NP-MRD: Showing NP-Card for (1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol (NP0321137)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 23:10:48 UTC

Updated at

2022-09-11 23:10:48 UTC

NP-MRD ID

NP0321137

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol

Description

CHEMBL483024 belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. (1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol is found in Antipathella subpinnata. Based on a literature review very few articles have been published on CHEMBL483024.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122201102D          

 31 34  0  0  1  0            999 V2000
    6.9960   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4249   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1394   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8538   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5683   -2.5011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.5683   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2828   -2.0886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3690   -1.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1760   -1.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5885   -1.8111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.3955   -1.9826    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.9475   -1.3695    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.6926   -0.5849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7545   -1.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0094   -2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8164   -2.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0713   -3.2818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.8783   -3.4534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5193   -3.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7123   -3.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4574   -2.9388    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9053   -3.5519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1603   -4.3365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6504   -2.7673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3955   -3.5519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0984   -3.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2914   -3.2088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0365   -2.4242    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4234   -2.9762    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
  2  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  6  0  0  0
  9  7  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
  9 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END

     RDKit          3D

 77 80  0  0  0  0  0  0  0  0999 V2000
    7.3032    1.0501    1.0574 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1021    0.7260   -0.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1155   -0.3559   -0.7561 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6921    0.1642   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7458    1.2220   -0.2204 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2802    0.8864   -0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9110   -0.3195    0.4180 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1984   -0.0365    1.8629 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6140   -0.9359    0.1086 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4262   -2.1445    1.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0396   -1.9270    1.6486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6378   -1.2663    0.5103 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0189   -0.8274    0.6809 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8712   -2.1006    0.8154 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6677   -2.6180    2.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3159   -1.6893    0.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7470   -0.6030    0.1410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2354   -0.3396    0.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7449   -0.0409   -1.2230 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.0285    0.4848   -1.0911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8415    0.8817   -2.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4053    0.4824   -1.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8533    0.3717   -0.5636 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9706    1.6977    0.1449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5979    1.6470    1.4772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4891   -0.1970   -0.6164 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5201   -1.2573   -1.5540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4990    0.8002   -1.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1145    0.1999   -1.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3634   -0.1685    0.1170 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2568    1.0409    0.9369 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3927    1.0095    1.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9448    2.0589    1.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8398    0.2610    1.7109 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2681    1.6540   -0.9885 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0066   -1.1370    0.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1269    0.0711   -0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8793   -0.8310   -1.7298 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6656   -0.7716   -0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6127    0.0166   -1.7447 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8883    1.5190    0.8382 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9757    2.1391   -0.8234 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0876    0.7924   -1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420    1.7773    0.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6810   -1.1016    0.1153 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2480    1.0745    2.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3921    2.1784 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -0.4536    2.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7065   -1.3744   -0.9348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3294   -3.0971    0.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2111   -2.2819    1.7509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3511   -2.9033    1.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1079   -1.3064    2.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6020   -1.9862   -0.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2548   -0.2473    1.5756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5934   -2.7786    0.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9874   -1.9331    2.7345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0679   -2.3300    1.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7838   -1.1997    0.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3882    0.5562    0.7972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8507   -1.0171   -1.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2543    1.0881   -1.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1653    0.8619   -3.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0092    1.9356   -1.6678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323    1.2664   -2.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3141   -0.5038   -2.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3863    2.4950   -0.3471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0287    2.0214    0.1176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3784    1.5334    2.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2587   -0.9178   -2.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8320    1.0239   -2.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4507    1.7378   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0986   -0.6898   -1.9298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5283    0.9670   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8640    1.1124    1.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3714    1.9508    0.2738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8117    1.1517    1.2967 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  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
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 24 25  1  0
 23 26  1  0
 26 27  1  6
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  1
 30  9  1  0
 30 12  1  0
 26 13  1  0
 23 17  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  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  6
 15 57  1  0
 16 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  6
 20 62  1  0
 21 63  1  0
 21 64  1  0
 22 65  1  0
 22 66  1  0
 24 67  1  0
 24 68  1  0
 25 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 31 75  1  0
 31 76  1  0
 31 77  1  0
M  END


