NP-MRD: Showing NP-Card for (3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione (NP0196796)

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Record Information

Version

2.0

Created at

2022-09-04 14:56:34 UTC

Updated at

2022-09-04 14:56:34 UTC

NP-MRD ID

NP0196796

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione

Description

Amphilactam B belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Based on a literature review very few articles have been published on Amphilactam B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216562D          

 44 45  0  0  0  0            999 V2000
    5.2520    2.5957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309042216562D          

 44 45  0  0  0  0            999 V2000
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    5.9670    1.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938    0.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2287    1.1309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9208    0.6819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7396   -0.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7590   -0.9410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4093   -1.7176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7033   -2.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8605   -2.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2515   -1.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4032   -1.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6235   -1.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0037   -1.7299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4309   -0.3654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0997    0.4477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3832   -0.0405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9120    0.6401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1188    0.8670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6858    0.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6415    1.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049    0.3151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4243    1.5480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2267    2.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4492    2.8366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8725    3.4265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0732    3.2220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4263    2.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4965    3.8119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6660    1.1828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4332    1.4862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8933    0.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1129    0.1265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1972   -0.3662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9690   -0.6578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4481   -0.7450    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650    1.4178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1559    2.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4704    2.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9047    2.6843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6976    2.3585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2639    1.5859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9681    0.8158    0.0000 C   0  0  0  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  1  0  0  0  0
  5  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 25 31  1  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
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 37 12  1  4  0  0  0
 17 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
  2 43  1  0  0  0  0
 43 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196796

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CCCCCC2=CC(=O)OC(C\C(C)=C/C=C(C)/C(=C)C1)\C=C(C)/CC(=O)OC(\C=C/C(C)C)C(C)C(O)C(O)=N2

> <INCHI_IDENTIFIER>
InChI=1S/C36H53NO7/c1-23(2)14-17-32-28(7)35(40)36(41)37-29-12-10-9-11-13-30(42-8)21-27(6)26(5)16-15-24(3)18-31(43-34(39)22-29)19-25(4)20-33(38)44-32/h14-17,19,22-23,28,30-32,35,40H,6,9-13,18,20-21H2,1-5,7-8H3,(H,37,41)/b17-14-,24-15-,25-19-,26-16+,29-22-

> <INCHI_KEY>
DPIUYTPGQBRNHI-NVWHZFMVSA-N

> <FORMULA>
C36H53NO7

> <MOLECULAR_WEIGHT>
611.82

> <EXACT_MASS>
611.382203051

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
68.62050598638398

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3Z,5E,15Z,24Z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1Z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione

> <JCHEM_LOGP>
6.240732430566331

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.755419017513688

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.22769815986634

> <JCHEM_PKA_STRONGEST_BASIC>
4.041521619957029

> <JCHEM_POLAR_SURFACE_AREA>
114.65

> <JCHEM_REFRACTIVITY>
178.66790000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3Z,5E,15Z,24Z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1Z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       9.804   4.845   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.656   3.312   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.138   2.690   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.122   1.411   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.494   2.111   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      14.786   1.273   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.581  -0.138   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.617  -1.756   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.964  -3.206   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.646  -4.044   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.073  -4.027   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.936  -2.938   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.353  -2.760   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.897  -2.213   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.740  -3.229   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       4.538  -0.682   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.919   0.836   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.582  -0.076   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.702   1.195   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.222   1.618   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.147   1.819   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.931   2.048   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.423   0.588   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.392   2.890   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.890   3.812   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.305   5.295   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.229   6.396   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.737   6.014   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.529   5.059   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.660   7.116   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.710   2.208   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.142   2.774   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.134   0.736   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.677   0.236   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.701  -0.684   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      11.142  -1.228   0.000  0.00  0.00           O+0
HETATM   37  N   UNK     0       8.303  -1.391   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0       3.855   2.647   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.024   4.255   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.745   5.112   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       5.422   5.011   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.902   4.403   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.959   2.960   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.407   1.523   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   43                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   37                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   38                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   25   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   12                                                       
CONECT   38   17   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42    2   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₅₃NO₇

Average Mass

611.8200 Da

Monoisotopic Mass

611.38220 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1CCCCCC2=CC(=O)OC(C\C(C)=C/C=C(C)/C(=C)C1)\C=C(C)/CC(=O)OC(\C=C/C(C)C)C(C)C(O)C(O)=N2

InChI Identifier

InChI=1S/C36H53NO7/c1-23(2)14-17-32-28(7)35(40)36(41)37-29-12-10-9-11-13-30(42-8)21-27(6)26(5)16-15-24(3)18-31(43-34(39)22-29)19-25(4)20-33(38)44-32/h14-17,19,22-23,28,30-32,35,40H,6,9-13,18,20-21H2,1-5,7-8H3,(H,37,41)/b17-14-,24-15-,25-19-,26-16+,29-22-

InChI Key

DPIUYTPGQBRNHI-NVWHZFMVSA-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 macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Dicarboxylic acid or derivatives
Cyclic carboximidic acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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

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

119080539

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione (NP0196796)

MOL for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

3D MOL for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

3D SDF for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

3D-SDF for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

PDB for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

3D PDB for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

SMILES for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

INCHI for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

Structure for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)

3D Structure for NP0196796 ((3z,5e,15z,24z)-17,18-dihydroxy-9-methoxy-3,6,19,24-tetramethyl-20-[(1z)-3-methylbut-1-en-1-yl]-7-methylidene-21,26-dioxa-16-azabicyclo[13.10.3]octacosa-3,5,15(28),16,24-pentaene-22,27-dione)