NP-MRD: Showing NP-Card for rosiridoside A (NP0037296)

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Record Information

Version

2.0

Created at

2021-06-20 20:15:10 UTC

Updated at

2021-06-30 00:09:25 UTC

NP-MRD ID

NP0037296

Secondary Accession Numbers

None

Natural Product Identification

Common Name

rosiridoside A

Provided By

JEOL Database JEOL Logo

Description

Rosiridoside A 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. rosiridoside A is found in Rhodiola sachalinensis. rosiridoside A was first documented in 2008 (Yoshikawa, M., et al.). Based on a literature review very few articles have been published on Rosiridoside A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202122153D          

 47 47  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306202122153D          

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  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
  9 35  1  0  0  0  0
  4 28  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
  7 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0037296

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]([H])(C(=C(/[H])C([H])([H])O[C@]1([H])OC([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])[C@@]1([H])O[H])\C([H])([H])[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O6/c1-9(2)4-5-11(16)10(3)6-7-20-15-14(19)13(18)12(17)8-21-15/h4,6,11-19H,5,7-8H2,1-3H3/b10-6+/t11-,12-,13-,14+,15+/m0/s1

> <INCHI_KEY>
QBKWSKLQLMCHEU-UEAYSTNJSA-N

> <FORMULA>
C15H26O6

> <MOLECULAR_WEIGHT>
302.367

> <EXACT_MASS>
302.172938557

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.714607524501844

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,4S,5S)-2-{[(2E,4S)-4-hydroxy-3,7-dimethylocta-2,6-dien-1-yl]oxy}oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.21

> <JCHEM_LOGP>
0.13107152533333427

> <ALOGPS_LOGS>
-1.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.375863188434888

