NP-MRD: Showing NP-Card for 16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone (NP0227799)

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Record Information

Version

2.0

Created at

2022-09-06 07:14:40 UTC

Updated at

2022-09-06 07:14:40 UTC

NP-MRD ID

NP0227799

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone

Description

16-Benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-4,20-dimethyl-13-(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]Hexacos-17-ene-2,5,12,15,21-pentone belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. Based on a literature review very few articles have been published on 16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-4,20-dimethyl-13-(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]Hexacos-17-ene-2,5,12,15,21-pentone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062209142D          

 50 53  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  2  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
  5  4  1  0
 46 41  1  0
 24 30  1  0
  7 12  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  0
  3 55  1  0
  3 56  1  0
  3 57  1  0
  4 58  1  1
 50100  1  0
 39 92  1  6
 40 93  1  0
 40 94  1  0
 42 95  1  0
 43 96  1  0
 44 97  1  0
 45 98  1  0
 46 99  1  0
 37 91  1  0
 35 89  1  0
 35 90  1  0
 34 86  1  0
 34 87  1  0
 34 88  1  0
 30 85  1  1
 29 83  1  0
 29 84  1  0
 27 81  1  1
 28 82  1  0
 26 79  1  0
 26 80  1  0
 25 78  1  0
 17 70  1  1
 16 67  1  0
 16 68  1  0
 16 69  1  0
 12 66  1  1
 11 64  1  0
 11 65  1  0
 10 62  1  0
 10 63  1  0
  9 60  1  0
  9 61  1  0
  8 59  1  0
 19 71  1  0
 19 72  1  0
 19 73  1  0
 20 74  1  0
 20 75  1  0
 20 76  1  0
 21 77  1  0
M  END


  Mrv1652309062209142D          

 50 53  0  0  0  0            999 V2000
    2.9388   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8862   -3.0590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448   -3.0546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -2.5559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -2.9684    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -1.7309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336    0.3316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2574   -2.0690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6836   -0.9772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -2.5559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4914   -1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -4.2059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -5.0309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -6.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -6.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -7.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -5.4434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -4.2059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -3.7934    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  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  1  0  0  0  0
 36 38  2  0  0  0  0
 38 39  1  4  0  0  0
 39 40  1  0  0  0  0
 40 41  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  2  0  0  0  0
 41 46  1  0  0  0  0
 39 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
  4 49  1  0  0  0  0
 49 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0227799

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1N(O)C(=O)C(CC2=CC=CC=C2)N=C(O)CN(C)C(=O)C2CC(O)CNN2C(=O)C(N(C)C(=O)C2CCCNN2C1=O)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C33H50N8O9/c1-19(2)26-31(47)39-23(13-10-14-34-39)30(46)38(6)27(33(3,4)49)32(48)40-24(16-21(42)17-35-40)29(45)37(5)18-25(43)36-22(28(44)41(26)50)15-20-11-8-7-9-12-20/h7-9,11-12,19,21-24,26-27,34-35,42,49-50H,10,13-18H2,1-6H3,(H,36,43)

> <INCHI_KEY>
FQDZOOBJRFYXQS-UHFFFAOYSA-N

> <FORMULA>
C33H50N8O9

> <MOLECULAR_WEIGHT>
702.81

> <EXACT_MASS>
702.370075222

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
70.43959552912813

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-4,20-dimethyl-13-(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacos-17-ene-2,5,12,15,21-pentone

> <JCHEM_LOGP>
-1.973390254694311

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.665640853648788

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.617369859844959

> <JCHEM_PKA_STRONGEST_BASIC>
3.880965854414629

> <JCHEM_POLAR_SURFACE_AREA>
218.89000000000001

> <JCHEM_REFRACTIVITY>
200.1114

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacos-17-ene-2,5,12,15,21-pentone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       5.486  -9.391   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.486  -7.851   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.819  -7.081   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.152  -7.081   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.521  -5.710   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.684  -5.702   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       2.818  -4.771   0.000  0.00  0.00           N+0
HETATM    8  N   UNK     0       4.152  -5.541   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       5.486  -4.771   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.486  -3.231   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.152  -2.461   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.818  -3.231   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.485  -2.461   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.485  -0.921   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0       0.151  -3.231   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       0.151  -4.771   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.183  -2.461   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.183  -0.921   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.723  -0.921   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.357  -0.921   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.183   0.619   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.347  -3.862   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.143  -1.824   0.000  0.00  0.00           O+0
HETATM   24  N   UNK     0      -2.516  -4.771   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0      -2.516  -3.231   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      -3.850  -2.461   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.184  -3.231   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.517  -2.461   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -5.184  -4.771   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.850  -5.541   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.850  -7.081   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -5.184  -7.851   0.000  0.00  0.00           O+0
HETATM   33  N   UNK     0      -2.516  -7.851   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0      -1.183  -7.081   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.516  -9.391   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.183 -10.161   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.183 -11.701   0.000  0.00  0.00           O+0
HETATM   38  N   UNK     0       0.151  -9.391   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0       1.485 -10.161   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.485 -11.701   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.818 -12.471   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.152 -11.701   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.486 -12.471   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.486 -14.011   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.152 -14.781   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.818 -14.011   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       2.818  -9.391   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       4.152 -10.161   0.000  0.00  0.00           O+0
HETATM   49  N   UNK     0       2.818  -7.851   0.000  0.00  0.00           N+0
HETATM   50  O   UNK     0       1.485  -7.081   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   49                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   17   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   24   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   47                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   46                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   41                                                       
CONECT   47   39   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47    4   50                                                  
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₅₀N₈O₉

Average Mass

702.8100 Da

Monoisotopic Mass

702.37008 Da

IUPAC Name

16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-4,20-dimethyl-13-(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacos-17-ene-2,5,12,15,21-pentone

Traditional Name

16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacos-17-ene-2,5,12,15,21-pentone

CAS Registry Number

Not Available

SMILES

CC(C)C1N(O)C(=O)C(CC2=CC=CC=C2)N=C(O)CN(C)C(=O)C2CC(O)CNN2C(=O)C(N(C)C(=O)C2CCCNN2C1=O)C(C)(C)O

InChI Identifier

InChI=1S/C33H50N8O9/c1-19(2)26-31(47)39-23(13-10-14-34-39)30(46)38(6)27(33(3,4)49)32(48)40-24(16-21(42)17-35-40)29(45)37(5)18-25(43)36-22(28(44)41(26)50)15-20-11-8-7-9-12-20/h7-9,11-12,19,21-24,26-27,34-35,42,49-50H,10,13-18H2,1-6H3,(H,36,43)

InChI Key

FQDZOOBJRFYXQS-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 oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Macrolactam
Alpha-amino acid or derivatives
Benzenoid
1,2-diazinane
Monocyclic benzene moiety
Tertiary carboxylic acid amide
Tertiary alcohol
Secondary carboxylic acid amide
Secondary alcohol
Lactam
Hydroxamic acid
Carboxylic acid hydrazide
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	-2	ChemAxon
pKa (Strongest Acidic)	4.62	ChemAxon
pKa (Strongest Basic)	3.88	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	218.89 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	200.11 m³·mol⁻¹	ChemAxon
Polarizability	70.44 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162816296

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone (NP0227799)

MOL for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

3D MOL for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

3D SDF for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

3D-SDF for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

PDB for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

3D PDB for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

SMILES for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

INCHI for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

Structure for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)

3D Structure for NP0227799 (16-benzyl-14,18,24-trihydroxy-3-(2-hydroxypropan-2-yl)-13-isopropyl-4,20-dimethyl-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacos-17-ene-2,5,12,15,21-pentone)