NP-MRD: Showing NP-Card for 2-pentadecylbenzene-1,3-diol (NP0145446)

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Record Information

Version

2.0

Created at

2022-09-02 00:38:44 UTC

Updated at

2022-09-02 00:38:44 UTC

NP-MRD ID

NP0145446

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-pentadecylbenzene-1,3-diol

Description

Pentadecylresorcinol belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3. 2-pentadecylbenzene-1,3-diol is found in Ginkgo biloba. 2-pentadecylbenzene-1,3-diol was first documented in 2019 (PMID: 30724178). Based on a literature review a small amount of articles have been published on pentadecylresorcinol (PMID: 35584958) (PMID: 35898902).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 59 59  0  0  0  0  0  0  0  0999 V2000
   -8.8767    0.2172    1.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0735   -0.1957    0.4579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6079   -0.2056    0.8604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8014   -0.6150   -0.3360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3029   -0.6562   -0.0281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7752    0.6396    0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3529    0.7358    0.7525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2707    0.6013   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1924   -0.6481   -0.9923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0099   -0.8514   -1.8617 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3416   -1.0659   -1.2966 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9745   -0.1026   -0.3859 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4028   -0.5222    0.0038 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2433   -0.5929   -1.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6911   -0.9506   -0.8822 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2251    0.1027    0.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6669    1.2967   -0.5548 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6630    1.5538   -1.8902 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1542    2.3147    0.2827 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1998    2.1450    1.6467 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7684    0.9743    2.2150 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2826   -0.0415    1.3935 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8404   -1.2304    1.9439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8727    1.3374    1.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9201   -0.1784    1.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3194   -0.1267    2.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3435   -1.2474    0.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2707    0.5058   -0.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3767    0.8185    1.2070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5162   -0.9719    1.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9882    0.0594   -1.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1170   -1.6332   -0.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8178   -1.0814   -0.8908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1697   -1.4025    0.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9785    1.4256   -0.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3615    1.0927    1.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1585    1.7070    1.3565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1159   -0.0311    1.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3352    0.9658    0.2612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4949    1.4640   -1.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0624   -0.5501   -1.7741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4615   -1.5446   -0.4054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0198    0.0211   -2.5934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2673   -1.7227   -2.5594 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988   -2.1077   -0.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -1.2007   -2.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4243   -0.0829    0.6330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0592    0.9169   -0.7929 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2932   -1.5163    0.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7901    0.2449    0.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8462   -1.4185   -1.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2283    0.3380   -1.7846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2365   -0.9534   -1.8538 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7415   -1.9533   -0.4537 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3532    0.8941   -2.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5052    3.2618   -0.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5843    2.9620    2.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7916    0.8091    3.2857 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4755   -2.0047    1.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 16  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 13 50  1  0
 14 51  1  0
 14 52  1  0
 15 53  1  0
 15 54  1  0
 18 55  1  0
 19 56  1  0
 20 57  1  0
 21 58  1  0
 23 59  1  0
M  END


  Mrv1652309022202382D          

 23 23  0  0  0  0            999 V2000
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  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
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0145446

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC1=C(O)C=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-20(22)17-15-18-21(19)23/h15,17-18,22-23H,2-14,16H2,1H3

> <INCHI_KEY>
NLCUMKKFPDGYTH-UHFFFAOYSA-N

> <FORMULA>
C21H36O2

> <MOLECULAR_WEIGHT>
320.517

> <EXACT_MASS>
320.271530399

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.91720361915325

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-pentadecylbenzene-1,3-diol

> <ALOGPS_LOGP>
8.07

> <JCHEM_LOGP>
8.103497872

> <ALOGPS_LOGS>
-5.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.958949821179129

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.610683654907042

> <JCHEM_PKA_STRONGEST_BASIC>
-5.6532742036392

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
99.475

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.24e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-pentadecylbenzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002 -16.940   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336 -16.170   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669 -16.940   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.003 -16.170   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.337 -16.940   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.670 -16.170   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.004 -16.940   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.338 -16.170   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.672 -16.940   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.005 -16.170   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.339 -16.940   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      22.673 -16.170   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      24.006 -16.940   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      25.340 -16.170   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.674 -16.940   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.007 -16.170   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      28.007 -14.630   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      29.341 -16.940   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.341 -18.480   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      28.007 -19.250   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      26.674 -18.480   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      25.340 -19.250   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₆O₂

Average Mass

320.5170 Da

Monoisotopic Mass

320.27153 Da

IUPAC Name

2-pentadecylbenzene-1,3-diol

Traditional Name

2-pentadecylbenzene-1,3-diol

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC1=C(O)C=CC=C1O

InChI Identifier

InChI=1S/C21H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-20(22)17-15-18-21(19)23/h15,17-18,22-23H,2-14,16H2,1H3

InChI Key

NLCUMKKFPDGYTH-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
Ginkgo biloba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Organic oxygen compound
Hydrocarbon derivative
Organooxygen 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	8.07	ALOGPS
logP	8.1	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	9.61	ChemAxon
pKa (Strongest Basic)	-5.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	99.48 m³·mol⁻¹	ChemAxon
Polarizability	41.92 Å³	ChemAxon
Number of Rings	1	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

C00002662

Chemspider ID

10752487

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

22016521

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

He Q, Ma P, Torshizi R: The Impact of Some Natural Phenolic Compounds on alpha-Glucosidase and Sorbitol Dehydrogenase Enzymes, and Anti-leukemia Cancer Potential, Spin Density Distributions, and in silico Studies. J Oleo Sci. 2022 Jun 3;71(6):863-873. doi: 10.5650/jos.ess22029. Epub 2022 May 18. [PubMed:35584958 ]
Wei L, Zhang Q, Xie A, Xiao Y, Guo K, Mu S, Xie Y, Li Z, He T: Isolation of Bioactive Compounds, Antibacterial Activity, and Action Mechanism of Spore Powder From Aspergillus niger xj. Front Microbiol. 2022 Jul 11;13:934857. doi: 10.3389/fmicb.2022.934857. eCollection 2022. [PubMed:35898902 ]
Arriola NDA, Chater PI, Wilcox M, Lucini L, Rocchetti G, Dalmina M, Pearson JP, de Mello Castanho Amboni RD: Encapsulation of stevia rebaudiana Bertoni aqueous crude extracts by ionic gelation - Effects of alginate blends and gelling solutions on the polyphenolic profile. Food Chem. 2019 Mar 1;275:123-134. doi: 10.1016/j.foodchem.2018.09.086. Epub 2018 Sep 14. [PubMed:30724178 ]
LOTUS database [Link]

Showing NP-Card for 2-pentadecylbenzene-1,3-diol (NP0145446)

MOL for NP0145446 (2-pentadecylbenzene-1,3-diol)

3D MOL for NP0145446 (2-pentadecylbenzene-1,3-diol)

3D SDF for NP0145446 (2-pentadecylbenzene-1,3-diol)

3D-SDF for NP0145446 (2-pentadecylbenzene-1,3-diol)

PDB for NP0145446 (2-pentadecylbenzene-1,3-diol)

3D PDB for NP0145446 (2-pentadecylbenzene-1,3-diol)

SMILES for NP0145446 (2-pentadecylbenzene-1,3-diol)

INCHI for NP0145446 (2-pentadecylbenzene-1,3-diol)

Structure for NP0145446 (2-pentadecylbenzene-1,3-diol)

3D Structure for NP0145446 (2-pentadecylbenzene-1,3-diol)