NP-MRD: Showing NP-Card for Hupehemonoside (NP0069949)

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Record Information

Version

2.0

Created at

2022-04-28 15:14:46 UTC

Updated at

2022-04-28 15:14:46 UTC

NP-MRD ID

NP0069949

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Hupehemonoside

Description

(1R,2S,6S,9R,10S,11R,14R,15R,18S,20S,23R,24R)-10-hydroxy-6,10,23-trimethyl-20-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-azahexacyclo[12.11.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁴.0¹⁸,²³]Pentacosan-17-one belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative. Hupehemonoside is found in Fritillaria hupehensis . Based on a literature review very few articles have been published on (1R,2S,6S,9R,10S,11R,14R,15R,18S,20S,23R,24R)-10-hydroxy-6,10,23-trimethyl-20-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-azahexacyclo[12.11.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁴.0¹⁸,²³]Pentacosan-17-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282217142D          

 42 48  0  0  1  0            999 V2000
    6.5397   -0.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1866    0.1082    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    6.3000    1.2287    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 41 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282217142D          

 42 48  0  0  1  0            999 V2000
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    7.1866    0.1082    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0668    0.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3000    1.2287    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6530    0.7168    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7729   -0.0994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8862    1.0212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7664    1.8374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4133    2.3493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1802    2.0450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8271    2.5569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9530    1.9757    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5702    1.2449    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1469    0.6550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7459    1.2110    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3044    1.9080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6873    2.6388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5116    2.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4801    1.8741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0973    1.1433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5388    0.4464    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3631    0.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1559   -0.2844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316   -0.3183    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1098    0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2730    1.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0512   -1.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4175    2.6967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7631    2.2822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0061    0.2049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9535   -0.1962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0733   -1.0124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8401   -1.3168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9600   -2.1330    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3130   -2.6449    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5462   -2.3406    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4263   -1.5243    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6595   -1.2200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8992   -2.8525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4328   -3.4612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7268   -2.4374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8466   -3.2536    0.0000 O   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
  7 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 12 18  1  6  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 15 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 26  1  0  0  0  0
 24 27  1  1  0  0  0
 19 28  1  1  0  0  0
 19 29  1  6  0  0  0
  5 30  1  1  0  0  0
  2 31  1  1  0  0  0
 32 31  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 32 37  1  0  0  0  0
 37 38  1  1  0  0  0
 36 39  1  6  0  0  0
 35 40  1  1  0  0  0
 34 41  1  6  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069949

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@H]2N(C1)C[C@H]1[C@@H]3C[C@@H]4[C@H](CC(=O)[C@H]5C[C@H](CC[C@]45C)O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3CC[C@H]1[C@]2(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C33H53NO8/c1-16-4-7-27-33(3,40)22-6-5-18-19(21(22)14-34(27)13-16)11-23-20(18)12-25(36)24-10-17(8-9-32(23,24)2)41-31-30(39)29(38)28(37)26(15-35)42-31/h16-24,26-31,35,37-40H,4-15H2,1-3H3/t16-,17-,18-,19+,20+,21-,22+,23+,24+,26+,27+,28+,29-,30+,31+,32+,33-/m0/s1

> <INCHI_KEY>
DHQFYEJMFMYGCV-KJZPUUMCSA-N

> <FORMULA>
C33H53NO8

> <MOLECULAR_WEIGHT>
591.786

> <EXACT_MASS>
591.377117671

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
67.72635052868685

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,6S,9R,10S,11R,14R,15R,18S,20S,23R,24R)-10-hydroxy-6,10,23-trimethyl-20-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-azahexacyclo[12.11.0.0^{2,11}.0^{4,9}.0^{15,24}.0^{18,23}]pentacosan-17-one

> <ALOGPS_LOGP>
1.40

> <JCHEM_LOGP>
1.449694365666665

> <ALOGPS_LOGS>
-3.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.163098271567886

