NP-MRD: Showing NP-Card for Aspidospermidose (NP0066868)

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Record Information

Version

2.0

Created at

2022-04-28 11:06:10 UTC

Updated at

2022-04-28 11:06:10 UTC

NP-MRD ID

NP0066868

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Aspidospermidose

Description

(2R,4S,5R,6S)-6-[(1R,9R,12S,19R)-12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]Nonadeca-2,4,6-trien-8-yl]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-one belongs to the class of organic compounds known as aspidospermatan-type alkaloids. These are tryptophan-derived alkaloids that are derived from the fusion of tryptamine and a terpene unit (generally either 9 or 10 carbons). Aspidospermine and aspidospermidine (along with tabersonine) are the archetypical members of the Aspidosperma alkaloids. Aspidospermidose is found in Rhazya sticta. Based on a literature review very few articles have been published on (2R,4S,5R,6S)-6-[(1R,9R,12S,19R)-12-ethyl-8,16-diazapentacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁶,¹⁹]Nonadeca-2,4,6-trien-8-yl]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282213062D          

 32 37  0  0  1  0            999 V2000
    5.4285    1.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0125    0.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7998   -0.1702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0031   -0.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4191    0.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6318    0.9952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6844   -0.1772    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8144   -0.9919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6293   -1.1201    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0047   -1.8548    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8286   -1.8971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2039   -2.6318    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7553   -3.3241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1306   -4.0588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9314   -3.2818    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5561   -2.5471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4828   -3.9742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6589   -3.9319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0278   -2.6741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2772   -1.2047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1738   -1.5118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4032   -1.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2733   -0.4022    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9139    0.1177    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7840    0.9324    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0135    1.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3729    0.7073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7529    1.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2030    0.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6327   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8622   -0.6272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  7  5  1  6  0  0  0
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  8  9  1  6  0  0  0
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 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 12 19  1  6  0  0  0
 11 20  1  6  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  7 24  1  0  0  0  0
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 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
 23 31  1  1  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

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    3.0247   -1.0395   -0.2302 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6977   -2.3661    0.9008 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0851   -2.3747    1.0863 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9238    0.0375    0.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5477    1.4225    0.3235 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3935    1.8741   -0.7068 O   0  0  0  0  0  0  0  0  0  0  0  0
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 32 66  1  1
M  END


  Mrv1652304282213062D          

 32 37  0  0  1  0            999 V2000
    5.4285    1.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0125    0.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7998   -0.1702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0031   -0.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4191    0.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6318    0.9952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8144   -0.9919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.1738   -1.5118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4032   -1.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2733   -0.4022    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9139    0.1177    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7840    0.9324    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0135    1.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3729    0.7073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7529    1.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2030    0.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6327   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8622   -0.6272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
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  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
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  1  6  1  0  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
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  8 21  1  0  0  0  0
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 22 23  1  0  0  0  0
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 27 28  1  0  0  0  0
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 25 29  1  0  0  0  0
 29 30  1  0  0  0  0
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 23 31  1  1  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066868

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@]12CCCN3CC[C@@]4([C@@H](CC1)N([C@H]1O[C@H](CO)C(=O)[C@@H](O)[C@H]1O)C1=CC=CC=C41)[C@@H]23

> <INCHI_IDENTIFIER>
InChI=1S/C25H34N2O5/c1-2-24-9-5-12-26-13-11-25(23(24)26)15-6-3-4-7-16(15)27(18(25)8-10-24)22-21(31)20(30)19(29)17(14-28)32-22/h3-4,6-7,17-18,20-23,28,30-31H,2,5,8-14H2,1H3/t17-,18-,20-,21-,22+,23-,24+,25-/m1/s1

> <INCHI_KEY>
ZIGOWDMHNDQEOB-WZZUFGGRSA-N

> <FORMULA>
C25H34N2O5

> <MOLECULAR_WEIGHT>
442.556

> <EXACT_MASS>
442.246772203

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.88493675220801

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4S,5R,6S)-6-[(1R,9R,12S,19R)-12-ethyl-8,16-diazapentacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{16,19}]nonadeca-2,4,6-trien-8-yl]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-one

> <ALOGPS_LOGP>
1.77

> <JCHEM_LOGP>
1.8263624283917401

> <ALOGPS_LOGS>
-1.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.616055003541732

