NP-MRD: Showing NP-Card for (3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one (NP0322559)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 01:23:59 UTC

Updated at

2022-09-12 01:24:00 UTC

NP-MRD ID

NP0322559

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one

Description

PUQIENINE B belongs to the class of organic compounds known as piperidines. Piperidines are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms. (3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one is found in Fritillaria puqiensis. (3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one was first documented in 2005 (PMID: 15730259). Based on a literature review very few articles have been published on PUQIENINE B (PMID: 19686814).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122203242D          

 32 36  0  0  1  0            999 V2000
    3.6701   -3.2268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7093   -2.4027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4426   -2.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2142   -2.3166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7303   -1.6730    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2776   -0.9832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6486   -0.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4723   -0.1992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8433    0.5377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9249   -0.8889    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7486   -0.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2012   -1.5315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.0249   -1.4844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8302   -2.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0066   -2.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5539   -1.6258    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1829   -2.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4818   -1.2006    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7877   -0.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0545   -1.1327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0152   -1.9568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2820   -2.3348    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2428   -3.1589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5879   -1.8888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8547   -2.2669    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8154   -3.0910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1606   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1998   -0.9969    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4943   -0.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9331   -0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6271   -1.0648    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3604   -0.6867    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  8  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  1  0  0  0
  6 18  1  0  0  0  0
 18  3  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  1  0  0  0
 24 22  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

 77 81  0  0  0  0  0  0  0  0999 V2000
    0.6314   -2.3647    0.6802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4153   -1.0047    0.1525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8229   -0.5821   -0.0695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1632   -1.2177    0.1012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0494    0.0039    0.1157 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4389    0.7949   -1.0205 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0961    2.1435   -1.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5654    1.9328   -1.1618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2240    2.4880   -2.0127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2166    1.0495   -0.1896 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6638    0.8205   -0.4577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2888   -0.0140    0.6084 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.5367   -0.4552    0.1102 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5156   -1.2326    0.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0295   -0.9842    1.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4955   -0.2909   -0.0846 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7468   -1.1566   -1.2960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0076    0.8241   -0.6090 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0386    0.9760   -1.7211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3703    0.9049   -1.1649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5832   -0.1263   -0.1174 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8755   -0.9060   -0.2362 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0454   -1.6384   -1.5208 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0669   -0.1919    0.2885 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6640    0.8654   -0.5608 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4805    0.3535   -1.5809 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6185    1.6861    0.3260 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6834    0.7477    0.8304 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5795    1.5074    1.7653 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9916   -0.3580    1.6032 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1225   -1.1009    0.7103 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5691   -2.1881    1.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3624   -2.8636    0.8860 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291   -3.0586   -0.0334 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1381   -2.3710    1.6685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2030   -1.7180    1.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3198   -1.8721   -0.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8921    0.5494    1.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5664    0.2925   -1.9978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8048    2.8134   -0.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7841    2.6448   -2.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1290    1.5290    0.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8592    0.4478   -1.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1684    1.8304   -0.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5495    0.6078    1.5026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3392   -1.0690   -0.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8779   -1.5498    2.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6953   -2.1053    0.3337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8145   -0.3466    2.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5238   -1.9512    1.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8584   -1.3250   -1.3576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3157   -2.1495   -1.0767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3238   -0.7235   -2.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8505    1.4995    0.2395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2308    0.1755   -2.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1246    1.9599   -2.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5795    1.9355   -0.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0380    0.7749   -2.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7122    0.4389    0.8728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7157   -1.7565    0.5357 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5934   -2.5826   -1.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6618   -1.0947   -2.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0515   -1.9123   -1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7332    0.3117    1.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9279    1.5833   -0.9448 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1359    1.0093   -1.9061 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0949    2.0971    1.1944 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0558    2.5188   -0.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2792    0.3101    0.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6379    2.5550    1.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6137    1.1044    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1924    1.5117    2.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3386    0.1229    2.3622 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7034   -1.0056    2.1348 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8120   -1.8076    2.2447 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4140   -2.5729    2.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2372   -3.0424    0.9348 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  6
 16  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
  2 21  1  0
 31 24  1  0
  3 18  1  0
  5  6  1  0
 16 10  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 22 60  1  1
 21 59  1  1
 20 57  1  0
 20 58  1  0
 19 55  1  0
 19 56  1  0
 18 54  1  1
  6 39  1  6
  7 40  1  0
  7 41  1  0
 10 42  1  1
 11 43  1  0
 11 44  1  0
 12 45  1  1
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 17 51  1  0
 17 52  1  0
 17 53  1  0
  5 38  1  1
  4 36  1  0
  4 37  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
 24 64  1  1
 25 65  1  6
 26 66  1  0
 27 67  1  0
 27 68  1  0
 28 69  1  6
 29 70  1  0
 29 71  1  0
 29 72  1  0
 30 73  1  0
 30 74  1  0
 32 75  1  0
 32 76  1  0
 32 77  1  0
M  END


