NP-MRD: Showing NP-Card for 5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol (NP0238218)

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Record Information

Version

2.0

Created at

2022-09-06 21:34:20 UTC

Updated at

2022-09-06 21:34:21 UTC

NP-MRD ID

NP0238218

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol

Description

5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol is found in Thelephora vialis. CHEMBL219810 is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652310101709312D          

 25 28  0  0  0  0            999 V2000
   -1.1544    1.5402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9614    1.7117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2585    0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995    0.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5134    1.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3464    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3204    1.2701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2575   -0.8137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7674    0.7556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3896   -0.8137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2243   -1.1567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2046    1.9817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    1.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  7  1  2  0  0  0  0
  7  2  1  0  0  0  0
  8  3  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  5  2  0  0  0  0
 11  6  2  0  0  0  0
 11 10  1  0  0  0  0
 12  6  1  0  0  0  0
 12  9  2  0  0  0  0
 13  7  1  0  0  0  0
 14  9  1  0  0  0  0
 15 13  2  0  0  0  0
 16 14  2  0  0  0  0
 16 15  1  0  0  0  0
 17 13  1  0  0  0  0
 18 14  1  0  0  0  0
 18 17  2  0  0  0  0
 19  8  1  0  0  0  0
 20 10  1  0  0  0  0
 21 11  1  0  0  0  0
 22 15  1  0  0  0  0
 23 16  1  0  0  0  0
 24 17  1  0  0  0  0
 25 12  1  0  0  0  0
 25 18  1  0  0  0  0
M  END

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
   -6.9770    0.1299    0.3787 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5907    0.0948    0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8079    0.8208    1.1527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4440    0.8171    1.0848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7806    0.0706    0.1068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3249    0.0552    0.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6897    1.2121   -0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4428    2.3068   -0.8224 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6833    1.2859   -0.5098 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3402    2.3907   -0.9633 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4264    0.1684   -0.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7926   -0.9678    0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162   -1.8488    0.6669 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -1.3826    0.4397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1612   -1.9500    0.6123 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2737   -1.2166    0.2863 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5116   -1.7639    0.4522 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1547    0.0797   -0.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2822    0.7967   -0.5344 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9123    0.6556   -0.3898 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7920   -0.0815   -0.0620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5856   -1.0361    0.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2289   -2.1656    0.9080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5752   -0.6444   -0.7640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9565   -0.6488   -0.7054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4010    0.6802    1.0959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2852    1.4178    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8102    1.3723    1.7594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1108    3.1713   -1.1744 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8983    3.2231   -1.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3090   -2.9487    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6772   -2.6915    0.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2179    1.7387   -0.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8071    1.6630   -0.7741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1995   -2.3166    1.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1238   -1.2506   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5247   -1.2373   -1.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5 24  1  0
 24 25  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  2  0
 11 21  1  0
 21 14  2  0
 14 13  1  0
 13 12  1  0
 12 22  2  0
 22 23  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  2  0
 25  2  1  0
 22  6  1  0
 12 11  1  0
 20 21  1  0
  1 26  1  0
  3 27  1  0
  4 28  1  0
 24 36  1  0
 25 37  1  0
  8 29  1  0
 10 30  1  0
 23 35  1  0
 15 31  1  0
 17 32  1  0
 19 33  1  0
 20 34  1  0
M  END


  Mrv1652310101709312D          

 25 28  0  0  0  0            999 V2000
   -1.1544    1.5402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9614    1.7117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2585    0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8995    0.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5134    1.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3464    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9604    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925    0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624   -0.2006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694   -0.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4595    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665    1.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3204    1.2701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2575   -0.8137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7674    0.7556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3896   -0.8137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2243   -1.1567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2046    1.9817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9339    1.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  7  1  2  0  0  0  0
  7  2  1  0  0  0  0
  8  3  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  5  2  0  0  0  0
 11  6  2  0  0  0  0
 11 10  1  0  0  0  0
 12  6  1  0  0  0  0
 12  9  2  0  0  0  0
 13  7  1  0  0  0  0
 14  9  1  0  0  0  0
 15 13  2  0  0  0  0
 16 14  2  0  0  0  0
 16 15  1  0  0  0  0
 17 13  1  0  0  0  0
 18 14  1  0  0  0  0
 18 17  2  0  0  0  0
 19  8  1  0  0  0  0
 20 10  1  0  0  0  0
 21 11  1  0  0  0  0
 22 15  1  0  0  0  0
 23 16  1  0  0  0  0
 24 17  1  0  0  0  0
 25 12  1  0  0  0  0
 25 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0238218