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.244118651714379

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9926560511273523

> <JCHEM_POLAR_SURFACE_AREA>
99.38000000000001

> <JCHEM_REFRACTIVITY>
79.14840000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.21e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S)-2-{[(2E,4S)-4-hydroxy-3,7-dimethylocta-2,6-dien-1-yl]oxy}oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 47  0  0  0  0  0  0  0  0999 V2000
    0.7339   -5.3734    1.6804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.9175    1.7844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0085   -3.6594    2.3265 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1711   -2.8906    1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5794   -2.9505    0.8990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6775   -2.6506   -0.6107 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0185   -2.8707   -1.0534 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2945   -1.2309   -0.9994 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1639   -0.1351   -0.4382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2322   -1.0138   -1.8051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.2928   -2.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320    0.2541   -2.0136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4158    1.3590   -2.6173 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9416    2.6044   -2.1186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6246    3.7285   -2.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1384    3.6792   -2.4590 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4285    3.8739   -1.0687 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7048    2.3310   -2.9029 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0807    2.2373   -2.4981 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9084    1.1787   -2.2937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4136   -0.0603   -2.8233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0342   -5.9108    1.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6839   -5.5504    1.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7985   -5.8174    2.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2363   -2.5904    2.3952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7620   -4.1185    1.6783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1064   -4.0849    3.3307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7859   -1.8754    1.5388 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0407   -3.9235    1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1990   -2.2453    1.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0527   -3.3719   -1.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2037   -3.8165   -0.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9678   -0.0030    0.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2245   -0.3740   -0.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0085    0.8290   -0.9277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6789   -1.8775   -2.1712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8493    0.3900   -3.3491 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1051    1.1504   -1.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2564    1.3016   -3.7026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2036    4.6237   -2.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3960    3.7672   -3.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6325    4.4971   -2.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3648    3.6067   -0.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6901    2.2578   -3.9972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3212    1.2982   -2.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675    1.1376   -1.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7988   -0.7421   -2.4824 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 20 13  1  0
 11 10  1  0
 20 18  1  0
 10  8  2  0
 16 18  1  0
  8  6  1  0
 16 15  1  0
  6  5  1  0
 15 14  1  0
  8  9  1  0
 14 13  1  0
  5  4  1  0
 16 17  1  0
  4  2  2  3
 18 19  1  0
  2  1  1  0
 20 21  1  0
  2  3  1  0
  6  7  1  0
 13 12  1  0
 17 43  1  0
 13 39  1  6
 16 42  1  6
 18 44  1  6
 19 45  1  0
 20 46  1  1
 21 47  1  0
 15 40  1  0
 15 41  1  0
 11 37  1  0
 11 38  1  0
 10 36  1  0
  6 31  1  6
  5 29  1  0
  5 30  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
  4 28  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  7 32  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       0.734  -5.373   1.680  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.374  -3.918   1.784  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.008  -3.659   2.326  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.171  -2.891   1.430  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.579  -2.950   0.899  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.678  -2.651  -0.611  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.019  -2.871  -1.053  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.295  -1.231  -0.999  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.164  -0.135  -0.438  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.232  -1.014  -1.805  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.670   0.293  -2.272  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.732   0.254  -2.014  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.416   1.359  -2.617  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.942   2.604  -2.119  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.625   3.728  -2.689  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.138   3.679  -2.459  0.00  0.00           C+0
HETATM   17  O   UNK     0      -3.429   3.874  -1.069  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.705   2.331  -2.903  0.00  0.00           C+0
HETATM   19  O   UNK     0      -5.081   2.237  -2.498  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.908   1.179  -2.294  0.00  0.00           C+0
HETATM   21  O   UNK     0      -3.414  -0.060  -2.823  0.00  0.00           O+0
HETATM   22  H   UNK     0      -0.034  -5.911   1.114  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.684  -5.550   1.171  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.799  -5.817   2.679  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.236  -2.590   2.395  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.762  -4.119   1.678  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.106  -4.085   3.331  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.786  -1.875   1.539  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.041  -3.924   1.100  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.199  -2.245   1.468  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.053  -3.372  -1.153  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.204  -3.817  -0.932  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.968  -0.003   0.630  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.224  -0.374  -0.567  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.009   0.829  -0.928  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.679  -1.878  -2.171  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.849   0.390  -3.349  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.105   1.150  -1.755  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.256   1.302  -3.703  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.204   4.624  -2.220  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.396   3.767  -3.760  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.632   4.497  -2.994  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.365   3.607  -0.965  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.690   2.258  -3.997  0.00  0.00           H+0
HETATM   45  H   UNK     0      -5.321   1.298  -2.638  0.00  0.00           H+0
HETATM   46  H   UNK     0      -3.067   1.138  -1.209  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.799  -0.742  -2.482  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    4    1    3                                                  
CONECT    3    2   25   26   27                                             
CONECT    4    5    2   28                                                  
CONECT    5    6    4   29   30                                             
CONECT    6    8    5    7   31                                             
CONECT    7    6   32                                                       
CONECT    8   10    6    9                                                  
CONECT    9    8   33   34   35                                             
CONECT   10   11    8   36                                                  
CONECT   11   12   10   37   38                                             
CONECT   12   11   13                                                       
CONECT   13   20   14   12   39                                             
CONECT   14   15   13                                                       
CONECT   15   16   14   40   41                                             
CONECT   16   18   15   17   42                                             
CONECT   17   16   43                                                       
CONECT   18   20   16   19   44                                             
CONECT   19   18   45                                                       
CONECT   20   13   18   21   46                                             
CONECT   21   20   47                                                       
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    5                                                            
CONECT   31    6                                                            
CONECT   32    7                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35    9                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   11                                                            
CONECT   39   13                                                            
CONECT   40   15                                                            
CONECT   41   15                                                            
CONECT   42   16                                                            
CONECT   43   17                                                            
CONECT   44   18                                                            
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   94    0
END

