NP-MRD: Showing NP-Card for 13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone (NP0170195)

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Record Information

Version

2.0

Created at

2022-09-03 06:18:20 UTC

Updated at

2022-09-03 06:18:20 UTC

NP-MRD ID

NP0170195

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone

Description

13-Benzyl-8-hydroxy-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3,10,16-tris(propan-2-yl)-1H,2H,3H,4H,6H,7H,10H,11H,12H,13H,14H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. 13-Benzyl-8-hydroxy-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3,10,16-tris(propan-2-yl)-1H,2H,3H,4H,6H,7H,10H,11H,12H,13H,14H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241512452D          

 52 54  0  0  0  0            999 V2000
   -3.1077    2.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3510    2.4363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6879    1.9455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8679    2.3232    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5095    3.0662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8999    3.7930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4547    2.1431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3126    2.1431    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
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 14 15  3  0  0  0  0
 10 16  1  0  0  0  0
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 19 20  1  0  0  0  0
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 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
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 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
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 41 42  1  0  0  0  0
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 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
  4 48  1  0  0  0  0
 48 49  2  0  0  0  0
 34 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
M  END

     RDKit          3D

110112  0  0  0  0  0  0  0  0999 V2000
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 28 84  1  0
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 28 86  1  0
M  END


  Mrv1533004241512452D          

 52 54  0  0  0  0            999 V2000
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    0.8098   -0.8925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2257   -1.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9893   -0.7731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1144   -1.9028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6474   -2.5325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2132   -3.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4118   -3.0379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3508   -2.2151    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6985   -1.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3081   -0.9832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0651   -2.0223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7174   -1.5172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1332   -1.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4810   -1.8295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8968   -1.6367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1470    0.6229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7993    1.1280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5629    0.8157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1764   -2.8398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9400   -3.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4758   -3.3449    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  3  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 40 45  1  0  0  0  0
 38 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
  4 48  1  0  0  0  0
 48 49  2  0  0  0  0
 34 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0170195

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1NC(=O)C(C)C(CCCC#C)OC(=O)C(C(C)C)N(C)C(=O)C2CCCN2C(=O)C(OC(=O)C(CC2=CC=CC=C2)N(C)C1=O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H58N4O8/c1-11-12-14-21-31-27(8)35(45)41-32(24(2)3)37(47)42(9)30(23-28-18-15-13-16-19-28)39(49)52-34(26(6)7)38(48)44-22-17-20-29(44)36(46)43(10)33(25(4)5)40(50)51-31/h1,13,15-16,18-19,24-27,29-34H,12,14,17,20-23H2,2-10H3,(H,41,45)

> <INCHI_KEY>
HGDNKULJQQBFCT-UHFFFAOYSA-N

> <FORMULA>
C40H58N4O8

> <MOLECULAR_WEIGHT>
722.924

> <EXACT_MASS>
722.425464844

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
110

> <JCHEM_AVERAGE_POLARIZABILITY>
79.13549804958853

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
13-benzyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3,10,16-tris(propan-2-yl)-octadecahydro-1H-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,8,11,14,17-hexone

> <ALOGPS_LOGP>
3.93

> <JCHEM_LOGP>
4.954920388

> <ALOGPS_LOGS>
-5.17

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.732335154303374

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.588384064414853

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0986873581703227

> <JCHEM_POLAR_SURFACE_AREA>
142.63000000000002

> <JCHEM_REFRACTIVITY>
194.9605

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.94e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-benzyl-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-decahydro-3H-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,8,11,14,17-hexone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -5.801   3.934   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.389   4.548   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.214   6.078   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.151   3.632   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      -1.620   4.337   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -0.951   5.724   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.680   7.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.575   5.516   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.640   6.628   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.849   4.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.182   4.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.516   4.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.850   4.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.183   4.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.517   3.230   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.135   2.912   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.927   1.386   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.502   0.803   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.145   0.443   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.570   1.026   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.788   0.083   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.778   2.552   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       2.937  -1.083   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       1.512  -1.666   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.155  -2.026   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.580  -1.443   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.947  -3.552   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.942  -4.727   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.131  -6.037   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.635  -5.671   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       2.521  -4.135   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       1.304  -3.192   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.575  -1.835   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -0.122  -3.775   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.339  -2.832   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -1.131  -1.306   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       0.294  -0.723   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -2.349  -0.363   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.774  -0.946   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -3.982  -2.472   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.764  -3.415   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.972  -4.941   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -4.398  -5.524   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -5.615  -4.581   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -5.407  -3.055   0.000  0.00  0.00           C+0
HETATM   46  N   UNK     0      -2.141   1.163   0.000  0.00  0.00           N+0
HETATM   47  C   UNK     0      -0.716   1.746   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -3.359   2.106   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -4.784   1.523   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -0.329  -5.301   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -1.755  -5.884   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       0.888  -6.244   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   48                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   10   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   27   32                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   50                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   46                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   45                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   40                                                       
CONECT   46   38   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46    4   49                                                  
CONECT   49   48                                                            
CONECT   50   34   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₅₈N₄O₈

Average Mass

722.9240 Da

Monoisotopic Mass

722.42546 Da

IUPAC Name

13-benzyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3,10,16-tris(propan-2-yl)-octadecahydro-1H-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,8,11,14,17-hexone

Traditional Name

13-benzyl-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-decahydro-3H-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,8,11,14,17-hexone

CAS Registry Number

Not Available

SMILES

CC(C)C1NC(=O)C(C)C(CCCC#C)OC(=O)C(C(C)C)N(C)C(=O)C2CCCN2C(=O)C(OC(=O)C(CC2=CC=CC=C2)N(C)C1=O)C(C)C

InChI Identifier

InChI=1S/C40H58N4O8/c1-11-12-14-21-31-27(8)35(45)41-32(24(2)3)37(47)42(9)30(23-28-18-15-13-16-19-28)39(49)52-34(26(6)7)38(48)44-22-17-20-29(44)36(46)43(10)33(25(4)5)40(50)51-31/h1,13,15-16,18-19,24-27,29-34H,12,14,17,20-23H2,2-10H3,(H,41,45)

InChI Key

HGDNKULJQQBFCT-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 depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Macrolide lactam
Alpha-amino acid ester
Macrolactam
Macrolide
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Carboxylic acid ester
Lactam
Lactone
Acetylide
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Carbonyl group
Organic nitrogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen 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	3.93	ALOGPS
logP	4.95	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	12.59	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	142.63 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	194.96 m³·mol⁻¹	ChemAxon
Polarizability	79.14 Å³	ChemAxon
Number of Rings	3	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone (NP0170195)

MOL for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

3D MOL for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

3D SDF for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

3D-SDF for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

PDB for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

3D PDB for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

SMILES for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

INCHI for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

Structure for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)

3D Structure for NP0170195 (13-benzyl-8-hydroxy-3,10,16-triisopropyl-2,7,12-trimethyl-6-(pent-4-yn-1-yl)-3h,6h,7h,10h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-f]1,10-dioxa-4,7,13,16-tetraazacyclononadecane-1,4,11,14,17-pentone)