NP-MRD: Showing NP-Card for (3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone (NP0311475)

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Record Information

Version

2.0

Created at

2022-09-11 07:29:41 UTC

Updated at

2022-09-11 07:29:41 UTC

NP-MRD ID

NP0311475

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone

Description

(3S,6S,9S,13S,16S,21aS)-3,16-dibenzyl-4,11-dihydroxy-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-13-(propan-2-yl)-1H,2H,3H,6H,7H,9H,10H,13H,14H,15H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone 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. Based on a literature review very few articles have been published on (3S,6S,9S,13S,16S,21aS)-3,16-dibenzyl-4,11-dihydroxy-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-13-(propan-2-yl)-1H,2H,3H,6H,7H,9H,10H,13H,14H,15H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112209292D          

 55 58  0  0  1  0            999 V2000
   15.2335   -1.1960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6713   -0.5922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1092    0.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3052   -0.1734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7430    0.4304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9390    0.2455    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.3848   -0.4487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8624   -1.0872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0719   -1.8852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.5977   -0.5476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7308    0.2666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8260   -0.8393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    7.8153    1.8339    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1768    2.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.8667    1.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0  0  0  0
  2  3  1  0  0  0  0
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  6  7  1  0  0  0  0
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  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
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 13 14  1  4  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
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 17 18  2  0  0  0  0
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 20 21  1  0  0  0  0
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 15 23  1  0  0  0  0
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 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
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 30 31  1  0  0  0  0
 27 31  1  6  0  0  0
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 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
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 51 53  1  0  0  0  0
  6 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  1  0  0  0  0
M  END

     RDKit          3D

112115  0  0  0  0  0  0  0  0999 V2000
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   -3.1896   -1.7120   -0.6994 N   0  0  0  0  0  0  0  0  0  0  0  0
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 43 97  1  0
M  END


  Mrv1652309112209292D          

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    5.9618   -0.2112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6821    1.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.8667    1.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
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 34 35  1  6  0  0  0
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 44 45  2  0  0  0  0
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 47 48  1  0  0  0  0
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 46 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  4  0  0  0
 51 53  1  0  0  0  0
  6 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0311475

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1N=C(O)C(C)(C)[C@H](CCCC#C)OC(=O)[C@H](C)N=C(O)[C@H](CC2=CC=CC=C2)N(C)C(=O)[C@@H]2CCCN2C(=O)[C@H](CC2=CC=CC=C2)N(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C43H57N5O7/c1-9-10-13-24-35-43(5,6)42(54)45-36(28(2)3)40(52)47(8)34(27-31-21-16-12-17-22-31)39(51)48-25-18-23-32(48)38(50)46(7)33(26-30-19-14-11-15-20-30)37(49)44-29(4)41(53)55-35/h1,11-12,14-17,19-22,28-29,32-36H,10,13,18,23-27H2,2-8H3,(H,44,49)(H,45,54)/t29-,32-,33-,34-,35-,36-/m0/s1

> <INCHI_KEY>
UQBZXGHVULROAE-UJARKJSPSA-N

> <FORMULA>
C43H57N5O7

> <MOLECULAR_WEIGHT>
755.957

> <EXACT_MASS>
755.425799195

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
80.39751520201312

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,9S,13S,16S,21aS)-3,16-dibenzyl-4,11-dihydroxy-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-13-(propan-2-yl)-1H,2H,3H,6H,7H,9H,10H,13H,14H,15H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone

> <JCHEM_LOGP>
6.302318264999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
5.085370936952666