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.207853396919674

> <JCHEM_PKA_STRONGEST_BASIC>
9.856668297206575

> <JCHEM_POLAR_SURFACE_AREA>
139.92000000000002

> <JCHEM_REFRACTIVITY>
154.8718

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.25e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,6S,9R,10S,11R,14R,15R,18S,20S,23R,24R)-10-hydroxy-6,10,23-trimethyl-20-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4-azahexacyclo[12.11.0.0^{2,11}.0^{4,9}.0^{15,24}.0^{18,23}]pentacosan-17-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      12.207  -0.754   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.415   0.202   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.191   1.726   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.760   2.294   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.552   1.338   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.776  -0.186   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.121   1.906   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.897   3.430   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.105   4.385   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.536   3.817   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.744   4.773   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.379   3.688   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.664   2.324   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.741   1.223   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.126   2.261   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.302   3.562   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.016   4.926   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.555   4.989   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.763   3.498   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.048   2.134   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       2.872   0.833   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       4.411   0.896   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.158  -0.531   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.619  -0.594   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.205   0.707   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.510   2.071   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.096  -1.958   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.646   5.034   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.425   4.260   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.345   0.383   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.846  -0.366   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      15.070  -1.890   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      16.502  -2.458   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      16.725  -3.982   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      15.518  -4.937   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      14.086  -4.369   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.862  -2.845   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.431  -2.277   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      12.879  -5.325   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      15.741  -6.461   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      18.157  -4.550   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      18.380  -6.073   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   30                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   14                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    7                                                       
CONECT   15   13   16   22                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17   12                                                       
CONECT   19   16   20   28   29                                             
CONECT   20   19   21   26                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21   15                                                       
CONECT   23   21   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25   20                                                       
CONECT   27   24                                                            
CONECT   28   19                                                            
CONECT   29   19                                                            
CONECT   30    5                                                            
CONECT   31    2   32                                                       
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   41                                                  
CONECT   35   34   36   40                                                  
CONECT   36   35   37   39                                                  
CONECT   37   36   32   38                                                  
CONECT   38   37                                                            
CONECT   39   36                                                            
CONECT   40   35                                                            
CONECT   41   34   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₅₃NO₈

Average Mass

591.7860 Da

Monoisotopic Mass

591.37712 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@H]2N(C1)C[C@H]1[C@@H]3C[C@@H]4[C@H](CC(=O)[C@H]5C[C@H](CC[C@]45C)O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3CC[C@H]1[C@]2(C)O

InChI Identifier

InChI=1S/C33H53NO8/c1-16-4-7-27-33(3,40)22-6-5-18-19(21(22)14-34(27)13-16)11-23-20(18)12-25(36)24-10-17(8-9-32(23,24)2)41-31-30(39)29(38)28(37)26(15-35)42-31/h16-24,26-31,35,37-40H,4-15H2,1-3H3/t16-,17-,18-,19+,20+,21-,22+,23+,24+,26+,27+,28+,29-,30+,31+,32+,33-/m0/s1

InChI Key

DHQFYEJMFMYGCV-KJZPUUMCSA-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
Fritillaria hupehensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal saponins

Alternative Parents

Substituents

Steroidal saponin
Diterpene glycoside
Cerveratrum-type alkaloid
Diterpenoid
Steroidal alkaloid
Terpene glycoside
Azasteroid
Hexose monosaccharide
O-glycosyl compound
Glycosyl compound
Quinolizidine
Alkaloid or derivatives
Piperidine
Oxane
Monosaccharide
Tertiary alcohol
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Ketone
1,2-aminoalcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Polyol
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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	1.4	ALOGPS
logP	1.45	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	9.86	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	139.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	154.87 m³·mol⁻¹	ChemAxon
Polarizability	67.73 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	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

163007868

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Hupehemonoside (NP0069949)

MOL for NP0069949 (Hupehemonoside)

3D MOL for NP0069949 (Hupehemonoside)

3D SDF for NP0069949 (Hupehemonoside)

3D-SDF for NP0069949 (Hupehemonoside)

PDB for NP0069949 (Hupehemonoside)

3D PDB for NP0069949 (Hupehemonoside)

SMILES for NP0069949 (Hupehemonoside)

INCHI for NP0069949 (Hupehemonoside)

Structure for NP0069949 (Hupehemonoside)

3D Structure for NP0069949 (Hupehemonoside)