NP-MRD: Showing NP-Card for 1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol (NP0149335)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 05:12:30 UTC

Updated at

2022-09-02 05:12:30 UTC

NP-MRD ID

NP0149335

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol

Description

14-(5-Ethyl-3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-3,5,7,8-tetrol belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24. 14-(5-Ethyl-3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-3,5,7,8-tetrol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191522022D          

 34 37  0  0  0  0            999 V2000
    8.2924   -0.1891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4674   -0.1891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0549   -0.9035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2299   -0.9035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8174   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2299   -2.3325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9924   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5799   -2.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5799   -0.9035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7594   -0.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879   -0.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    0.4022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4739    1.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8608    1.7612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0323    2.5681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4192    3.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8170    2.8231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2039    3.3751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9885    3.6301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7731    3.8850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9446    4.6920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3862    3.3330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2147    2.5260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8278    1.9740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4301    2.2711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0432    1.7190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2585    1.4641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8716    0.9121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7001    0.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9155   -0.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4675   -0.7630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4674   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2924   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0549   -2.3325    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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  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
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END

     RDKit          3D

 86 89  0  0  0  0  0  0  0  0999 V2000
    4.7204    2.3278   -0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7053    1.2710    0.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3230    0.2221    1.0546 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3061   -0.7655    0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784   -0.5405    0.5195 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3652   -1.9394    0.6227 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5418   -0.2437   -0.9304 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9636   -1.4862   -1.7104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2671    0.3211   -1.2906 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0479    1.6557   -0.6171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2371    2.0836   -1.3488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989    0.7947   -1.5486 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1488    0.8083   -0.5845 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0409    1.9594   -1.0175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4919    1.6608   -0.8628 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9963    0.9701   -1.9377 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6491    0.8748    0.4196 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8007    1.4087    1.4125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0369    0.9749    0.9499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1685    0.0989    2.1764 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5197   -0.0210    2.4649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6087   -1.2634    1.9875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1540   -1.2438    1.4985 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4139   -0.6069    2.4564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1650   -0.5251    0.1548 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1960   -1.3086   -0.6771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8626   -0.5185   -0.5524 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8811   -1.5294   -0.0931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4392   -1.2180   -0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0274   -0.3566   -1.3895 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1478   -1.1401   -2.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6614   -0.5731    1.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6900    0.3824    1.8383 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4564   -1.7350    2.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1481    3.3198    0.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7674    2.1868    0.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095    2.4292   -1.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6884    1.7596    0.3643 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9703    0.7680   -0.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1746    0.7719    2.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6752   -1.4688   -0.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3708   -1.5517    1.7028 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3617   -0.0271    1.2790 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0957   -2.5346    0.8200 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3086    0.4801   -1.2660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5145   -1.4630   -2.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7857   -2.4194   -1.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0473   -1.4053   -1.9005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4241    0.6804   -2.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8108    2.4075   -0.9309 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8021    1.6303    0.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0114    2.5854   -2.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8159    2.8083   -0.7423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3965    0.8473   -2.5820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7251    0.9832    0.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8662    2.2275   -2.0864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8175    2.8413   -0.3566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0649    2.6145   -0.7173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2397    1.5254   -2.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2490    2.2025    1.8025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1526    2.0339    1.3312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8353    0.8406    0.2183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7099    0.6125    3.0672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9639   -0.3346    1.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2493   -1.8660    1.3403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5574   -1.7493    2.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9236   -2.3388    1.3786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8970   -0.3038    3.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8685   -1.3553   -1.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2089   -0.9434   -0.5407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2004   -2.3908   -0.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0775   -0.7434   -1.6428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0218   -1.7823    1.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1767   -2.5043   -0.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0715   -0.7497    0.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0243   -2.2317   -0.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2266   -2.1565   -2.6196 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4165   -0.6180   -3.5269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2009   -1.1230   -3.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9647   -0.9296    0.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2717   -0.1654    2.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1681    1.2033    2.3772 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3799    0.7628    1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4681   -2.0672    2.5808 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0476   -2.6414    1.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8147   -1.4571    3.0764 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
  5  7  1  0
  7  8  1  0
  7  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
 15 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  6
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  6
  3 32  1  0
 32 33  1  0
 32 34  1  0
 30  9  1  0
 30 12  1  0
 27 13  1  0
 25 17  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  3 40  1  1
  4 41  1  0
  4 42  1  0
  5 43  1  1
  6 44  1  0
  7 45  1  6
  8 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  6
 10 50  1  0
 10 51  1  0
 11 52  1  0
 11 53  1  0
 12 54  1  6
 13 55  1  1
 14 56  1  0
 14 57  1  0
 15 58  1  1
 16 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 20 63  1  1
 21 64  1  0
 22 65  1  0
 22 66  1  0
 23 67  1  6
 24 68  1  0
 26 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  6
 28 73  1  0
 28 74  1  0
 29 75  1  0
 29 76  1  0
 31 77  1  0
 31 78  1  0
 31 79  1  0
 32 80  1  0
 33 81  1  0
 33 82  1  0
 33 83  1  0
 34 84  1  0
 34 85  1  0
 34 86  1  0
M  END


