NP-MRD: Showing NP-Card for 3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one (NP0171908)

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Record Information

Version

2.0

Created at

2022-09-03 08:37:10 UTC

Updated at

2022-09-03 08:37:11 UTC

NP-MRD ID

NP0171908

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one

Description

3-[(4-Hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-1H,2H,3H,4H-cyclopenta[b]indol-1-ylidene}-3-methoxy-1H,2H,3H,4H-cyclopenta[b]indol-2-one belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. Based on a literature review very few articles have been published on 3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-1H,2H,3H,4H-cyclopenta[b]indol-1-ylidene}-3-methoxy-1H,2H,3H,4H-cyclopenta[b]indol-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032210372D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309032210372D          

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   10.1768   -2.7261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4472   -3.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9073   -4.1294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1777   -4.9088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0971   -3.9738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8268   -3.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2861   -1.6355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2160   -2.4575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4691   -2.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5255   -0.8460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3049   -0.5756    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8486   -0.3743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8324    0.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1555    0.9222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3760    0.6519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3949    1.7117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5847    1.8673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0449    1.2434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4650    2.5337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2119    2.8841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2819    3.7061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7881    3.0054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0412    2.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3643    3.1267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4343    3.9487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7575    4.4204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1813    4.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8581    3.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2197    1.7280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8775    2.2260    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.5544    1.7543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3578    1.9417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9218    1.3396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6824    0.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8790    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3149    0.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4901    0.9485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1909   -0.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4612   -1.6517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8035   -2.1497    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1266   -1.6780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3232   -1.8654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7592   -1.2633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9986   -0.4738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8020   -0.2864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3660   -0.8885    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 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
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
 20 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 35 40  1  0  0  0  0
 40 41  1  0  0  0  0
 33 41  2  0  0  0  0
 17 41  1  0  0  0  0
 16 42  1  0  0  0  0
 42 43  2  0  0  0  0
 11 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 42 50  1  0  0  0  0
 45 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171908

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(C1=CC=C(O)C=C1)C1(OC)C(=O)C(C2=C1NC1=CC=CC=C21)=C1C(=O)C(OC)(C(OC)C2=CC=C(O)C=C2)C2=C1C1=CC=CC=C1N2

> <INCHI_IDENTIFIER>
InChI=1S/C40H34N2O8/c1-47-37(21-13-17-23(43)18-14-21)39(49-3)33-29(25-9-5-7-11-27(25)41-33)31(35(39)45)32-30-26-10-6-8-12-28(26)42-34(30)40(50-4,36(32)46)38(48-2)22-15-19-24(44)20-16-22/h5-20,37-38,41-44H,1-4H3

> <INCHI_KEY>
JJTLRFUXUFDNRP-UHFFFAOYSA-N

> <FORMULA>
C40H34N2O8

> <MOLECULAR_WEIGHT>
670.718

> <EXACT_MASS>
670.231516063

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
72.06359977969346

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-1H,2H,3H,4H-cyclopenta[b]indol-1-ylidene}-3-methoxy-1H,2H,3H,4H-cyclopenta[b]indol-2-one

> <ALOGPS_LOGP>
5.16

> <JCHEM_LOGP>
6.589477208666667

> <ALOGPS_LOGS>
-5.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.770214350894038

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.168246630107786

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6165757374703147

> <JCHEM_POLAR_SURFACE_AREA>
143.1

> <JCHEM_REFRACTIVITY>
186.59179999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.70e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4H-cyclopenta[b]indol-1-ylidene}-3-methoxy-4H-cyclopenta[b]indol-2-one

> <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      19.500  -2.469   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      17.987  -2.179   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      16.980  -3.343   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.484  -4.798   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.997  -5.089   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.501  -6.544   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      18.494  -7.708   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      18.998  -9.163   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      16.981  -7.418   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.477  -5.963   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.467  -3.053   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      15.337  -4.587   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      13.942  -5.241   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.914  -1.579   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      17.369  -1.074   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      14.651  -0.699   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.620   0.841   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.357   1.721   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.902   1.217   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.804   3.195   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.291   3.486   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.284   2.321   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.935   4.730   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      15.329   5.384   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      15.460   6.918   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.671   5.610   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.277   4.956   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.013   5.837   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.144   7.371   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.881   8.251   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      11.538   8.025   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.802   7.145   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.344   3.226   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0      16.571   4.155   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0      17.835   3.275   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      19.335   3.624   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      20.387   2.501   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      19.940   1.027   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      18.441   0.677   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      17.388   1.801   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      15.848   1.771   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      13.423  -1.628   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      13.928  -3.083   0.000  0.00  0.00           C+0
HETATM   44  N   UNK     0      12.700  -4.013   0.000  0.00  0.00           N+0
HETATM   45  C   UNK     0      11.436  -3.132   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       9.937  -3.482   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.884  -2.358   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       9.331  -0.885   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      10.830  -0.535   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      11.883  -1.659   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9    4                                                       
CONECT   11    3   12   14   43                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   42                                                  
CONECT   17   16   18   41                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   23   33                                             
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   26                                                       
CONECT   33   20   34   41                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   35   41                                                  
CONECT   41   40   33   17                                                  
CONECT   42   16   43   50                                                  
CONECT   43   42   11   44                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46   50                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   42   45                                                  
MASTER        0    0    0    0    0    0    0    0   50    0  114    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₃₄N₂O₈

Average Mass

670.7180 Da

Monoisotopic Mass

670.23152 Da

IUPAC Name

3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-1H,2H,3H,4H-cyclopenta[b]indol-1-ylidene}-3-methoxy-1H,2H,3H,4H-cyclopenta[b]indol-2-one

Traditional Name

3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4H-cyclopenta[b]indol-1-ylidene}-3-methoxy-4H-cyclopenta[b]indol-2-one

CAS Registry Number

Not Available

SMILES

COC(C1=CC=C(O)C=C1)C1(OC)C(=O)C(C2=C1NC1=CC=CC=C21)=C1C(=O)C(OC)(C(OC)C2=CC=C(O)C=C2)C2=C1C1=CC=CC=C1N2

InChI Identifier

InChI=1S/C40H34N2O8/c1-47-37(21-13-17-23(43)18-14-21)39(49-3)33-29(25-9-5-7-11-27(25)41-33)31(35(39)45)32-30-26-10-6-8-12-28(26)42-34(30)40(50-4,36(32)46)38(48-2)22-15-19-24(44)20-16-22/h5-20,37-38,41-44H,1-4H3

InChI Key

JJTLRFUXUFDNRP-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 indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

Indoles

Alternative Parents

Substituents

Benzylether
Indole
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Pyrrole
Ketone
Cyclic ketone
Dialkyl ether
Ether
Azacycle
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
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	5.16	ALOGPS
logP	6.59	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	9.17	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	143.1 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	186.59 m³·mol⁻¹	ChemAxon
Polarizability	72.06 Å³	ChemAxon
Number of Rings	8	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

85111534

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one (NP0171908)

MOL for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

3D MOL for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

3D SDF for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

3D-SDF for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

PDB for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

3D PDB for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

SMILES for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

INCHI for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

Structure for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)

3D Structure for NP0171908 (3-[(4-hydroxyphenyl)(methoxy)methyl]-1-{3-[(4-hydroxyphenyl)(methoxy)methyl]-3-methoxy-2-oxo-4h-cyclopenta[b]indol-1-ylidene}-3-methoxy-4h-cyclopenta[b]indol-2-one)