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.3215955132572486

> <JCHEM_PKA_STRONGEST_BASIC>
1.5870814035817389

> <JCHEM_POLAR_SURFACE_AREA>
152.40999999999997

> <JCHEM_REFRACTIVITY>
209.08250000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,9S,13S,16S,21aS)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3H,6H,9H,13H,16H,19H,20H,21H,21aH-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      28.436  -2.233   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      27.386  -1.106   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      26.337   0.022   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.836  -0.324   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      23.787   0.803   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.286   0.458   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      23.118  -0.838   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      22.143  -2.029   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      22.534  -3.519   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      20.708  -1.470   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.749   0.069   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      19.108  -1.997   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      17.916  -1.022   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      18.164   0.498   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      16.475  -1.567   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.227  -3.087   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.418  -4.062   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.859  -3.517   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      20.051  -4.492   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      19.802  -6.012   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.362  -6.557   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.170  -5.582   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      15.283  -0.592   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      15.532   0.928   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.843  -1.136   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      13.594  -2.656   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.651  -0.161   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.129  -0.394   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.436   0.981   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.531   2.065   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0      12.899   1.359   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0      14.340   1.903   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      15.877   1.815   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      14.589   3.423   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.397   4.398   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.645   5.918   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.453   6.893   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.702   8.413   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      14.142   8.958   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      15.334   7.983   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      15.086   6.463   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0      16.029   3.968   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0      16.278   5.488   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.221   2.993   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      16.972   1.473   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      18.661   3.537   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      18.910   5.057   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      20.350   5.602   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      17.718   6.032   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      19.853   2.562   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      21.294   3.107   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      21.542   4.627   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      22.486   2.132   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      23.482   3.305   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      24.018   1.977   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   53                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   15   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   42                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   36                                                       
CONECT   42   34   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   50                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   46   51                                                       
CONECT   51   50   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51    6   54   55                                             
CONECT   54   53                                                            
CONECT   55   53                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  116    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₃H₅₇N₅O₇

Average Mass

755.9570 Da

Monoisotopic Mass

755.42580 Da

IUPAC Name

(3S,9S,13S,16S,21aS)-3,16-dibenzyl-4,11-dihydroxy-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-13-(propan-2-yl)-1H,2H,3H,6H,7H,9H,10H,13H,14H,15H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone

Traditional Name

(3S,9S,13S,16S,21aS)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3H,6H,9H,13H,16H,19H,20H,21H,21aH-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1N=C(O)C(C)(C)[C@H](CCCC#C)OC(=O)[C@H](C)N=C(O)[C@H](CC2=CC=CC=C2)N(C)C(=O)[C@@H]2CCCN2C(=O)[C@H](CC2=CC=CC=C2)N(C)C1=O

InChI Identifier

InChI=1S/C43H57N5O7/c1-9-10-13-24-35-43(5,6)42(54)45-36(28(2)3)40(52)47(8)34(27-31-21-16-12-17-22-31)39(51)48-25-18-23-32(48)38(50)46(7)33(26-30-19-14-11-15-20-30)37(49)44-29(4)41(53)55-35/h1,11-12,14-17,19-22,28-29,32-36H,10,13,18,23-27H2,2-8H3,(H,44,49)(H,45,54)/t29-,32-,33-,34-,35-,36-/m0/s1

InChI Key

UQBZXGHVULROAE-UJARKJSPSA-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
Macrolactam
Alpha-amino acid ester
Alpha-amino acid or derivatives
Benzenoid
Monocyclic benzene moiety
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Pyrrolidine
Lactone
Lactam
Carboxylic acid ester
Carboxamide group
Acetylide
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	6.3	ChemAxon
pKa (Strongest Acidic)	4.32	ChemAxon
pKa (Strongest Basic)	1.59	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	152.41 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	209.08 m³·mol⁻¹	ChemAxon
Polarizability	80.4 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	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

70951803

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163114089

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone (NP0311475)

MOL for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

3D MOL for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

3D SDF for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

3D-SDF for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

PDB for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

3D PDB for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

SMILES for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

INCHI for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

Structure for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)

3D Structure for NP0311475 ((3s,6s,9s,13s,16s,21as)-3,16-dibenzyl-4,11-dihydroxy-13-isopropyl-2,6,10,10,15-pentamethyl-9-(pent-4-yn-1-yl)-3h,6h,9h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-i]1-oxa-4,7,10,13,16-pentaazacyclononadecane-1,7,14,17-tetrone)