NP-MRD: Showing NP-Card for (-)-Schleicherastatin 5 (NP0081178)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 02:08:46 UTC

Updated at

2022-04-29 02:08:46 UTC

NP-MRD ID

NP0081178

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Schleicherastatin 5

Description

SCHLEICHERASTATIN 5 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. (-)-Schleicherastatin 5 is found in Schleichera oleosa . Based on a literature review very few articles have been published on SCHLEICHERASTATIN 5.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204082D          

 32 35  0  0  1  0            999 V2000
   -2.5161    0.5961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6876   -0.2108    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0745   -0.7629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2899   -0.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6768   -1.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1078   -0.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7209   -1.3571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794    0.0019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3337    0.5540    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1183    0.2990    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7314    0.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9468    1.1060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1622    1.3609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6224    1.6159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2355    1.0639    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0640    0.2569    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7785   -0.1556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3916    0.3964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    1.1501    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4685    1.8646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2935    1.8646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7060    2.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5310    2.5790    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9435    3.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7685    3.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5310    4.0080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9435    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5310    1.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7060    1.1501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    2.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4905    1.8485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4722   -0.4658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 10 12  1  1  0  0  0
  9 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 29  1  1  0  0  0
 20 30  1  6  0  0  0
 15 31  1  1  0  0  0
  2 32  1  1  0  0  0
M  END

     RDKit          3D

 80 83  0  0  0  0  0  0  0  0999 V2000
    6.1554   -0.9174    2.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1149   -1.1666    1.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0523   -0.2601   -0.0443 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9763   -0.6469   -1.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5661   -0.6937   -0.5334 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4441   -1.6346    0.4803 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1719    0.6478    0.0323 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3254    1.7447   -0.9992 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9094    0.6841    0.8073 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7409    2.1168    1.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6359    2.5713    0.8130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3340    1.2468    0.8500 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6782    1.1489    0.2935 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6495    2.0399    1.0388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2089    2.8137    1.8945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0396    1.8833    0.6555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4291    0.7648    0.0758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8541    0.5611   -0.3340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4788   -0.5884    0.4342 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.0784   -1.4339   -0.4837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3742   -1.2745    1.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2677   -1.6284    0.2227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5103   -0.3834   -0.2211 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2624   -0.4401   -1.7045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2133   -0.2333    0.5221 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2749   -1.3636    0.3476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8698   -1.0832    0.8331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3740    0.2538    0.2322 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4893    0.0976   -1.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3619   -0.0600   -0.7995 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4656    0.5431    0.0036 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7812   -1.3426   -1.4910 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0458    0.0321    2.7083 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9424   -1.6999    2.9678 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1822   -1.1564    1.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1335   -2.2424    0.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1318   -1.0314    1.6776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8097    0.7819    0.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0815    0.0219   -1.9218 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1988   -1.6687   -1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8928   -1.0360   -1.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3493   -2.5634    0.1483 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9474    0.8635    0.7945 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4778    2.4359   -0.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5020    1.3429   -2.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2347    2.3894   -0.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0809    0.0504    1.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7634    2.1434    2.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5085    2.8087    0.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0091    3.2294    1.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6375    3.0757   -0.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4338    1.0149    1.9643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7992    1.5288   -0.7499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7467    2.7032    0.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4223    1.5195   -0.1629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9271    0.3962   -1.4476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2337   -0.1510    1.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2626   -0.9478   -1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7723   -2.2150    1.6094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9880   -0.5756    1.9575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6409   -2.3962    0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7779   -2.0781   -0.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8224    0.4674   -2.1205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7206   -1.3782   -1.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2514   -0.5519   -2.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5257   -0.2369    1.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1921   -1.7501   -0.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6362   -2.2241    0.9549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2202   -1.8791    0.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8093   -1.0429    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1990    0.6945   -1.8533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4589   -0.9864   -1.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4996    0.3880   -1.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1069    0.6569   -1.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1688    1.0331    0.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3568   -0.1468    0.1134 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9446    1.4039   -0.5919 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4553   -1.3871   -2.5488 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3414   -2.2344   -0.9963 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8894   -1.3688   -1.4902 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 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 25 23  1  0
 23 24  1  6
 23 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  1  0
 19 18  1  0
 18 17  1  0
 17 16  2  0
 16 14  1  0
 14 15  2  0
  3 30  1  0
 30 31  1  0
 30 32  1  0
 28  9  1  0
 17 23  1  0
 28 12  1  0
 14 13  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  1
  4 39  1  0
  4 40  1  0
  5 41  1  6
  6 42  1  0
  7 43  1  1
  8 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  1
 10 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  1
 13 53  1  6
 25 66  1  1
 26 67  1  0
 26 68  1  0
 27 69  1  0
 27 70  1  0
 29 71  1  0
 29 72  1  0
 29 73  1  0
 24 63  1  0
 24 64  1  0
 24 65  1  0
 22 61  1  0
 22 62  1  0
 21 59  1  0
 21 60  1  0
 19 57  1  1
 20 58  1  0
 18 55  1  0
 18 56  1  0
 16 54  1  0
 30 74  1  6
 31 75  1  0
 31 76  1  0
 31 77  1  0
 32 78  1  0
 32 79  1  0
 32 80  1  0
M  END


