NP-MRD: Showing NP-Card for 16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol (NP0207998)

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Record Information

Version

2.0

Created at

2022-09-05 04:50:00 UTC

Updated at

2022-09-05 04:50:00 UTC

NP-MRD ID

NP0207998

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol

Description

16-(Dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]Icosane-18,20-diol belongs to the class of organic compounds known as conanine-type alkaloids. These are alkaloids with a structure based on the conanine skeleton. 16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol is found in Holarrhena pubescens. 16-(Dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]Icosane-18,20-diol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171518022D          

 29 33  0  0  0  0            999 V2000
   -0.0401   -0.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7847   -0.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2813    0.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2958    1.2411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0847    1.4822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5579    0.8064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3767    0.7057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8733    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5510    2.1240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6921    1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    0.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5110    1.1633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8332    0.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3298    1.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1555   -0.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6590   -1.0144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8401   -0.9138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5178   -0.1543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0213   -0.8131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6990   -0.0537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2024   -0.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3836   -0.6119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0613    0.1475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0468   -0.6773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579   -0.9185    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9892   -1.6985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9744   -0.4562    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4709    0.2027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2966   -1.2156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
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  3 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
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  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 73 77  0  0  0  0  0  0  0  0999 V2000
   -6.2873   -0.3655    1.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6541    1.4283    0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2000    1.6757    0.3468 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3897    0.4049    0.1125 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6268   -0.4811    1.3417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0849    0.7521    0.0638 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5813    1.0326    1.4793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9594    1.6716    1.2574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8708    0.7248    0.5454 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7070    1.5800   -0.4163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0643    1.2196   -0.2045 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6102    0.3674   -1.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2277   -2.0950   -2.5548 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004171518022D          

 29 33  0  0  0  0            999 V2000
   -0.0401   -0.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7847   -0.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2813    0.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2958    1.2411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0847    1.4822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5579    0.8064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3767    0.7057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8733    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5510    2.1240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6921    1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    0.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5110    1.1633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8332    0.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3298    1.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1555   -0.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6590   -1.0144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8401   -0.9138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0213   -0.8131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0613    0.1475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.2966   -1.2156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207998

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2CCC3C4C(O)CC5(O)C(C)C(CCC5(C)C4CCC23CN1C)N(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H44N2O2/c1-15-20(26(4)5)10-11-23(3)18-9-12-24-14-27(6)16(2)17(24)7-8-19(24)22(18)21(28)13-25(15,23)29/h15-22,28-29H,7-14H2,1-6H3

> <INCHI_KEY>
OXOKQBJXPMVNLS-UHFFFAOYSA-N

> <FORMULA>
C25H44N2O2

> <MOLECULAR_WEIGHT>
404.639

> <EXACT_MASS>
404.340278665

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
49.005049305873804

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol

> <ALOGPS_LOGP>
2.62

> <JCHEM_LOGP>
2.3004070983333333

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
15.00518497390894

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.99278661446166

> <JCHEM_PKA_STRONGEST_BASIC>
10.281158695968301

> <JCHEM_POLAR_SURFACE_AREA>
46.940000000000005

> <JCHEM_REFRACTIVITY>
118.35159999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.96e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -0.075  -0.426   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.465  -0.453   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.392   0.777   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.419   2.317   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.892   2.767   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.775   1.505   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.303   1.317   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.230   2.547   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.629   3.965   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.759   2.359   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.360   0.942   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.287   2.172   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.889   0.754   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.816   1.984   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.490  -0.664   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.563  -1.894   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.035  -1.706   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.433  -0.288   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.506  -1.518   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.905  -0.100   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.978  -1.330   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.449  -1.142   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.848   0.275   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.821  -1.264   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       2.348  -1.714   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       1.847  -3.171   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0      13.019  -0.852   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      13.946   0.378   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.620  -2.269   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8   20                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13   18                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   27                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   11   19   20                                             
CONECT   19   18                                                            
CONECT   20   18    7   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    3    6   24                                             
CONECT   24   23   25                                                       
CONECT   25   24    2   26                                                  
CONECT   26   25                                                            
CONECT   27   15   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₄₄N₂O₂

Average Mass

404.6390 Da

Monoisotopic Mass

404.34028 Da

IUPAC Name

16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol

Traditional Name

16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol

CAS Registry Number

Not Available

SMILES

CC1C2CCC3C4C(O)CC5(O)C(C)C(CCC5(C)C4CCC23CN1C)N(C)C

InChI Identifier

InChI=1S/C25H44N2O2/c1-15-20(26(4)5)10-11-23(3)18-9-12-24-14-27(6)16(2)17(24)7-8-19(24)22(18)21(28)13-25(15,23)29/h15-22,28-29H,7-14H2,1-6H3

InChI Key

OXOKQBJXPMVNLS-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Holarrhena pubescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as conanine-type alkaloids. These are alkaloids with a structure based on the conanine skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Conanine-type alkaloids

Alternative Parents

Substituents

Conanine skeleton
5-hydroxysteroid
Hydroxysteroid
7-hydroxysteroid
Azasteroid
Azaspirodecane
Alkaloid or derivatives
N-alkylpyrrolidine
Cyclic alcohol
Pyrrolidine
Tertiary alcohol
Tertiary aliphatic amine
Secondary alcohol
Tertiary amine
Organoheterocyclic compound
Azacycle
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Alcohol
Amine
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
logP	2.62	ALOGPS
logP	2.3	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	13.99	ChemAxon
pKa (Strongest Basic)	10.28	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	46.94 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	118.35 m³·mol⁻¹	ChemAxon
Polarizability	49.01 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14543695

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol (NP0207998)

MOL for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

3D MOL for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

3D SDF for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

3D-SDF for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

PDB for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

3D PDB for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

SMILES for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

INCHI for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

Structure for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)

3D Structure for NP0207998 (16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosane-18,20-diol)