NP-MRD: Showing NP-Card for 3-heptadecylcatechol (NP0326350)

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Record Information

Version

1.0

Created at

2022-09-12 07:49:39 UTC

Updated at

2022-09-12 07:49:39 UTC

NP-MRD ID

NP0326350

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-heptadecylcatechol

Description

3-Heptadecylcatechol, also known as HDC, belongs to the class of organic compounds known as catechols. Catechols are compounds containing a 1,2-benzenediol moiety. 3-Heptadecylcatechol is an extremely weak basic (essentially neutral) compound (based on its pKa). It was first documented in 1984 (PMID: 6231243). Catechol substituted at position 3 with a heptadecyl group (PMID: 3742608).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 65 65  0  0  0  0  0  0  0  0999 V2000
    7.5357    0.8164   -3.6691 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6783    1.0950   -2.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3969    0.6241   -1.5015 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5593    0.9073   -0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3221    0.4745    0.7565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0580   -0.9635    0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9897   -1.6135    1.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5679   -1.2280    1.2999 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2312    0.1194    1.7788 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7275    0.4143    1.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0772   -0.5409    2.4841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5846   -0.2590    2.4144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0876   -0.3585    1.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5620   -0.0665    0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3648   -1.0291    1.6861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8380   -0.8868    1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5196   -1.1482    0.3535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1782   -0.3714   -0.8302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5737   -0.9928   -1.9111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3011   -0.3001   -3.0553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6373    1.0246   -3.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2480    1.6980   -2.0546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5672    3.0296   -2.1619 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5070    0.9676   -0.9184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1031    1.5309    0.1807 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1559    1.4959   -4.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8266   -0.2582   -3.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4572    0.8960   -3.9113 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5688    0.6418   -1.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7513    2.2011   -1.9969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3186   -0.4834   -1.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5644    1.1727   -1.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7379    1.9845    0.1005 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4573    0.3675    0.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5066    1.0150    0.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3187    0.8727    1.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8446   -1.2165   -0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0053   -1.5692    0.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0853   -2.7695    1.2727 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3082   -1.5582    2.5169 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -1.3850    0.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0023   -1.9913    1.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4700    0.2910    2.8504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6921    0.9089    1.1846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5950    1.4361    2.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4143    0.4304    0.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2360   -0.6445    3.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0302   -1.5700    2.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7599    0.7665    2.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1215   -1.0026    3.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5612    0.3512    0.3204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9062   -1.4049    0.6316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7370    0.9507    1.3922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8692    0.0622   -0.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0228   -0.9292    2.7654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1239   -2.0931    1.4080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0607    0.1603    2.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2402   -1.5782    2.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6298   -0.9939    0.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4553   -2.2717    0.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3283   -2.0397   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8283   -0.8231   -3.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4280    1.5922   -4.0181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0038    3.5515   -1.4319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3696    2.4905    0.1941 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  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 24 18  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 13 51  1  0
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 15 56  1  0
 16 57  1  0
 16 58  1  0
 17 59  1  0
 17 60  1  0
 19 61  1  0
 20 62  1  0
 21 63  1  0
 23 64  1  0
 25 65  1  0
M  END


  Mrv1533004151518252D          

 25 25  0  0  0  0            999 V2000
    4.2868   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -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
   15.0039  -10.3125    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
   16.4328  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -11.5500    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  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 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
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326350

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCC1=CC=CC(O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18-21-19-17-20-22(24)23(21)25/h17,19-20,24-25H,2-16,18H2,1H3

> <INCHI_KEY>
DXRKLUVKXMAMOV-UHFFFAOYSA-N

> <FORMULA>
C23H40O2

> <MOLECULAR_WEIGHT>
348.571

> <EXACT_MASS>
348.302830528

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
46.37421110265963

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
8.77

> <JCHEM_LOGP>
8.992635202

> <ALOGPS_LOGS>
-6.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.983379271693696

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.548682588024976

> <JCHEM_PKA_STRONGEST_BASIC>
-6.279935694325503

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
108.67699999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.12e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-heptadecylcatechol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       8.002 -18.480   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336 -19.250   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669 -18.480   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003 -19.250   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.337 -18.480   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.670 -19.250   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.004 -18.480   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.338 -19.250   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.672 -18.480   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.005 -19.250   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.339 -18.480   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.673 -19.250   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.006 -18.480   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.340 -19.250   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      26.674 -18.480   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.007 -19.250   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      29.341 -18.480   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.675 -19.250   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      32.008 -18.480   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      33.342 -19.250   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      33.342 -20.790   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      32.008 -21.560   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      32.008 -23.100   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      30.675 -20.790   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      29.341 -21.560   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                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   18   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Value	Source
3-Heptadecyl-1,2-benzenediol	ChEBI
3-Heptadecylpyrocatechol	ChEBI
3-N-Heptadecylcatechol	ChEBI
3-N-Heptadecylpyrocatechol	ChEBI
HDC	ChEBI
Heptadecylcatechol	MeSH

Chemical Formula

C₂₃H₄₀O₂

Average Mass

348.5710 Da

Monoisotopic Mass

348.30283 Da

IUPAC Name

3-heptadecylbenzene-1,2-diol

Traditional Name

3-heptadecylcatechol

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCC1=CC=CC(O)=C1O

InChI Identifier

InChI=1S/C23H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18-21-19-17-20-22(24)23(21)25/h17,19-20,24-25H,2-16,18H2,1H3

InChI Key

DXRKLUVKXMAMOV-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as catechols. Catechols are compounds containing a 1,2-benzenediol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Catechol
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

catechols (CHEBI:59112 )

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	8.77	ALOGPS
logP	8.99	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	9.55	ChemAxon
pKa (Strongest Basic)	-6.3	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	16	ChemAxon
Refractivity	108.68 m³·mol⁻¹	ChemAxon
Polarizability	46.37 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

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

119222

PDB ID

Not Available

ChEBI ID

59112

Good Scents ID

Not Available

References

General References

Dunn IS, Liberato DJ, Castagnoli N Jr, Byers VS: Influence of chemical reactivity of urushiol-type haptens on sensitization and the induction of tolerance. Cell Immunol. 1986 Jan;97(1):189-96. doi: 10.1016/0008-8749(86)90388-6. [PubMed:3742608 ]
Dunn IS, Liberato DJ, Castagnoli N, Byers VS: Induction of suppressor T cells for lymph node cell proliferation after contact sensitization of mice with a poison oak urushiol component. Immunology. 1984 Apr;51(4):773-81. [PubMed:6231243 ]
LOTUS database [Link]

Showing NP-Card for 3-heptadecylcatechol (NP0326350)

MOL for NP0326350 (3-heptadecylcatechol)

3D MOL for NP0326350 (3-heptadecylcatechol)

3D SDF for NP0326350 (3-heptadecylcatechol)

3D-SDF for NP0326350 (3-heptadecylcatechol)

PDB for NP0326350 (3-heptadecylcatechol)

3D PDB for NP0326350 (3-heptadecylcatechol)

SMILES for NP0326350 (3-heptadecylcatechol)

INCHI for NP0326350 (3-heptadecylcatechol)

Structure for NP0326350 (3-heptadecylcatechol)

3D Structure for NP0326350 (3-heptadecylcatechol)