NP-MRD: Showing NP-Card for 4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate) (NP0182372)

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Record Information

Version

2.0

Created at

2022-09-03 21:02:36 UTC

Updated at

2022-09-03 21:02:37 UTC

NP-MRD ID

NP0182372

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate)

Description

4-(2-Hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate) belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). Based on a literature review very few articles have been published on 4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032223022D          

 61 64  0  0  0  0            999 V2000
   -0.9288    3.9600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143    3.5475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143    2.7225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001    2.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001    1.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143    1.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143    0.2475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -0.1650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2146    0.2475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2146   -1.4025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2146   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -2.6400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -3.4650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9288   -2.6400    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6433   -2.2275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143   -1.4025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9288    1.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9288    2.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6969    3.9600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1259    2.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259    1.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4114    1.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4114    0.2475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259   -0.1650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8403    0.2475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8403   -1.4025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8403   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259   -2.6400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259   -3.4650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6969   -2.6400    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9825   -2.2275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4114   -1.4025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6969    1.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6969    2.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6197   -5.1150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9053   -5.5275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9053   -6.3525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1908   -6.7650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1908   -7.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4763   -8.0025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9053   -8.0025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6197   -7.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6197   -6.7650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3342   -6.3525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 15 18  2  0  0  0  0
 10 18  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 20  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
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 30 38  1  0  0  0  0
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 23 40  1  0  0  0  0
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 58 59  1  0  0  0  0
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 43 60  1  0  0  0  0
 60 61  1  0  0  0  0
M  END

     RDKit          3D

 94 97  0  0  0  0  0  0  0  0999 V2000
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   -1.3641    0.3161    0.2871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0023    0.5424    0.2034 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0800    0.5842   -0.2424 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2531    1.0290   -2.3655 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.2263    0.3355    0.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11 10  2  0
 10 18  1  0
 18 15  2  0
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  8  9  2  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
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  4  3  2  0
  3  2  1  0
  2  1  2  3
  3 20  1  0
 20 19  2  0
 34 33  1  0
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 32 31  1  0
 31 30  2  0
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 59 93  1  0
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 44 84  1  0
 57 91  1  0
 56 90  1  0
M  END


  Mrv1652309032223022D          

 61 64  0  0  0  0            999 V2000
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    0.5001    1.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143    1.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143    0.2475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -0.1650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2146    0.2475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2146   -1.4025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2146   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -2.6400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5001   -3.4650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9288   -2.6400    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6433   -2.2275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9288    1.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4114    1.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1259   -0.1650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8403    0.2475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8403   -1.4025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8403   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259   -2.6400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1259   -3.4650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4114   -2.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6969   -2.6400    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9825   -2.2275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4114   -1.4025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6969    1.4850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6969    2.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6197   -5.1150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9053   -5.5275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9053   -6.3525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1908   -6.7650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1908   -7.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4763   -8.0025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4763   -8.8275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2382   -7.5900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9526   -8.0025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6671   -7.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816   -8.0025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816   -8.8275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960   -9.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0960  -10.0650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8105  -10.4775    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6671   -9.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9526   -8.8275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9053   -8.0025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6197   -7.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6197   -6.7650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3342   -6.3525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 15 18  2  0  0  0  0
 10 18  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 20  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 35 38  2  0  0  0  0
 30 38  1  0  0  0  0
 26 39  1  0  0  0  0
 39 40  2  0  0  0  0
 23 40  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 53 54  2  0  0  0  0
 54 55  1  4  0  0  0
 52 56  1  0  0  0  0
 56 57  2  0  0  0  0
 49 57  1  0  0  0  0
 45 58  2  0  0  0  0
 58 59  1  0  0  0  0
 59 60  2  0  0  0  0
 43 60  1  0  0  0  0
 60 61  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0182372

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1N=O)C(=O)OC1=CC=C(C=C)C=C1.OC1=CC=C(C=C1N=O)C(=O)OC1=CC=C(C=C)C=C1.OC=CC1=CC=C(OC(=O)C2=CC=C(O)C(=C2)N=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H11NO5.2C15H11NO4/c17-8-7-10-1-4-12(5-2-10)21-15(19)11-3-6-14(18)13(9-11)16-20;2*1-2-10-3-6-12(7-4-10)20-15(18)11-5-8-14(17)13(9-11)16-19/h1-9,17-18H;2*2-9,17H,1H2

> <INCHI_KEY>
LVHCQRYOLLLGLT-UHFFFAOYSA-N

> <FORMULA>
C45H33N3O13

> <MOLECULAR_WEIGHT>
823.767

> <EXACT_MASS>
823.201338135

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
28.270359430712492

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate)

> <JCHEM_LOGP>
3.555113567666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.409114307655803