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.571960233364026

> <JCHEM_PKA_STRONGEST_BASIC>
9.69764852168661

> <JCHEM_POLAR_SURFACE_AREA>
93.47

> <JCHEM_REFRACTIVITY>
119.15369999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.75e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4S,5R,6S)-6-[(1R,9R,12S,19R)-12-ethyl-8,16-diazapentacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{16,19}]nonadeca-2,4,6-trien-8-yl]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      10.133   2.258   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.223   1.170   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.826  -0.318   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.339  -0.718   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.249   0.370   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.646   1.858   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.878  -0.331   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.120  -1.852   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       8.641  -2.091   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       9.342  -3.462   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.880  -3.541   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.581  -4.913   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.743  -6.205   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.444  -7.576   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.205  -6.126   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.505  -4.755   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.368  -7.419   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.830  -7.340   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      13.119  -4.992   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      11.717  -2.249   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.924  -2.822   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.486  -2.272   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.244  -0.751   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.439   0.220   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       5.197   1.740   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       3.759   2.291   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.563   1.320   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.805  -0.200   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.005   2.158   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.846   0.867   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.048  -1.721   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.609  -1.171   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   24   30                                             
CONECT    8    7    9   21                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12   20                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15   10                                                       
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   12                                                            
CONECT   20   11                                                            
CONECT   21    8   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   28   31                                             
CONECT   24   23    7   25                                                  
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   23                                                       
CONECT   29   25   30                                                       
CONECT   30   29    7                                                       
CONECT   31   23   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₄N₂O₅

Average Mass

442.5560 Da

Monoisotopic Mass

442.24677 Da

IUPAC Name

(2R,4S,5R,6S)-6-[(1R,9R,12S,19R)-12-ethyl-8,16-diazapentacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{16,19}]nonadeca-2,4,6-trien-8-yl]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-one

Traditional Name

(2R,4S,5R,6S)-6-[(1R,9R,12S,19R)-12-ethyl-8,16-diazapentacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{16,19}]nonadeca-2,4,6-trien-8-yl]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-one

CAS Registry Number

Not Available

SMILES

CC[C@]12CCCN3CC[C@@]4([C@@H](CC1)N([C@H]1O[C@H](CO)C(=O)[C@@H](O)[C@H]1O)C1=CC=CC=C41)[C@@H]23

InChI Identifier

InChI=1S/C25H34N2O5/c1-2-24-9-5-12-26-13-11-25(23(24)26)15-6-3-4-7-16(15)27(18(25)8-10-24)22-21(31)20(30)19(29)17(14-28)32-22/h3-4,6-7,17-18,20-23,28,30-31H,2,5,8-14H2,1H3/t17-,18-,20-,21-,22+,23-,24+,25-/m1/s1

InChI Key

ZIGOWDMHNDQEOB-WZZUFGGRSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rhazya sticta	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aspidospermatan-type alkaloids. These are tryptophan-derived alkaloids that are derived from the fusion of tryptamine and a terpene unit (generally either 9 or 10 carbons). Aspidospermine and aspidospermidine (along with tabersonine) are the archetypical members of the Aspidosperma alkaloids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aspidospermatan-type alkaloids

Sub Class

Not Available

Direct Parent

Aspidospermatan-type alkaloids

Alternative Parents

Substituents

Aspidosperma alkaloid
Plumeran-type alkaloid
Carbazole
N-glycosyl compound
Glycosyl compound
Quinolidine
Indolizidine
Indole or derivatives
Dialkylarylamine
Aralkylamine
Benzenoid
N-alkylpyrrolidine
Piperidine
Oxane
Pyrrolidine
Cyclic ketone
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Ketone
Oxacycle
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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
logP	1.77	ALOGPS
logP	1.83	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	10.57	ChemAxon
pKa (Strongest Basic)	9.7	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	93.47 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	119.15 m³·mol⁻¹	ChemAxon
Polarizability	47.88 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

163085846

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Aspidospermidose (NP0066868)

MOL for NP0066868 (Aspidospermidose)

3D MOL for NP0066868 (Aspidospermidose)

3D SDF for NP0066868 (Aspidospermidose)

3D-SDF for NP0066868 (Aspidospermidose)

PDB for NP0066868 (Aspidospermidose)

3D PDB for NP0066868 (Aspidospermidose)

SMILES for NP0066868 (Aspidospermidose)

INCHI for NP0066868 (Aspidospermidose)

Structure for NP0066868 (Aspidospermidose)

3D Structure for NP0066868 (Aspidospermidose)