  Mrv1533004191522022D          

 34 37  0  0  0  0            999 V2000
    8.2924   -0.1891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4674   -0.1891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0549   -0.9035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2299   -0.9035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8174   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2299   -2.3325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9924   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5799   -2.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5799   -0.9035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7594   -0.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879   -0.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    0.4022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4739    1.2091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8608    1.7612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0323    2.5681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4192    3.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8170    2.8231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2039    3.3751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9885    3.6301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7731    3.8850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9446    4.6920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3862    3.3330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2147    2.5260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8278    1.9740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4301    2.2711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0432    1.7190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2585    1.4641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8716    0.9121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7001    0.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9155   -0.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4675   -0.7630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4674   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2924   -1.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0549   -2.3325    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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  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
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0149335

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(CC(O)C(C)C1CCC2C3CC(O)C4(O)CC(O)CC(O)C4(C)C3CCC12C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C29H52O5/c1-7-18(16(2)3)12-24(31)17(4)21-8-9-22-20-14-26(33)29(34)15-19(30)13-25(32)28(29,6)23(20)10-11-27(21,22)5/h16-26,30-34H,7-15H2,1-6H3

> <INCHI_KEY>
SENGWVUFOJLNFP-UHFFFAOYSA-N

> <FORMULA>
C29H52O5

> <MOLECULAR_WEIGHT>
480.73

> <EXACT_MASS>
480.381474774

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
57.62302445410637

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-3,5,7,8-tetrol

> <ALOGPS_LOGP>
3.23

> <JCHEM_LOGP>
3.330689025333335

> <ALOGPS_LOGS>
-4.36

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.359144228118762

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.202036981809798

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6624374602467146

> <JCHEM_POLAR_SURFACE_AREA>
101.15

> <JCHEM_REFRACTIVITY>
134.8265

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.11e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-3,5,7,8-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      15.479  -0.353   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.939  -0.353   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.169  -1.687   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.629  -1.687   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.859  -3.020   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.629  -4.354   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       9.319  -3.020   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.549  -4.354   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.549  -1.687   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.018  -1.526   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.697  -0.019   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.031   0.751   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.351   2.257   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.207   3.288   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.527   4.794   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.383   5.824   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.992   5.270   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.847   6.300   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.312   6.776   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.776   7.252   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.097   8.758   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.921   6.222   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.601   4.715   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.745   3.685   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.136   4.239   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.281   3.209   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.816   2.733   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.960   1.702   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.640   0.196   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.176  -0.280   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.206  -1.424   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.939  -3.020   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.479  -3.020   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.169  -4.354   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   30                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   30                                                  
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   25                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   13   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    9   12   31                                             
CONECT   31   30                                                            
CONECT   32    3   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₅₂O₅

Average Mass

480.7300 Da

Monoisotopic Mass

480.38147 Da

IUPAC Name

14-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-3,5,7,8-tetrol

Traditional Name

14-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-3,5,7,8-tetrol

CAS Registry Number

Not Available

SMILES

CCC(CC(O)C(C)C1CCC2C3CC(O)C4(O)CC(O)CC(O)C4(C)C3CCC12C)C(C)C

InChI Identifier

InChI=1S/C29H52O5/c1-7-18(16(2)3)12-24(31)17(4)21-8-9-22-20-14-26(33)29(34)15-19(30)13-25(32)28(29,6)23(20)10-11-27(21,22)5/h16-26,30-34H,7-15H2,1-6H3

InChI Key

SENGWVUFOJLNFP-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 stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Stigmastanes and derivatives

Direct Parent

Stigmastanes and derivatives

Alternative Parents

Substituents

C24-propyl-sterol-skeleton
Triterpenoid
Stigmastane-skeleton
Pentahydroxy bile acid, alcohol, or derivatives
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
22-hydroxysteroid
3-hydroxysteroid
1-hydroxysteroid
6-hydroxysteroid
5-hydroxysteroid
Hydroxysteroid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Polyol
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	3.23	ALOGPS
logP	3.33	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	13.2	ChemAxon
pKa (Strongest Basic)	-0.66	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	101.15 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	134.83 m³·mol⁻¹	ChemAxon
Polarizability	57.62 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

75021374

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol (NP0149335)

MOL for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

3D MOL for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

3D SDF for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

3D-SDF for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

PDB for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

3D PDB for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

SMILES for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

INCHI for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

Structure for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)

3D Structure for NP0149335 (1-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthrene-5,5a,7,9-tetrol)