NP-MRD: Showing NP-Card for 3-hydroxydocosanoic acid (NP0244316)

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Record Information

Version

2.0

Created at

2022-09-07 05:05:08 UTC

Updated at

2022-09-07 05:05:08 UTC

NP-MRD ID

NP0244316

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxydocosanoic acid

Description

3-Hydroxydocosanoic acid belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms. 3-hydroxydocosanoic acid is found in Centaurea aspera. 3-Hydroxydocosanoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 69 68  0  0  0  0  0  0  0  0999 V2000
   -9.5704   -0.1737    2.1825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3706   -1.3587    1.2981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6717   -1.1248    0.0193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2777   -0.6327    0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0039    0.6675    0.6933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5259    0.9950    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6154    0.0014    1.1945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1471    0.4034    1.0355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7651    0.5034   -0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2526    0.9152   -0.4495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8168    1.0302   -1.8515 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5095    1.5254   -2.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7249    0.8531   -1.6861 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9790    1.0187   -0.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0857    0.2173    0.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4717    0.2687   -0.1477 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8340   -0.2224   -1.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2625   -0.0706   -1.8843 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3591   -0.7155   -1.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6876   -0.4315    0.2232 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9737    0.9445    0.4014 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1062   -1.0687    0.5000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4190   -0.7769    1.9008 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6381   -0.1382    2.6408 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6176   -1.2180    2.4363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9159   -0.2355    3.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5199    0.7711    1.6370 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6167   -0.1709    2.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4105   -1.7244    1.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9474   -2.2334    1.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6475   -2.1200   -0.5245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3308   -0.4952   -0.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6083   -1.4144    0.4773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9400   -0.5483   -1.0245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5450    1.5016    0.1928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1849    0.6690    1.7939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2876    1.0923   -0.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3557    2.0163    0.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8278    0.0122    2.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6998   -1.0165    0.8197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9028    1.3148    1.6126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5376   -0.4259    1.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8519   -0.4414   -0.9527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3010    1.3510   -0.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1419    1.8124    0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7589   -0.0036    0.0038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5664    1.7092   -2.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0254    0.0032   -2.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6291    1.6174   -3.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5500    2.6150   -1.8453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8192   -0.1820   -2.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6159    1.4045   -2.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0745    0.8387    0.3694 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579    2.1495   -0.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1324    0.4136    1.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7981   -0.9091    0.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0392   -0.3970    0.5955 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9678    1.2682    0.0037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6018   -1.3580   -1.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2403    0.1782   -2.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2830   -0.4354   -2.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4692    1.0459   -2.0686 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3228   -0.4898   -1.7722 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2941   -1.8495   -1.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0796   -0.7762    1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7366    1.1417   -0.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9391   -2.1486    0.2944 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7983   -0.6460   -0.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6232   -1.8725    3.2003 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  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 25  1  0
 23 24  2  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
 18 61  1  0
 18 62  1  0
 19 63  1  0
 19 64  1  0
 20 65  1  1
 21 66  1  0
 22 67  1  0
 22 68  1  0
 25 69  1  0
M  END

  Mrv1533004251513392D          

 25 24  0  0  0  0            999 V2000
   11.6605    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0895    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8039    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5184    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2329    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9474    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6618    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3763    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.0908    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8052    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5197    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2342    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9487    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6631    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3776    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0921    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8065    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.5210    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.2355    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.2355    6.3197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.9499    7.5572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.6644    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.3789    7.5572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.6644    6.3197    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  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0244316

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCC(O)CC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H44O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-21(23)20-22(24)25/h21,23H,2-20H2,1H3,(H,24,25)

> <INCHI_KEY>
PNPWTPYWWUOMDS-UHFFFAOYSA-N

> <FORMULA>
C22H44O3

> <MOLECULAR_WEIGHT>
356.591

> <EXACT_MASS>
356.329045277

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
47.75943385581212

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-hydroxydocosanoic acid

> <ALOGPS_LOGP>
8.36

> <JCHEM_LOGP>
7.693183700666668

> <ALOGPS_LOGS>
-6.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.288498288670866

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.671850167040888

> <JCHEM_PKA_STRONGEST_BASIC>
-2.798587426318786

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
106.20509999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.86e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxydocosanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      21.766  14.107   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      23.100  13.337   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      24.434  14.107   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      25.767  13.337   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      27.101  14.107   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      28.435  13.337   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      29.768  14.107   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      31.102  13.337   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      32.436  14.107   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      33.769  13.337   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      35.103  14.107   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      36.437  13.337   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      37.770  14.107   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      39.104  13.337   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      40.438  14.107   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      41.772  13.337   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      43.105  14.107   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      44.439  13.337   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      45.773  14.107   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      47.106  13.337   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      47.106  11.797   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      48.440  14.107   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      49.774  13.337   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      51.107  14.107   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      49.774  11.797   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                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Value	Source
3-Hydroxydocosanoate	Generator

Chemical Formula

C₂₂H₄₄O₃

Average Mass

356.5910 Da

Monoisotopic Mass

356.32905 Da

IUPAC Name

3-hydroxydocosanoic acid

Traditional Name

3-hydroxydocosanoic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCC(O)CC(O)=O

InChI Identifier

InChI=1S/C22H44O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-21(23)20-22(24)25/h21,23H,2-20H2,1H3,(H,24,25)

InChI Key

PNPWTPYWWUOMDS-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
Centaurea aspera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Very long-chain fatty acids

Alternative Parents

Substituents

Very long-chain fatty acid
Hydroxy fatty acid
Beta-hydroxy acid
Hydroxy acid
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

3-hydroxy monocarboxylic acid (CHEBI:52348 )
Hydroxy fatty acids (LMFA01050078 )

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	8.36	ALOGPS
logP	7.69	ChemAxon
logS	-6.3	ALOGPS
pKa (Strongest Acidic)	4.67	ChemAxon
pKa (Strongest Basic)	-2.8	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	20	ChemAxon
Refractivity	106.21 m³·mol⁻¹	ChemAxon
Polarizability	47.76 Å³	ChemAxon
Number of Rings	0	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

5282921

PDB ID

Not Available

ChEBI ID

52348

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-hydroxydocosanoic acid (NP0244316)

MOL for NP0244316 (3-hydroxydocosanoic acid)

3D MOL for NP0244316 (3-hydroxydocosanoic acid)

3D SDF for NP0244316 (3-hydroxydocosanoic acid)

3D-SDF for NP0244316 (3-hydroxydocosanoic acid)

PDB for NP0244316 (3-hydroxydocosanoic acid)

3D PDB for NP0244316 (3-hydroxydocosanoic acid)

SMILES for NP0244316 (3-hydroxydocosanoic acid)

INCHI for NP0244316 (3-hydroxydocosanoic acid)

Structure for NP0244316 (3-hydroxydocosanoic acid)

3D Structure for NP0244316 (3-hydroxydocosanoic acid)