NP-MRD: Showing NP-Card for (1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate (NP0296121)

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Record Information

Version

1.0

Created at

2022-09-10 05:31:01 UTC

Updated at

2022-09-10 05:31:02 UTC

NP-MRD ID

NP0296121

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate

Description

(1R,4S,5S,11R,14S,15S)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]Docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate belongs to the class of organic compounds known as epipolythiodioxopiperazines. Epipolythiodioxopiperazines are compounds containing an epipolythiodioxopiperazine moiety, which consists of a 2,3-dithia-5,7-diazabicyclo[2.2.2]Octane-6,8-dione ring system. One distinct characteristics of Epipolythiodioxopiperazines is the presence of unique di- or polysulfide bridges. Based on a literature review very few articles have been published on (1R,4S,5S,11R,14S,15S)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]Docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102207312D          

 44 51  0  0  1  0            999 V2000
    8.4502    4.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7443    3.9722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5588    3.8415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0793    4.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7852    5.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3057    5.8925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1203    5.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4144    4.9910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8939    4.3509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2238    3.3321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5179    2.5613    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.3325    2.4306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6266    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1061    1.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2915    1.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5982    0.6749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8517    1.0980    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    6.4056    2.1038    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.6803    2.4044    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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 17 43  1  1  0  0  0
 44 43  1  6  0  0  0
 15 44  1  0  0  0  0
 11 44  1  0  0  0  0
M  END

     RDKit          3D

 72 79  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309102207312D          

 44 51  0  0  1  0            999 V2000
    8.4502    4.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7443    3.9722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9117    1.9372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    1.1608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0024    1.0141    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2813    0.2377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7484   -0.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9365   -0.2454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0272   -1.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4943   -1.7983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7732   -2.5747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2402   -3.2044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4283   -3.0577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1495   -2.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6824   -1.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5354    1.6438    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3918    1.5400    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664    0.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7258    0.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5548    2.6940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    3.4851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1368    1.9679    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9974    1.9212    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  2 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 26 37  1  0  0  0  0
 22 37  1  0  0  0  0
 37 38  1  6  0  0  0
 20 38  1  1  0  0  0
 38 39  1  0  0  0  0
 17 39  1  0  0  0  0
 39 40  2  0  0  0  0
 20 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 17 43  1  1  0  0  0
 44 43  1  6  0  0  0
 15 44  1  0  0  0  0
 11 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0296121

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C(CC1=CC=CC=C1)O[C@H]1C=CC=C2C[C@@]34SS[C@]5(CC6=CC=C[C@H](OC(=O)CC7=CC=CC=C7)[C@H]6N5C3=O)C(=O)N4[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C34H28N2O6S2/c37-27(17-21-9-3-1-4-10-21)41-25-15-7-13-23-19-33-32(40)36-30-24(20-34(36,44-43-33)31(39)35(33)29(23)25)14-8-16-26(30)42-28(38)18-22-11-5-2-6-12-22/h1-16,25-26,29-30H,17-20H2/t25-,26-,29-,30-,33+,34+/m0/s1

> <INCHI_KEY>
QFNXGJMEFDFWRJ-GJQRYMIASA-N

> <FORMULA>
C34H28N2O6S2

> <MOLECULAR_WEIGHT>
624.73

> <EXACT_MASS>
624.138878978

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
62.32503495863571

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4S,5S,11R,14S,15S)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate

> <JCHEM_LOGP>
5.076034343999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.415507776136661

