NP-MRD: Showing NP-Card for n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid (NP0258834)

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Record Information

Version

2.0

Created at

2022-09-08 00:29:03 UTC

Updated at

2022-09-08 00:29:03 UTC

NP-MRD ID

NP0258834

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082202292D          

 40 42  0  0  0  0            999 V2000
    5.7364    0.4889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4188    1.2503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6006    1.3559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2830    2.1173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4648    2.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9642    1.5672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818    0.8058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1000    0.7002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176   -0.0612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9170   -0.7170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0988   -0.6113    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5982   -1.2671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9158   -2.0285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7800   -1.1614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2937   -1.8279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6278   -2.5823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4481   -2.6701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3966   -0.3441    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510    0.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5675    0.9798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7285    3.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0461    4.1528    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8643    4.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5455    4.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2739    3.0743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5915    3.8357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5443    2.9686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1460    1.6729    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 11 10  1  4  0  0  0
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 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
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 16 18  1  0  0  0  0
 19 14  1  4  0  0  0
 19 20  2  0  0  0  0
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 34 35  1  0  0  0  0
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 29 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 23 40  1  0  0  0  0
  6 40  1  0  0  0  0
M  END

     RDKit          3D

 83 85  0  0  0  0  0  0  0  0999 V2000
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   -6.0747    0.9561    1.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309082202292D          

 40 42  0  0  0  0            999 V2000
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    0.3613    1.5515    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4569    1.6571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9576    1.0014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7745    2.4186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5927    2.5242    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9103    3.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4097    3.9414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7285    3.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0461    4.1528    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8643    4.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5455    4.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2739    3.0743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5915    3.8357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5443    2.9686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1460    1.6729    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 19 14  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 30 29  1  4  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 29 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 23 40  1  0  0  0  0
  6 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258834

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2OC3CCN(C3C(O)=NC(CC(C)C)C(O)=N\C=C/C1=C2)C(=O)C(N=C(O)CN(C)C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C29H43N5O6/c1-17(2)14-21-27(36)30-12-10-19-15-20(8-9-22(19)39-7)40-23-11-13-34(26(23)28(37)31-21)29(38)25(18(3)4)32-24(35)16-33(5)6/h8-10,12,15,17-18,21,23,25-26H,11,13-14,16H2,1-7H3,(H,30,36)(H,31,37)(H,32,35)/b12-10-

> <INCHI_KEY>
YRWFYJHVFNQJOK-BENRWUELSA-N

> <FORMULA>
C29H43N5O6

> <MOLECULAR_WEIGHT>
557.692

> <EXACT_MASS>
557.321334125

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
60.2893220459124

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-{1-[(13Z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid

> <JCHEM_LOGP>
-4.290096352726575

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
-4.972792537689849

> <JCHEM_PKA_STRONGEST_ACIDIC>
-7.2331991220635965

> <JCHEM_PKA_STRONGEST_BASIC>
14.93796366357399

> <JCHEM_POLAR_SURFACE_AREA>
139.78

> <JCHEM_REFRACTIVITY>
152.0509

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-{1-[(13Z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      10.708   0.913   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.115   2.334   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.588   2.531   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.995   3.952   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.468   4.150   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.533   2.926   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.126   1.504   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.653   1.307   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.246  -0.114   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.312  -1.338   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       5.784  -1.141   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       4.850  -2.365   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.443  -3.787   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.323  -2.168   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.415  -3.412   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.038  -4.820   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.570  -4.984   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.131  -6.064   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       2.607  -0.642   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       1.215   0.017   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.136  -0.721   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.413   1.545   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.926   1.829   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.123   3.356   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.732   4.016   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       0.674   2.896   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0      -0.853   3.093   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.787   1.869   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.446   4.515   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      -2.973   4.712   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      -3.566   6.133   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.631   7.357   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -5.093   6.330   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0      -5.686   7.752   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0      -7.213   7.949   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.752   8.976   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.511   5.739   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -1.104   7.160   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.016   5.541   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       4.006   3.123   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   40                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   26                                                  
CONECT   23   22   24   40                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22   27                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   37                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   29   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   23    6                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₃N₅O₆

Average Mass

557.6920 Da

Monoisotopic Mass

557.32133 Da

IUPAC Name

N-{1-[(13Z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC=C2OC3CCN(C3C(O)=NC(CC(C)C)C(O)=N\C=C/C1=C2)C(=O)C(N=C(O)CN(C)C)C(C)C

InChI Identifier

InChI=1S/C29H43N5O6/c1-17(2)14-21-27(36)30-12-10-19-15-20(8-9-22(19)39-7)40-23-11-13-34(26(23)28(37)31-21)29(38)25(18(3)4)32-24(35)16-33(5)6/h8-10,12,15,17-18,21,23,25-26H,11,13-14,16H2,1-7H3,(H,30,36)(H,31,37)(H,32,35)/b12-10-

InChI Key

YRWFYJHVFNQJOK-BENRWUELSA-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

Species Name	Source	Reference
Ziziphus jujuba	LOTUS Database	35616633
Zizyphus rugosa	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	-4.3	ChemAxon
pKa (Strongest Acidic)	-7.2	ChemAxon
pKa (Strongest Basic)	14.94	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	139.78 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	152.05 m³·mol⁻¹	ChemAxon
Polarizability	60.29 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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid (NP0258834)

MOL for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

3D MOL for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

3D SDF for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

3D-SDF for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

PDB for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

3D PDB for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

SMILES for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

INCHI for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

Structure for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)

3D Structure for NP0258834 (n-{1-[(13z)-8,11-dihydroxy-16-methoxy-10-(2-methylpropyl)-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-3-methyl-1-oxobutan-2-yl}-2-(dimethylamino)ethanimidic acid)