NP-MRD: Showing NP-Card for 9e-heptadecenoic acid (NP0207228)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 03:45:36 UTC

Updated at

2022-09-05 03:45:37 UTC

NP-MRD ID

NP0207228

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9e-heptadecenoic acid

Description

9E-Heptadecenoic acid, also known as (e)-heptadec-9-enoate or fa(17:1(9E)), 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. 9E-Heptadecenoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, 9E-Heptadecenoic acid has been detected, but not quantified in, a few different foods, such as fats and oils, italian sweet red peppers, and milk (cow). 9e-heptadecenoic acid is found in Osmerus mordax and Anthracocystis flocculosa. This could make 9E-heptadecenoic acid a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 50  0  0  0  0  0  0  0  0999 V2000
    7.1289    0.5152    0.1553 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5942    0.5642    0.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0673   -0.4738    0.9269 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6266   -0.7237    1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6980    0.2904    1.5215 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5490    1.5916    0.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1705    1.4530   -0.5809 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9197    0.9112   -1.0325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1353    0.4850   -0.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3416   -0.0505   -1.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5254   -1.4625   -0.6811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6855   -2.1662   -1.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0102   -1.4960   -1.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2937   -1.4347    0.4503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6121   -0.7840    0.7352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7282    0.6141    0.2499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7309    1.5133    0.8610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057    1.1393    1.7228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6989    2.8497    0.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4248    0.3219    1.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4925   -0.2880   -0.4849 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5779    1.4664   -0.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3258    0.2778   -1.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2806    1.5953    0.1807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5730   -1.4506    0.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4969   -0.3681    1.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2208   -1.0404   -0.0084 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4261   -1.6648    1.6266 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7016   -0.2243    1.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0230    0.5335    2.6106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4058    2.2490    1.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7260    2.1184    1.4299 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2452    2.4899   -1.0597 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9921    0.9047   -1.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289    0.8406   -2.1493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1270    0.5488    0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1267    0.0456   -2.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2522    0.5230   -0.8416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5991   -2.0362   -0.9702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5451   -1.4848    0.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5196   -2.2941   -2.3964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7377   -3.1846   -0.8712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0689   -0.4866   -1.4795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8016   -2.1166   -1.5019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4381   -0.9624    0.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3898   -2.5204    0.7843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4639   -1.3600    0.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384   -0.7932    1.8423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7543    1.0344    0.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5802    0.6461   -0.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5850    3.3443    0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  8  9  2  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 19  1  0
 17 18  2  0
  8 35  1  0
  7 33  1  0
  7 34  1  0
  6 31  1  0
  6 32  1  0
  5 29  1  0
  5 30  1  0
  4 27  1  0
  4 28  1  0
  3 25  1  0
  3 26  1  0
  2 23  1  0
  2 24  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 19 51  1  0
M  END

  Mrv1652306251823492D          

 21 20  0  0  0  0            999 V2000
   -3.4322    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0033    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2888    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5743    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    3.3809    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    1.3184    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  2  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  2  0  0  0  0
 19 17  1  0  0  0  0
 20  8  1  0  0  0  0
 21  9  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207228

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(CCCCCCC)=C(\[H])CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19/h8-9H,2-7,10-16H2,1H3,(H,18,19)/b9-8+

> <INCHI_KEY>
QSBYPNXLFMSGKH-CMDGGOBGSA-N

> <FORMULA>
C17H32O2

> <MOLECULAR_WEIGHT>
268.4348

> <EXACT_MASS>
268.240230268

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.52862338489056

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9E)-heptadec-9-enoic acid

> <ALOGPS_LOGP>
7.22

> <JCHEM_LOGP>
6.339229786

> <ALOGPS_LOGS>
-6.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.988167283903808

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
82.8012

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.23e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9E-heptadecenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-JUN-18   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-JUN-18         0                                  
HETATM    1  C   UNK     0      -6.407   4.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.073   4.771   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.739   4.001   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.406   4.771   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.072   4.001   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.262   4.771   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.595   4.001   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.929   4.771   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.263   4.001   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      16.266   4.771   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      14.932   2.461   0.000  0.00  0.00           O+0
HETATM   20  H   UNK     0       2.929   6.311   0.000  0.00  0.00           H+0
HETATM   21  H   UNK     0       4.263   2.461   0.000  0.00  0.00           H+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   20                                                  
CONECT    9    8   10   21                                                  
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   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    8                                                            
CONECT   21    9                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
9E-Heptadecenoate	Generator
(9E)-9-Heptadecenoic acid	HMDB
(e)-9-Heptadecenoic acid	HMDB
FA(17:1(9E))	HMDB
9E-Heptadecenoic acid	HMDB

Chemical Formula

C₁₇H₃₂O₂

Average Mass

268.4348 Da

Monoisotopic Mass

268.24023 Da

IUPAC Name

(9E)-heptadec-9-enoic acid

Traditional Name

9E-heptadecenoic acid

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCCCC)=C(\[H])CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C17H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19/h8-9H,2-7,10-16H2,1H3,(H,18,19)/b9-8+

InChI Key

QSBYPNXLFMSGKH-CMDGGOBGSA-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
Osmerus mordax	LOTUS Database	35616633
Pseudozyma flocculosa	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
Unsaturated fatty acid
Straight chain fatty acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

long-chain fatty acid (CHEBI:80550 )
Monounsaturated fatty acids (C16536 )
Unsaturated fatty acids (LMFA01030289 )

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	7.22	ALOGPS
logP	6.34	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	4.99	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	82.8 m³·mol⁻¹	ChemAxon
Polarizability	35.53 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

HMDB0031046

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB003041

KNApSAcK ID

Not Available

Chemspider ID

4471865

KEGG Compound ID

C16536

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5312440

PDB ID

Not Available

ChEBI ID

80550

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9e-heptadecenoic acid (NP0207228)

MOL for NP0207228 (9e-heptadecenoic acid)

3D MOL for NP0207228 (9e-heptadecenoic acid)

3D SDF for NP0207228 (9e-heptadecenoic acid)

3D-SDF for NP0207228 (9e-heptadecenoic acid)

PDB for NP0207228 (9e-heptadecenoic acid)

3D PDB for NP0207228 (9e-heptadecenoic acid)

SMILES for NP0207228 (9e-heptadecenoic acid)

INCHI for NP0207228 (9e-heptadecenoic acid)

Structure for NP0207228 (9e-heptadecenoic acid)

3D Structure for NP0207228 (9e-heptadecenoic acid)