RDKit          3D

47 47  0  0  0  0  0  0  0  0999 V2000
    0.7339   -5.3734    1.6804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.9175    1.7844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0085   -3.6594    2.3265 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1711   -2.8906    1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5794   -2.9505    0.8990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6775   -2.6506   -0.6107 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0185   -2.8707   -1.0534 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2945   -1.2309   -0.9994 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1639   -0.1351   -0.4382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2322   -1.0138   -1.8051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.2928   -2.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320    0.2541   -2.0136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4158    1.3590   -2.6173 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9416    2.6044   -2.1186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6246    3.7285   -2.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1384    3.6792   -2.4590 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4285    3.8739   -1.0687 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7048    2.3310   -2.9029 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0807    2.2373   -2.4981 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9084    1.1787   -2.2937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4136   -0.0603   -2.8233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0342   -5.9108    1.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6839   -5.5504    1.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7985   -5.8174    2.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2363   -2.5904    2.3952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7620   -4.1185    1.6783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1064   -4.0849    3.3307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7859   -1.8754    1.5388 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0407   -3.9235    1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1990   -2.2453    1.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0527   -3.3719   -1.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2037   -3.8165   -0.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9678   -0.0030    0.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2245   -0.3740   -0.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0085    0.8290   -0.9277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6789   -1.8775   -2.1712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8493    0.3900   -3.3491 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1051    1.1504   -1.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2564    1.3016   -3.7026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2036    4.6237   -2.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3960    3.7672   -3.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6325    4.4971   -2.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3648    3.6067   -0.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6901    2.2578   -3.9972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3212    1.2982   -2.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675    1.1376   -1.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7988   -0.7421   -2.4824 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 20 13  1  0
 11 10  1  0
 20 18  1  0
 10  8  2  0
 16 18  1  0
  8  6  1  0
 16 15  1  0
  6  5  1  0
 15 14  1  0
  8  9  1  0
 14 13  1  0
  5  4  1  0
 16 17  1  0
  4  2  2  3
 18 19  1  0
  2  1  1  0
 20 21  1  0
  2  3  1  0
  6  7  1  0
 13 12  1  0
 17 43  1  0
 13 39  1  6
 16 42  1  6
 18 44  1  6
 19 45  1  0
 20 46  1  1
 21 47  1  0
 15 40  1  0
 15 41  1  0
 11 37  1  0
 11 38  1  0
 10 36  1  0
  6 31  1  6
  5 29  1  0
  5 30  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
  4 28  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  7 32  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₆O₆

Average Mass

302.3670 Da

Monoisotopic Mass

302.17294 Da

IUPAC Name

(2R,3R,4S,5S)-2-{[(2E,4S)-4-hydroxy-3,7-dimethylocta-2,6-dien-1-yl]oxy}oxane-3,4,5-triol

Traditional Name

(2R,3R,4S,5S)-2-{[(2E,4S)-4-hydroxy-3,7-dimethylocta-2,6-dien-1-yl]oxy}oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

[H]O[C@]([H])(C(=C(/[H])C([H])([H])O[C@]1([H])OC([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])[C@@]1([H])O[H])\C([H])([H])[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C15H26O6/c1-9(2)4-5-11(16)10(3)6-7-20-15-14(19)13(18)12(17)8-21-15/h4,6,11-19H,5,7-8H2,1-3H3/b10-6+/t11-,12-,13-,14+,15+/m0/s1

InChI Key

QBKWSKLQLMCHEU-UEAYSTNJSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rhodiola sachalinensis	JEOL database	Yoshikawa, M., et al, Chem. Pharm. Bull. 56, 695 (2008)

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

O-glycosyl compound
Pentose monosaccharide
Monoterpenoid
Monocyclic monoterpenoid
Oxane
Monosaccharide
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-0.21	ALOGPS
logP	0.13	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	12.24	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	99.38 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	79.15 m³·mol⁻¹	ChemAxon
Polarizability	32.71 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

101849416

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yoshikawa, M., et al. (2008). Yoshikawa, M., et al, Chem. Pharm. Bull. 56, 695 (2008). Chem. Pharm. Bull..

Showing NP-Card for rosiridoside A (NP0037296)

MOL for NP0037296 (rosiridoside A)

3D MOL for NP0037296 (rosiridoside A)

3D SDF for NP0037296 (rosiridoside A)

3D-SDF for NP0037296 (rosiridoside A)

PDB for NP0037296 (rosiridoside A)

3D PDB for NP0037296 (rosiridoside A)

SMILES for NP0037296 (rosiridoside A)

INCHI for NP0037296 (rosiridoside A)

Structure for NP0037296 (rosiridoside A)

3D Structure for NP0037296 (rosiridoside A)