NP-MRD: Showing NP-Card for hovetrichoside d (NP0191972)

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Record Information

Version

2.0

Created at

2022-09-04 09:04:39 UTC

Updated at

2022-09-04 09:04:39 UTC

NP-MRD ID

NP0191972

Secondary Accession Numbers

None

Natural Product Identification

Common Name

hovetrichoside d

Description

Hovetrichoside D belongs to the class of organic compounds known as aurone o-glycosides. These are aurone flavonoids containing a carbohydrate moiety O-glycosidically bound to the aurone skeleton. hovetrichoside d is found in Hovenia trichocarpa. Based on a literature review very few articles have been published on Hovetrichoside D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042211042D          

 42 46  0  0  1  0            999 V2000
   -5.0101   -3.2895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2255   -3.0345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0539   -2.2276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2693   -1.9726    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0978   -1.1657    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3132   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1416   -0.1038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3570    0.1512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7439   -0.4008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0407   -0.1459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0407   -1.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0668   -3.9979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668   -4.8229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6562   -2.5247    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.2146   -3.8837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6124   -3.5866    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7839   -4.3936    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
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
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 19 32  2  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  0  0  0  0
 11 33  1  0  0  0  0
 33 34  2  0  0  0  0
  9 35  1  0  0  0  0
 35 36  2  0  0  0  0
  6 36  1  0  0  0  0
  4 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
  2 41  1  0  0  0  0
 41 42  1  1  0  0  0
M  END

     RDKit          3D

 74 78  0  0  0  0  0  0  0  0999 V2000
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    5.8242    0.0618   -0.3179 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7814    0.2769   -1.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309042211042D          

 42 46  0  0  1  0            999 V2000
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   -4.2255   -3.0345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9154   -1.2078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7001   -1.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6562   -2.5247    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8716   -2.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8277   -3.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2146   -3.8837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6124   -3.5866    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7839   -4.3936    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
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 19 32  2  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  0  0  0  0
 11 33  1  0  0  0  0
 33 34  2  0  0  0  0
  9 35  1  0  0  0  0
 35 36  2  0  0  0  0
  6 36  1  0  0  0  0
  4 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
  2 41  1  0  0  0  0
 41 42  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0191972

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1O[C@@H](OC2=CC=C(CC3(O)OC4=CC(O)=CC(O[C@@H]5OC(CO)[C@@H](O)[C@H](O)C5O)=C4C3=O)C=C2)[C@@H](O)C(O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H32O15/c1-10-18(30)20(32)22(34)25(38-10)39-13-4-2-11(3-5-13)8-27(37)24(36)17-14(6-12(29)7-15(17)42-27)40-26-23(35)21(33)19(31)16(9-28)41-26/h2-7,10,16,18-23,25-26,28-35,37H,8-9H2,1H3/t10?,16?,18-,19+,20?,21-,22-,23?,25-,26+,27?/m0/s1

> <INCHI_KEY>
GRXIBUCMIOIMAU-CRGPTENZSA-N

> <FORMULA>
C27H32O15

> <MOLECULAR_WEIGHT>
596.538

> <EXACT_MASS>
596.17412033

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
57.19386832423578

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,6-dihydroxy-4-{[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-[(4-{[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)methyl]-2,3-dihydro-1-benzofuran-3-one

> <JCHEM_LOGP>
-1.3664767733333325

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.946962195901595

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.562205307479706

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6122003585840474

> <JCHEM_POLAR_SURFACE_AREA>
245.28999999999996

> <JCHEM_REFRACTIVITY>
135.81840000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
hovetrichoside D

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -9.352  -6.140   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.888  -5.664   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -7.567  -4.158   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -6.103  -3.682   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.783  -2.176   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.318  -1.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.998  -0.194   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.533   0.282   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.389  -0.748   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.076  -0.272   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.076  -2.333   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       2.126  -0.057   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.591   0.237   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.924  -4.383   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.258  -5.153   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.591  -4.383   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.925  -5.153   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.259  -4.383   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.592  -5.153   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.925  -6.693   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.259  -7.463   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.591  -7.463   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.591  -9.003   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.258  -6.693   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.924  -7.463   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       1.650  -4.013   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -1.709  -2.255   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.173  -2.730   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -4.958  -4.713   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -3.494  -4.237   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -5.278  -6.219   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -4.134  -7.250   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -6.743  -6.695   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -7.063  -8.201   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   41                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   37                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   36                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   35                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13   33                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   32                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   21   31                                                  
CONECT   31   30                                                            
CONECT   32   19   14   33                                                  
CONECT   33   32   11   34                                                  
CONECT   34   33                                                            
CONECT   35    9   36                                                       
CONECT   36   35    6                                                       
CONECT   37    4   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39    2   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₂O₁₅

Average Mass

596.5380 Da

Monoisotopic Mass

596.17412 Da

IUPAC Name

2,6-dihydroxy-4-{[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-[(4-{[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)methyl]-2,3-dihydro-1-benzofuran-3-one

Traditional Name

hovetrichoside D

CAS Registry Number

Not Available

SMILES

CC1O[C@@H](OC2=CC=C(CC3(O)OC4=CC(O)=CC(O[C@@H]5OC(CO)[C@@H](O)[C@H](O)C5O)=C4C3=O)C=C2)[C@@H](O)C(O)[C@H]1O

InChI Identifier

InChI=1S/C27H32O15/c1-10-18(30)20(32)22(34)25(38-10)39-13-4-2-11(3-5-13)8-27(37)24(36)17-14(6-12(29)7-15(17)42-27)40-26-23(35)21(33)19(31)16(9-28)41-26/h2-7,10,16,18-23,25-26,28-35,37H,8-9H2,1H3/t10?,16?,18-,19+,20?,21-,22-,23?,25-,26+,27?/m0/s1

InChI Key

GRXIBUCMIOIMAU-CRGPTENZSA-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
Hovenia trichocarpa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aurone o-glycosides. These are aurone flavonoids containing a carbohydrate moiety O-glycosidically bound to the aurone skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Aurone O-glycosides

Alternative Parents

Substituents

Aurone-4-o-glycoside
Auronol
Aurone
Phenolic glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Coumaran
Benzofuran
Phenoxy compound
Aryl alkyl ketone
Aryl ketone
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Acyloin
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Monosaccharide
Oxane
Ketone
Hemiacetal
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Aldehyde
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Primary alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Aurone flavonoids (LMPK12130071 )

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	ChemAxon
pKa (Strongest Acidic)	7.56	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	245.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	135.82 m³·mol⁻¹	ChemAxon
Polarizability	57.19 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

C00014671

Chemspider ID

24846208

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42607793

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for hovetrichoside d (NP0191972)

MOL for NP0191972 (hovetrichoside d)

3D MOL for NP0191972 (hovetrichoside d)

3D SDF for NP0191972 (hovetrichoside d)

3D-SDF for NP0191972 (hovetrichoside d)

PDB for NP0191972 (hovetrichoside d)

3D PDB for NP0191972 (hovetrichoside d)

SMILES for NP0191972 (hovetrichoside d)

INCHI for NP0191972 (hovetrichoside d)

Structure for NP0191972 (hovetrichoside d)

3D Structure for NP0191972 (hovetrichoside d)