NP-MRD: Showing NP-Card for 13-methylpentadecanoic acid (NP0154798)

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Record Information

Version

2.0

Created at

2022-09-02 11:45:46 UTC

Updated at

2022-09-02 11:45:46 UTC

NP-MRD ID

NP0154798

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-methylpentadecanoic acid

Description

13-Methylpentadecanoic acid, also known as anteisopalmitic acid or C15:0-13-Methyl, 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. 13-methylpentadecanoic acid was first documented in 1979 (PMID: 115510). 13-Methylpentadecanoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 49  0  0  0  0  0  0  0  0999 V2000
   -5.0106    2.0285   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4691    0.7672    0.1762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3067   -0.1491    0.4927 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8647   -1.3642    1.1806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5556   -0.4890   -0.7697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3848   -1.4002   -0.5191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3697   -0.8306    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7573    0.4541   -0.0739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0603    0.3122   -1.3828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0322   -0.7076   -1.3069 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0825   -0.3175   -0.2729 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1837   -1.3759   -0.2594 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2140   -1.0265    0.7623 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8390    0.3057    0.4338 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066    0.6390    1.4684 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4941    1.9395    1.1201 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4009    2.4162    1.8397 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0520    2.6297    0.0112 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7270    1.7753   -1.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2469    2.5680    0.0383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9000    2.7001   -0.5867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0122    0.9837    1.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1299    0.2013   -0.5206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6446    0.3799    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7274   -1.0325    1.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2719   -2.0290    0.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1349   -1.8589    1.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2675   -0.9366   -1.4922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2027    0.4626   -1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9497   -1.6401   -1.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7210   -2.3726   -0.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5632   -1.5652    0.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8566   -0.6541    1.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269    1.2797   -0.1107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0399    0.7994    0.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7463    0.0525   -2.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3398    1.3267   -1.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6788   -1.7093   -1.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5498   -0.8264   -2.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5744   -0.2843    0.7076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4661    0.6936   -0.4952 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6924   -1.2818   -1.2651 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7715   -2.3831   -0.1598 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9791   -1.8186    0.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6663   -0.8781    1.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0814    1.1394    0.5165 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2323    0.3620   -0.6008 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4031    0.6455    2.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6473   -0.1730    1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1599    2.2424   -0.9174 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
  3  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 18  1  0
 16 17  2  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  1
  4 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 15 49  1  0
 18 50  1  0
M  END

  Mrv1533004241519342D          

 18 17  0  0  0  0            999 V2000
    5.9961    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7105    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1395    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8539    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5684    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2829    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1408    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8552    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5697    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2842    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7131    4.6993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    3.4618    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
  3  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  2  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154798

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)CCCCCCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H32O2/c1-3-15(2)13-11-9-7-5-4-6-8-10-12-14-16(17)18/h15H,3-14H2,1-2H3,(H,17,18)

> <INCHI_KEY>
WWASUAHHCLARMF-UHFFFAOYSA-N

> <FORMULA>
C16H32O2

> <MOLECULAR_WEIGHT>
256.43

> <EXACT_MASS>
256.24023027

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
33.940681990473166

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
13-methylpentadecanoic acid

> <ALOGPS_LOGP>
7.13

> <JCHEM_LOGP>
6.099033209

> <ALOGPS_LOGS>
-5.99

> <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>
77.03119999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.62e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-methylpentadecanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      11.193   8.002   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.526   8.772   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.860   8.002   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.860   6.462   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.194   8.772   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.527   8.002   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.861   8.772   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.195   8.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.528   8.772   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.862   8.002   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      23.196   8.772   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      24.529   8.002   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.863   8.772   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      27.197   8.002   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      28.530   8.772   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      29.864   8.002   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      31.198   8.772   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      29.864   6.462   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    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   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   34    0
END

View in JSmol

Synonyms

Value	Source
Anteisopalmitic acid	ChEBI
C15:0-13-Methyl	ChEBI
Anteisopalmitate	Generator
13-Methylpentadecanoate	Generator
Anteisohexadecanoate	Generator

Chemical Formula

C₁₆H₃₂O₂

Average Mass

256.4300 Da

Monoisotopic Mass

256.24023 Da

IUPAC Name

13-methylpentadecanoic acid

Traditional Name

13-methylpentadecanoic acid

CAS Registry Number

Not Available

SMILES

CCC(C)CCCCCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C16H32O2/c1-3-15(2)13-11-9-7-5-4-6-8-10-12-14-16(17)18/h15H,3-14H2,1-2H3,(H,17,18)

InChI Key

WWASUAHHCLARMF-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

Not Available

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
Methyl-branched 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 (LMFA01020192 )

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	7.13	ALOGPS
logP	6.1	ChemAxon
logS	-6	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	13	ChemAxon
Refractivity	77.03 m³·mol⁻¹	ChemAxon
Polarizability	33.94 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

146501

PDB ID

Not Available

ChEBI ID

131414

Good Scents ID

Not Available

References

General References

Smith A, Calder AG, Morrsion ER, Garton GA: Identification of branched chain fatty acids in baboon liver lipids. Biomed Mass Spectrom. 1979 Aug;6(8):345-6. doi: 10.1002/bms.1200060807. [PubMed:115510 ]
LOTUS database [Link]

Showing NP-Card for 13-methylpentadecanoic acid (NP0154798)

MOL for NP0154798 (13-methylpentadecanoic acid)

3D MOL for NP0154798 (13-methylpentadecanoic acid)

3D SDF for NP0154798 (13-methylpentadecanoic acid)

3D-SDF for NP0154798 (13-methylpentadecanoic acid)

PDB for NP0154798 (13-methylpentadecanoic acid)

3D PDB for NP0154798 (13-methylpentadecanoic acid)

SMILES for NP0154798 (13-methylpentadecanoic acid)

INCHI for NP0154798 (13-methylpentadecanoic acid)

Structure for NP0154798 (13-methylpentadecanoic acid)

3D Structure for NP0154798 (13-methylpentadecanoic acid)