NP-MRD: Showing NP-Card for Scabroside (NP0057580)

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Record Information

Version

2.0

Created at

2022-04-28 02:59:52 UTC

Updated at

2022-04-28 02:59:52 UTC

NP-MRD ID

NP0057580

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Scabroside

Description

(2S,3S,4S,5S,6R)-2-{[(1R,2R,4S,5R,6R,10S)-5,6-dihydroxy-7-methyl-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Scabroside is found in Deutzia scabra and Gentiana scabra . Based on a literature review very few articles have been published on (2S,3S,4S,5S,6R)-2-{[(1R,2R,4S,5R,6R,10S)-5,6-dihydroxy-7-methyl-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -4.8717    1.9038    0.7855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4729    1.3996    0.8104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5233    2.2537    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2230    1.7849    1.1250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7991    0.6120    0.4802 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2469    0.0692    1.2042 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4565    0.1015    0.5239 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9931   -1.1668    0.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1374   -1.0182   -0.4520 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6077   -2.3327   -1.0303 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7524   -2.0920   -1.7873 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1836   -0.3558    0.3929 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4466   -0.3888   -0.1907 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7244    1.0900    0.6035 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6190    1.8071    1.3702 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3859    0.9832    1.3324 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5704    0.4951    2.6169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445   -0.4037    0.2571 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7798   -0.8841   -1.1992 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5223   -2.1587   -1.3796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0197   -0.8407   -1.7504 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0255   -0.3640   -0.7347 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9560   -1.3665   -0.5111 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2392   -0.0077    0.5111 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8125   -0.7588    1.5618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1693    2.2892   -0.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6096    1.1293    1.0644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9792    2.7272    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7406    3.2987    1.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3537    0.9430   -0.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3531    0.5614   -0.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8780   -0.3165   -1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8240   -2.6614   -1.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7188   -3.1180   -0.2852 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0176   -2.8940   -2.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2171   -0.8326    1.3991 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0973   -0.3579    0.5595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5098    1.5372   -0.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0776    2.5205    1.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9190    1.9956    1.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4055   -0.4776    2.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6282   -1.3301    0.8622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7601   -0.9122   -1.5828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2621   -0.8039   -2.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5341    0.5212   -1.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6011   -1.9660    0.1946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4143   -0.2146    2.1145 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  5 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  1
 24  2  1  0
 16  7  1  0
 24 18  1  0
 21 19  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  5 30  1  6
  7 31  1  6
  9 32  1  6
 10 33  1  0
 10 34  1  0
 11 35  1  0
 12 36  1  1
 13 37  1  0
 14 38  1  6
 15 39  1  0
 16 40  1  1
 17 41  1  0
 18 42  1  1
 19 43  1  6
 21 44  1  6
 22 45  1  6
 23 46  1  0
 25 47  1  0
M  END


  Mrv1652304282204592D          

 25 28  0  0  1  0            999 V2000
    0.7327   -1.5964    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5364   -0.7950    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1323   -0.2244    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9243   -0.4551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1206   -1.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5248   -1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7210   -2.6284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9360    0.5769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.1475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3356    1.9488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9314    2.5194    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7235    2.2887    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9198    1.4874    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3239    0.9168    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5202    0.1155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7119    1.2567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3194    2.8594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7352    3.3208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310    3.8914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2863   -0.7341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5986   -1.4977    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0312   -2.0306    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0298   -2.8534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1038   -0.8455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8441   -2.4138    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  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  3  8  1  6  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 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
  9 14  1  0  0  0  0
 14 15  1  6  0  0  0
 13 16  1  6  0  0  0
 12 17  1  1  0  0  0
 11 18  1  6  0  0  0
 18 19  1  0  0  0  0
  2 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  1 22  1  0  0  0  0
 22 23  1  6  0  0  0
 21 24  1  6  0  0  0
 20 24  1  6  0  0  0
  1 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0057580