  Mrv1652304292204082D          

 32 35  0  0  1  0            999 V2000
   -2.5161    0.5961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6876   -0.2108    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0745   -0.7629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2899   -0.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6768   -1.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1078   -0.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7209   -1.3571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794    0.0019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3337    0.5540    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1183    0.2990    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7314    0.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9468    1.1060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1622    1.3609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6224    1.6159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2355    1.0639    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0640    0.2569    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7785   -0.1556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3916    0.3964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    1.1501    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4685    1.8646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2935    1.8646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7060    2.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5310    2.5790    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9435    3.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7685    3.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5310    4.0080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9435    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5310    1.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7060    1.1501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    2.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4905    1.8485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4722   -0.4658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 10 12  1  1  0  0  0
  9 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 29  1  1  0  0  0
 20 30  1  6  0  0  0
 15 31  1  1  0  0  0
  2 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0081178

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C[C@@H](O)[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@H](O)CC1=CC3=O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C29H48O3/c1-7-19(17(2)3)14-25(31)18(4)22-8-9-23-27-24(11-13-29(22,23)6)28(5)12-10-21(30)15-20(28)16-26(27)32/h16-19,21-25,27,30-31H,7-15H2,1-6H3/t18-,19+,21-,22+,23-,24-,25+,27-,28-,29+/m0/s1

> <INCHI_KEY>
XWLHFTUCQDCSTJ-PNGDTKJZSA-N

> <FORMULA>
C29H48O3

> <MOLECULAR_WEIGHT>
444.7

> <EXACT_MASS>
444.360345406

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
54.6153516305378

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,10S,11S,14R,15R)-14-[(2S,3R,5R)-5-ethyl-3-hydroxy-6-methylheptan-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one

> <ALOGPS_LOGP>
5.01

> <JCHEM_LOGP>
5.972206598000001

> <ALOGPS_LOGS>
-5.16

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.270745923091404

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.38833010645442

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5843642472725484

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
132.00259999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.10e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,10S,11S,14R,15R)-14-[(2S,3R,5R)-5-ethyl-3-hydroxy-6-methylheptan-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -4.697   1.113   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.017  -0.394   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.872  -1.424   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.408  -0.948   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.263  -1.979   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.201  -1.503   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.346  -2.533   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.521   0.004   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.623   1.034   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.088   0.558   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.232   1.589   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.767   2.065   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.303   2.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.162   3.016   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.306   1.986   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.986   0.480   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.320  -0.290   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.464   0.740   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.838   2.147   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.608   3.481   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.148   3.481   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.918   4.814   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.458   4.814   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.228   6.148   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.768   6.148   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.458   7.482   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.228   3.481   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.458   2.147   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.918   2.147   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.838   4.814   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.782   3.450   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -6.481  -0.869   0.000  0.00  0.00           O+0
CONECT    1    2   11                                                       
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   16                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9    4   11   12                                             
CONECT   11   10    1                                                       
CONECT   12   10                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19   31                                             
CONECT   16   15    8   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   15   20                                                  
CONECT   20   19   21   30                                                  
CONECT   21   20   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   23   28                                                       
CONECT   28   27                                                            
CONECT   29   21                                                            
CONECT   30   20                                                            
CONECT   31   15                                                            
CONECT   32    2                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₈O₃

Average Mass

444.7000 Da

Monoisotopic Mass

444.36035 Da

IUPAC Name

(1S,2R,5S,10S,11S,14R,15R)-14-[(2S,3R,5R)-5-ethyl-3-hydroxy-6-methylheptan-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one

Traditional Name

(1S,2R,5S,10S,11S,14R,15R)-14-[(2S,3R,5R)-5-ethyl-3-hydroxy-6-methylheptan-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one

CAS Registry Number

Not Available

SMILES

CC[C@H](C[C@@H](O)[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@H](O)CC1=CC3=O)C(C)C

InChI Identifier

InChI=1S/C29H48O3/c1-7-19(17(2)3)14-25(31)18(4)22-8-9-23-27-24(11-13-29(22,23)6)28(5)12-10-21(30)15-20(28)16-26(27)32/h16-19,21-25,27,30-31H,7-15H2,1-6H3/t18-,19+,21-,22+,23-,24-,25+,27-,28-,29+/m0/s1

InChI Key

XWLHFTUCQDCSTJ-PNGDTKJZSA-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
Schleichera oleosa	Plant	KNApSAcK

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
Stigmastane-skeleton
Triterpenoid
Dihydroxy bile acid, alcohol, or derivatives
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
22-hydroxysteroid
3-hydroxy-delta-5-steroid
3-hydroxysteroid
7-oxosteroid
Hydroxysteroid
Oxosteroid
3-beta-hydroxysteroid
3-beta-hydroxy-delta-5-steroid
Delta-5-steroid
Cyclohexenone
Cyclic alcohol
Ketone
Secondary alcohol
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Carbonyl group
Organic oxide
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	5.01	ALOGPS
logP	5.97	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	17.39	ChemAxon
pKa (Strongest Basic)	-0.58	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	132 m³·mol⁻¹	ChemAxon
Polarizability	54.62 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

C00046914

Chemspider ID

9972239

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11797567

PDB ID

Not Available

ChEBI ID

169002

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-Schleicherastatin 5 (NP0081178)

MOL for NP0081178 ((-)-Schleicherastatin 5)

3D MOL for NP0081178 ((-)-Schleicherastatin 5)

3D SDF for NP0081178 ((-)-Schleicherastatin 5)

3D-SDF for NP0081178 ((-)-Schleicherastatin 5)

PDB for NP0081178 ((-)-Schleicherastatin 5)

3D PDB for NP0081178 ((-)-Schleicherastatin 5)

SMILES for NP0081178 ((-)-Schleicherastatin 5)

INCHI for NP0081178 ((-)-Schleicherastatin 5)

Structure for NP0081178 ((-)-Schleicherastatin 5)

3D Structure for NP0081178 ((-)-Schleicherastatin 5)