  Mrv1652309122203242D          

 32 36  0  0  1  0            999 V2000
    3.6701   -3.2268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7093   -2.4027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4426   -2.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2142   -2.3166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7303   -1.6730    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2776   -0.9832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6486   -0.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4723   -0.1992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8433    0.5377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9249   -0.8889    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7486   -0.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2012   -1.5315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.0249   -1.4844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8302   -2.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0066   -2.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5539   -1.6258    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1829   -2.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4818   -1.2006    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7877   -0.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0545   -1.1327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0152   -1.9568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2820   -2.3348    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2428   -3.1589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5879   -1.8888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8547   -2.2669    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8154   -3.0910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1606   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1998   -0.9969    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4943   -0.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9331   -0.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6271   -1.0648    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3604   -0.6867    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  8  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  1  0  0  0
  6 18  1  0  0  0  0
 18  3  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  1  0  0  0
 24 22  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322559

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]([C@H]1CC[C@H]2[C@@H]3CC(=O)[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC2=C1C)[C@@H]1[C@H](O)C[C@@H](C)CN1C

> <INCHI_IDENTIFIER>
InChI=1S/C28H45NO3/c1-15-10-26(32)27(29(5)14-15)17(3)19-6-7-20-21(16(19)2)12-23-22(20)13-25(31)24-11-18(30)8-9-28(23,24)4/h15,17-20,22-24,26-27,30,32H,6-14H2,1-5H3/t15-,17-,18+,19+,20-,22+,23+,24-,26-,27-,28-/m1/s1

> <INCHI_KEY>
RITHKXDOKOLLCZ-PXRUYVGHSA-N

> <FORMULA>
C28H45NO3

> <MOLECULAR_WEIGHT>
443.672

> <EXACT_MASS>
443.339944313

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
52.89628088291674

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,7S,10R,11S,14R)-5-hydroxy-14-[(1R)-1-[(2R,3R,5R)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadec-15-en-8-one

> <JCHEM_LOGP>
3.617882951333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.32069086261788

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.490614154481694

> <JCHEM_PKA_STRONGEST_BASIC>
9.532158643564355

> <JCHEM_POLAR_SURFACE_AREA>
60.77

> <JCHEM_REFRACTIVITY>
129.36189999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,7S,10R,11S,14R)-5-hydroxy-14-[(1R)-1-[(2R,3R,5R)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadec-15-en-8-one

> <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       6.851  -6.023   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.924  -4.485   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.293  -3.779   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.733  -4.324   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.697  -3.123   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.852  -1.835   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.544  -0.460   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.082  -0.372   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.774   1.004   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      12.927  -1.659   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.464  -1.571   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.309  -2.859   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      16.846  -2.771   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.616  -4.234   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.079  -4.322   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.234  -3.035   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.541  -4.410   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.366  -2.241   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.070  -1.409   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.702  -2.114   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.628  -3.653   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.260  -4.358   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.187  -5.897   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.964  -3.526   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.595  -4.232   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.522  -5.770   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.300  -3.399   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.373  -1.861   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.923  -1.028   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.742  -1.155   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       3.037  -1.988   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       4.406  -1.282   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   16                                                  
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10    5   17                                             
CONECT   17   16                                                            
CONECT   18    6    3   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    2   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   31                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   24   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₄₅NO₃

Average Mass

443.6720 Da

Monoisotopic Mass

443.33994 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]([C@H]1CC[C@H]2[C@@H]3CC(=O)[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC2=C1C)[C@@H]1[C@H](O)C[C@@H](C)CN1C

InChI Identifier

InChI=1S/C28H45NO3/c1-15-10-26(32)27(29(5)14-15)17(3)19-6-7-20-21(16(19)2)12-23-22(20)13-25(31)24-11-18(30)8-9-28(23,24)4/h15,17-20,22-24,26-27,30,32H,6-14H2,1-5H3/t15-,17-,18+,19+,20-,22+,23+,24-,26-,27-,28-/m1/s1

InChI Key

RITHKXDOKOLLCZ-PXRUYVGHSA-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
Fritillaria puqiensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as piperidines. Piperidines are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Piperidines

Sub Class

Not Available

Direct Parent

Piperidines

Alternative Parents

Substituents

Piperidine
Cyclic alcohol
1,2-aminoalcohol
Ketone
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Azacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Amine
Alcohol
Organic nitrogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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

C00028890

Chemspider ID

9594275

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11419389

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Jiang Y, Li H, Li P, Cai Z, Ye W: Steroidal alkaloids from the bulbs of Fritillaria puqiensis. J Nat Prod. 2005 Feb;68(2):264-7. doi: 10.1021/np0497649. [PubMed:15730259 ]
An JJ, Zhou JL, Li HJ, Jiang Y, Li P: Puqienine E: an angiotensin converting enzyme inhibitory steroidal alkaloid from Fritillaria puqiensis. Fitoterapia. 2010 Apr;81(3):149-52. doi: 10.1016/j.fitote.2009.08.012. Epub 2009 Aug 15. [PubMed:19686814 ]
LOTUS database [Link]

Showing NP-Card for (3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one (NP0322559)

MOL for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

3D MOL for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

3D SDF for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

3D-SDF for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

PDB for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

3D PDB for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

SMILES for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

INCHI for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

Structure for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)

3D Structure for NP0322559 ((3s,4as,6ar,6bs,9r,11as,11br)-3-hydroxy-9-[(1r)-1-[(2r,3r,5r)-3-hydroxy-1,5-dimethylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,4ah,6h,6ah,6bh,7h,8h,9h,11h,11ah-cyclohexa[a]fluoren-5-one)