NP-MRD: Showing NP-Card for octadecatetraenoic acid (NP0148959)

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Record Information

Version

2.0

Created at

2022-09-02 04:47:01 UTC

Updated at

2022-09-02 04:47:01 UTC

NP-MRD ID

NP0148959

Secondary Accession Numbers

None

Natural Product Identification

Common Name

octadecatetraenoic acid

Description

Trans-parinaric acid, also known as all-trans-parinarate or b-parinarate, belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. octadecatetraenoic acid is found in Impatiens balsamina. octadecatetraenoic acid was first documented in 2019 (PMID: 31610877). Based on a literature review a small amount of articles have been published on trans-parinaric acid (PMID: 35218738) (PMID: 32755561) (PMID: 31424941) (PMID: 31133285).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 47  0  0  0  0  0  0  0  0999 V2000
    5.6383   -5.0322   -6.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6526   -3.5219   -6.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5254   -3.0818   -5.2862 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6949   -2.3627   -4.2024 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5818   -1.9577   -3.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7128   -1.2350   -2.2790 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5029   -0.8886   -1.5276 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5555   -0.1705   -0.4165 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3771    0.1886    0.3489 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4745    0.9001    1.4485 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3057    1.2967    2.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9356    0.7688    1.6371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2007    1.0879    2.3686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4534    2.5515    2.5227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7398    2.8471    3.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9407    2.2992    2.5804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2210    2.5872    3.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3501    2.0470    4.6396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4578    1.3406    5.1506 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4862    2.3173    5.3809 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6261   -5.4530   -5.8654 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4846   -5.4222   -7.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8501   -5.4554   -5.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4987   -3.1725   -7.2120 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6115   -3.1091   -5.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5143   -3.3595   -5.5357 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6894   -2.0631   -3.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5851   -2.2616   -3.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6936   -0.9195   -1.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5211   -1.2004   -1.8426 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5370    0.1502   -0.0869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3973   -0.1237    0.0262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4761    1.2020    1.7509 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794    2.3698    2.4878 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4308    0.7348    3.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0405    1.1867    0.6075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8764   -0.3475    1.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0309    0.6535    1.7440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2781    0.5863    3.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4556    3.0525    1.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5731    2.9701    3.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6308    2.3703    4.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8318    3.9391    3.4374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8357    1.1786    2.5093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0657    2.7240    1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0433    2.2117    2.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3851    3.6942    3.3291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3843    1.8823    5.2424 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  2  0
  6  7  1  0
  7  8  2  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 20  1  0
 18 19  2  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  4 27  1  0
  5 28  1  0
  6 29  1  0
  7 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 14 41  1  0
 15 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 20 48  1  0
M  END


  Mrv1652309022206472D          

 20 19  0  0  0  0            999 V2000
   -4.1467    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -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  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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  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
 18 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0148959

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C\C=C\C=C\C=C\CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h3-10H,2,11-17H2,1H3,(H,19,20)/b4-3+,6-5+,8-7+,10-9+

> <INCHI_KEY>
IJTNSXPMYKJZPR-BYFNFPHLSA-N

> <FORMULA>
C18H28O2

> <MOLECULAR_WEIGHT>
276.42

> <EXACT_MASS>
276.208930142

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
35.92825815039204

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9E,11E,13E,15E)-octadeca-9,11,13,15-tetraenoic acid

> <ALOGPS_LOGP>
6.32

> <JCHEM_LOGP>
5.698033481

> <ALOGPS_LOGS>
-5.81

> <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>
90.752

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.25e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
trans-parinaric acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.740   4.771   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.407   4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.073   4.771   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.739   4.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.406   4.771   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.072   4.001   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.262   4.771   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.595   4.001   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.929   4.771   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.263   4.001   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      16.266   4.771   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      14.932   2.461   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   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   38    0
END

