NP-MRD: Showing NP-Card for (9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one (NP0259490)

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Record Information

Version

2.0

Created at

2022-09-08 01:22:51 UTC

Updated at

2022-09-08 01:22:51 UTC

NP-MRD ID

NP0259490

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one

Description

Cotylelophenol F belongs to the class of organic compounds known as dibenzocycloheptenes. Dibenzocycloheptenes are compounds containing a dibenzocycloheptene moiety, which consists of two benzene rings connected by a cycloheptene ring. (9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one is found in Cotylelobium lanceolatum. Based on a literature review very few articles have been published on Cotylelophenol F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082203222D          

 44 50  0  0  1  0            999 V2000
    0.8935   -1.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8538   -0.2148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926    0.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2043   -0.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6155   -0.7246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1630    0.6586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5513    1.2121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3688    1.6688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7660    0.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2436    1.5975    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5922    2.3452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5171    3.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2894    3.8407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6380    4.5884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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 38 44  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309082203222D          

 44 50  0  0  1  0            999 V2000
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   -2.2524    2.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9038    2.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6680    2.4309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7911    3.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0270    3.8702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9143    4.6875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3756    3.3640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0444    2.2699    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2357    3.0459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2962    3.6765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0160    4.4525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7961    4.5978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0762    5.3738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3280    3.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0478    3.1912    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  2  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 36  1  0  0  0  0
 28 37  1  0  0  0  0
 19 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 38 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259490

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)[C@H]1[C@@H]2[C@@H](C3=CC=C(O)C=C3)C3=C(O)C=C(O)C=C3C(=O)C3=C2C([C@@H]1C1=CC(O)=CC(O)=C1)=C(O)C=C3O

> <INCHI_IDENTIFIER>
InChI=1S/C35H26O9/c36-18-5-1-15(2-6-18)27-29(17-9-20(38)11-21(39)10-17)31-25(42)14-26(43)32-34(31)33(27)28(16-3-7-19(37)8-4-16)30-23(35(32)44)12-22(40)13-24(30)41/h1-14,27-29,33,36-43H/t27-,28+,29-,33-/m1/s1

> <INCHI_KEY>
ZKVAIORTZTYFSI-VGBJTSDXSA-N

> <FORMULA>
C35H26O9

> <MOLECULAR_WEIGHT>
590.584

> <EXACT_MASS>
590.157682417

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
59.67088636419794

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9S,10R,11S,12S)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0^{3,8}.0^{13,17}]heptadeca-1(17),3,5,7,13,15-hexaen-2-one

> <JCHEM_LOGP>
6.816376946

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.732759715190655

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.058761668666751

> <JCHEM_PKA_STRONGEST_BASIC>
-5.000688183819897

> <JCHEM_POLAR_SURFACE_AREA>
178.91

> <JCHEM_REFRACTIVITY>
162.47929999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(9S,10R,11S,12S)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0^{3,8}.0^{13,17}]heptadeca-1(17),3,5,7,13,15-hexaen-2-one

> <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  O   UNK     0       1.668  -1.992   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.594  -0.401   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.973   0.285   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.115  -0.749   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.581  -0.276   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.749  -1.353   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.904   1.229   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.762   2.263   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.288   3.115   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.297   1.790   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.321   2.982   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.972   4.378   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.181   5.442   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.832   6.838   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.274   7.169   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.924   8.565   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.157   5.908   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.506   4.512   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.782   2.963   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.163   1.747   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.198   0.250   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.069  -0.762   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.372  -2.323   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.518  -0.239   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.789   1.277   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.357   0.853   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.612   2.270   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.562   3.809   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.778   4.754   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.205   4.173   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -5.421   5.118   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -6.847   4.538   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -5.210   6.644   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -3.784   7.224   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -3.573   8.750   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -2.568   6.279   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.083   4.237   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.440   5.686   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -0.553   6.863   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -0.030   8.311   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.486   8.583   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       2.009  10.031   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       2.479   7.405   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.956   5.957   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    3   11                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   12                                                       
CONECT   19   11   20   37                                                  
CONECT   20   19   21   27                                                  
CONECT   21   20    2   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   20   28                                                  
CONECT   28   27   29   37                                                  
CONECT   29   28   30   36                                                  
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   29                                                       
CONECT   37   28   19   38                                                  
CONECT   38   37   39   44                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   38                                                       
MASTER        0    0    0    0    0    0    0    0   44    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₂₆O₉

Average Mass

590.5840 Da

Monoisotopic Mass

590.15768 Da

IUPAC Name

(9S,10R,11S,12S)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0^{3,8}.0^{13,17}]heptadeca-1(17),3,5,7,13,15-hexaen-2-one

Traditional Name

(9S,10R,11S,12S)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0^{3,8}.0^{13,17}]heptadeca-1(17),3,5,7,13,15-hexaen-2-one

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)[C@H]1[C@@H]2[C@@H](C3=CC=C(O)C=C3)C3=C(O)C=C(O)C=C3C(=O)C3=C2C([C@@H]1C1=CC(O)=CC(O)=C1)=C(O)C=C3O

InChI Identifier

InChI=1S/C35H26O9/c36-18-5-1-15(2-6-18)27-29(17-9-20(38)11-21(39)10-17)31-25(42)14-26(43)32-34(31)33(27)28(16-3-7-19(37)8-4-16)30-23(35(32)44)12-22(40)13-24(30)41/h1-14,27-29,33,36-43H/t27-,28+,29-,33-/m1/s1

InChI Key

ZKVAIORTZTYFSI-VGBJTSDXSA-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
Cotylelobium lanceolatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzocycloheptenes. Dibenzocycloheptenes are compounds containing a dibenzocycloheptene moiety, which consists of two benzene rings connected by a cycloheptene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Dibenzocycloheptenes

Sub Class

Not Available

Direct Parent

Dibenzocycloheptenes

Alternative Parents

Substituents

Dibenzocycloheptene
Stilbene
Indane
Aryl ketone
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Vinylogous acid
Ketone
Polyol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	6.82	ChemAxon
pKa (Strongest Acidic)	8.06	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	178.91 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	162.48 m³·mol⁻¹	ChemAxon
Polarizability	59.67 Å³	ChemAxon
Number of Rings	7	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

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

102253982

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one (NP0259490)

MOL for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

3D MOL for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

3D SDF for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

3D-SDF for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

PDB for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

3D PDB for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

SMILES for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

INCHI for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

Structure for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)

3D Structure for NP0259490 ((9s,10r,11s,12s)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.0³,⁸.0¹³,¹⁷]heptadeca-1(17),3,5,7,13,15-hexaen-2-one)