> <JCHEM_POLAR_SURFACE_AREA>
93.21999999999998

> <JCHEM_REFRACTIVITY>
170.10379999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4S,5S,11R,14S,15S)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosa-6,8,16,18-tetraen-5-yl phenylacetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  O   UNK     0      15.774   8.854   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      16.323   7.415   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.843   7.171   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.815   8.366   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.266   9.805   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.237  10.999   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.758  10.755   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.307   9.317   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.335   8.122   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      15.351   6.220   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      15.900   4.781   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.421   4.537   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.970   3.098   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.998   1.903   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.477   2.147   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.183   1.260   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.790   2.050   0.000  0.00  0.00           C+0
HETATM   18  S   UNK     0      11.446   2.616   0.000  0.00  0.00           S+0
HETATM   19  S   UNK     0      11.957   3.927   0.000  0.00  0.00           S+0
HETATM   20  C   UNK     0      10.603   4.488   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.270   5.352   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.946   4.518   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.430   4.792   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.435   3.616   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.956   2.167   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.471   1.893   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.992   0.444   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.997  -0.732   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.481  -0.458   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.518  -2.181   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.523  -3.357   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.043  -4.806   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.048  -5.982   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.533  -5.708   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.012  -4.258   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.007  -3.083   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.466   3.068   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      10.065   2.875   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      11.137   1.525   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      10.688   0.052   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      12.236   5.029   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      12.672   6.505   0.000  0.00  0.00           O+0
HETATM   43  N   UNK     0      13.322   3.673   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0      14.928   3.586   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    4                                                       
CONECT   10    2   11                                                       
CONECT   11   10   12   44                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   44                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   39   43                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   38   41                                             
CONECT   21   20   22                                                       
CONECT   22   21   23   37                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   37                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   26   22   38                                                  
CONECT   38   37   20   39                                                  
CONECT   39   38   17   40                                                  
CONECT   40   39                                                            
CONECT   41   20   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   17   44                                                  
CONECT   44   43   15   11                                                  
MASTER        0    0    0    0    0    0    0    0   44    0  102    0
END

View in JSmol

Synonyms

Value	Source
(1R,4S,5S,11R,14S,15S)-2,12-Dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0,.0,.0,.0,]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetic acid	Generator

Chemical Formula

C₃₄H₂₈N₂O₆S₂

Average Mass

624.7300 Da

Monoisotopic Mass

624.13888 Da

IUPAC Name

(1R,4S,5S,11R,14S,15S)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate

Traditional Name

(1R,4S,5S,11R,14S,15S)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosa-6,8,16,18-tetraen-5-yl phenylacetate

CAS Registry Number

Not Available

SMILES

O=C(CC1=CC=CC=C1)O[C@H]1C=CC=C2C[C@@]34SS[C@]5(CC6=CC=C[C@H](OC(=O)CC7=CC=CC=C7)[C@H]6N5C3=O)C(=O)N4[C@H]12

InChI Identifier

InChI=1S/C34H28N2O6S2/c37-27(17-21-9-3-1-4-10-21)41-25-15-7-13-23-19-33-32(40)36-30-24(20-34(36,44-43-33)31(39)35(33)29(23)25)14-8-16-26(30)42-28(38)18-22-11-5-2-6-12-22/h1-16,25-26,29-30H,17-20H2/t25-,26-,29-,30-,33+,34+/m0/s1

InChI Key

QFNXGJMEFDFWRJ-GJQRYMIASA-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 epipolythiodioxopiperazines. Epipolythiodioxopiperazines are compounds containing an epipolythiodioxopiperazine moiety, which consists of a 2,3-dithia-5,7-diazabicyclo[2.2.2]Octane-6,8-dione ring system. One distinct characteristics of Epipolythiodioxopiperazines is the presence of unique di- or polysulfide bridges.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazinanes

Sub Class

Piperazines

Direct Parent

Epipolythiodioxopiperazines

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Epipolythiodioxopiperazine
Indole or derivatives
N-alkylpiperazine
Monocyclic benzene moiety
Dithiazinane
Dicarboxylic acid or derivatives
Benzenoid
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Carboxylic acid ester
Organic disulfide
Lactam
Carboxylic acid derivative
Azacycle
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Carbonyl group
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	5.08	ChemAxon
pKa (Strongest Basic)	-6.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	93.22 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	170.1 m³·mol⁻¹	ChemAxon
Polarizability	62.33 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28295226

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14589903

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate (NP0296121)

MOL for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

3D MOL for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

3D SDF for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

3D-SDF for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

PDB for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

3D PDB for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

SMILES for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

INCHI for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

Structure for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)

3D Structure for NP0296121 ((1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate)