NP-MRD: Showing NP-Card for 3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione (NP0157104)

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Record Information

Version

2.0

Created at

2022-09-02 14:25:20 UTC

Updated at

2022-09-02 14:25:20 UTC

NP-MRD ID

NP0157104

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione

Description

3,24-Dibenzyl-21-(butan-2-yl)-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]Triaconta-4,13,22,25-tetraene-2,11,20-trione belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. 3,24-Dibenzyl-21-(butan-2-yl)-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]Triaconta-4,13,22,25-tetraene-2,11,20-trione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251511452D          

 63 69  0  0  0  0            999 V2000
    1.2373    1.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7650    0.7832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5781    0.9231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1058    0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8634    1.6972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6765    1.8371    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1038    1.1313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7062    0.4084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3559    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9583   -0.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9880   -1.7088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1632   -1.7259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7359   -1.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1335   -0.2973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.3070    4.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9247    6.1274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4262    5.4680    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7350    5.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5228    6.7157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  9 17  1  0  0  0  0
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 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
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 25 27  1  0  0  0  0
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  5 62  1  0  0  0  0
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M  END

     RDKit          3D

122128  0  0  0  0  0  0  0  0999 V2000
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 60121  1  0
 60122  1  0
M  END


  Mrv1533004251511452D          

 63 69  0  0  0  0            999 V2000
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    3.5228    6.7157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3081    5.9956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5 62  1  0  0  0  0
 62 63  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0157104

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C1NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C(=O)C(CC2=CC=C(O)C=C2)NC(=O)C2CCCN2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C48H59N7O8/c1-3-30(2)41-48(63)55-26-12-19-40(55)45(60)51-37(29-33-20-22-34(56)23-21-33)47(62)54-25-11-18-39(54)44(59)50-36(28-32-15-8-5-9-16-32)46(61)53-24-10-17-38(53)43(58)49-35(42(57)52-41)27-31-13-6-4-7-14-31/h4-9,13-16,20-23,30,35-41,56H,3,10-12,17-19,24-29H2,1-2H3,(H,49,58)(H,50,59)(H,51,60)(H,52,57)

> <INCHI_KEY>
ZLIGMNGUSFAVFH-UHFFFAOYSA-N

> <FORMULA>
C48H59N7O8

> <MOLECULAR_WEIGHT>
862.041

> <EXACT_MASS>
861.442511888

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
122

> <JCHEM_AVERAGE_POLARIZABILITY>
88.89713155501644

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,24-dibenzyl-21-(butan-2-yl)-12-[(4-hydroxyphenyl)methyl]-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triacontane-2,5,11,14,20,23,26-heptone

> <ALOGPS_LOGP>
3.20

> <JCHEM_LOGP>
3.059841419333333

> <ALOGPS_LOGS>
-4.15

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.715383957378677

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.50082990497477

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1466917462949726

> <JCHEM_POLAR_SURFACE_AREA>
197.56

> <JCHEM_REFRACTIVITY>
233.58360000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.05e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,24-dibenzyl-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triacontane-2,5,11,14,20,23,26-heptone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.310   2.646   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.295   1.462   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.812   1.723   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.797   0.539   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.345   3.168   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       6.863   3.429   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       7.660   2.112   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.918   0.762   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.200   2.144   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.998   0.826   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.255  -0.523   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.053  -1.840   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.311  -3.190   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.771  -3.222   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.974  -1.904   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.716  -0.555   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       9.942   3.493   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0      11.469   3.295   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      12.062   1.874   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      12.404   4.519   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.939   4.643   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.296   6.141   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.295   6.642   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      11.812   5.941   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      12.919   7.011   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      14.458   7.066   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.545   8.505   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.652   9.576   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      15.133   9.153   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      16.239  10.224   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.720   9.800   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      18.094   8.306   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.987   7.236   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.506   7.659   0.000  0.00  0.00           C+0
HETATM   35  N   UNK     0      11.064   8.929   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0      10.917  10.462   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.171  11.355   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.516  11.101   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.054  12.570   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.514  12.584   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.326  11.438   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0       8.262  10.207   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0       6.972  11.048   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       6.576  12.536   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       5.599  10.351   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.309  11.192   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.392  12.730   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       3.101  13.570   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       3.185  15.108   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       4.558  15.805   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       4.641  17.343   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       5.848  14.964   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       5.765  13.426   0.000  0.00  0.00           C+0
HETATM   54  N   UNK     0       5.516   8.813   0.000  0.00  0.00           N+0
HETATM   55  C   UNK     0       4.054   8.329   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0       2.903   9.353   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0       3.742   6.821   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0       2.413   6.043   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       2.742   4.538   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0       3.960   4.688   0.000  0.00  0.00           C+0
HETATM   61  N   UNK     0       4.893   5.797   0.000  0.00  0.00           N+0
HETATM   62  C   UNK     0       4.360   4.352   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0       2.997   3.634   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   62                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    9   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29                                                       
CONECT   35   27   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   42                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   38   43                                                  
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   54                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48   53                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   53                                                       
CONECT   53   52   47                                                       
CONECT   54   45   55                                                       
CONECT   55   54   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   58   61                                                  
CONECT   58   57   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59   61                                                       
CONECT   61   60   57   62                                                  
CONECT   62   61    5   63                                                  
CONECT   63   62                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  138    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₈H₅₉N₇O₈

Average Mass

862.0410 Da

Monoisotopic Mass

861.44251 Da

IUPAC Name

3,24-dibenzyl-21-(butan-2-yl)-12-[(4-hydroxyphenyl)methyl]-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triacontane-2,5,11,14,20,23,26-heptone

Traditional Name

3,24-dibenzyl-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triacontane-2,5,11,14,20,23,26-heptone

CAS Registry Number

Not Available

SMILES

CCC(C)C1NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C(=O)C(CC2=CC=C(O)C=C2)NC(=O)C2CCCN2C1=O

InChI Identifier

InChI=1S/C48H59N7O8/c1-3-30(2)41-48(63)55-26-12-19-40(55)45(60)51-37(29-33-20-22-34(56)23-21-33)47(62)54-25-11-18-39(54)44(59)50-36(28-32-15-8-5-9-16-32)46(61)53-24-10-17-38(53)43(58)49-35(42(57)52-41)27-31-13-6-4-7-14-31/h4-9,13-16,20-23,30,35-41,56H,3,10-12,17-19,24-29H2,1-2H3,(H,49,58)(H,50,59)(H,51,60)(H,52,57)

InChI Key

ZLIGMNGUSFAVFH-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 cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Alpha-amino acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Carboxamide group
Lactam
Organoheterocyclic compound
Azacycle
Polyol
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
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	3.2	ALOGPS
logP	3.06	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	9.5	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	197.56 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	233.58 m³·mol⁻¹	ChemAxon
Polarizability	88.9 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	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

74065844

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione (NP0157104)

MOL for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

3D MOL for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

3D SDF for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

3D-SDF for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

PDB for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

3D PDB for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

SMILES for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

INCHI for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

Structure for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)

3D Structure for NP0157104 (3,24-dibenzyl-5,14,23,26-tetrahydroxy-12-[(4-hydroxyphenyl)methyl]-21-(sec-butyl)-1,4,10,13,19,22,25-heptaazatetracyclo[25.3.0.0⁶,¹⁰.0¹⁵,¹⁹]triaconta-4,13,22,25-tetraene-2,11,20-trione)