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)C1=C(O)C(O)=C2C3=C(OC2=C1O)C=C(O)C(O)=C3

> <INCHI_IDENTIFIER>
InChI=1S/C18H12O7/c19-8-3-1-7(2-4-8)13-15(22)16(23)14-9-5-10(20)11(21)6-12(9)25-18(14)17(13)24/h1-6,19-24H

> <INCHI_KEY>
KPLKPGSATMNRTH-UHFFFAOYSA-N

> <FORMULA>
C18H12O7

> <MOLECULAR_WEIGHT>
340.287

> <EXACT_MASS>
340.058302726

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
33.83838843856849

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6,10,12-hexaene-3,4,6,11,12-pentol

> <ALOGPS_LOGP>
2.41

> <JCHEM_LOGP>
2.9770805289999998

> <ALOGPS_LOGS>
-2.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.89375635845238

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.914167579350141

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9259919029212726

> <JCHEM_POLAR_SURFACE_AREA>
134.52

> <JCHEM_REFRACTIVITY>
88.2484

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6,10,12-hexaene-3,4,6,11,12-pentol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-OCT-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-OCT-17         0                                  
HETATM    1  C   UNK     0      -2.155   2.875   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.709   0.266   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.661   3.195   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.216   0.586   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.410  -0.695   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.362   2.235   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.679   1.410   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.692   2.051   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.380   0.450   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.917  -0.374   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.393   1.090   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.856   1.914   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.173   1.090   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.840   0.450   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.303  -0.374   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.810  -0.695   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.858   2.235   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.364   1.914   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.198   2.371   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.947  -1.519   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.899   1.410   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -0.727  -1.519   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.285  -2.159   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.382   3.699   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.610   2.820   0.000  0.00  0.00           O+0
CONECT    1    3    7                                                       
CONECT    2    4    7                                                       
CONECT    3    1    8                                                       
CONECT    4    2    8                                                       
CONECT    5    9   10                                                       
CONECT    6   11   12                                                       
CONECT    7    1    2   13                                                  
CONECT    8    3    4   19                                                  
CONECT    9    5   12   14                                                  
CONECT   10    5   11   20                                                  
CONECT   11    6   10   21                                                  
CONECT   12    6    9   25                                                  
CONECT   13    7   15   17                                                  
CONECT   14    9   16   18                                                  
CONECT   15   13   16   22                                                  
CONECT   16   14   15   23                                                  
CONECT   17   13   18   24                                                  
CONECT   18   14   17   25                                                  
CONECT   19    8                                                            
CONECT   20   10                                                            
CONECT   21   11                                                            
CONECT   22   15                                                            
CONECT   23   16                                                            
CONECT   24   17                                                            
CONECT   25   12   18                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₂O₇

Average Mass

340.2870 Da

Monoisotopic Mass

340.05830 Da

IUPAC Name

5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6,10,12-hexaene-3,4,6,11,12-pentol

Traditional Name

5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6,10,12-hexaene-3,4,6,11,12-pentol

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)C1=C(O)C(O)=C2C3=C(OC2=C1O)C=C(O)C(O)=C3

InChI Identifier

InChI=1S/C18H12O7/c19-8-3-1-7(2-4-8)13-15(22)16(23)14-9-5-10(20)11(21)6-12(9)25-18(14)17(13)24/h1-6,19-24H

InChI Key

KPLKPGSATMNRTH-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
Thelephora vialis	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	2.41	ALOGPS
logP	2.98	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	7.91	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	134.52 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.25 m³·mol⁻¹	ChemAxon
Polarizability	33.84 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0178594

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

10065824

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol (NP0238218)

MOL for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

3D MOL for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

3D SDF for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

3D-SDF for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

PDB for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

3D PDB for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

SMILES for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

INCHI for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

Structure for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)

3D Structure for NP0238218 (5-(4-hydroxyphenyl)-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-3,4,6,11,12-pentol)