NP-MRD: Showing NP-Card for (+)-Balanophotannin B (NP0071980)

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Record Information

Version

2.0

Created at

2022-04-28 17:22:15 UTC

Updated at

2022-04-28 17:22:15 UTC

NP-MRD ID

NP0071980

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Balanophotannin B

Description

(8R,9S,10R,11S,13R)-2,3,9,10,19,20-hexahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]Tetracosa-1(23),2,4,17,19,21-hexaen-11-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. (+)-Balanophotannin B is found in Balanophora japonica. Based on a literature review very few articles have been published on (8R,9S,10R,11S,13R)-2,3,9,10,19,20-hexahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]Tetracosa-1(23),2,4,17,19,21-hexaen-11-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219222D          

 45 50  0  0  1  0            999 V2000
    2.7573   -1.7314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4609   -0.9567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1060   -1.2160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5739   -1.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9017   -1.4921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3516   -0.8005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4690   -2.0995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2881   -1.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.3560   -4.1405    0.0000 C   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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M  END

     RDKit          3D

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M  END


  Mrv1652304282219222D          

 45 50  0  0  1  0            999 V2000
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    6.6927    0.2968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8801    0.5098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0593    1.3151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0342    0.6653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2148    0.3670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5889    0.9297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8496    0.5197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7656    1.7490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5465    2.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1743    1.4925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951    2.8435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1441    2.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6461   -0.8271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2343   -2.3695    0.0000 O   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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  6  0  0  0
 15 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 25 28  1  0  0  0  0
 24 29  1  0  0  0  0
 14 30  1  1  0  0  0
 13 31  1  1  0  0  0
 12 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
 35 36  1  0  0  0  0
  4 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
  3 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 35 41  2  0  0  0  0
 40 42  1  0  0  0  0
 39 43  1  0  0  0  0
  2 44  1  0  0  0  0
  1 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0071980

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1[C@H](OC(=O)\C=C\C2=CC(O)=C(O)C=C2)O[C@@H]2COC(=O)C3=CC(O)=C(O)C4=C3C3=C(O4)C(O)=C(O)C=C3C(=O)O[C@@H]2[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C29H22O16/c30-12-3-1-9(5-13(12)31)2-4-17(34)43-29-23(38)22(37)24-16(42-29)8-41-27(39)10-6-14(32)20(35)25-18(10)19-11(28(40)45-24)7-15(33)21(36)26(19)44-25/h1-7,16,22-24,29-33,35-38H,8H2/b4-2+/t16-,22+,23-,24+,29+/m1/s1

> <INCHI_KEY>
JYYDBEUJTVLEFP-DSWRNUMTSA-N

> <FORMULA>
C29H22O16

> <MOLECULAR_WEIGHT>
626.479

> <EXACT_MASS>
626.090784628

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
59.14318086437463

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(8R,9S,10R,11S,13R)-2,3,9,10,19,20-hexahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0^{5,23}.0^{8,13}.0^{17,22}]tetracosa-1(23),2,4,17,19,21-hexaen-11-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
2.49

> <JCHEM_LOGP>
2.0753147323333327

> <ALOGPS_LOGS>
-2.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.597353933859551

