NP-MRD: Showing NP-Card for Cathidine D (NP0059582)

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Record Information

Version

2.0

Created at

2022-04-28 04:48:42 UTC

Updated at

2022-04-28 04:48:42 UTC

NP-MRD ID

NP0059582

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cathidine D

Description

(1R,2S,3S,4S,5R,6R,7S,9R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-4-(benzoyloxy)-2,3-dihydroxy-2,10,10-trimethyl-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). Cathidine D is found in Catha edulis . Based on a literature review very few articles have been published on (1R,2S,3S,4S,5R,6R,7S,9R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-4-(benzoyloxy)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl pyridine-3-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282206482D          

 44 48  0  0  1  0            999 V2000
    1.5308    0.0357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2124   -0.5456    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6196   -1.3335    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1620   -2.0848    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3043   -2.0169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9362   -1.2343    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7709   -0.3870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0516   -0.4512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6141   -0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2649   -3.4696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4613   -1.3590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  3  4  1  0  0  0  0
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  6 10  1  6  0  0  0
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  3 20  1  0  0  0  0
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 20 36  1  6  0  0  0
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  3 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282206482D          

 44 48  0  0  1  0            999 V2000
    1.5308    0.0357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4613   -1.3590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9107   -0.6592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5375    0.0833    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7127    0.1338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7501    0.9580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0562    0.6334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9918    0.7720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7345   -0.7025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1840   -0.0107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8096    0.7245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0078   -0.0540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4573    0.6378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2811    0.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6556   -0.1406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2061   -0.8324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3822   -0.7891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8459   -2.0889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -2.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1101   -1.4228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0548   -2.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2177   -1.9019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0245   -2.7039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6226   -3.2722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4137   -3.0385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4294   -4.0743    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
  1  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  6  0  0  0
  2 10  1  6  0  0  0
  4 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 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
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
  3 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
  2 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  1  0  0  0
 22 26  1  1  0  0  0
 21 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 20 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
  3 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0059582

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@]12[C@H](C[C@@H]3C[C@]1(OC3(C)C)[C@@](C)(O)[C@@H](O)[C@H](OC(=O)C1=CC=CC=C1)[C@@H]2OC(C)=O)OC(=O)C1=CN=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H37NO11/c1-18(34)40-17-31-23(42-28(38)21-12-9-13-33-16-21)14-22-15-32(31,44-29(22,3)4)30(5,39)25(36)24(26(31)41-19(2)35)43-27(37)20-10-7-6-8-11-20/h6-13,16,22-26,36,39H,14-15,17H2,1-5H3/t22-,23+,24+,25+,26+,30+,31-,32+/m1/s1

> <INCHI_KEY>
IBYLVJWSADDHAM-VFYMZHOQSA-N

> <FORMULA>
C32H37NO11

> <MOLECULAR_WEIGHT>
611.644

> <EXACT_MASS>
611.236661015

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
61.178409083866086

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3S,4S,5R,6R,7S,9R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-4-(benzoyloxy)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl pyridine-3-carboxylate

> <ALOGPS_LOGP>
2.47

> <JCHEM_LOGP>
1.8752240076666669

> <ALOGPS_LOGS>
-4.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.938149343037423

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.562134129618187

> <JCHEM_PKA_STRONGEST_BASIC>
3.240858452629817

> <JCHEM_POLAR_SURFACE_AREA>
167.78

> <JCHEM_REFRACTIVITY>
151.06390000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.99e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,4S,5R,6R,7S,9R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-4-(benzoyloxy)-2,3-dihydroxy-2,10,10-trimethyl-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  O   UNK     0       2.857   0.067   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.130  -1.019   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.890  -2.489   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.036  -3.892   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.435  -3.765   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.747  -2.304   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.439  -0.722   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.096  -0.842   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.541   0.529   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.013  -1.746   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.736  -5.263   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.899  -6.555   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.600  -7.927   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.361  -6.477   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.660  -5.105   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       0.122  -5.026   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -0.715  -6.319   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.014  -7.690   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.524  -7.769   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.461  -2.537   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.300  -1.230   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.603   0.156   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.064   0.250   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.134   1.788   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.838   1.182   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.451   1.441   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.838  -1.311   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.677  -0.020   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.978   1.352   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.215  -0.101   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.054   1.191   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.591   1.110   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.290  -0.262   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.451  -1.554   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.914  -1.473   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       7.179  -3.899   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       8.718  -3.959   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       9.539  -2.656   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       9.436  -5.321   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.006  -3.550   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       5.646  -5.047   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       6.762  -6.108   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       8.239  -5.672   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       6.402  -7.605   0.000  0.00  0.00           C+0
CONECT    1    2    7                                                       
CONECT    2    1    3   10   23                                             
CONECT    3    2    4   20   40                                             
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    1    8    9                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    6    2                                                       
CONECT   11    4   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20    3   21   36                                                  
CONECT   21   20   22   27                                                  
CONECT   22   21   23   26                                                  
CONECT   23   22    2   24   25                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   22                                                            
CONECT   27   21   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   30                                                       
CONECT   36   20   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40    3   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   96    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,3S,4S,5R,6R,7S,9R)-5-(Acetyloxy)-6-[(acetyloxy)methyl]-4-(benzoyloxy)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0,]dodecan-7-yl pyridine-3-carboxylic acid	Generator

Chemical Formula

C₃₂H₃₇NO₁₁

Average Mass

611.6440 Da

Monoisotopic Mass

611.23666 Da

IUPAC Name

(1R,2S,3S,4S,5R,6R,7S,9R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-4-(benzoyloxy)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl pyridine-3-carboxylate

Traditional Name

(1R,2S,3S,4S,5R,6R,7S,9R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-4-(benzoyloxy)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-7-yl pyridine-3-carboxylate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@]12[C@H](C[C@@H]3C[C@]1(OC3(C)C)[C@@](C)(O)[C@@H](O)[C@H](OC(=O)C1=CC=CC=C1)[C@@H]2OC(C)=O)OC(=O)C1=CN=CC=C1

InChI Identifier

InChI=1S/C32H37NO11/c1-18(34)40-17-31-23(42-28(38)21-12-9-13-33-16-21)14-22-15-32(31,44-29(22,3)4)30(5,39)25(36)24(26(31)41-19(2)35)43-27(37)20-10-7-6-8-11-20/h6-13,16,22-26,36,39H,14-15,17H2,1-5H3/t22-,23+,24+,25+,26+,30+,31-,32+/m1/s1

InChI Key

IBYLVJWSADDHAM-VFYMZHOQSA-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
Catha edulis	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
Benzoate ester
Pyridine carboxylic acid or derivatives
Pyridine carboxylic acid
Benzoic acid or derivatives
Benzoyl
Oxepane
Benzenoid
Pyridine
Monocyclic benzene moiety
Cyclitol or derivatives
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
1,2-diol
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
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	2.47	ALOGPS
logP	1.88	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	12.56	ChemAxon
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	167.78 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	151.06 m³·mol⁻¹	ChemAxon
Polarizability	61.18 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	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

162889326

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Cathidine D (NP0059582)

MOL for NP0059582 (Cathidine D)

3D MOL for NP0059582 (Cathidine D)

3D SDF for NP0059582 (Cathidine D)

3D-SDF for NP0059582 (Cathidine D)

PDB for NP0059582 (Cathidine D)

3D PDB for NP0059582 (Cathidine D)

SMILES for NP0059582 (Cathidine D)

INCHI for NP0059582 (Cathidine D)

Structure for NP0059582 (Cathidine D)

3D Structure for NP0059582 (Cathidine D)