NP-MRD: Showing NP-Card for (11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione (NP0259405)

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Record Information

Version

2.0

Created at

2022-09-08 01:15:48 UTC

Updated at

2022-09-08 01:15:48 UTC

NP-MRD ID

NP0259405

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082203152D          

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M  END

     RDKit          3D

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  Mrv1652309082203152D          

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   -6.5130   -5.7078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3211   -5.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9304   -6.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4129   -4.7219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6616   -4.3812    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4120   -3.5949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6062   -3.4178    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3567   -2.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2707   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4649   -3.7511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2154   -2.9648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0913   -4.3604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971   -4.1834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1466   -3.3970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 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  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  2  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 36 35  1  6  0  0  0
 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 27 38  1  0  0  0  0
 38 39  1  1  0  0  0
 16 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 14 43  1  0  0  0  0
 43 44  1  0  0  0  0
 10 44  1  0  0  0  0
 44 45  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0259405

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@H]2CC(=O)O[C@H]2C2=C1C(=O)C1=CC(=CC(O)=C1C2=O)C1=CC(O)=C2C(=O)C3=C([C@H](C)O[C@H]4CC(=O)O[C@@H]34)C(=O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H22O13/c1-8-19-24(31-15(42-8)6-17(35)44-31)29(40)21-12(27(19)38)3-10(4-13(21)33)11-5-14(34)22-23(26(11)37)28(39)20-9(2)43-16-7-18(36)45-32(16)25(20)30(22)41/h3-5,8-9,15-16,31-34,37H,6-7H2,1-2H3/t8-,9-,15-,16-,31+,32+/m0/s1

> <INCHI_KEY>
AVIMZSKCFXRKQP-HQEAHUMCSA-N

> <FORMULA>
C32H22O13

> <MOLECULAR_WEIGHT>
614.515

> <EXACT_MASS>
614.106040768

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
60.04544007364954

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(11S,15S,17S)-4,7-dihydroxy-5-[(11S,15S,17S)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione

> <JCHEM_LOGP>
2.935392601666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.039683854445586

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.3688826623583585

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9199100127439483

> <JCHEM_POLAR_SURFACE_AREA>
200.02999999999994

> <JCHEM_REFRACTIVITY>
149.58089999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(11S,15S,17S)-4,7-dihydroxy-5-[(11S,15S,17S)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione

> <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       2.819 -13.019   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.285 -11.552   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.789 -11.221   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.255  -9.753   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.658  -9.117   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.486  -7.587   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.624  -6.549   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       4.978  -7.277   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.217  -8.616   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.713  -8.946   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.247 -10.414   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.743 -10.745   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.277 -12.213   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.295  -9.607   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.800  -9.938   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.838  -8.800   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.342  -9.131   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.808 -10.599   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.312 -10.929   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -6.778 -12.397   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -7.350  -9.792   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.884  -8.324   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.380  -7.994   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.914  -6.526   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -7.923  -7.187   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -7.457  -5.719   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -9.427  -7.517   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.893  -8.985   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -8.854 -10.122   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -9.320 -11.590   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0     -11.397  -9.316   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0     -12.158 -10.655   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0     -13.666 -10.345   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0     -14.803 -11.383   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0     -13.837  -8.814   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -12.435  -8.178   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0     -11.969  -6.710   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0     -10.465  -6.380   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -9.999  -4.912   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.372  -7.333   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -0.868  -7.002   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -0.402  -5.534   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       0.170  -8.140   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.675  -7.809   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       2.140  -6.341   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9   11   44                                                  
CONECT   11   10    2   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   43                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   40                                                  
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   29                                                  
CONECT   22   21   23   25                                                  
CONECT   23   22   17   24                                                  
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   38                                                  
CONECT   28   27   29   31                                                  
CONECT   29   28   21   30                                                  
CONECT   30   29                                                            
CONECT   31   28   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   31   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   27   39                                                  
CONECT   39   38                                                            
CONECT   40   16   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   14   44                                                  
CONECT   44   43   10   45                                                  
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₂₂O₁₃

Average Mass

614.5150 Da

Monoisotopic Mass

614.10604 Da

IUPAC Name

(11S,15S,17S)-4,7-dihydroxy-5-[(11S,15S,17S)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,15}]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@H]2CC(=O)O[C@H]2C2=C1C(=O)C1=CC(=CC(O)=C1C2=O)C1=CC(O)=C2C(=O)C3=C([C@H](C)O[C@H]4CC(=O)O[C@@H]34)C(=O)C2=C1O

InChI Identifier

InChI=1S/C32H22O13/c1-8-19-24(31-15(42-8)6-17(35)44-31)29(40)21-12(27(19)38)3-10(4-13(21)33)11-5-14(34)22-23(26(11)37)28(39)20-9(2)43-16-7-18(36)45-32(16)25(20)30(22)41/h3-5,8-9,15-16,31-34,37H,6-7H2,1-2H3/t8-,9-,15-,16-,31+,32+/m0/s1

InChI Key

AVIMZSKCFXRKQP-HQEAHUMCSA-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

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	2.94	ChemAxon
pKa (Strongest Acidic)	7.37	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	200.03 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	149.58 m³·mol⁻¹	ChemAxon
Polarizability	60.05 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	No	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione (NP0259405)

MOL for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D MOL for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D SDF for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D-SDF for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

PDB for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D PDB for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

SMILES for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

INCHI for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

Structure for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D Structure for NP0259405 ((11s,15s,17s)-4,7-dihydroxy-5-[(11s,15s,17s)-7-hydroxy-17-methyl-2,9,13-trioxo-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraen-5-yl]-17-methyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)