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H]2[C@H]3O[C@H]3[C@@H](O)[C@]12O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O10/c1-4-3-22-13(6-10-11(24-10)12(20)15(4,6)21)25-14-9(19)8(18)7(17)5(2-16)23-14/h3,5-14,16-21H,2H2,1H3/t5-,6+,7-,8+,9+,10-,11-,12-,13+,14+,15+/m1/s1

> <INCHI_KEY>
RTVGHDMOWLNNHR-OLLCSRHOSA-N

> <FORMULA>
C15H22O10

> <MOLECULAR_WEIGHT>
362.331

> <EXACT_MASS>
362.121296908

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.04927783235908

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5S,6R)-2-{[(1R,2R,4S,5R,6R,10S)-5,6-dihydroxy-7-methyl-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-1.95

> <JCHEM_LOGP>
-3.735878189000001

> <ALOGPS_LOGS>
-0.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.583050268633947

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.022102708335023

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981084760230427

> <JCHEM_POLAR_SURFACE_AREA>
161.6

> <JCHEM_REFRACTIVITY>
76.43469999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.06e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5S,6R)-2-{[(1R,2R,4S,5R,6R,10S)-5,6-dihydroxy-7-methyl-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <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       1.368  -2.980   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.001  -1.484   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.114  -0.419   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.592  -0.850   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.958  -2.345   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.846  -3.411   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.213  -4.906   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.747   1.077   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.859   2.142   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.493   3.638   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.605   4.703   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.084   4.272   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.450   2.777   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.338   1.711   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.704   0.216   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.929   2.346   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.196   5.337   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.239   6.199   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.351   7.264   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.534  -1.370   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.117  -2.796   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.058  -3.790   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.056  -5.326   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -2.060  -1.578   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       1.576  -4.506   0.000  0.00  0.00           O+0
CONECT    1    2    6   22   25                                             
CONECT    2    1    3   20                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    3    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13    9   15                                                  
CONECT   15   14                                                            
CONECT   16   13                                                            
CONECT   17   12                                                            
CONECT   18   11   19                                                       
CONECT   19   18                                                            
CONECT   20    2   21   24                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21    1   23                                                  
CONECT   23   22                                                            
CONECT   24   21   20                                                       
CONECT   25    1                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₁₀

Average Mass

362.3310 Da

Monoisotopic Mass

362.12130 Da

IUPAC Name

(2S,3S,4S,5S,6R)-2-{[(1R,2R,4S,5R,6R,10S)-5,6-dihydroxy-7-methyl-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,3S,4S,5S,6R)-2-{[(1R,2R,4S,5R,6R,10S)-5,6-dihydroxy-7-methyl-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H]2[C@H]3O[C@H]3[C@@H](O)[C@]12O

InChI Identifier

InChI=1S/C15H22O10/c1-4-3-22-13(6-10-11(24-10)12(20)15(4,6)21)25-14-9(19)8(18)7(17)5(2-16)23-14/h3,5-14,16-21H,2H2,1H3/t5-,6+,7-,8+,9+,10-,11-,12-,13+,14+,15+/m1/s1

InChI Key

RTVGHDMOWLNNHR-OLLCSRHOSA-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
Deutzia scabra	Plant	KNApSAcK
Gentiana scabra	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
O-glycosyl compound
Oxane
Monosaccharide
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Oxirane
Dialkyl ether
Acetal
Hydrocarbon derivative
Primary alcohol
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	-2	ALOGPS
logP	-3.7	ChemAxon
logS	-0.07	ALOGPS
pKa (Strongest Acidic)	12.02	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	161.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	76.43 m³·mol⁻¹	ChemAxon
Polarizability	34.05 Å³	ChemAxon
Number of Rings	4	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

154497435

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Scabroside (NP0057580)

MOL for NP0057580 (Scabroside)

3D MOL for NP0057580 (Scabroside)

3D SDF for NP0057580 (Scabroside)

3D-SDF for NP0057580 (Scabroside)

PDB for NP0057580 (Scabroside)

3D PDB for NP0057580 (Scabroside)

SMILES for NP0057580 (Scabroside)

INCHI for NP0057580 (Scabroside)

Structure for NP0057580 (Scabroside)

3D Structure for NP0057580 (Scabroside)