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9332   -0.0343   -1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6109    0.7125   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1438    1.4693   -0.6417 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.5696    0.4929   -0.3747 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5394   -0.7639    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7290   -1.4789    0.3628 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9472   -0.9341   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1466   -1.6038    0.1420 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9775    0.3183   -0.5738 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7902    1.0121   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1536    0.9054    1.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1492    0.7996    1.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3114    0.3982    0.9977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5006    0.0605   -0.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6771   -0.1548   -0.9665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0218   -0.0432   -0.4303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8365   -1.1238   -0.1819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1225   -1.0165    0.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6569    0.2256    0.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9406    0.3504    1.0459 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6050   -1.2036    0.4862 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7214   -2.4578    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5551   -2.2227   -0.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9229    0.7682   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8905    2.0105   -1.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9027    1.1792    1.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2644    1.0752    2.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2272    0.3211    1.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4596   -2.1296   -0.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7378   -1.9037    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2357    0.3684    1.9887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2646    2.3215    0.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9349    2.0926   -0.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
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 21 36  1  0
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 24 38  1  0
 25 39  1  0
 26 40  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  O   UNK     0      -3.159  -0.740  -3.177  0.00  0.00           O+0
HETATM    2  C   UNK     0      -2.328  -0.474  -2.283  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.033  -0.452  -2.426  0.00  0.00           O+0
HETATM    4  C   UNK     0      -0.433  -0.146  -1.324  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.933  -0.034  -1.141  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.611   0.713  -0.164  0.00  0.00           C+0
HETATM    7  S   UNK     0       3.144   1.469  -0.642  0.00  0.00           S+0
HETATM    8  C   UNK     0       4.570   0.493  -0.375  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.539  -0.764   0.184  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.729  -1.479   0.363  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.947  -0.934  -0.017  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.147  -1.604   0.142  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.978   0.318  -0.574  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.790   1.012  -0.744  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.154   0.905   1.120  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.149   0.800   1.630  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.311   0.398   0.998  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.501   0.061  -0.322  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.677  -0.155  -0.967  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.022  -0.043  -0.430  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.837  -1.124  -0.182  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.122  -1.016   0.303  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.657   0.226   0.565  0.00  0.00           C+0
HETATM   24  O   UNK     0      -7.941   0.350   1.046  0.00  0.00           O+0
HETATM   25  C   UNK     0      -5.847   1.337   0.321  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.569   1.218  -0.161  0.00  0.00           C+0
HETATM   27  H   UNK     0       1.573  -0.554  -1.806  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.605  -1.204   0.486  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.721  -2.458   0.797  0.00  0.00           H+0
HETATM   30  H   UNK     0       8.555  -2.223  -0.560  0.00  0.00           H+0
HETATM   31  H   UNK     0       7.923   0.768  -0.884  0.00  0.00           H+0
HETATM   32  H   UNK     0       5.891   2.010  -1.200  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.903   1.179   1.830  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.264   1.075   2.687  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.227   0.321   1.565  0.00  0.00           H+0
HETATM   36  H   UNK     0      -4.460  -2.130  -0.373  0.00  0.00           H+0
HETATM   37  H   UNK     0      -6.738  -1.904   0.486  0.00  0.00           H+0
HETATM   38  H   UNK     0      -8.236   0.368   1.989  0.00  0.00           H+0
HETATM   39  H   UNK     0      -6.265   2.321   0.528  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.935   2.093  -0.351  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   18                                                  
CONECT    5    4    6   27                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   28                                                  
CONECT   10    9   11   29                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11   30                                                       
CONECT   13   11   14   31                                                  
CONECT   14   13    8   32                                                  
CONECT   15    6   16   33                                                  
CONECT   16   15   17   34                                                  
CONECT   17   16   18   35                                                  
CONECT   18   17   19    4                                                  
CONECT   19   18   20    2                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20   22   36                                                  
CONECT   22   21   23   37                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   38                                                       
CONECT   25   23   26   39                                                  
CONECT   26   25   20   40                                                  
CONECT   27    5                                                            
CONECT   28    9                                                            
CONECT   29   10                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
CONECT   33   15                                                            
CONECT   34   16                                                            
CONECT   35   17                                                            
CONECT   36   21                                                            
CONECT   37   22                                                            
CONECT   38   24                                                            
CONECT   39   25                                                            
CONECT   40   26                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

