NP-MRD: Showing NP-Card for 17-hydroxystearic acid (NP0314257)

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Record Information

Version

2.0

Created at

2022-09-11 12:15:57 UTC

Updated at

2022-09-11 12:15:57 UTC

NP-MRD ID

NP0314257

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-hydroxystearic acid

Description

17-Hydroxy stearic acid belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. 17-hydroxystearic acid is found in Starmerella magnoliae. 17-Hydroxy stearic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 57 56  0  0  0  0  0  0  0  0999 V2000
    7.2149   -0.0046    0.8571 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9602   -0.7219    1.3540 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3159   -1.7018    2.3102 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2816   -1.4486    0.2313 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8478   -0.5600   -0.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8605    0.4708   -0.3273 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4564    1.3395   -1.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4803    2.4092   -1.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2122    1.8031   -0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5662    0.9274   -1.5471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6907    0.2892   -1.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6746    1.3624   -0.6552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9750    0.7515   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7035   -0.0857    1.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9811   -0.6671    1.5870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6283   -1.5354    0.5561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9175   -2.1781    1.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8719   -1.0710    1.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1345   -0.2514    0.2346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4063    0.6876   -0.1723 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2752   -0.5028   -0.5427 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8877   -0.6703    0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7300    0.4119    1.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8515    0.7682    0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3437    0.0179    1.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1994   -2.0836    2.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0058   -2.2093   -0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3705   -1.9288    0.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2719   -1.1802   -1.6075 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6558   -0.0870   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9999   -0.0585    0.1158 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3206    1.0937    0.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1200    0.7048   -2.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3780    1.8684   -1.8770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1709    2.9948   -1.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9217    3.1134   -0.3691 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5204    2.6743   -0.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4435    1.2763    0.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2283    0.0992   -1.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3831    1.5447   -2.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4236   -0.3924   -0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1976   -0.3238   -1.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3110    2.0418    0.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9276    1.9100   -1.5847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6773    1.5786    0.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3630    0.1529   -1.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1786    0.4659    1.8583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0938   -0.9762    0.7229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6204    0.2161    1.8569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8130   -1.1943    2.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8160   -0.9934   -0.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9778   -2.4036    0.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2974   -2.8180    0.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6216   -2.7903    1.9390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8265   -1.5920    1.7324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4466   -0.5140    2.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1482   -0.0300   -0.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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 21  1  0
 19 20  2  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  1
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 16 52  1  0
 17 53  1  0
 17 54  1  0
 18 55  1  0
 18 56  1  0
 21 57  1  0
M  END

  Mrv1652310091719302D          

 21 20  0  0  0  0            999 V2000
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6158    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9013    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3302    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0447    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4724    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17  1  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 17  1  0  0  0  0
 20 18  2  0  0  0  0
 21 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0314257

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H36O3/c1-17(19)15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18(20)21/h17,19H,2-16H2,1H3,(H,20,21)

> <INCHI_KEY>
CKGPXFKOAGKQDN-UHFFFAOYSA-N

> <FORMULA>
C18H36O3

> <MOLECULAR_WEIGHT>
300.483

> <EXACT_MASS>
300.266445019

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
39.476474402136525

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
17-hydroxyoctadecanoic acid

> <ALOGPS_LOGP>
6.71

> <JCHEM_LOGP>
5.681047850666667

> <ALOGPS_LOGS>
-5.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.683061087845683

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.952019770185588

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6252291951333233

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
88.03209999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17-hydroxy stearic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-OCT-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-OCT-17         0                                  
HETATM    1  C   UNK     0      17.146  11.439   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      29.149  10.669   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      27.816  11.439   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      30.483  11.439   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      26.482  10.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      31.817  10.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      25.148  11.439   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      33.150  11.439   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.815  10.669   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      34.484  10.669   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.481  11.439   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      35.818  11.439   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      21.147  10.669   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      37.152  10.669   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.814  11.439   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      38.485  11.439   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      39.819  10.669   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      18.480   9.129   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      41.153  11.439   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      39.819   9.129   0.000  0.00  0.00           O+0
CONECT    1   17                                                            
CONECT    2    3    4                                                       
CONECT    3    2    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   14                                                       
CONECT   13   11   15                                                       
CONECT   14   12   16                                                       
CONECT   15   13   17                                                       
CONECT   16   14   18                                                       
CONECT   17    1   15   19                                                  
CONECT   18   16   20   21                                                  
CONECT   19   17                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
17-Hydroxy stearate	Generator
17-Hydroxystearate	Generator

Chemical Formula

C₁₈H₃₆O₃

Average Mass

300.4830 Da

Monoisotopic Mass

300.26645 Da

IUPAC Name

17-hydroxyoctadecanoic acid

Traditional Name

17-hydroxy stearic acid

CAS Registry Number

Not Available

SMILES

CC(O)CCCCCCCCCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H36O3/c1-17(19)15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18(20)21/h17,19H,2-16H2,1H3,(H,20,21)

InChI Key

CKGPXFKOAGKQDN-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
Starmerella magnoliae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Hydroxy fatty 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

Other Octadecanoids (LMFA02000135 )

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	6.71	ALOGPS
logP	5.68	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	4.95	ChemAxon
pKa (Strongest Basic)	-1.6	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	16	ChemAxon
Refractivity	88.03 m³·mol⁻¹	ChemAxon
Polarizability	39.48 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

HMDB0171068

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

5282914

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17-hydroxystearic acid (NP0314257)

MOL for NP0314257 (17-hydroxystearic acid)

3D MOL for NP0314257 (17-hydroxystearic acid)

3D SDF for NP0314257 (17-hydroxystearic acid)

3D-SDF for NP0314257 (17-hydroxystearic acid)

PDB for NP0314257 (17-hydroxystearic acid)

3D PDB for NP0314257 (17-hydroxystearic acid)

SMILES for NP0314257 (17-hydroxystearic acid)

INCHI for NP0314257 (17-hydroxystearic acid)

Structure for NP0314257 (17-hydroxystearic acid)

3D Structure for NP0314257 (17-hydroxystearic acid)