NP-MRD: Showing NP-Card for Celapanine (NP0051068)

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Record Information

Version

2.0

Created at

2022-04-27 22:30:32 UTC

Updated at

2022-04-27 22:30:32 UTC

NP-MRD ID

NP0051068

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Celapanine

Description

(1R,2R,5R,6R,7R,8R,9S,12R)-5,8-bis(acetyloxy)-12-(furan-3-carbonyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl pyridine-3-carboxylate belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). Celapanine is found in Celastrus paniculata. Based on a literature review very few articles have been published on (1R,2R,5R,6R,7R,8R,9S,12R)-5,8-bis(acetyloxy)-12-(furan-3-carbonyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl pyridine-3-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282200302D          

 41 45  0  0  1  0            999 V2000
    1.0812    0.0746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9060    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    0.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298    1.5673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9881    1.5419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5808    0.7540    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1007    0.1726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8607    0.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954    1.4426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3272    2.2252    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5304    2.2931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8621    3.1866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4348    4.0918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1097    4.7940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0609    4.5788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7109    5.3259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1828    6.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2508    1.8757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7316    0.5798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7629    1.7632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6738    1.7253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2900    2.3359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0736   -0.7922    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
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
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 10 21  1  1  0  0  0
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 22 24  1  0  0  0  0
  9 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  1  0  0  0
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 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
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 29 33  1  0  0  0  0
  8 34  1  0  0  0  0
  8 35  1  0  0  0  0
  5 36  1  6  0  0  0
  4 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
  1 41  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282200302D          

 41 45  0  0  1  0            999 V2000
    1.0812    0.0746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9060    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7981    3.9647    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0916    3.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4490    2.6763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2555   -0.1886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7316    0.5798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6994    2.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7629    1.7632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6738    1.7253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2900    2.3359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2383    1.0886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0736   -0.7922    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
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 10 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  9 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 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
 32 33  2  0  0  0  0
 29 33  1  0  0  0  0
  8 34  1  0  0  0  0
  8 35  1  0  0  0  0
  5 36  1  6  0  0  0
  4 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
  1 41  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0051068

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@H](OC(C)=O)[C@]2(C)[C@@H](OC(=O)C3=CC=CN=C3)[C@H](OC(C)=O)[C@H]3[C@@H](OC(=O)C4=COC=C4)[C@@]12OC3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C30H35NO10/c1-16-9-10-21(37-17(2)32)29(6)25(40-26(34)19-8-7-12-31-14-19)23(38-18(3)33)22-24(30(16,29)41-28(22,4)5)39-27(35)20-11-13-36-15-20/h7-8,11-16,21-25H,9-10H2,1-6H3/t16-,21-,22+,23-,24-,25+,29-,30+/m1/s1

> <INCHI_KEY>
MHXMEJIEIHJTGN-WXXSSFMASA-N

> <FORMULA>
C30H35NO10

> <MOLECULAR_WEIGHT>
569.607

> <EXACT_MASS>
569.226096331

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
57.987188601013884

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5R,6R,7R,8R,9S,12R)-5,8-bis(acetyloxy)-12-(furan-3-carbonyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl pyridine-3-carboxylate

> <ALOGPS_LOGP>
3.85

> <JCHEM_LOGP>
3.446361407666667

> <ALOGPS_LOGS>
-4.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.2398580888374977

> <JCHEM_POLAR_SURFACE_AREA>
140.46

> <JCHEM_REFRACTIVITY>
140.12290000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.09e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5R,6R,7R,8R,9S,12R)-5,8-bis(acetyloxy)-12-(furan-3-carbonyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl pyridine-3-carboxylate

> <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       2.018   0.139   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.558   0.233   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.254   1.619   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.416   2.926   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.844   2.878   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.084   1.407   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.188   0.322   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.607   1.111   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.298   2.693   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.611   4.154   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.990   4.280   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.609   5.948   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.812   7.638   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.205   8.949   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.980   8.547   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.327   9.942   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.208  11.205   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.742  11.073   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       4.396   9.679   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       3.515   8.416   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.863   4.935   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -3.855   4.809   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.016   3.590   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -5.054   6.226   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.033   2.135   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.468   3.501   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.043   5.138   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.693   6.525   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.416   5.838   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.818   7.325   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -3.356   7.401   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -3.904   5.962   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.705   4.996   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.344  -0.352   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.232   1.082   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.172   4.034   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.157   3.291   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       6.858   3.221   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       8.008   4.360   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       7.911   2.032   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.004  -1.479   0.000  0.00  0.00           C+0
CONECT    1    2    6   41                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   37                                                  
CONECT    5    4    6   11   36                                             
CONECT    6    5    1    7   25                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   34   35                                             
CONECT    9    8   10   25                                                  
CONECT   10    9   11   21                                                  
CONECT   11   10    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   10   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    9    6   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   33                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   29                                                       
CONECT   34    8                                                            
CONECT   35    8                                                            
CONECT   36    5                                                            
CONECT   37    4   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41    1                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,5R,6R,7R,8R,9S,12R)-5,8-Bis(acetyloxy)-12-(furan-3-carbonyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0,]dodecan-7-yl pyridine-3-carboxylic acid	Generator

Chemical Formula

C₃₀H₃₅NO₁₀

Average Mass

569.6070 Da

Monoisotopic Mass

569.22610 Da

IUPAC Name

(1R,2R,5R,6R,7R,8R,9S,12R)-5,8-bis(acetyloxy)-12-(furan-3-carbonyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl pyridine-3-carboxylate

Traditional Name

(1R,2R,5R,6R,7R,8R,9S,12R)-5,8-bis(acetyloxy)-12-(furan-3-carbonyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl pyridine-3-carboxylate

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@H](OC(C)=O)[C@]2(C)[C@@H](OC(=O)C3=CC=CN=C3)[C@H](OC(C)=O)[C@H]3[C@@H](OC(=O)C4=COC=C4)[C@@]12OC3(C)C

InChI Identifier

InChI=1S/C30H35NO10/c1-16-9-10-21(37-17(2)32)29(6)25(40-26(34)19-8-7-12-31-14-19)23(38-18(3)33)22-24(30(16,29)41-28(22,4)5)39-27(35)20-11-13-36-15-20/h7-8,11-16,21-25H,9-10H2,1-6H3/t16-,21-,22+,23-,24-,25+,29-,30+/m1/s1

InChI Key

MHXMEJIEIHJTGN-WXXSSFMASA-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
Celastrus paniculata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Tetracarboxylic acid or derivatives
Furoic acid ester
Pyridine carboxylic acid or derivatives
Pyridine carboxylic acid
Furoic acid or derivatives
Furan-3-carboxylic acid ester
Furan-3-carboxylic acid or derivatives
Oxepane
Pyridine
Heteroaromatic compound
Tetrahydrofuran
Furan
Carboxylic acid ester
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	3.85	ALOGPS
logP	3.45	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	140.46 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	140.12 m³·mol⁻¹	ChemAxon
Polarizability	57.99 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162927704

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Celapanine (NP0051068)

MOL for NP0051068 (Celapanine)

3D MOL for NP0051068 (Celapanine)

3D SDF for NP0051068 (Celapanine)

3D-SDF for NP0051068 (Celapanine)

PDB for NP0051068 (Celapanine)

3D PDB for NP0051068 (Celapanine)

SMILES for NP0051068 (Celapanine)

INCHI for NP0051068 (Celapanine)

Structure for NP0051068 (Celapanine)

3D Structure for NP0051068 (Celapanine)