NP-MRD: Showing NP-Card for tetracosyl acetate (NP0223747)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 01:55:53 UTC

Updated at

2022-09-06 01:55:53 UTC

NP-MRD ID

NP0223747

Secondary Accession Numbers

None

Natural Product Identification

Common Name

tetracosyl acetate

Description

Tetracosyl acetate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. tetracosyl acetate is found in Gisekia pharnaceoides. Tetracosyl acetate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

  Mrv1533004171519182D          

 28 27  0  0  0  0            999 V2000
   14.1355    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5645    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2789    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9934    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7079    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4224    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1368    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8513    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5658    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2802    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9947    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7092    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4237    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1381    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.8526    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5671    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.7105    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.4249    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.1394    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.8539    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.5684    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.2828    8.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.9973    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7118    8.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.9973    7.7487    0.0000 C   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
 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
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 80 79  0  0  0  0  0  0  0  0999 V2000
    7.7612   -2.8998    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7577   -1.8228   -0.3831 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1637   -0.7861   -1.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9810   -0.1030   -0.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4321    0.5512    0.6328 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4376    1.2824    1.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7180    2.4280    0.9350 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8005    2.5011   -0.1819 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5267    1.7487   -0.1759 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6691    0.2893   -0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3185   -0.4358   -0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4948   -0.0683    1.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1922   -0.8147    0.9989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5637   -0.4694   -0.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741    1.0111   -0.3559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6277    1.2522   -1.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8760    0.5208   -1.7674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9892    0.7645   -0.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9334    0.5268    0.5828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3117    0.8573    1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4150    0.0243    0.5849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1498   -1.4234    0.8397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1441   -2.3964    0.3242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4994   -2.2042    0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0856   -0.9795    0.6221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3754   -0.5446   -0.6819 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0020    0.7811   -0.8732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1071   -1.2662   -1.6515 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0028   -2.9480   -0.7968 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2916   -2.6697    0.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2528   -3.9048    0.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2926   -1.4083    0.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5413   -2.3506   -1.0043 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9238   -0.0001   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8125   -1.2481   -2.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4898    0.4934   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2672   -0.9180   -0.3221 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3650    1.1781    0.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8460   -0.2903    1.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0489    1.7268    2.3603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8477    0.5133    2.0323 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5253    3.2639    0.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1688    2.9160    1.8353 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2829    2.4229   -1.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4497    3.6236   -0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9165    2.1499    0.6868 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9874    2.0591   -1.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1732   -0.0206   -1.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2404   -0.1358    0.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4834   -1.5297   -0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8345   -0.1931   -1.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0167   -0.4143    1.9638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2513    1.0187    1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4297   -0.5464    1.8812 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3546   -1.9209    1.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0704   -0.7652   -1.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5553   -1.0118   -0.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2505    1.4211    0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1638    1.5034   -0.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7633    2.3652   -1.7986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9752    0.9711   -2.5192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6663   -0.6185   -1.8072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2964    0.6532   -2.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3602    1.8270   -1.0472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8454    0.0838   -1.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2594    1.1864    1.1773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6401   -0.5018    0.8365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2797    0.6886    2.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4601    1.9399    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6450    0.2836   -0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3265    0.2916    1.1902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1517   -1.7463    0.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0684   -1.5887    1.9437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7816   -3.4306    0.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1812   -2.3967   -0.8013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4008   -2.2657    2.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1862   -3.0142    0.5335 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1177    1.3229    0.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0053    0.6769   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4132    1.4361   -1.5482 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 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 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 13 54  1  0
 13 55  1  0
 14 56  1  0
 14 57  1  0
 15 58  1  0
 15 59  1  0
 16 60  1  0
 16 61  1  0
 17 62  1  0
 17 63  1  0
 18 64  1  0
 18 65  1  0
 19 66  1  0
 19 67  1  0
 20 68  1  0
 20 69  1  0
 21 70  1  0
 21 71  1  0
 22 72  1  0
 22 73  1  0
 23 74  1  0
 23 75  1  0
 24 76  1  0
 24 77  1  0
 27 78  1  0
 27 79  1  0
 27 80  1  0
M  END

  Mrv1533004171519182D          

 28 27  0  0  0  0            999 V2000
   14.1355    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5645    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2789    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9934    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7079    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4224    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1368    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8513    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5658    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2802    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9947    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7092    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4237    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1381    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.8526    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5671    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.7105    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.4249    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.1394    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.8539    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.5684    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.2828    8.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.9973    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7118    8.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.9973    7.7487    0.0000 C   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
 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
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223747

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCCCCCCOC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H52O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-28-26(2)27/h3-25H2,1-2H3

> <INCHI_KEY>
YNNTYKYGOBKPFT-UHFFFAOYSA-N

> <FORMULA>
C26H52O2

> <MOLECULAR_WEIGHT>
396.7

> <EXACT_MASS>
396.396730914

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
55.90188174497869

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
tetracosyl acetate

> <ALOGPS_LOGP>
10.12

> <JCHEM_LOGP>
10.137820656333332

> <ALOGPS_LOGS>
-7.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.993812176968582

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
123.30639999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.24e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
tetracosyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      26.386  16.774   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      27.720  16.004   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      29.054  16.774   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      30.387  16.004   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      31.721  16.774   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      33.055  16.004   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      34.388  16.774   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      35.722  16.004   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      37.056  16.774   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      38.389  16.004   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      39.723  16.774   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      41.057  16.004   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      42.390  16.774   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      43.724  16.004   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      45.058  16.774   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      46.392  16.004   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      47.725  16.774   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      49.059  16.004   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      50.393  16.774   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      51.726  16.004   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      53.060  16.774   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      54.394  16.004   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      55.727  16.774   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      57.061  16.004   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      58.395  16.774   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      59.728  16.004   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      61.062  16.774   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      59.728  14.464   0.000  0.00  0.00           C+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                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   54    0
END

View in JSmol

Synonyms

Value	Source
Tetracosyl acetic acid	Generator

Chemical Formula

C₂₆H₅₂O₂

Average Mass

396.7000 Da

Monoisotopic Mass

396.39673 Da

IUPAC Name

tetracosyl acetate

Traditional Name

tetracosyl acetate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCOC(C)=O

InChI Identifier

InChI=1S/C26H52O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-28-26(2)27/h3-25H2,1-2H3

InChI Key

YNNTYKYGOBKPFT-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
Gisekia pharnaceoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohol esters

Direct Parent

Fatty alcohol esters

Alternative Parents

Substituents

Fatty alcohol ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Wax monoesters (LMFA07010406 )

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	10.12	ALOGPS
logP	10.14	ChemAxon
logS	-7.5	ALOGPS
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	123.31 m³·mol⁻¹	ChemAxon
Polarizability	55.9 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

13908471

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for tetracosyl acetate (NP0223747)

MOL for NP0223747 (tetracosyl acetate)

3D MOL for NP0223747 (tetracosyl acetate)

3D SDF for NP0223747 (tetracosyl acetate)

3D-SDF for NP0223747 (tetracosyl acetate)

PDB for NP0223747 (tetracosyl acetate)

3D PDB for NP0223747 (tetracosyl acetate)

SMILES for NP0223747 (tetracosyl acetate)

INCHI for NP0223747 (tetracosyl acetate)

Structure for NP0223747 (tetracosyl acetate)

3D Structure for NP0223747 (tetracosyl acetate)