NP-MRD: Showing NP-Card for (9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one (NP0313181)

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Record Information

Version

2.0

Created at

2022-09-11 10:33:23 UTC

Updated at

2022-09-11 10:33:23 UTC

NP-MRD ID

NP0313181

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one

Description

(9S)-5,9-dihydroxy-2-methyl-9-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-4H,8H,9H-oxepino[2,3-h]chromen-4-one belongs to the class of organic compounds known as benzoxepines. These are organic compounds containing a benzene ring fused to an oxepine ring (an unsaturated seven-membered heterocycle with one oxygen atom replacing a carbon atom). (9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one is found in Eranthis cilicica. Based on a literature review very few articles have been published on (9S)-5,9-dihydroxy-2-methyl-9-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-4H,8H,9H-oxepino[2,3-h]chromen-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112212332D          

 43 47  0  0  1  0            999 V2000
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 16 42  1  0  0  0  0
 42 43  1  0  0  0  0
 10 43  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309112212332D          

 43 47  0  0  1  0            999 V2000
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    2.2214    0.6093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112   -0.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2431    0.3354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0552    0.1901    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5870    0.8208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3991    0.6756    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9309    1.3063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6506    2.0823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1825    2.7130    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9021    3.4889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4340    4.1196    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1537    4.8955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6855    5.5262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2461    3.9744    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7779    4.6051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5264    3.1985    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3385    3.0533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9946    2.5678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2749    1.7918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6794   -0.1003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4915   -0.2455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1476   -0.7310    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4279   -1.5069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3355   -0.5858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8037   -1.2165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9383   -0.9742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -1.5186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  1  0  0  0
 18 19  1  0  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  1  0  0  0
 22 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 20 40  1  0  0  0  0
 40 41  1  1  0  0  0
 16 42  1  0  0  0  0
 42 43  1  0  0  0  0
 10 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0313181

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(=O)C2=C(O)C=C3OC[C@](O)(CO[C@@H]4O[C@H](CO[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=CC3=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O16/c1-10-4-12(29)17-13(30)5-14-11(24(17)41-10)2-3-27(37,8-39-14)9-40-26-23(36)21(34)19(32)16(43-26)7-38-25-22(35)20(33)18(31)15(6-28)42-25/h2-5,15-16,18-23,25-26,28,30-37H,6-9H2,1H3/t15-,16-,18-,19-,20+,21+,22-,23-,25-,26-,27+/m1/s1

> <INCHI_KEY>
JOBWUMLSLUCCJM-OHJXWDBTSA-N

> <FORMULA>
C27H34O16

> <MOLECULAR_WEIGHT>
614.553

> <EXACT_MASS>
614.184685015

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
58.98471168040102

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9S)-5,9-dihydroxy-2-methyl-9-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-4H,8H,9H-oxepino[2,3-h]chromen-4-one

> <JCHEM_LOGP>
-2.516879875

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.862442364159973

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.611863999027389

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6483773177512537

> <JCHEM_POLAR_SURFACE_AREA>
254.51999999999995

> <JCHEM_REFRACTIVITY>
141.39550000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(9S)-5,9-dihydroxy-2-methyl-9-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8H-oxepino[2,3-h]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.334   1.583   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.600   0.229   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.407  -1.083   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.673  -2.437   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -4.479  -3.750   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.134  -2.479   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.401  -3.834   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.207  -5.146   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.139  -3.876   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.945  -2.564   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.212  -1.209   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.328  -1.167   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.061   0.187   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.813   0.208   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.297   0.622   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.545  -0.280   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.147   1.137   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.061  -0.551   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.054   0.626   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.570   0.355   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.562   1.532   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.078   1.261   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.071   2.439   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.548   3.887   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.541   5.064   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      11.017   6.513   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.010   7.690   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.487   9.138   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      12.480  10.316   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      13.526   7.419   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.519   8.596   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      14.049   5.970   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      15.565   5.699   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      13.057   4.793   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      13.580   3.345   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      10.602  -0.187   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.118  -0.458   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.609  -1.365   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      10.132  -2.813   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       8.093  -1.093   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       7.100  -2.271   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       3.618  -1.819   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       2.461  -2.835   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   12                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   43                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11    6   13                                                  
CONECT   13   12    2                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   42                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   40                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   36                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   34                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   25   35                                                  
CONECT   35   34                                                            
CONECT   36   22   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   20   41                                                  
CONECT   41   40                                                            
CONECT   42   16   43                                                       
CONECT   43   42   10                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₄O₁₆

Average Mass

614.5530 Da

Monoisotopic Mass

614.18469 Da

IUPAC Name

Traditional Name

(9S)-5,9-dihydroxy-2-methyl-9-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8H-oxepino[2,3-h]chromen-4-one

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)C2=C(O)C=C3OC[C@](O)(CO[C@@H]4O[C@H](CO[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=CC3=C2O1

InChI Identifier

InChI=1S/C27H34O16/c1-10-4-12(29)17-13(30)5-14-11(24(17)41-10)2-3-27(37,8-39-14)9-40-26-23(36)21(34)19(32)16(43-26)7-38-25-22(35)20(33)18(31)15(6-28)42-25/h2-5,15-16,18-23,25-26,28,30-37H,6-9H2,1H3/t15-,16-,18-,19-,20+,21+,22-,23-,25-,26-,27+/m1/s1

InChI Key

JOBWUMLSLUCCJM-OHJXWDBTSA-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
Eranthis cilicica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoxepines. These are organic compounds containing a benzene ring fused to an oxepine ring (an unsaturated seven-membered heterocycle with one oxygen atom replacing a carbon atom).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxepines

Sub Class

Not Available

Direct Parent

Benzoxepines

Alternative Parents

Substituents

Benzoxepine
Chromone
Disaccharide
Glycosyl compound
O-glycosyl compound
Benzopyran
1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Oxane
Pyran
Heteroaromatic compound
Vinylogous acid
Tertiary alcohol
Secondary alcohol
Ether
Oxacycle
Acetal
Polyol
Organooxygen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Primary 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	-2.5	ChemAxon
pKa (Strongest Acidic)	7.61	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	254.52 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	141.4 m³·mol⁻¹	ChemAxon
Polarizability	58.98 Å³	ChemAxon
Number of Rings	5	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

162842172

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one (NP0313181)

MOL for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

3D MOL for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

3D SDF for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

3D-SDF for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

PDB for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

3D PDB for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

SMILES for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

INCHI for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

Structure for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)

3D Structure for NP0313181 ((9s)-5,9-dihydroxy-2-methyl-9-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}methyl)-8h-oxepino[2,3-h]chromen-4-one)