NP-MRD: Showing NP-Card for 3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate (NP0325049)

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Record Information

Version

2.0

Created at

2022-09-12 05:30:39 UTC

Updated at

2022-09-12 05:30:40 UTC

NP-MRD ID

NP0325049

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate

Description

3-Hydroxy-5-[(2S)-2-hydroxytetradecyl]phenyl acetate 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. 3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate is found in Ardisia virens. Based on a literature review very few articles have been published on 3-hydroxy-5-[(2S)-2-hydroxytetradecyl]phenyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122207302D          

 26 26  0  0  1  0            999 V2000
   -4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   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   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -9.4875    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
    7.1447   -9.9000    0.0000 O   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
  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  6  0  0  0
 13 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
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  2  0  0  0  0
 16 26  1  0  0  0  0
M  END

     RDKit          3D

 62 62  0  0  0  0  0  0  0  0999 V2000
    7.5358    0.6407    3.0823 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3942    0.3225    1.8733 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7041    0.7385    0.5907 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3651   -0.0105    0.4479 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7160    0.4329   -0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4086   -0.2865   -1.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4115   -0.0393    0.0504 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0942   -0.7535   -0.1283 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4542   -0.3091   -1.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0988   -0.9799   -1.6592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8165   -0.6433   -0.5433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1893   -1.2198   -0.6511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9841   -0.8280   -1.8383 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4393   -1.1585   -3.0549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4520    0.6224   -1.8082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3101    0.8523   -0.6117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7708    1.2586    0.5769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5917    1.4644    1.6738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0967    1.8763    2.9021 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9458    1.2587    1.5609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5190    0.8455    0.3633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8720    0.6303    0.2166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4418   -0.5874    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9021   -0.7632    0.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7647   -1.5786    0.8168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6911    0.6473   -0.7099 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1020    1.6650    2.9265 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1523    0.5886    3.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7385   -0.1163    3.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5412   -0.7798    1.8110 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3561    0.8671    1.9036 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3329    0.4014   -0.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5183    1.8203    0.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5400   -1.0946    0.4864 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7439    0.2636    1.3450 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5170    1.5408   -0.7887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3834    0.2027   -1.6863 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6631   -1.3840   -1.0625 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0105   -0.0728   -2.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8591   -0.2545    1.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1598    1.0619    0.0029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2015   -1.8547   -0.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4800   -0.4347    0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1237   -0.6254   -2.2489 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3877    0.7790   -1.4143 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3093   -2.0444   -1.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2517   -0.5044   -2.6214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3787   -1.0995    0.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8210    0.4401   -0.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1158   -2.3389   -0.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7480   -0.9593    0.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9495   -1.4177   -1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4959   -0.3847   -3.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5892    1.3187   -1.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0994    0.7624   -2.6977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7000    1.4331    0.7062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8120    1.1966    3.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6383    1.4026    2.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1050   -1.7483   -0.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4006   -0.7975    1.2709 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3171    0.0467   -0.3277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0936    0.3220   -1.6746 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
 13 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21 26  2  0
 26 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  1
 14 53  1  0
 15 54  1  0
 15 55  1  0
 17 56  1  0
 19 57  1  0
 20 58  1  0
 24 59  1  0
 24 60  1  0
 24 61  1  0
 26 62  1  0
M  END


  Mrv1652309122207302D          

 26 26  0  0  1  0            999 V2000
   -4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   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   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -9.4875    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
    7.1447   -9.9000    0.0000 O   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
  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  6  0  0  0
 13 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
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  2  0  0  0  0
 16 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325049

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H36O4/c1-3-4-5-6-7-8-9-10-11-12-13-20(24)14-19-15-21(25)17-22(16-19)26-18(2)23/h15-17,20,24-25H,3-14H2,1-2H3/t20-/m0/s1

> <INCHI_KEY>
QHWJHYOFDSCFLI-FQEVSTJZSA-N

> <FORMULA>
C22H36O4

> <MOLECULAR_WEIGHT>
364.526

> <EXACT_MASS>
364.261359639

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.0651053518918

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-hydroxy-5-[(2S)-2-hydroxytetradecyl]phenyl acetate

> <JCHEM_LOGP>
6.183036975999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.148806606166037

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.072607132983746

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7484125725200848

> <JCHEM_POLAR_SURFACE_AREA>
66.75999999999999

> <JCHEM_REFRACTIVITY>
105.695

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-5-[(2S)-2-hydroxytetradecyl]phenyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002 -15.400   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668 -16.170   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335 -15.400   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001 -16.170   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667 -15.400   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000 -15.400   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334 -16.170   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667 -15.400   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335 -15.400   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002 -15.400   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.002 -13.860   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669 -15.400   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003 -13.090   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.337 -13.860   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.337 -15.400   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      14.670 -16.170   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      14.670 -17.710   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.004 -18.480   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.337 -18.480   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.003 -16.170   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   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   16                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

View in JSmol

Synonyms

Value	Source
3-Hydroxy-5-[(2S)-2-hydroxytetradecyl]phenyl acetic acid	Generator

Chemical Formula

C₂₂H₃₆O₄

Average Mass

364.5260 Da

Monoisotopic Mass

364.26136 Da

IUPAC Name

3-hydroxy-5-[(2S)-2-hydroxytetradecyl]phenyl acetate

Traditional Name

3-hydroxy-5-[(2S)-2-hydroxytetradecyl]phenyl acetate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H36O4/c1-3-4-5-6-7-8-9-10-11-12-13-20(24)14-19-15-21(25)17-22(16-19)26-18(2)23/h15-17,20,24-25H,3-14H2,1-2H3/t20-/m0/s1

InChI Key

QHWJHYOFDSCFLI-FQEVSTJZSA-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
Phenol ester
Phenoxy compound
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
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	6.18	ChemAxon
pKa (Strongest Acidic)	9.07	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	105.7 m³·mol⁻¹	ChemAxon
Polarizability	45.07 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

91405049

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate (NP0325049)

MOL for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

3D MOL for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

3D SDF for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

3D-SDF for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

PDB for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

3D PDB for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

SMILES for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

INCHI for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

Structure for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)

3D Structure for NP0325049 (3-hydroxy-5-[(2s)-2-hydroxytetradecyl]phenyl acetate)