NP-MRD: Showing NP-Card for 5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol (NP0146099)

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Record Information

Version

2.0

Created at

2022-09-02 01:25:48 UTC

Updated at

2022-09-02 01:25:48 UTC

NP-MRD ID

NP0146099

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol

Description

5-(2R-hydroxy-pentadecyl)resorcinol belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. 5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol is found in Ardisia virens. Based on a literature review very few articles have been published on 5-(2r-hydroxy-pentadecyl)resorcinol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 60 60  0  0  0  0  0  0  0  0999 V2000
   -6.2196    2.7091   -1.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4241    2.4086   -0.5406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0765    1.3016    0.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2040    0.0291   -0.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9036   -0.5568   -0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9449   -0.8803    0.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6766   -1.4879   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9790   -0.5631   -1.3526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7190   -1.1936   -1.8855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2135   -1.5014   -0.7407 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4959   -2.1178   -1.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -2.4295   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982   -1.2127    0.6515 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7400   -1.5923    1.7915 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8775   -2.1621    1.2615 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0497   -0.3714    2.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6986    0.7096    1.8637 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0727    0.7271    1.7890 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7124    1.7169    1.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1136    1.7593    0.9865 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9426    2.6718    0.4585 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5626    2.6655    0.5258 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8464    3.6740   -0.1344 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9505    1.6735    1.2355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7850    2.2258   -2.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1683    3.7997   -1.9655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2709    2.3676   -1.6545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3796    3.3267    0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3829    2.1626   -0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1046    1.6657    0.5014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5696    1.2081    1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6835   -0.7163    0.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9027    0.1873   -1.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4612    0.2249   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0799   -1.4452   -1.5813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6221    0.0886    0.6018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3210   -1.5871    0.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0401   -1.7676    0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9638   -2.4548   -0.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7296    0.3632   -0.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6459   -0.2343   -2.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2724   -0.4670   -2.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0096   -2.1305   -2.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4116   -0.5374   -0.2356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1968   -2.2100   -0.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9600   -1.3854   -1.9881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2244   -3.0663   -1.7774 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8950   -3.1852    0.4939 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3286   -2.9120   -0.5940 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9165   -0.7444    1.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2687   -0.4926   -0.0245 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2643   -2.3274    2.4701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9086   -3.1261    1.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1444    0.0153    3.1309 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7453   -0.7355    3.4464 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6470   -0.0394    2.2898 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6122    2.2832    1.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4440    3.4663   -0.1097 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5845    3.4765   -1.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8859    1.6395    1.3074 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
 14 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 24 17  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  1
 15 53  1  0
 16 54  1  0
 16 55  1  0
 18 56  1  0
 20 57  1  0
 21 58  1  0
 23 59  1  0
 24 60  1  0
M  END

  Mrv1652309022203252D          

 24 24  0  0  1  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  1  0  0  0  0  0  0  0  0  0
   12.8605   -9.9000    0.0000 O   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
   15.7184   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -8.6625    0.0000 O   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
   15.0039  -11.1375    0.0000 O   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
  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  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 17 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146099

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCC[C@@H](O)CC1=CC(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-19(22)14-18-15-20(23)17-21(24)16-18/h15-17,19,22-24H,2-14H2,1H3/t19-/m1/s1

> <INCHI_KEY>
IYXFMXYFVCIIAN-LJQANCHMSA-N

> <FORMULA>
C21H36O3

> <MOLECULAR_WEIGHT>
336.516

> <EXACT_MASS>
336.266445019

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.95732204678879

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[(2R)-2-hydroxypentadecyl]benzene-1,3-diol

> <ALOGPS_LOGP>
6.91

> <JCHEM_LOGP>
6.716779345000001

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.758113428236893

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.305318180406852

> <JCHEM_PKA_STRONGEST_BASIC>
-2.745818493421341

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
101.14449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.82e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(2R)-2-hydroxypentadecyl]benzene-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  O   UNK     0      24.006 -18.480   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      25.340 -16.170   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.674 -16.940   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.007 -16.170   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      29.341 -16.940   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      30.675 -16.170   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      29.341 -18.480   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      28.007 -19.250   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      28.007 -20.790   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      26.674 -18.480   0.000  0.00  0.00           C+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   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   17                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₆O₃

Average Mass

336.5160 Da

Monoisotopic Mass

336.26645 Da

IUPAC Name

5-[(2R)-2-hydroxypentadecyl]benzene-1,3-diol

Traditional Name

5-[(2R)-2-hydroxypentadecyl]benzene-1,3-diol

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCC[C@@H](O)CC1=CC(O)=CC(O)=C1

InChI Identifier

InChI=1S/C21H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-19(22)14-18-15-20(23)17-21(24)16-18/h15-17,19,22-24H,2-14H2,1H3/t19-/m1/s1

InChI Key

IYXFMXYFVCIIAN-LJQANCHMSA-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
Ardisia virens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	6.91	ALOGPS
logP	6.72	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.31	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	101.14 m³·mol⁻¹	ChemAxon
Polarizability	42.96 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

Not Available

Chemspider ID

57512796

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71414613

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol (NP0146099)

MOL for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

3D MOL for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

3D SDF for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

3D-SDF for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

PDB for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

3D PDB for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

SMILES for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

INCHI for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

Structure for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)

3D Structure for NP0146099 (5-[(2r)-2-hydroxypentadecyl]benzene-1,3-diol)