NP-MRD: Showing NP-Card for 4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid (NP0227470)

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Record Information

Version

2.0

Created at

2022-09-06 06:48:12 UTC

Updated at

2022-09-06 06:48:12 UTC

NP-MRD ID

NP0227470

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid

Description

56882-00-9, Also known as turbinaric acid, belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. 56882-00-9 Is a weakly acidic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181501462D          

 29 28  0  0  0  0            999 V2000
   11.1375    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    4.2868    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
    7.0125    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 10 27  1  0  0  0  0
  6 28  1  0  0  0  0
  2 29  1  0  0  0  0
M  END

     RDKit          3D

 73 72  0  0  0  0  0  0  0  0999 V2000
   -9.6245    1.2039   -2.1255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6905    0.6905   -1.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9070    1.0941    0.3457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6978   -0.1061   -1.4109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7822   -0.6057   -0.3559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3560   -0.1760   -0.6178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4911   -0.7022    0.4593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7361   -0.3097    1.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4977   -1.5237    0.1618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5844   -2.0979    1.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1416   -1.7580    0.9444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8928   -0.3213    1.0206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5294    0.6143    0.0354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0927    0.2116    1.9219 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6483   -0.5157    2.9549 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1408   -0.2722    2.7134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5326   -0.7523    1.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0486   -0.0260    0.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3833   -0.7308   -0.8611 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3211    1.3987    0.5653 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7921    1.7640    0.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3486    1.4071   -0.8998 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3362    0.5063   -1.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8980   -0.1690    0.1443 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8249    0.1761   -2.3986 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2180    0.4918   -2.7195 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3250   -0.1565   -2.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3243   -1.1191   -1.2882 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6136    0.3849   -2.3246 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6311    2.3032   -2.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6332    0.7763   -2.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2730    0.9258   -3.1380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8041    1.7307    0.4200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0371    1.6910    0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0527    0.1770    0.9856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5635   -0.3827   -2.4406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8149   -1.7305   -0.3845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0749   -0.2182    0.6387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0058   -0.4676   -1.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3544    0.9469   -0.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9860   -1.2236    2.4564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6150    0.3657    1.9344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8355    0.1558    2.3032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3707   -1.7876   -0.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7296   -3.2162    1.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8935   -1.6458    2.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4824   -2.3813    1.6044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9003   -2.1235   -0.1282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9373    0.0735   -0.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7394    1.3445   -0.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3290    1.1455    0.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0656    1.3189    1.9382 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5059   -1.5822    3.0143 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4689   -0.0411    3.9670 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7046   -0.8423    3.5217 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3048    0.7773    2.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3624   -1.8368    1.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2227   -1.4396   -0.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5068   -0.0129   -1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4888   -1.3490   -1.1266 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0457    1.7869    1.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7428    2.0200   -0.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3907    1.5150    1.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7442    2.9204    0.3801 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9875    1.8631   -1.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.2230    0.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0483   -1.2605   -0.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1531   -0.1939    0.9888 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6494   -0.9512   -2.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0902    0.5971   -3.1346 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4007    1.6252   -2.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3425    0.3079   -3.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2468    0.5079   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 29  1  0
 27 28  2  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  8 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 13 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 17 57  1  0
 19 58  1  0
 19 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  0
 21 64  1  0
 22 65  1  0
 24 66  1  0
 24 67  1  0
 24 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 29 73  1  0
M  END


  Mrv1533004181501462D          

 29 28  0  0  0  0            999 V2000
   11.1375    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    4.2868    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
    7.0125    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 10 27  1  0  0  0  0
  6 28  1  0  0  0  0
  2 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0227470

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H44O2/c1-22(2)12-9-15-25(5)18-10-16-23(3)13-7-8-14-24(4)17-11-19-26(6)20-21-27(28)29/h12-14,18-19H,7-11,15-17,20-21H2,1-6H3,(H,28,29)

> <INCHI_KEY>
BJHPHCBHTOHNEI-UHFFFAOYSA-N

> <FORMULA>
C27H44O2

> <MOLECULAR_WEIGHT>
400.647

> <EXACT_MASS>
400.334130657

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
51.34638044007455

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid

> <ALOGPS_LOGP>
7.58

> <JCHEM_LOGP>
8.331192842666667

> <ALOGPS_LOGS>
-5.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.928870878433938

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
131.68259999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.12e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      20.790  12.003   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.020  10.669   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.710   9.336   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.400   8.002   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.860   8.002   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.090   6.668   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.780   5.335   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.850   4.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000  -2.667   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.770  -4.001   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.000  -5.335   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -2.310  -4.001   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      11.550   4.001   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.170   6.668   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      20.790   9.336   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   10                                                            
CONECT   28    6                                                            
CONECT   29    2                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   56    0
END

View in JSmol

Synonyms

Value	Source
4,8,13,17,21-Pentamethyl-4,8,12,16,20-docosapentaenoic acid	MeSH
Turbinaric acid	MeSH
4,8,13,17,21-Pentamethyl-4,8,12,16,20-docosapentaenoate	Generator

Chemical Formula

C₂₇H₄₄O₂

Average Mass

400.6470 Da

Monoisotopic Mass

400.33413 Da

IUPAC Name

4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid

Traditional Name

4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC(O)=O

InChI Identifier

InChI=1S/C27H44O2/c1-22(2)12-9-15-25(5)18-10-16-23(3)13-7-8-14-24(4)17-11-19-26(6)20-21-27(28)29/h12-14,18-19H,7-11,15-17,20-21H2,1-6H3,(H,28,29)

InChI Key

BJHPHCBHTOHNEI-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 sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Very long-chain fatty acid
Branched fatty acid
Methyl-branched fatty acid
Unsaturated fatty acid
Fatty acyl
Fatty acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

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	7.58	ALOGPS
logP	8.33	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.93	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	15	ChemAxon
Refractivity	131.68 m³·mol⁻¹	ChemAxon
Polarizability	51.35 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

124342

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid (NP0227470)

MOL for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

3D MOL for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

3D SDF for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

3D-SDF for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

PDB for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

3D PDB for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

SMILES for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

INCHI for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

Structure for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)

3D Structure for NP0227470 (4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenoic acid)