NP-MRD: Showing NP-Card for 2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid (NP0257515)

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Record Information

Version

2.0

Created at

2022-09-07 22:39:36 UTC

Updated at

2022-09-07 22:39:36 UTC

NP-MRD ID

NP0257515

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid

Description

6-((8Z,11z,14z)-heptadeca-8,11,14-trien-1-yl)salicylic acid belongs to the class of organic compounds known as salicylic acids. These are ortho-hydroxylated benzoic acids. 2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid is found in Philodendron hederaceum and Spondias mombin. Based on a literature review very few articles have been published on 6-((8z,11z,14z)-heptadeca-8,11,14-trien-1-yl)salicylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082200392D          

 27 27  0  0  0  0            999 V2000
   -0.2083   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3318   -4.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0618   -5.1157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6019   -5.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4120   -5.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9521   -6.2071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7622   -6.0512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0323   -5.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424   -5.1157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124   -4.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424   -2.9329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6525   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1926   -3.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0028   -3.2448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -3.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3530   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -4.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7032   -4.1802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2433   -4.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9732   -5.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1631   -5.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -6.5189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6230   -5.1157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8129   -5.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2728   -4.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -6.0512    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 61 61  0  0  0  0  0  0  0  0999 V2000
    7.7535    2.3672    0.5712 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2455    0.9303    0.4935 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3187    0.0413    1.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6778   -0.9451    0.6154 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7535   -1.3341   -0.7647 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6229   -1.3316   -1.6555 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3941   -0.9763   -1.4392 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8722   -0.4610   -0.1433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8353   -1.3424    0.4189 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6002   -1.0070    0.7197 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0825    0.3584    0.5258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0736    0.3722   -0.4663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2348   -0.4689   -0.0455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3157   -0.3730   -1.1022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5262   -1.1989   -0.7620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6545   -1.1265   -1.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4709    0.1137   -1.7182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2470    0.2861   -0.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3968   -0.5482   -0.4401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1888   -0.6854    0.6623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8360    0.0204    1.7747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7014    0.8588    1.7827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4394    1.5098    2.9323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9183    0.9782    0.6409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8235    1.9274    0.6365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0398    2.1581   -0.2954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5369    2.7270    1.7749 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3401    2.6826   -0.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0133    2.4458    1.3806 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5679    3.0857    0.7936 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5998    0.6495   -0.4793 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1862    0.9483    1.1473 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1287    0.1889    2.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0172   -1.5730    1.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2487   -2.3858   -0.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5813   -0.7266   -1.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8338   -1.6915   -2.6954 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6791   -1.0669   -2.2898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5646    0.0000    0.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2665    0.4659   -0.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1230   -2.3891    0.6074 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8939   -1.7522    1.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7987    1.1206    0.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5902    0.7167    1.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3252    0.0283   -1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4284    1.4151   -0.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5793   -0.1807    0.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9126   -1.5258   -0.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8642   -0.9535   -2.0118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4644    0.6398   -1.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8341   -0.9737    0.3057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1923   -2.2883   -0.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2973   -2.0406   -1.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2330   -1.2499   -2.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8464    0.9890   -1.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2141    0.0259   -2.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6475   -1.0934   -1.3430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0728   -1.3375    0.6495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4381   -0.0644    2.6690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8140    2.1011    3.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6725    2.4447    2.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  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
 25 27  1  0
 25 26  2  0
 24 18  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  0
 16 54  1  0
 17 55  1  0
 17 56  1  0
 19 57  1  0
 20 58  1  0
 21 59  1  0
 23 60  1  0
 27 61  1  0
M  END


  Mrv1652309082200392D          

 27 27  0  0  0  0            999 V2000
   -0.2083   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3318   -4.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0618   -5.1157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6019   -5.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4120   -5.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9521   -6.2071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7622   -6.0512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0323   -5.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424   -5.1157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124   -4.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424   -2.9329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6525   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1926   -3.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0028   -3.2448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -3.8684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3530   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -4.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7032   -4.1802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2433   -4.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9732   -5.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1631   -5.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -6.5189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6230   -5.1157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8129   -5.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2728   -4.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -6.0512    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0257515

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C/C\C=C/C\C=C/CCCCCCCC1=CC=CC(O)=C1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18-21-19-17-20-22(25)23(21)24(26)27/h3-4,6-7,9-10,17,19-20,25H,2,5,8,11-16,18H2,1H3,(H,26,27)/b4-3-,7-6-,10-9-

> <INCHI_KEY>
MBYMHCHZLAJVRK-PDBXOOCHSA-N

> <FORMULA>
C24H34O3

> <MOLECULAR_WEIGHT>
370.533

> <EXACT_MASS>
370.250794955

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
44.19332030441211

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(8Z,11Z,14Z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid

> <JCHEM_LOGP>
8.518018461666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.364273313389209

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.640733551078049

> <JCHEM_PKA_STRONGEST_BASIC>
-6.287065354678508

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
117.30209999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(8Z,11Z,14Z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.389  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.619  -8.094   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.115  -9.549   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.123 -10.713   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.636 -10.422   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.644 -11.587   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.156 -11.295   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.660  -9.840   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.172  -9.549   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.677  -8.094   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.172  -5.475   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.685  -5.184   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.693  -6.348   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.205  -6.057   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.213  -7.221   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.726  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.734  -8.094   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.246  -7.803   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.254  -8.967   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.750 -10.422   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.238 -10.713   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      14.734 -12.169   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      14.230  -9.549   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.717  -9.840   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      11.709  -8.676   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      12.213 -11.295   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   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Value	Source
6-((8Z,11Z,14Z)-Heptadeca-8,11,14-trien-1-yl)salicylate	Generator
SB 202742, (Z,Z,Z)-Isomer	MeSH

Chemical Formula

C₂₄H₃₄O₃

Average Mass

370.5330 Da

Monoisotopic Mass

370.25079 Da

IUPAC Name

2-[(8Z,11Z,14Z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid

Traditional Name

2-[(8Z,11Z,14Z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid

CAS Registry Number

Not Available

SMILES

CC\C=C/C\C=C/C\C=C/CCCCCCCC1=CC=CC(O)=C1C(O)=O

InChI Identifier

InChI=1S/C24H34O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18-21-19-17-20-22(25)23(21)24(26)27/h3-4,6-7,9-10,17,19-20,25H,2,5,8,11-16,18H2,1H3,(H,26,27)/b4-3-,7-6-,10-9-

InChI Key

MBYMHCHZLAJVRK-PDBXOOCHSA-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
Philodendron scandens	LOTUS Database	35616633
Spondias mombin	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as salicylic acids. These are ortho-hydroxylated benzoic acids.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Salicylic acids

Alternative Parents

Substituents

Salicylic acid
Benzoic acid
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Vinylogous acid
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
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	8.52	ChemAxon
pKa (Strongest Acidic)	2.64	ChemAxon
pKa (Strongest Basic)	-6.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	117.3 m³·mol⁻¹	ChemAxon
Polarizability	44.19 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

8243312

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10067772

PDB ID

Not Available

ChEBI ID

186627

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid (NP0257515)

MOL for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

3D MOL for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

3D SDF for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

3D-SDF for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

PDB for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

3D PDB for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

SMILES for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

INCHI for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

Structure for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)

3D Structure for NP0257515 (2-[(8z,11z,14z)-heptadeca-8,11,14-trien-1-yl]-6-hydroxybenzoic acid)