NP-MRD: Showing NP-Card for (3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol (NP0313878)

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Record Information

Version

2.0

Created at

2022-09-11 11:40:55 UTC

Updated at

2022-09-11 11:40:56 UTC

NP-MRD ID

NP0313878

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol

Description

(3R,4R,4'S,6R,6''S,9S,9''S,9aR,9''aR)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizine]-4-ol belongs to the class of organic compounds known as quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom. (3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol is found in Nuphar lutea. Based on a literature review very few articles have been published on (3R,4R,4'S,6R,6''S,9S,9''S,9aR,9''aR)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizine]-4-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112213402D          

 36 42  0  0  1  0            999 V2000
    6.0735    2.0609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1094    1.2367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8411    0.8557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8770    0.0315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1811   -0.4117    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2170   -1.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9049   -1.6914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6843   -2.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8601   -2.5222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5713   -1.7494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4494   -0.0307    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7535   -0.4738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0218   -0.0928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9859    0.7314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6818    1.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4135    0.7935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.7294   -0.4268    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2739   -1.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4505   -1.0642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0825   -0.3259    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.3465    1.1509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1699    1.1004    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6254    1.7883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3366    2.5611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6702    2.6191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4496    1.8241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5379    0.3620    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3614    0.3115    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8168    0.9994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2542    0.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
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  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  2  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 13 14  1  0  0  0  0
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 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 11  1  6  0  0  0
 13 17  1  6  0  0  0
 17 18  1  0  0  0  0
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 19 20  1  0  0  0  0
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 23 24  1  1  0  0  0
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 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
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 33 34  1  0  0  0  0
 19 34  1  0  0  0  0
 34 35  1  6  0  0  0
 19 36  1  0  0  0  0
 13 36  1  0  0  0  0
M  END

     RDKit          3D

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    0.1586   -0.5617    0.1275 C   0  0  0  0  0  0  0  0  0  0  0  0
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  8 47  1  0
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M  END


  Mrv1652309112213402D          

 36 42  0  0  1  0            999 V2000
    6.0735    2.0609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6254    1.7883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3366    2.5611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9823    3.0746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6702    2.6191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4496    1.8241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5379    0.3620    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3614    0.3115    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8168    0.9994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2542    0.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  2  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 11  1  6  0  0  0
 13 17  1  6  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 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 28 32  2  0  0  0  0
 27 33  1  0  0  0  0
 22 33  1  6  0  0  0
 33 34  1  0  0  0  0
 19 34  1  0  0  0  0
 34 35  1  6  0  0  0
 19 36  1  0  0  0  0
 13 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0313878

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@H](N2C[C@]3(CS[C@@]4(C3)CC[C@@H]3[C@@H](C)CC[C@@H](N3[C@@H]4O)C3=COC=C3)CC[C@H]12)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H42N2O3S/c1-20-3-5-26(22-9-13-34-15-22)31-18-29(11-7-24(20)31)17-30(36-19-29)12-8-25-21(2)4-6-27(32(25)28(30)33)23-10-14-35-16-23/h9-10,13-16,20-21,24-28,33H,3-8,11-12,17-19H2,1-2H3/t20-,21-,24+,25+,26-,27+,28+,29-,30+/m0/s1

> <INCHI_KEY>
GAKRXIIHJWAJNM-JTRVWZDJSA-N

> <FORMULA>
C30H42N2O3S

> <MOLECULAR_WEIGHT>
510.74

> <EXACT_MASS>
510.291614394

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
58.15893166756513

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,4R,4'S,6R,6''S,9S,9''S,9aR,9''aR)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizine]-4-ol

> <JCHEM_LOGP>
5.7991872493333325

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.830234024688327

> <JCHEM_PKA_STRONGEST_BASIC>
9.070838800063065

> <JCHEM_POLAR_SURFACE_AREA>
52.99000000000001

> <JCHEM_REFRACTIVITY>
144.1799

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R,4'S,6R,6''S,9S,9''S,9aR,9''aR)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizine]-4-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      11.337   3.847   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.404   2.309   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.770   1.597   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.837   0.059   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.538  -0.769   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.605  -2.307   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.889  -3.157   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.477  -4.641   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.939  -4.708   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      10.400  -3.266   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      10.172  -0.057   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       8.873  -0.885   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.507  -0.173   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.440   1.365   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.739   2.193   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.105   1.481   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.413  -1.710   0.000  0.00  0.00           C+0
HETATM   18  S   UNK     0       5.922  -2.096   0.000  0.00  0.00           S+0
HETATM   19  C   UNK     0       5.095  -0.797   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.245  -2.081   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.708  -1.987   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.021  -0.608   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.484  -0.514   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.367  -1.798   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.203   0.864   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.647   2.148   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.184   2.054   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.034   3.338   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.495   4.781   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.700   5.739   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.984   4.889   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.573   3.405   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0       2.871   0.676   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0       4.408   0.582   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.258   1.866   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.075   0.391   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6                                                       
CONECT   11    5   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   17   36                                             
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    2   11                                                  
CONECT   17   13   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   34   36                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   33                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   33                                                  
CONECT   28   27   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   28                                                       
CONECT   33   27   22   34                                                  
CONECT   34   33   19   35                                                  
CONECT   35   34                                                            
CONECT   36   19   13                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂N₂O₃S

Average Mass

510.7400 Da

Monoisotopic Mass

510.29161 Da

IUPAC Name

(3R,4R,4'S,6R,6''S,9S,9''S,9aR,9''aR)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizine]-4-ol

Traditional Name

(3R,4R,4'S,6R,6''S,9S,9''S,9aR,9''aR)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizine]-4-ol

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@H](N2C[C@]3(CS[C@@]4(C3)CC[C@@H]3[C@@H](C)CC[C@@H](N3[C@@H]4O)C3=COC=C3)CC[C@H]12)C1=COC=C1

InChI Identifier

InChI=1S/C30H42N2O3S/c1-20-3-5-26(22-9-13-34-15-22)31-18-29(11-7-24(20)31)17-30(36-19-29)12-8-25-21(2)4-6-27(32(25)28(30)33)23-10-14-35-16-23/h9-10,13-16,20-21,24-28,33H,3-8,11-12,17-19H2,1-2H3/t20-,21-,24+,25+,26-,27+,28+,29-,30+/m0/s1

InChI Key

GAKRXIIHJWAJNM-JTRVWZDJSA-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
Nuphar lutea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizines

Sub Class

Not Available

Direct Parent

Quinolizines

Alternative Parents

Substituents

Azaspirodecane
Quinolizidine
Quinolizine
Aralkylamine
Piperidine
Furan
Heteroaromatic compound
Thiolane
Hemiaminal
Tertiary amine
Tertiary aliphatic amine
Alkanolamine
Oxacycle
Azacycle
Dialkylthioether
Thioether
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Amine
Organic nitrogen compound
Organic oxygen 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
logP	5.8	ChemAxon
pKa (Strongest Acidic)	12.83	ChemAxon
pKa (Strongest Basic)	9.07	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	52.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	144.18 m³·mol⁻¹	ChemAxon
Polarizability	58.16 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

162856136

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol (NP0313878)

MOL for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

3D MOL for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

3D SDF for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

3D-SDF for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

PDB for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

3D PDB for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

SMILES for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

INCHI for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

Structure for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)

3D Structure for NP0313878 ((3r,4r,4's,6r,6''s,9s,9''s,9ar,9''ar)-6,6''-bis(furan-3-yl)-9,9''-dimethyl-hexadecahydrodispiro[quinolizine-3,2'-thiolane-4',3''-quinolizin]-4-ol)