  Mrv1652309122201102D          

 31 34  0  0  1  0            999 V2000
    6.9960   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7104   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4249   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1394   -2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8538   -2.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5683   -2.5011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.5683   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2828   -2.0886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3690   -1.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1760   -1.0966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5885   -1.8111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.3955   -1.9826    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.9475   -1.3695    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.6926   -0.5849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7545   -1.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0094   -2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8164   -2.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0713   -3.2818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.8783   -3.4534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5193   -3.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7123   -3.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4574   -2.9388    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9053   -3.5519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1603   -4.3365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6504   -2.7673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3955   -3.5519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0984   -3.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2914   -3.2088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0365   -2.4242    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4234   -2.9762    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
  2  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  6  0  0  0
  9  7  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
  9 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0321137

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C=C4C[C@@H](O)CC[C@]4(CO)[C@@]3(O)CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H46O4/c1-17(2)6-5-7-18(3)21-8-9-22-24-23(30)15-19-14-20(29)10-11-26(19,16-28)27(24,31)13-12-25(21,22)4/h15,17-18,20-24,28-31H,5-14,16H2,1-4H3/t18-,20+,21-,22+,23+,24-,25-,26-,27-/m1/s1

> <INCHI_KEY>
IHAYVMNCCIGXGO-VHTRLTIZSA-N

> <FORMULA>
C27H46O4

> <MOLECULAR_WEIGHT>
434.661

> <EXACT_MASS>
434.339609961

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
52.58361023570666

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,5S,9S,10R,11S,14R,15R)-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-1,5,9-triol

> <JCHEM_LOGP>
3.5615174990000007

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.552638137581152

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.796513136876044

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3973697656503297

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
125.25899999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5S,9S,10R,11S,14R,15R)-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-1,5,9-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      13.059  -3.899   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.393  -4.669   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.393  -6.209   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.726  -3.899   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.060  -4.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.394  -3.899   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.728  -4.669   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.728  -6.209   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.061  -3.899   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.222  -2.367   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.729  -2.047   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      23.499  -3.381   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.005  -3.701   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.035  -2.556   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      25.559  -1.092   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      27.542  -2.877   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.018  -4.341   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      29.524  -4.661   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      30.000  -6.126   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      31.506  -6.446   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      28.969  -7.271   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      27.463  -6.950   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      26.987  -5.486   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.957  -6.630   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      26.433  -8.095   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      25.481  -5.166   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      25.005  -6.630   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      24.450  -6.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      22.944  -5.990   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      22.468  -4.525   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      21.324  -5.556   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    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   26                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   17   24   26                                             
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   13   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   12    9   31                                             
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₆O₄

Average Mass

434.6610 Da

Monoisotopic Mass

434.33961 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C=C4C[C@@H](O)CC[C@]4(CO)[C@@]3(O)CC[C@]12C

InChI Identifier

InChI=1S/C27H46O4/c1-17(2)6-5-7-18(3)21-8-9-22-24-23(30)15-19-14-20(29)10-11-26(19,16-28)27(24,31)13-12-25(21,22)4/h15,17-18,20-24,28-31H,5-14,16H2,1-4H3/t18-,20+,21-,22+,23+,24-,25-,26-,27-/m1/s1

InChI Key

IHAYVMNCCIGXGO-VHTRLTIZSA-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
Antipathella subpinnata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholesterols and derivatives

Alternative Parents

Substituents

Cholesterol
Cholesterol-skeleton
19-hydroxysteroid
3-hydroxy-delta-5-steroid
3-hydroxysteroid
7-hydroxysteroid
Hydroxysteroid
3-beta-hydroxy-delta-5-steroid
3-beta-hydroxysteroid
7-alpha-hydroxysteroid
Delta-5-steroid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Polyol
Organooxygen compound
Alcohol
Primary alcohol
Organic oxygen compound
Hydrocarbon derivative
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

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

24700838

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44576100

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol (NP0321137)

MOL for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

3D MOL for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

3D SDF for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

3D-SDF for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

PDB for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

3D PDB for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

SMILES for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

INCHI for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

Structure for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)

3D Structure for NP0321137 ((1r,3as,3br,4s,7s,9as,9br,11ar)-9a-(hydroxymethyl)-11a-methyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7,9b-triol)