NP-MRD: Showing NP-Card for 2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0186589)

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Record Information

Version

2.0

Created at

2022-09-04 02:29:36 UTC

Updated at

2022-09-04 02:29:36 UTC

NP-MRD ID

NP0186589

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

2-{[(6AR,11aS)-9-[(1S)-1-[(2S)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1H,2H,3H,4H,6H,6aH,11H,11aH,11bH-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as fluorenes. Fluorenes are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene. 2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Veratrum dahuricum and Veratrum nigrum. Based on a literature review very few articles have been published on 2-{[(6aR,11aS)-9-[(1S)-1-[(2S)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1H,2H,3H,4H,6H,6aH,11H,11aH,11bH-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042204292D          

 41 46  0  0  1  0            999 V2000
    4.4220    2.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309042204292D          

 41 46  0  0  1  0            999 V2000
    4.4220    2.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8493    1.9927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5041    0.7227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2374    1.1007    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9315    0.6548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8923   -0.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5863   -0.6153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1590   -0.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4649   -0.1014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7317   -0.4795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0376   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3043   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6103    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6495    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8779    1.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3618    0.5068    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8144   -0.1829    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4434   -0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6198   -0.9670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1671   -0.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3435   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1092    0.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9328    0.3182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3855    1.0079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2091    0.9608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6618    1.6505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4854    1.6034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8564    0.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2908    2.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7435    3.0771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4671    2.4345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0961    3.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0145    1.7448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1908    1.7920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2618    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0855    1.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5381    0.4596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9091    1.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  4  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
  3 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 16  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 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
 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 27 36  1  0  0  0  0
 36 37  1  0  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 23 40  1  0  0  0  0
 19 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0186589

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]([C@@H]1NCC(C)CC1O)C1=C(C)C2=C(C=C1)[C@@H]1CC=C3CC(CCC3(C)[C@H]1C2)OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C33H49NO7/c1-16-11-26(36)28(34-14-16)18(3)21-7-8-22-23-6-5-19-12-20(9-10-33(19,4)25(23)13-24(22)17(21)2)40-32-31(39)30(38)29(37)27(15-35)41-32/h5,7-8,16,18,20,23,25-32,34-39H,6,9-15H2,1-4H3/t16?,18-,20?,23-,25-,26?,27?,28-,29?,30?,31?,32?,33?/m0/s1

> <INCHI_KEY>
WXQHVBNTINGJJR-NHJAXKLSSA-N

> <FORMULA>
C33H49NO7

> <MOLECULAR_WEIGHT>
571.755

> <EXACT_MASS>
571.350902922

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
65.46050684183733

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[(1S,10R)-14-[(1S)-1-[(2S)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-7,11(16),12,14-tetraen-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
2.6423507343333337

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.1841900723728

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210645040195384

> <JCHEM_PKA_STRONGEST_BASIC>
9.911003422147147

> <JCHEM_POLAR_SURFACE_AREA>
131.64000000000001

> <JCHEM_REFRACTIVITY>
156.50220000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{[(1S,10R)-14-[(1S)-1-[(2S)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-7,11(16),12,14-tetraen-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       8.254   3.847   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.181   2.308   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.477   1.476   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.845   2.181   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.919   3.720   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.141   1.349   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      13.510   2.055   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      14.805   1.222   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.732  -0.316   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.028  -1.149   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.363  -1.022   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.068  -0.189   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.699  -0.895   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.404  -0.063   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.035  -0.768   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.739   0.064   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.812   1.603   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.372   2.147   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.409   0.946   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.254  -0.341   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.561  -1.717   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.024  -1.805   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.179  -0.517   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.641  -0.606   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.204   0.682   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.741   0.594   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.586   1.881   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -4.124   1.793   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.969   3.081   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.506   2.993   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -7.199   1.617   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -4.276   4.456   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -5.121   5.744   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -2.739   4.544   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.046   5.920   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -1.894   3.257   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.356   3.345   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       0.489   2.057   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.026   2.146   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.871   0.858   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.564   2.234   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4   14                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12                                                            
CONECT   14    3   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   20                                                  
CONECT   17   16    2   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   40                                                  
CONECT   20   19   16   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   40                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   38                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   36                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   27   37                                                  
CONECT   37   36                                                            
CONECT   38   25   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   23   19   41                                             
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₉NO₇

Average Mass

571.7550 Da

Monoisotopic Mass

571.35090 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]([C@@H]1NCC(C)CC1O)C1=C(C)C2=C(C=C1)[C@@H]1CC=C3CC(CCC3(C)[C@H]1C2)OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C33H49NO7/c1-16-11-26(36)28(34-14-16)18(3)21-7-8-22-23-6-5-19-12-20(9-10-33(19,4)25(23)13-24(22)17(21)2)40-32-31(39)30(38)29(37)27(15-35)41-32/h5,7-8,16,18,20,23,25-32,34-39H,6,9-15H2,1-4H3/t16?,18-,20?,23-,25-,26?,27?,28-,29?,30?,31?,32?,33?/m0/s1

InChI Key

WXQHVBNTINGJJR-NHJAXKLSSA-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
Veratrum dahuricum	LOTUS Database	35616633
Veratrum nigrum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fluorenes. Fluorenes are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Fluorenes

Sub Class

Not Available

Direct Parent

Fluorenes

Alternative Parents

Substituents

Fluorene
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Indane
Aralkylamine
Monosaccharide
Oxane
Piperidine
1,2-aminoalcohol
Secondary alcohol
Azacycle
Acetal
Secondary aliphatic amine
Organoheterocyclic compound
Oxacycle
Secondary amine
Polyol
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Amine
Organonitrogen compound
Organooxygen compound
Alcohol
Primary alcohol
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

Not Available

Chemspider ID

9730

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10136

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0186589)

MOL for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0186589 (2-{[(6ar,11as)-9-[(1s)-1-[(2s)-3-hydroxy-5-methylpiperidin-2-yl]ethyl]-10,11b-dimethyl-1h,2h,3h,4h,6h,6ah,11h,11ah-cyclohexa[a]fluoren-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)