NP-MRD: Showing NP-Card for 3-Methyl-tricosane (NP0044956)

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Record Information

Version

2.0

Created at

2022-03-10 18:51:46 UTC

Updated at

2022-03-10 22:17:19 UTC

NP-MRD ID

NP0044956

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-Methyl-tricosane

Description

3-Methyl-tricosane is a methylated derivative of tricosane. Tricosane, also known as CH3-[CH2]21-CH3, belongs to the class of organic compounds known as alkanes and consists of a straight chain alkane containing 23 carbon atoms. Alkanes are acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2, and therefore consisting entirely of hydrogen atoms and saturated carbon atoms. Tricosane is considered to be a hydrocarbon lipid molecule. It is a very hydrophobic molecule, practically insoluble in water and relatively neutral. Tricosane is an odorless, alkane tasting compound, which is solid at room temperature. Tricosane has been detected, but not quantified in, common hazelnuts. This could make tricosane a potential biomarker for the consumption of these foods. 3-Methyl-tricosane is one of many hydrocarbons that are known in Cannabis plants (PMID: 6991645 ).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 74 73  0  0  0  0  0  0  0  0999 V2000
    9.4951   -2.6898   -0.1487 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6765   -1.2736   -0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2612   -0.6972   -0.8063 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6588   -0.7443    0.5698 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2268   -0.1626    0.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3450   -0.9308   -0.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216   -0.5536   -0.4422 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4740    0.7496   -0.9138 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8256    1.9917   -0.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3241    1.9116    1.2485 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8280    1.7376    1.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0647    2.8486    0.6786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4141    2.5818    0.8114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8587    1.3131    0.1610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3763    1.2290    0.3994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8898   -0.0214   -0.2273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4005   -0.2075   -0.0444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1439    0.9098   -0.6511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6042    0.9296   -0.5375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4812   -0.0813   -1.1207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4081   -1.4972   -0.7206 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6325   -1.7301    0.7501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5180   -2.2874   -1.4884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8752   -1.8024   -1.0927 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5596   -3.1482   -0.4829 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4597   -2.6522    0.9706 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3330   -3.3098   -0.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1919   -0.6209    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2285   -1.2306   -1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7383   -1.3717   -1.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3053    0.3224   -1.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6005   -1.7957    0.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2471   -0.1226    1.2499 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4317    0.8988    0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8508   -0.1931    1.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7982   -1.0499   -1.3956 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3744   -2.0084    0.0193 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4236   -0.7494    0.5755 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -1.3329   -1.0743 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8069    0.8468   -2.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3427    0.6885   -1.0513 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8479    2.3263   -0.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2634    2.8809   -0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6433    2.7853    1.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7938    1.0221    1.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5672    1.7432    2.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5970    0.7856    0.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2858    3.8244    1.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2495    2.9176   -0.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6720    2.6010    1.9099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378    3.4767    0.3977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7445    1.4330   -0.9342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3556    0.4179    0.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7762    2.1578   -0.0030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5988    1.2026    1.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6222   -0.0436   -1.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4048   -0.8960    0.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5865   -1.2070   -0.4674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6218   -0.2819    1.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8975    0.9862   -1.7518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7723    1.8547   -0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9180    1.9753   -0.9324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8240    1.0906    0.5776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3997    0.0189   -2.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5614    0.2905   -0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4965   -1.9847   -1.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2658   -0.9638    1.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6479   -1.8625    1.2856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1495   -2.7048    0.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3914   -3.3363   -1.1960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3682   -2.0895   -2.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2639   -1.0169   -1.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5845   -2.6534   -1.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9252   -1.4445   -0.0443 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  1  0
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  3  2  1  0
  2  1  1  0
 21 66  1  6
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 12 48  1  0
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 10 44  1  0
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  9 42  1  0
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  8 40  1  0
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  7 38  1  0
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  6 36  1  0
  6 37  1  0
  5 34  1  0
  5 35  1  0
  4 32  1  0
  4 33  1  0
  3 30  1  0
  3 31  1  0
  2 28  1  0
  2 29  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
M  END


  Mrv1652307312018382D          

 25 24  0  0  1  0            999 V2000
   11.2480   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9664   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5374   -5.1927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2519   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6770   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3914   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1059   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8204   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5349   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2493   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9638   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6783   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3927   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1072   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8217   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5362   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2506   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9651   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6796   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.3940   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1085   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.8230   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5374   -6.0177    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.2519   -5.6052    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  2  1  0  0  0  0
  6  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  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  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24  3  1  1  0  0  0
 24  5  1  0  0  0  0
 24 23  1  0  0  0  0
 24 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0044956

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@](C)(CC)CCCCCCCCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C24H50/c1-4-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(3)5-2/h24H,4-23H2,1-3H3/t24-/m0/s1

> <INCHI_KEY>
WCAGWYVPTZQWEN-DEOSSOPVSA-N

> <FORMULA>
C24H50

> <MOLECULAR_WEIGHT>
338.664

> <EXACT_MASS>
338.39125161

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
50.16877476303612

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S)-3-methyltricosane

> <ALOGPS_LOGP>
10.48

> <JCHEM_LOGP>
10.975824294

> <ALOGPS_LOGS>
-7.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
112.17379999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.33e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-methyltricosane

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 31-JUL-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-JUL-20         0                                  
HETATM    1  C   UNK     0      20.996 -11.233   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      50.337 -11.233   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      47.670  -9.693   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      22.330 -12.003   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      49.004 -12.003   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.664 -11.233   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      24.997 -12.003   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      26.331 -11.233   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      27.665 -12.003   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      28.998 -11.233   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      30.332 -12.003   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      31.666 -11.233   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      32.999 -12.003   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      34.333 -11.233   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      35.667 -12.003   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      37.001 -11.233   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      38.334 -12.003   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      39.668 -11.233   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      41.002 -12.003   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      42.335 -11.233   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      43.669 -12.003   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      45.003 -11.233   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      46.336 -12.003   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      47.670 -11.233   0.000  0.00  0.00           C+0
HETATM   25  H   UNK     0      49.004 -10.463   0.000  0.00  0.00           H+0
CONECT    1    4                                                            
CONECT    2    5                                                            
CONECT    3   24                                                            
CONECT    4    1    6                                                       
CONECT    5    2   24                                                       
CONECT    6    4    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                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24    3    5   23   25                                             
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₅₀

Average Mass

338.6640 Da

Monoisotopic Mass

338.39125 Da

IUPAC Name

(3S)-3-methyltricosane

Traditional Name

(3S)-3-methyltricosane

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)CCCCCCCCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C24H50/c1-4-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(3)5-2/h24H,4-23H2,1-3H3/t24-/m0/s1

InChI Key

WCAGWYVPTZQWEN-DEOSSOPVSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Cannabis sativa	NULL	Not Available

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	10.48	ALOGPS
logP	10.98	ChemAxon
logS	-7.9	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	112.17 m³·mol⁻¹	ChemAxon
Polarizability	50.17 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3-Methyl-tricosane (NP0044956)

MOL for NP0044956 (3-Methyl-tricosane)

3D MOL for NP0044956 (3-Methyl-tricosane)

3D SDF for NP0044956 (3-Methyl-tricosane)

3D-SDF for NP0044956 (3-Methyl-tricosane)

PDB for NP0044956 (3-Methyl-tricosane)

3D PDB for NP0044956 (3-Methyl-tricosane)

SMILES for NP0044956 (3-Methyl-tricosane)

INCHI for NP0044956 (3-Methyl-tricosane)

Structure for NP0044956 (3-Methyl-tricosane)

3D Structure for NP0044956 (3-Methyl-tricosane)