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.75584663548875

> <JCHEM_PKA_STRONGEST_BASIC>
-3.694111205868066

> <JCHEM_POLAR_SURFACE_AREA>
263.10999999999996

> <JCHEM_REFRACTIVITY>
146.13130000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.08e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(8R,9S,10R,11S,13R)-2,3,9,10,19,20-hexahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0^{5,23}.0^{8,13}.0^{17,22}]tetracosa-1(23),2,4,17,19,21-hexaen-11-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.147  -3.232   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.594  -1.786   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.582  -0.566   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.134  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.665  -2.270   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.671  -3.491   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.150  -2.785   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.990  -1.494   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      10.209  -3.919   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.738  -3.609   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.660  -2.343   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.132  -0.877   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.638  -0.553   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.671  -1.695   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.198  -3.161   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.693  -3.485   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      16.232  -4.303   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      15.759  -5.769   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      14.254  -6.092   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      16.792  -6.911   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.298  -6.587   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.331  -7.729   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      20.837  -7.405   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      21.870  -8.547   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      21.398 -10.013   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      19.892 -10.337   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      18.859  -9.195   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      22.431 -11.155   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      23.376  -8.223   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      17.176  -1.371   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      15.110   0.913   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      12.493   0.554   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      10.976   0.952   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      11.311   2.455   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.397   1.242   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.868   0.685   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.699   1.735   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       5.319   0.970   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       7.029   3.265   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.487   3.793   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.659   2.786   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.764   5.308   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       5.869   4.278   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       3.073  -1.544   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       4.171  -4.423   0.000  0.00  0.00           O+0
CONECT    1    2    6   45                                                  
CONECT    2    1    3   44                                                  
CONECT    3    2    4   38                                                  
CONECT    4    3    5   36                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   32                                                  
CONECT   13   12   14   31                                                  
CONECT   14   13   15   30                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15   11                                                       
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26   22                                                       
CONECT   28   25                                                            
CONECT   29   24                                                            
CONECT   30   14                                                            
CONECT   31   13                                                            
CONECT   32   12   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   41                                                  
CONECT   36   35    4   37                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37    3                                                       
CONECT   39   37   40   43                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40   35                                                       
CONECT   42   40                                                            
CONECT   43   39                                                            
CONECT   44    2                                                            
CONECT   45    1                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  100    0
END

View in JSmol

Synonyms

Value	Source
(8R,9S,10R,11S,13R)-2,3,9,10,19,20-Hexahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0,.0,.0,]tetracosa-1(23),2,4,17,19,21-hexaen-11-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₉H₂₂O₁₆

Average Mass

626.4790 Da

Monoisotopic Mass

626.09078 Da

IUPAC Name

(8R,9S,10R,11S,13R)-2,3,9,10,19,20-hexahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0^{5,23}.0^{8,13}.0^{17,22}]tetracosa-1(23),2,4,17,19,21-hexaen-11-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

O[C@H]1[C@H](OC(=O)\C=C\C2=CC(O)=C(O)C=C2)O[C@@H]2COC(=O)C3=CC(O)=C(O)C4=C3C3=C(O4)C(O)=C(O)C=C3C(=O)O[C@@H]2[C@H]1O

InChI Identifier

InChI=1S/C29H22O16/c30-12-3-1-9(5-13(12)31)2-4-17(34)43-29-23(38)22(37)24-16(42-29)8-41-27(39)10-6-14(32)20(35)25-18(10)19-11(28(40)45-24)7-15(33)21(36)26(19)44-25/h1-7,16,22-24,29-33,35-38H,8H2/b4-2+/t16-,22+,23-,24+,29+/m1/s1

InChI Key

JYYDBEUJTVLEFP-DSWRNUMTSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Balanophora japonica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Hydroxycinnamic acid glycoside
Dibenzofuran
Cinnamic acid ester
Hydroxycinnamic acid or derivatives
Gallic acid or derivatives
Coumaric acid or derivatives
Cinnamic acid or derivatives
Dihydroxybenzoic acid
Tricarboxylic acid or derivatives
Benzofuran
Styrene
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acid ester
Fatty acyl
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Furan
Secondary alcohol
Lactone
Carboxylic acid ester
1,2-diol
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	2.49	ALOGPS
logP	2.08	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	6.76	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	263.11 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	146.13 m³·mol⁻¹	ChemAxon
Polarizability	59.14 Å³	ChemAxon
Number of Rings	6	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

163030653

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Balanophotannin B (NP0071980)

MOL for NP0071980 ((+)-Balanophotannin B)

3D MOL for NP0071980 ((+)-Balanophotannin B)

3D SDF for NP0071980 ((+)-Balanophotannin B)

3D-SDF for NP0071980 ((+)-Balanophotannin B)

PDB for NP0071980 ((+)-Balanophotannin B)

3D PDB for NP0071980 ((+)-Balanophotannin B)

SMILES for NP0071980 ((+)-Balanophotannin B)

INCHI for NP0071980 ((+)-Balanophotannin B)

Structure for NP0071980 ((+)-Balanophotannin B)

3D Structure for NP0071980 ((+)-Balanophotannin B)