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.538444038698343

> <JCHEM_PKA_STRONGEST_BASIC>
-0.312834828227753

> <JCHEM_POLAR_SURFACE_AREA>
96.19000000000001

> <JCHEM_REFRACTIVITY>
77.07920000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate)

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.734   7.392   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.400   6.622   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.400   5.082   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.934   4.312   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.934   2.772   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.400   2.002   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.400   0.462   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.934  -0.308   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.267   0.462   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.934  -1.848   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.267  -2.618   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.267  -4.158   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.934  -4.928   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.934  -6.468   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.400  -4.158   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -1.734  -4.928   0.000  0.00  0.00           N+0
HETATM   17  O   UNK     0      -3.067  -4.158   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.400  -2.618   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.734   2.772   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.734   4.312   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.901   7.392   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.235   6.622   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.235   5.082   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.568   4.312   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.568   2.772   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.235   2.002   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.235   0.462   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.568  -0.308   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.902   0.462   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.568  -1.848   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.902  -2.618   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.902  -4.158   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.568  -4.928   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       9.568  -6.468   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.235  -4.158   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0       6.901  -4.928   0.000  0.00  0.00           N+0
HETATM   37  O   UNK     0       5.567  -4.158   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       8.235  -2.618   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.901   2.772   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.901   4.312   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -4.890  -9.548   0.000  0.00  0.00           O+0
HETATM   42  N   UNK     0      -3.556 -10.318   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0      -3.556 -11.858   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -2.223 -12.628   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -2.223 -14.168   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -0.889 -14.938   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -0.889 -16.478   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0       0.445 -14.168   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       1.778 -14.938   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       3.112 -14.168   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       4.446 -14.938   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       4.446 -16.478   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       5.779 -17.248   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       5.779 -18.788   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       7.113 -19.558   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       3.112 -17.248   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       1.778 -16.478   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -3.556 -14.938   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -4.890 -14.168   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      -4.890 -12.628   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      -6.224 -11.858   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   10                                                       
CONECT   19    6   20                                                       
CONECT   20   19    3                                                       
CONECT   21   22                                                            
CONECT   22   21   23                                                       
CONECT   23   22   24   40                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   39                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   38                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   30                                                       
CONECT   39   26   40                                                       
CONECT   40   39   23                                                       
CONECT   41   42                                                            
CONECT   42   41   43                                                       
CONECT   43   42   44   60                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46   58                                                  
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49                                                       
CONECT   49   48   50   57                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53   56                                                  
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54                                                            
CONECT   56   52   57                                                       
CONECT   57   56   49                                                       
CONECT   58   45   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59   43   61                                                  
CONECT   61   60                                                            
MASTER        0    0    0    0    0    0    0    0   61    0  128    0
END

View in JSmol

Synonyms

Value	Source
4-(2-Hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoic acid; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoic acid)	Generator

Chemical Formula

C₄₅H₃₃N₃O₁₃

Average Mass

823.7670 Da

Monoisotopic Mass

823.20134 Da

IUPAC Name

4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate)

Traditional Name

4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate)

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1N=O)C(=O)OC1=CC=C(C=C)C=C1.OC1=CC=C(C=C1N=O)C(=O)OC1=CC=C(C=C)C=C1.OC=CC1=CC=C(OC(=O)C2=CC=C(O)C(=C2)N=O)C=C1

InChI Identifier

InChI=1S/C15H11NO5.2C15H11NO4/c17-8-7-10-1-4-12(5-2-10)21-15(19)11-3-6-14(18)13(9-11)16-20;2*1-2-10-3-6-12(7-4-10)20-15(18)11-5-8-14(17)13(9-11)16-19/h1-9,17-18H;2*2-9,17H,1H2

InChI Key

LVHCQRYOLLLGLT-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depside backbone
P-hydroxybenzoic acid ester
Phenol ester
Benzoate ester
Benzoic acid or derivatives
Phenoxy compound
Styrene
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Carboxylic acid ester
Organic nitroso compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Enol
Carboxylic acid derivative
C-nitroso compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Not Available

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	3.56	ChemAxon
pKa (Strongest Acidic)	6.54	ChemAxon
pKa (Strongest Basic)	-0.31	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96.19 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	77.08 m³·mol⁻¹	ChemAxon
Polarizability	28.27 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163192689

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate) (NP0182372)

MOL for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

3D MOL for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

3D SDF for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

3D-SDF for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

PDB for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

3D PDB for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

SMILES for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

INCHI for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

Structure for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))

3D Structure for NP0182372 (4-(2-hydroxyethenyl)phenyl 4-hydroxy-3-nitrosobenzoate; bis(4-ethenylphenyl 4-hydroxy-3-nitrosobenzoate))