NP-MRD: Showing NP-Card for 17-methyloctadecanoic acid (NP0317154)

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Record Information

Version

2.0

Created at

2022-09-11 16:50:28 UTC

Updated at

2022-09-11 16:50:28 UTC

NP-MRD ID

NP0317154

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-methyloctadecanoic acid

Description

17-Methyloctadecanoic acid, also known as 17-methylstearic acid or isononadecanoic 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. A branched-chain saturated fatty acid that is octadecanoic (stearic) acid carrying a methyl substituent at position 17. 17-Methyloctadecanoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, 17-Methyloctadecanoic acid has been detected, but not quantified in, fishes. 17-methyloctadecanoic acid is found in Callyspongia fallax and Ectyoplasia ferox. This could make 17-methyloctadecanoic acid a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 59 58  0  0  0  0  0  0  0  0999 V2000
    6.3234    0.6166    0.5048 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4882   -0.4765   -0.5236 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0790    0.0827   -1.8013 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2420   -1.2794   -0.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0791   -0.5008   -1.2502 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9059   -1.4849   -1.4288 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6688   -0.7680   -1.9294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2512    0.3203   -0.9480 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9247   -0.2245    0.4053 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5599    0.9001    1.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5970    1.7344    0.8845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8883    0.9689    0.7245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2424    0.3288    2.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5530   -0.4378    1.9506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6902    0.4781    1.6186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9897   -0.2460    1.5140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9651   -1.3136    0.4254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6111   -0.6575   -0.9158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6194    0.3640   -1.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8492    0.1279   -1.1640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1806    1.6294   -1.6269 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8667    0.3644    1.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8683    1.5113    0.1266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2798    0.8331    0.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2514   -1.1843   -0.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8643    0.8048   -1.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3695    0.6530   -2.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5828   -0.7373   -2.3414 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9514   -1.7477    0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5067   -2.0700   -1.4893 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7639    0.2402   -0.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2264    0.0484   -2.1800 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7617   -1.9656   -0.4499 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1809   -2.2459   -2.1799 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8703   -1.4977   -2.0094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8938   -0.2921   -2.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9836    1.1187   -0.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3014    0.7422   -1.3614 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1431   -0.9936    0.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8317   -0.7076    0.8350 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3249    0.4950    2.3353 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4434    1.5909    1.3644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3790    2.3296   -0.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7720    2.4792    1.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6529    1.6422    0.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6795    0.2109   -0.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4599   -0.4561    2.2327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1896    1.0362    2.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4204   -1.2912    1.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7164   -0.8407    2.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5472    1.0912    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7978    1.1591    2.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3397   -0.7183    2.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7754    0.4925    1.1959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3325   -2.1700    0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0158   -1.6722    0.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7111   -1.4697   -1.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5835   -0.2974   -0.9627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2293    1.9574   -1.4103 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  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  0
 16 54  1  0
 17 55  1  0
 17 56  1  0
 18 57  1  0
 18 58  1  0
 21 59  1  0
M  END


  Mrv1652305062021412D          

 21 20  0  0  0  0            999 V2000
 9989.4860 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.1995 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.9152 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9991.6328 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9990.9152 9985.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9988.7704 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9988.0547 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9987.3412 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9986.6255 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9985.9120 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9985.1964 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9984.4816 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9983.7668 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9983.0519 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9982.3370 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9981.6222 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9980.9074 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9980.1924 9984.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9979.4777 9984.9749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9978.7608 9984.5632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9979.4777 9985.8005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  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
 19 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0317154

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H38O2/c1-18(2)16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-19(20)21/h18H,3-17H2,1-2H3,(H,20,21)

> <INCHI_KEY>
YETXGSGCWODRAA-UHFFFAOYSA-N

> <FORMULA>
C19H38O2

> <MOLECULAR_WEIGHT>
298.5038

> <EXACT_MASS>
298.28718046

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.509088625069595

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
17-methyloctadecanoic acid

> <ALOGPS_LOGP>
8.22

> <JCHEM_LOGP>
7.432739204

> <ALOGPS_LOGS>
-6.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.952019655228562

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
90.83419999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.08e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17-methyloctadecanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-20         0                                  
HETATM    1  C   UNK     0    8647.0418638.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8648.3728637.851   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8649.7088638.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8651.0488637.851   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8649.7088640.161   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8645.7058637.851   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8644.3698638.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8643.0378637.851   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8641.7018638.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8640.3698637.851   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8639.0338638.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8637.6998637.851   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8636.3658638.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8635.0308637.851   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8633.6968638.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8632.3618637.851   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8631.0278638.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8629.6928637.851   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8628.3588638.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0    8627.0208637.851   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0    8628.3588640.161   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    1    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   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
17-Methyl-octadecanoic acid	ChEBI
17-Methylstearic acid	ChEBI
Isononadecanoic acid	ChEBI
17-Methyl-octadecanoate	Generator
17-Methylstearate	Generator
Isononadecanoate	Generator
17-methyloctadecanoate	Generator
XI-17-methyloctadecanoate	HMDB
17-Methyloctadecanoic acid	HMDB
FA(i-19:0)	HMDB
I19:0	HMDB
XI-17-methyloctadecanoic acid	HMDB

Chemical Formula

C₁₉H₃₈O₂

Average Mass

298.5038 Da

Monoisotopic Mass

298.28718 Da

IUPAC Name

17-methyloctadecanoic acid

Traditional Name

17-methyloctadecanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)CCCCCCCCCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C19H38O2/c1-18(2)16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-19(20)21/h18H,3-17H2,1-2H3,(H,20,21)

InChI Key

YETXGSGCWODRAA-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
Callyspongia fallax	LOTUS Database	35616633
Ectyoplasia ferox	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
Branched 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

Branched fatty acids (LMFA01020096 )

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	8.22	ALOGPS
logP	7.43	ChemAxon
logS	-6.7	ALOGPS
pKa (Strongest Acidic)	4.95	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	16	ChemAxon
Refractivity	90.83 m³·mol⁻¹	ChemAxon
Polarizability	40.51 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

HMDB0037397

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB016440

KNApSAcK ID

Not Available

Chemspider ID

2340933

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3083779

PDB ID

Not Available

ChEBI ID

133136

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17-methyloctadecanoic acid (NP0317154)

MOL for NP0317154 (17-methyloctadecanoic acid)

3D MOL for NP0317154 (17-methyloctadecanoic acid)

3D SDF for NP0317154 (17-methyloctadecanoic acid)

3D-SDF for NP0317154 (17-methyloctadecanoic acid)

PDB for NP0317154 (17-methyloctadecanoic acid)

3D PDB for NP0317154 (17-methyloctadecanoic acid)

SMILES for NP0317154 (17-methyloctadecanoic acid)

INCHI for NP0317154 (17-methyloctadecanoic acid)

Structure for NP0317154 (17-methyloctadecanoic acid)

3D Structure for NP0317154 (17-methyloctadecanoic acid)