NP-MRD: Showing NP-Card for (1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione (NP0192579)

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Record Information

Version

2.0

Created at

2022-09-04 09:49:41 UTC

Updated at

2022-09-04 09:49:41 UTC

NP-MRD ID

NP0192579

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione

Description

19,21-Dibromooscillatoxin A 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 19,21-Dibromooscillatoxin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042211492D          

 43 46  0  0  1  0            999 V2000
   -2.1960   -3.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3804   -3.0113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4469   -2.9342    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3253   -3.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3395   -3.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9154   -3.0113    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8327   -2.9117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3091   -2.2724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.6994   -0.3293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 42 43  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309042211492D          

 43 46  0  0  1  0            999 V2000
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    3.5653   -0.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8515    0.4084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2539   -0.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5931   -1.6881    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4761   -1.5493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1072   -0.9640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5062   -2.5210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0122   -3.2003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6391   -3.8172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368   -3.5339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3914   -3.3999    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7286   -4.2457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1432   -2.6199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7564   -3.9374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9371   -4.8367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9552   -3.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7515   -2.8955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0312   -2.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1175   -3.3938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3923   -1.4055    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1557   -1.6686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0585   -2.0383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8729   -1.9064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1658   -1.1351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9539   -1.1496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6444   -0.4958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8167    0.3748    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.1700   -0.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4629   -1.3990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3193   -1.1756    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  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
 12 11  1  6  0  0  0
 12 13  1  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  6  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 10 26  1  1  0  0  0
 24 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 10 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 12 33  1  0  0  0  0
  8 33  1  0  0  0  0
 33 34  1  6  0  0  0
  3 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 35 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0192579

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H](CC[C@H](C)C1O[C@@]23C[C@H](OC(=O)C[C@H](CO)OC(=O)C[C@](O)(O2)[C@H](C)CC3(C)C)[C@@H]1C)C1=CC(O)=C(Br)C=C1Br

> <INCHI_IDENTIFIER>
InChI=1S/C31H44Br2O10/c1-16(7-8-24(39-6)20-10-23(35)22(33)11-21(20)32)28-18(3)25-13-31(42-28)29(4,5)12-17(2)30(38,43-31)14-27(37)40-19(15-34)9-26(36)41-25/h10-11,16-19,24-25,28,34-35,38H,7-9,12-15H2,1-6H3/t16-,17+,18-,19+,24-,25-,28?,30-,31-/m0/s1

> <INCHI_KEY>
DDGGYVOCCJLZJL-YJMWZKKWSA-N

> <FORMULA>
C31H44Br2O10

> <MOLECULAR_WEIGHT>
736.491

> <EXACT_MASS>
734.130124

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
67.9814410696378

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4S,5S,9R,13S,14R)-3-[(2S,5S)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1^{1,5}]octadecane-7,11-dione

> <JCHEM_LOGP>
6.387388337999997

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.51749273594585

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.535997270976156

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9597089139064368

> <JCHEM_POLAR_SURFACE_AREA>
140.98

> <JCHEM_REFRACTIVITY>
162.91730000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,5S,9R,13S,14R)-3-[(2S,5S)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1^{1,5}]octadecane-7,11-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      -4.099  -6.139   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.577  -5.621   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.834  -5.477   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.607  -6.789   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.500  -6.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.575  -5.621   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.288  -5.435   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.456  -3.824   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.532  -2.857   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.444  -4.242   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.639  -2.275   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.510  -1.184   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.039  -0.615   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.655  -0.774   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.189   0.762   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.941  -1.715   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.574  -3.151   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.222  -2.892   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.400  -1.800   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       8.412  -4.706   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.489  -5.974   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.660  -7.125   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.042  -6.597   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.464  -6.347   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.093  -7.925   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       4.001  -4.890   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.279  -7.350   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.616  -9.028   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.783  -6.910   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.403  -5.405   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.058  -4.833   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.219  -6.335   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.466  -2.624   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.891  -3.115   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.109  -3.805   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.629  -3.559   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.176  -2.119   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.647  -2.146   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.203  -0.926   0.000  0.00  0.00           C+0
HETATM   40 Br   UNK     0       1.525   0.700   0.000  0.00  0.00          Br+0
HETATM   41  C   UNK     0      -0.317  -1.172   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.864  -2.611   0.000  0.00  0.00           C+0
HETATM   43 Br   UNK     0      -2.463  -2.195   0.000  0.00  0.00          Br+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   35                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   33                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   26   30                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   33                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24   10                                                       
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   10   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   12    8   34                                                  
CONECT   34   33                                                            
CONECT   35    3   36   42                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   35   43                                                  
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₄Br₂O₁₀

Average Mass

736.4910 Da

Monoisotopic Mass

734.13012 Da

IUPAC Name

(1S,4S,5S,9R,13S,14R)-3-[(2S,5S)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1^{1,5}]octadecane-7,11-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@@H](CC[C@H](C)C1O[C@@]23C[C@H](OC(=O)C[C@H](CO)OC(=O)C[C@](O)(O2)[C@H](C)CC3(C)C)[C@@H]1C)C1=CC(O)=C(Br)C=C1Br

InChI Identifier

InChI=1S/C31H44Br2O10/c1-16(7-8-24(39-6)20-10-23(35)22(33)11-21(20)32)28-18(3)25-13-31(42-28)29(4,5)12-17(2)30(38,43-31)14-27(37)40-19(15-34)9-26(36)41-25/h10-11,16-19,24-25,28,34-35,38H,7-9,12-15H2,1-6H3/t16-,17+,18-,19+,24-,25-,28?,30-,31-/m0/s1

InChI Key

DDGGYVOCCJLZJL-YJMWZKKWSA-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
Benzylether
4-bromophenol
2-bromophenol
2-halophenol
4-halophenol
1-hydroxy-2-unsubstituted benzenoid
Ketal
Phenol
Halobenzene
Bromobenzene
Benzenoid
Oxane
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Aryl halide
Aryl bromide
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organobromide
Organohalogen compound
Carbonyl group
Alcohol
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	6.39	ChemAxon
pKa (Strongest Acidic)	7.54	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	140.98 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	162.92 m³·mol⁻¹	ChemAxon
Polarizability	67.98 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

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

139584730

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione (NP0192579)

MOL for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

3D MOL for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

3D SDF for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

3D-SDF for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

PDB for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

3D PDB for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

SMILES for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

INCHI for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

Structure for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)

3D Structure for NP0192579 ((1s,4s,5s,9r,13s,14r)-3-[(2s,5s)-5-(2,4-dibromo-5-hydroxyphenyl)-5-methoxypentan-2-yl]-13-hydroxy-9-(hydroxymethyl)-4,14,16,16-tetramethyl-2,6,10,17-tetraoxatricyclo[11.3.1.1¹,⁵]octadecane-7,11-dione)