RDKit          3D

40 43  0  0  0  0  0  0  0  0999 V2000
   -3.1594   -0.7401   -3.1768 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3284   -0.4736   -2.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0334   -0.4523   -2.4255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333   -0.1457   -1.3239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9332   -0.0343   -1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6109    0.7125   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1438    1.4693   -0.6417 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.5696    0.4929   -0.3747 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5394   -0.7639    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7290   -1.4789    0.3628 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9472   -0.9341   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1466   -1.6038    0.1420 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9775    0.3183   -0.5738 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7902    1.0121   -0.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1536    0.9054    1.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1492    0.7996    1.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3114    0.3982    0.9977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5006    0.0605   -0.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6771   -0.1548   -0.9665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0218   -0.0432   -0.4303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8365   -1.1238   -0.1819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1225   -1.0165    0.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6569    0.2256    0.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9406    0.3504    1.0459 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8474    1.3370    0.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5689    1.2180   -0.1612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5732   -0.5541   -1.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6050   -1.2036    0.4862 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7214   -2.4578    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5551   -2.2227   -0.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9229    0.7682   -0.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8905    2.0105   -1.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9027    1.1792    1.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2644    1.0752    2.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2272    0.3211    1.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4596   -2.1296   -0.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7378   -1.9037    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2357    0.3684    1.9887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2646    2.3215    0.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9349    2.0926   -0.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
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 13 14  2  0
  6 15  2  0
 15 16  1  0
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 25 26  2  0
 19  2  1  0
 26 20  1  0
 18  4  1  0
 14  8  1  0
  5 27  1  0
  9 28  1  0
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 12 30  1  0
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 17 35  1  0
 21 36  1  0
 22 37  1  0
 24 38  1  0
 25 39  1  0
 26 40  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-(4-Hydroxyphenyl)-7-[(4-hydroxyphenyl)sulphanyl]-2H-cyclohepta[b]furan-2-one	Generator

Chemical Formula

C₂₁H₁₄O₄S

Average Mass

362.4000 Da

Monoisotopic Mass

362.06128 Da

IUPAC Name

3-(4-hydroxyphenyl)-7-[(4-hydroxyphenyl)sulfanyl]-2H-cyclohepta[b]furan-2-one

Traditional Name

3-(4-hydroxyphenyl)-7-[(4-hydroxyphenyl)sulfanyl]cyclohepta[b]furan-2-one

CAS Registry Number

Not Available

SMILES

OC1=CC=C(SC2=CC=CC3=C(C(=O)OC3=C2)C2=CC=C(O)C=C2)C=C1

InChI Identifier

InChI=1S/C21H14O4S/c22-14-6-4-13(5-7-14)20-18-3-1-2-17(12-19(18)25-21(20)24)26-16-10-8-15(23)9-11-16/h1-12,22-23H

InChI Key

DFIZEAKYMXSEJA-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
Phaeobacter gallaeciensis	NPAtlas	21928816

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	5.32	ALOGPS
logP	4.07	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.72	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	106.61 m³·mol⁻¹	ChemAxon
Polarizability	39.05 Å³	ChemAxon
Number of Rings	4	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

NPA014126

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78434975

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

87112883

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Roseobacticide H (NP0010336)

MOL for NP0010336 (Roseobacticide H)

3D MOL for NP0010336 (Roseobacticide H)

3D SDF for NP0010336 (Roseobacticide H)

3D-SDF for NP0010336 (Roseobacticide H)

PDB for NP0010336 (Roseobacticide H)

3D PDB for NP0010336 (Roseobacticide H)

SMILES for NP0010336 (Roseobacticide H)

INCHI for NP0010336 (Roseobacticide H)

Structure for NP0010336 (Roseobacticide H)

3D Structure for NP0010336 (Roseobacticide H)