View in JSmol

Synonyms

Value	Source
(e,e,e,e)-Octadeca-9,11,13,15-tetraenoic acid	ChEBI
all-trans-9,11,13,15-Octadecatetraenoic acid	ChEBI
all-trans-Octadeca-9,11,13,15-tetraenoic acid	ChEBI
all-trans-Parinaric acid	ChEBI
beta-Parinaric acid	ChEBI
Octadeca-9t,11t,13t,15t-tetraenoic acid	ChEBI
Octadeca-9t,11t,13t,15t-tetraensaeure	ChEBI
(e,e,e,e)-Octadeca-9,11,13,15-tetraenoate	Generator
all-trans-9,11,13,15-Octadecatetraenoate	Generator
all-trans-Octadeca-9,11,13,15-tetraenoate	Generator
all-trans-Parinarate	Generator
b-Parinarate	Generator
b-Parinaric acid	Generator
beta-Parinarate	Generator
Β-parinarate	Generator
Β-parinaric acid	Generator
Octadeca-9t,11t,13t,15t-tetraenoate	Generator
trans-Parinarate	Generator
Parinaric acid, (Z,Z,e,e)-isomer	MeSH
Parinaric acid, (all-e)-isomer	MeSH
Paranaric acid	MeSH
Parinaric acid	MeSH
cis-Parinaric acid	MeSH
Octadecatetraenoic acid	MeSH

Chemical Formula

C₁₈H₂₈O₂

Average Mass

276.4200 Da

Monoisotopic Mass

276.20893 Da

IUPAC Name

(9E,11E,13E,15E)-octadeca-9,11,13,15-tetraenoic acid

Traditional Name

trans-parinaric acid

CAS Registry Number

Not Available

SMILES

CC\C=C\C=C\C=C\C=C\CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h3-10H,2,11-17H2,1H3,(H,19,20)/b4-3+,6-5+,8-7+,10-9+

InChI Key

IJTNSXPMYKJZPR-BYFNFPHLSA-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
Impatiens balsamina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Long-chain fatty acid
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

parinaric acid (CHEBI:32410 )
Unsaturated fatty acids (LMFA01030171 )

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	6.32	ALOGPS
logP	5.7	ChemAxon
logS	-5.8	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	12	ChemAxon
Refractivity	90.75 m³·mol⁻¹	ChemAxon
Polarizability	35.93 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

4445965

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5282838

PDB ID

Not Available

ChEBI ID

32410

Good Scents ID

Not Available

References

General References

Hanashima S, Ikeda R, Matsubara Y, Yasuda T, Tsuchikawa H, Slotte JP, Murata M: Effect of cholesterol on the lactosylceramide domains in phospholipid bilayers. Biophys J. 2022 Apr 5;121(7):1143-1155. doi: 10.1016/j.bpj.2022.02.037. Epub 2022 Feb 23. [PubMed:35218738 ]
Engberg O, Lin KL, Hautala V, Slotte JP, Nyholm TKM: Sphingomyelin Acyl Chains Influence the Formation of Sphingomyelin- and Cholesterol-Enriched Domains. Biophys J. 2020 Sep 1;119(5):913-923. doi: 10.1016/j.bpj.2020.07.014. Epub 2020 Jul 24. [PubMed:32755561 ]
Nyholm TKM, Engberg O, Hautala V, Tsuchikawa H, Lin KL, Murata M, Slotte JP: Impact of Acyl Chain Mismatch on the Formation and Properties of Sphingomyelin-Cholesterol Domains. Biophys J. 2019 Nov 5;117(9):1577-1588. doi: 10.1016/j.bpj.2019.09.025. Epub 2019 Sep 25. [PubMed:31610877 ]
Engberg O, Scheidt HA, Nyholm TKM, Slotte JP, Huster D: Membrane Localization and Lipid Interactions of Common Lipid-Conjugated Fluorescence Probes. Langmuir. 2019 Sep 10;35(36):11902-11911. doi: 10.1021/acs.langmuir.9b01202. Epub 2019 Aug 29. [PubMed:31424941 ]
Al Sazzad MA, Yasuda T, Nyholm TKM, Slotte JP: Lateral Segregation of Palmitoyl Ceramide-1-Phosphate in Simple and Complex Bilayers. Biophys J. 2019 Jul 9;117(1):36-45. doi: 10.1016/j.bpj.2019.05.015. Epub 2019 May 21. [PubMed:31133285 ]
LOTUS database [Link]

Showing NP-Card for octadecatetraenoic acid (NP0148959)

MOL for NP0148959 (octadecatetraenoic acid)

3D MOL for NP0148959 (octadecatetraenoic acid)

3D SDF for NP0148959 (octadecatetraenoic acid)

3D-SDF for NP0148959 (octadecatetraenoic acid)

PDB for NP0148959 (octadecatetraenoic acid)

3D PDB for NP0148959 (octadecatetraenoic acid)

SMILES for NP0148959 (octadecatetraenoic acid)

INCHI for NP0148959 (octadecatetraenoic acid)

Structure for NP0148959 (octadecatetraenoic acid)

3D Structure for NP0148959 (octadecatetraenoic acid)