NP-MRD: Showing NP-Card for (-)-Upunaphenol I (NP0072530)

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Record Information

Version

2.0

Created at

2022-04-28 17:52:31 UTC

Updated at

2022-04-28 17:52:31 UTC

NP-MRD ID

NP0072530

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Upunaphenol I

Description

(1R,2R,3R,10R,11R,22R,23R,30R)-3,11,22,30-tetrakis(4-hydroxyphenyl)-12,21-dioxanonacyclo[18.10.2.2¹³,¹⁶.0²,¹⁵.0⁴,⁹.0¹⁰,¹⁴.0¹⁷,³¹.0²³,³².0²⁴,²⁹]Tetratriaconta-4(9),5,7,13,15,17(31),18,20(32),24(29),25,27,33-dodecaene-5,7,18,26,28,33-hexol belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. (-)-Upunaphenol I is found in Upuna borneensis. Based on a literature review very few articles have been published on (1R,2R,3R,10R,11R,22R,23R,30R)-3,11,22,30-tetrakis(4-hydroxyphenyl)-12,21-dioxanonacyclo[18.10.2.2¹³,¹⁶.0²,¹⁵.0⁴,⁹.0¹⁰,¹⁴.0¹⁷,³¹.0²³,³².0²⁴,²⁹]Tetratriaconta-4(9),5,7,13,15,17(31),18,20(32),24(29),25,27,33-dodecaene-5,7,18,26,28,33-hexol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219522D          

 68 80  0  0  1  0            999 V2000
    3.4207    1.9727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6774    1.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0572    2.9019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.4822    2.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2705    3.0388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9071    2.6889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5597    3.1937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1814    5.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4244    6.6166    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
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  5  6  1  6  0  0  0
  1  6  2  0  0  0  0
  6  7  1  0  0  0  0
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  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  1 10  1  0  0  0  0
 10 11  1  0  0  0  0
  8 12  1  0  0  0  0
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M  END

     RDKit          3D

108120  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652304282219522D          

 68 80  0  0  1  0            999 V2000
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 65 68  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0072530

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)[C@@H]1OC2=C3[C@H]1C1=C([C@H]([C@H]4[C@@H]5[C@H](C6=CC=C(O)C=C6)C6=C(C=C(O)C=C6O)[C@H]6[C@@H](OC7=C6C5=C(C(O)=C7)C(C(O)=C2)=C34)C2=CC=C(O)C=C2)C2=CC=C(O)C=C2)C(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C56H40O12/c57-27-9-1-23(2-10-27)41-43-33(17-31(61)19-35(43)63)45-49-39(67-55(45)25-5-13-29(59)14-6-25)21-37(65)47-48-38(66)22-40-50-46(56(68-40)26-7-15-30(60)16-8-26)34-18-32(62)20-36(64)44(34)42(24-3-11-28(58)12-4-24)52(54(48)50)51(41)53(47)49/h1-22,41-42,45-46,51-52,55-66H/t41-,42-,45-,46-,51+,52+,55+,56+/m1/s1

> <INCHI_KEY>
GNHFEBBJYOONPN-YHTMVWKPSA-N

> <FORMULA>
C56H40O12

> <MOLECULAR_WEIGHT>
904.924

> <EXACT_MASS>
904.251976728

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
95.83099573650208

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,10R,11R,22R,23R,30R)-3,11,22,30-tetrakis(4-hydroxyphenyl)-12,21-dioxanonacyclo[18.10.2.2^{13,16}.0^{2,15}.0^{4,9}.0^{10,14}.0^{17,31}.0^{23,32}.0^{24,29}]tetratriaconta-4(9),5,7,13,15,17(31),18,20(32),24(29),25,27,33-dodecaene-5,7,18,26,28,33-hexol

> <ALOGPS_LOGP>
5.98

> <JCHEM_LOGP>
10.104341265333332

> <ALOGPS_LOGS>
-5.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
13

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.925955947262329

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.497757912377134

> <JCHEM_PKA_STRONGEST_BASIC>
-5.453838334816322

> <JCHEM_POLAR_SURFACE_AREA>
220.75999999999996

> <JCHEM_REFRACTIVITY>
252.18819999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,10R,11R,22R,23R,30R)-3,11,22,30-tetrakis(4-hydroxyphenyl)-12,21-dioxanonacyclo[18.10.2.2^{13,16}.0^{2,15}.0^{4,9}.0^{10,14}.0^{17,31}.0^{23,32}.0^{24,29}]tetratriaconta-4(9),5,7,13,15,17(31),18,20(32),24(29),25,27,33-dodecaene-5,7,18,26,28,33-hexol

