NP-MRD: Showing NP-Card for 2-methyldecanoic acid; capric acid (NP0308687)

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Record Information

Version

2.0

Created at

2022-09-11 02:39:40 UTC

Updated at

2022-09-11 02:39:40 UTC

NP-MRD ID

NP0308687

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-methyldecanoic acid; capric acid

Description

2-methyldecanoic acid; capric acid is found in Houttuynia cordata.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 67 65  0  0  0  0  0  0  0  0999 V2000
   -4.1320    0.4186   -0.6625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4745    0.8464    0.6313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4458   -0.1978    1.0620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3930   -0.3331   -0.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4069   -1.3744    0.4660 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7013   -1.6170   -0.5055 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5311   -0.4033   -0.8106 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2091    0.2019    0.3572 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0022    1.4061   -0.0764 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0649    1.1389   -1.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6707    2.1782   -1.4884 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4833   -0.0736   -1.5173 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5097    0.1485   -1.1609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5111   -0.1208    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0805    0.1132    0.8108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2091   -0.8426    0.0685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7476   -0.7252    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2121    0.6605    0.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2263    0.7702    0.5710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1016   -0.2014   -0.1812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5239    0.0344    0.3150 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8778    1.4787    0.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4948   -0.8673   -0.3175 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4557   -0.3921   -0.9949 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4054   -2.2301   -0.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8623   -0.6298   -0.9493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2536    0.4710   -0.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8757    1.1342   -1.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2459    0.9650    1.4221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9673    1.8207    0.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9277   -1.1875    1.1751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0031    0.1026    2.0262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101    0.6079   -0.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7924   -0.6699   -0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9736   -2.3214    0.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0821   -1.0767    1.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3542   -2.4444   -0.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2367   -1.9444   -1.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9208    0.3714   -1.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2940   -0.7297   -1.5409 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8887   -0.5474    0.8276 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5332    0.5450    1.1638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    2.1497   -0.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3867    1.8976    0.8521 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1153   -0.7048   -1.0495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7216    0.8829   -1.3922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2403   -0.7975   -1.6775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5138    0.4382   -1.5310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1364    0.6301    0.8498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8425   -1.1567    0.4937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0066    0.0228    1.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8632    1.1679    0.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5035   -1.8983    0.2352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3171   -0.6385   -1.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1314   -1.4320   -0.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789   -0.9717    1.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8511    1.4387    0.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2461    0.8770   -0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6100    1.7846    0.3458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3176    0.5136    1.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1161   -0.0041   -1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8570   -1.2696    0.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5066   -0.1672    1.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9888    1.5651   -0.0876 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3533    1.8302   -0.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5611    2.0808    0.8774 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8266   -2.7221    0.4642 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
  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 12  1  0
 10 11  2  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 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 25  1  0
 23 24  2  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 12 45  1  0
 13 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
 19 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  1
 22 64  1  0
 22 65  1  0
 22 66  1  0
 25 67  1  0
M  END


  Mrv1652309112204392D          

 25 23  0  0  0  0            999 V2000
   -3.9571    0.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2426   -0.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5281    0.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8137   -0.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0992    0.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3847   -0.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3298    0.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0442   -0.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7587    0.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7587    1.0154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4732   -0.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1876    0.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4732   -1.0471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5448    0.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2593   -0.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9737    0.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6882   -0.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4027    0.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1171   -0.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8316    0.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5461   -0.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2606    0.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9750   -0.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6895    0.2750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9750   -0.9625    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
  4  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
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  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
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0308687

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCC(O)=O.CCCCCCCCC(C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C11H22O2.C10H20O2/c1-3-4-5-6-7-8-9-10(2)11(12)13;1-2-3-4-5-6-7-8-9-10(11)12/h10H,3-9H2,1-2H3,(H,12,13);2-9H2,1H3,(H,11,12)

> <INCHI_KEY>
VCUJGEVICOMMPM-UHFFFAOYSA-N

> <FORMULA>
C21H42O4

> <MOLECULAR_WEIGHT>
358.563

> <EXACT_MASS>
358.308309832

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
23.3483699350935

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-methyldecanoic acid; decanoic acid

> <JCHEM_LOGP>
4.1321570659999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.957336805313909

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
54.0521

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-methyldecanoic acid; capric acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.387   0.355   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.053  -0.415   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.719   0.355   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.385  -0.415   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.052   0.355   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.718  -0.415   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.616   0.355   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.949  -0.415   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.283   0.355   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.283   1.895   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.617  -0.415   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.950   0.355   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       4.617  -1.955   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.350   0.513   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.684  -0.257   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.018   0.513   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.351  -0.257   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.685   0.513   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.019  -0.257   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.352   0.513   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.686  -0.257   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      21.020   0.513   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.353  -0.257   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      23.687   0.513   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      22.353  -1.797   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   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   15                                                            
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₄₂O₄

Average Mass

358.5630 Da

Monoisotopic Mass

358.30831 Da

IUPAC Name

2-methyldecanoic acid; decanoic acid

Traditional Name

2-methyldecanoic acid; capric acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCC(O)=O.CCCCCCCCC(C)C(O)=O

InChI Identifier

InChI=1S/C11H22O2.C10H20O2/c1-3-4-5-6-7-8-9-10(2)11(12)13;1-2-3-4-5-6-7-8-9-10(11)12/h10H,3-9H2,1-2H3,(H,12,13);2-9H2,1H3,(H,11,12)

InChI Key

VCUJGEVICOMMPM-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
Houttuynia cordata	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	4.13	ChemAxon
pKa (Strongest Acidic)	4.96	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	54.05 m³·mol⁻¹	ChemAxon
Polarizability	23.35 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-methyldecanoic acid; capric acid (NP0308687)

MOL for NP0308687 (2-methyldecanoic acid; capric acid)

3D MOL for NP0308687 (2-methyldecanoic acid; capric acid)

3D SDF for NP0308687 (2-methyldecanoic acid; capric acid)

3D-SDF for NP0308687 (2-methyldecanoic acid; capric acid)

PDB for NP0308687 (2-methyldecanoic acid; capric acid)

3D PDB for NP0308687 (2-methyldecanoic acid; capric acid)

SMILES for NP0308687 (2-methyldecanoic acid; capric acid)

INCHI for NP0308687 (2-methyldecanoic acid; capric acid)

Structure for NP0308687 (2-methyldecanoic acid; capric acid)

3D Structure for NP0308687 (2-methyldecanoic acid; capric acid)