NP-MRD: Showing NP-Card for 4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol (NP0225346)

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Record Information

Version

2.0

Created at

2022-09-06 04:02:25 UTC

Updated at

2022-09-06 04:02:25 UTC

NP-MRD ID

NP0225346

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol

Description

4'-[2,4-Dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol belongs to the class of organic compounds known as tannins. These are naturally occurring polyphenols which be categorized into four main classes: Hydrolyzable tannin (based on ellagic acid or gallic acid), condensed tannins (made of oligomeric or polymeric proanthocyanidins), complex tannins (made of a catechin bound to a gallotannin or elagitannin), and phlorotannins (oligomers of phloroglucinol). 4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol is found in Cystophora torulosa. Based on a literature review very few articles have been published on 4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062206022D          

 36 39  0  0  0  0            999 V2000
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -13.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -13.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2 36  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
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   -0.2327   -2.4404   -2.0265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7740   -1.4116   -0.5382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1615   -0.1953   -0.8758 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1572    0.0187   -0.4776 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1682    0.1168   -1.4419 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4692    0.3234   -1.0515 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5034    0.4255   -2.0025 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8456    0.4426    0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2282    0.6608    0.6514 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1193   -0.3589    0.9091 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.8481    1.2293    1.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1528    1.5343    1.7379 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2270    1.1643   -0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2502    4.2998   -1.7281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1528    3.7599   -0.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8333    1.5999    1.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3819   -4.7034   -1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2056   -3.1847   -2.5135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858    0.0266   -2.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3050    0.3477   -3.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2594   -2.4700    0.9672 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1078   -0.8940    1.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4602    2.4921    1.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2632    3.2711    1.1953 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4987    0.3949    3.2449 H   0  0  0  0  0  0  0  0  0  0  0  0
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 30 50  1  0
 35 53  1  0
 36 54  1  0
M  END


  Mrv1652309062206022D          

 36 39  0  0  0  0            999 V2000
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0225346

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC(O)=C(OC2=CC(O)=CC(O)=C2OC2=CC(O)=C(C(O)=C2)C2=C(O)C=C(O)C=C2O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H18O12/c25-9-1-13(28)21(14(29)2-9)22-15(30)7-12(8-16(22)31)35-24-19(34)5-11(27)6-20(24)36-23-17(32)3-10(26)4-18(23)33/h1-8,25-34H

> <INCHI_KEY>
LWTNYFVJYLWADS-UHFFFAOYSA-N

> <FORMULA>
C24H18O12

> <MOLECULAR_WEIGHT>
498.396

> <EXACT_MASS>
498.07982602

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
46.74540152644568

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol

> <JCHEM_LOGP>
3.5853923273333326

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.846301640086555

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.702890090672704

> <JCHEM_PKA_STRONGEST_BASIC>
-5.3749289846217065

> <JCHEM_POLAR_SURFACE_AREA>
220.75999999999996

> <JCHEM_REFRACTIVITY>
123.48479999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.001 -14.630   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334 -16.170   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000 -16.940   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001 -16.170   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.667 -18.480   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334 -19.250   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.334 -20.790   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.000 -18.480   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.334 -19.250   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.334 -20.790   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667 -21.560   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667 -23.100   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.001 -23.870   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334 -23.870   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334 -25.410   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667 -26.180   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.001 -25.410   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.667 -27.720   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334 -28.490   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.334 -30.030   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.000 -27.720   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.000 -26.180   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.334 -25.410   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.000 -23.100   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.334 -23.870   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       0.000 -21.560   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.334 -14.630   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   34                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    8   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   33                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   31                                                  
CONECT   22   21   23   29                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   22   30                                                  
CONECT   30   29                                                            
CONECT   31   21   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   17                                                       
CONECT   34    6   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34    2                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₁₈O₁₂

Average Mass

498.3960 Da

Monoisotopic Mass

498.07983 Da

IUPAC Name

4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol

Traditional Name

4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol

CAS Registry Number

Not Available

SMILES

OC1=CC(O)=C(OC2=CC(O)=CC(O)=C2OC2=CC(O)=C(C(O)=C2)C2=C(O)C=C(O)C=C2O)C(O)=C1

InChI Identifier

InChI=1S/C24H18O12/c25-9-1-13(28)21(14(29)2-9)22-15(30)7-12(8-16(22)31)35-24-19(34)5-11(27)6-20(24)36-23-17(32)3-10(26)4-18(23)33/h1-8,25-34H

InChI Key

LWTNYFVJYLWADS-UHFFFAOYSA-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
Cystophora torulosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tannins. These are naturally occurring polyphenols which be categorized into four main classes: Hydrolyzable tannin (based on ellagic acid or gallic acid), condensed tannins (made of oligomeric or polymeric proanthocyanidins), complex tannins (made of a catechin bound to a gallotannin or elagitannin), and phlorotannins (oligomers of phloroglucinol).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Not Available

Direct Parent

Tannins

Alternative Parents

Substituents

Tannin
Diphenylether
Biphenyl
Diaryl ether
Benzenetriol
Phloroglucinol derivative
Phenoxy compound
Resorcinol
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Polyol
Ether
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	3.59	ChemAxon
pKa (Strongest Acidic)	6.7	ChemAxon
pKa (Strongest Basic)	-5.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	220.76 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	123.48 m³·mol⁻¹	ChemAxon
Polarizability	46.75 Å³	ChemAxon
Number of Rings	4	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

10477266

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21775035

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol (NP0225346)

MOL for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

3D MOL for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

3D SDF for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

3D-SDF for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

PDB for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

3D PDB for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

SMILES for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

INCHI for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

Structure for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)

3D Structure for NP0225346 (4'-[2,4-dihydroxy-6-(2,4,6-trihydroxyphenoxy)phenoxy]-[1,1'-biphenyl]-2,2',4,6,6'-pentol)