> <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       6.385   3.682   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.998   3.014   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.725   3.881   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.840   5.417   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.227   6.085   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.500   5.218   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.972   5.672   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.160   5.019   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.045   3.484   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.658   2.815   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.543   1.279   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      10.378   5.962   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.858   7.411   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.534   7.106   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.764   8.440   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.241   8.669   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.112   7.621   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.678   8.183   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.475   7.223   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.041   7.785   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.811   9.308   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.015  10.269   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.449   9.706   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.623   9.870   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.678  10.102   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.638  11.306   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.161  11.077   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.724   9.644   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.121  12.281   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       4.155  10.331   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      10.597   8.763   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.795  10.078   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.534  11.429   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.073  11.466   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.874  10.151   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.136   8.799   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.812  12.817   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       2.711   6.464   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.188   6.234   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.418   4.901   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.981   3.467   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.453   3.013   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.223   1.677   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.496   0.810   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.883   1.478   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       6.156   0.611   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       0.727   1.312   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -0.083   2.622   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -1.600   2.886   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -2.588   1.705   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -4.105   1.970   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -4.634   3.416   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -3.646   4.597   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -2.129   4.333   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -6.151   3.681   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      -1.122   4.900   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -1.892   6.234   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -1.122   7.568   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       0.418   7.568   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0       1.188   8.902   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      -3.432   6.234   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0       3.165   7.936   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0       2.117   9.065   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0       2.571  10.536   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0       4.072  10.879   0.000  0.00  0.00           C+0
HETATM   66  C   UNK     0       5.120   9.751   0.000  0.00  0.00           C+0
HETATM   67  C   UNK     0       4.666   8.279   0.000  0.00  0.00           C+0
HETATM   68  O   UNK     0       4.526  12.351   0.000  0.00  0.00           O+0
CONECT    1    2    6   10                                                  
CONECT    2    1    3   45                                                  
CONECT    3    2    4   42                                                  
CONECT    4    3    5   38                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8   14                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9    1   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14   31                                                  
CONECT   14   13    7   15                                                  
CONECT   15   14   16   28                                                  
CONECT   16   15   17   25                                                  
CONECT   17   16    5   18                                                  
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   21                                                            
CONECT   25   16   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27   15                                                       
CONECT   29   27                                                            
CONECT   30   25                                                            
CONECT   31   13   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   34                                                            
CONECT   38    4   39   62                                                  
CONECT   39   38   40   59                                                  
CONECT   40   39   41   56                                                  
CONECT   41   40   42   48                                                  
CONECT   42   41    3   43                                                  
CONECT   43   42   44   47                                                  
CONECT   44   43   45                                                       
CONECT   45   44    2   46                                                  
CONECT   46   45                                                            
CONECT   47   43   48                                                       
CONECT   48   47   41   49                                                  
CONECT   49   48   50   54                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53   55                                                  
CONECT   53   52   54                                                       
CONECT   54   53   49                                                       
CONECT   55   52                                                            
CONECT   56   40   57                                                       
CONECT   57   56   58   61                                                  
CONECT   58   57   59                                                       
CONECT   59   58   39   60                                                  
CONECT   60   59                                                            
CONECT   61   57                                                            
CONECT   62   38   63   67                                                  
CONECT   63   62   64                                                       
CONECT   64   63   65                                                       
CONECT   65   64   66   68                                                  
CONECT   66   65   67                                                       
CONECT   67   66   62                                                       
CONECT   68   65                                                            
MASTER        0    0    0    0    0    0    0    0   68    0  160    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₆H₄₀O₁₂

Average Mass

904.9240 Da

Monoisotopic Mass

904.25198 Da

IUPAC Name

(1R,2R,3R,10R,11R,22R,23R,30R)-3,11,22,30-tetrakis(4-hydroxyphenyl)-12,21-dioxanonacyclo[18.10.2.2^{13,16}.0^{2,15}.0^{4,9}.0^{10,14}.0^{17,31}.0^{23,32}.0^{24,29}]tetratriaconta-4(9),5,7,13,15,17(31),18,20(32),24(29),25,27,33-dodecaene-5,7,18,26,28,33-hexol

Traditional Name

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)[C@@H]1OC2=C3[C@H]1C1=C([C@H]([C@H]4[C@@H]5[C@H](C6=CC=C(O)C=C6)C6=C(C=C(O)C=C6O)[C@H]6[C@@H](OC7=C6C5=C(C(O)=C7)C(C(O)=C2)=C34)C2=CC=C(O)C=C2)C2=CC=C(O)C=C2)C(O)=CC(O)=C1

InChI Identifier

InChI=1S/C56H40O12/c57-27-9-1-23(2-10-27)41-43-33(17-31(61)19-35(43)63)45-49-39(67-55(45)25-5-13-29(59)14-6-25)21-37(65)47-48-38(66)22-40-50-46(56(68-40)26-7-15-30(60)16-8-26)34-18-32(62)20-36(64)44(34)42(24-3-11-28(58)12-4-24)52(54(48)50)51(41)53(47)49/h1-22,41-42,45-46,51-52,55-66H/t41-,42-,45-,46-,51+,52+,55+,56+/m1/s1

InChI Key

GNHFEBBJYOONPN-YHTMVWKPSA-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
Upuna borneensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
4-prenylated 2-arybenzofuran
Linear 1,7-diphenylheptane skeleton
Dibenzocycloheptene
Phenanthrene
Naphthofuran
1-naphthol
Naphthalene
Coumaran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	5.98	ALOGPS
logP	10.1	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	8.5	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	220.76 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	252.19 m³·mol⁻¹	ChemAxon
Polarizability	95.83 Å³	ChemAxon
Number of Rings	13	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

163104153

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Upunaphenol I (NP0072530)

MOL for NP0072530 ((-)-Upunaphenol I)

3D MOL for NP0072530 ((-)-Upunaphenol I)

3D SDF for NP0072530 ((-)-Upunaphenol I)

3D-SDF for NP0072530 ((-)-Upunaphenol I)

PDB for NP0072530 ((-)-Upunaphenol I)

3D PDB for NP0072530 ((-)-Upunaphenol I)

SMILES for NP0072530 ((-)-Upunaphenol I)

INCHI for NP0072530 ((-)-Upunaphenol I)

Structure for NP0072530 ((-)-Upunaphenol I)

3D Structure for NP0072530 ((-)-Upunaphenol I)