NP-MRD: Showing NP-Card for Glutinoside (NP0057482)

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Record Information

Version

2.0

Created at

2022-04-28 02:54:48 UTC

Updated at

2022-04-28 02:54:48 UTC

NP-MRD ID

NP0057482

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Glutinoside

Description

(2S,3S,4S,5S,6R)-2-{[(1R,4S,5R,6S,7R,8S,9S)-5-chloro-4,6-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,⁸]Undecan-9-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. Glutinoside is found in Rehmannia glutinosa . Based on a literature review very few articles have been published on (2S,3S,4S,5S,6R)-2-{[(1R,4S,5R,6S,7R,8S,9S)-5-chloro-4,6-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,⁸]Undecan-9-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282204542D          

 26 29  0  0  1  0            999 V2000
    1.2283    0.4317    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7910   -0.2230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5787   -0.7735    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2926   -0.2940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8866    0.4649    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4287    1.2079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5733    1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3626   -0.2216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7417   -0.9575    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8809   -0.8505    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5373   -0.0712    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2593    0.1433    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.3885   -1.5124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5711   -1.5984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8528   -2.0043    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1422   -1.5853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4239   -1.9912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4163   -2.8161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -3.2352    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8452   -2.8293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5558   -3.2484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1194   -4.0602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3019   -3.2220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2867   -1.5721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0049   -1.9780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867    0.9504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  5  8  1  0  0  0  0
  9  8  1  1  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 11 12  1  1  0  0  0
 10 13  1  6  0  0  0
  3 14  1  1  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  1  0  0  0
 19 22  1  1  0  0  0
 18 23  1  6  0  0  0
 17 24  1  1  0  0  0
 24 25  1  0  0  0  0
  1 26  1  6  0  0  0
M  END

     RDKit          3D

 49 52  0  0  0  0  0  0  0  0999 V2000
    2.9278    2.5193    1.9529 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8933    1.7936    1.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3064    0.4465    0.9014 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1892    0.5508    0.1057 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5009   -0.6736    0.1910 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3854   -0.6243   -0.6048 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8120   -0.7920    0.1293 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3905   -1.9660   -0.4074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7272   -1.9412    0.0141 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4809   -1.0509   -0.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6482    0.1668   -1.2943 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4715    1.4334   -1.2037 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6751    2.4575   -1.7530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6073    1.6762    0.2657 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2521    1.3862    0.8543 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.5902    0.7782    0.9605 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8743    1.5705    1.8607 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2496   -0.3794    1.6495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7483   -1.6036    1.3322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6679    0.3890   -0.1454 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3811   -1.8070   -0.3142 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7944   -2.4464   -1.4234 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7297   -1.3075   -0.7812 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6090   -0.7514   -2.0713 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3647   -0.3653    0.1896 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0988   -1.0799    1.1135 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928    3.0681    1.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2202    2.2837    0.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7676    1.5970    1.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0525   -0.0706    1.8458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1895   -0.8360    1.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5996   -0.9300    1.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1281   -2.9853   -0.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6426   -1.6141   -1.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4823   -0.7598   -0.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1246    0.0437   -2.2392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4348    1.3611   -1.7413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1616    2.9312   -1.0272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3835    2.7614    0.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2779    1.3980    2.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1361   -0.2324    2.7443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3605   -0.4105    1.4759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0602    1.2672   -0.4293 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4976   -2.5208    0.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3766   -1.7168   -1.9625 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3748   -2.2168   -0.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7825   -0.2044   -2.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0821    0.3177   -0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0699   -0.9111    1.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  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
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 16 20  1  0
  5 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25  3  1  0
 20  7  1  0
 19  9  1  0
 20 11  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  1
  5 31  1  1
  7 32  1  1
  9 33  1  1
 10 34  1  0
 10 35  1  0
 11 36  1  6
 12 37  1  6
 13 38  1  0
 14 39  1  6
 17 40  1  0
 18 41  1  0
 18 42  1  0
 20 43  1  6
 21 44  1  1
 22 45  1  0
 23 46  1  6
 24 47  1  0
 25 48  1  6
 26 49  1  0
M  END


  Mrv1652304282204542D          

 26 29  0  0  1  0            999 V2000
    1.2283    0.4317    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7910   -0.2230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5787   -0.7735    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2926   -0.2940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8866    0.4649    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4287    1.2079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5733    1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3626   -0.2216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7417   -0.9575    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8809   -0.8505    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5373   -0.0712    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2593    0.1433    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.3885   -1.5124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5711   -1.5984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8528   -2.0043    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1422   -1.5853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4239   -1.9912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4163   -2.8161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -3.2352    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8452   -2.8293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5558   -3.2484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1194   -4.0602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3019   -3.2220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2867   -1.5721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0049   -1.9780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867    0.9504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  5  8  1  0  0  0  0
  9  8  1  1  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 11 12  1  1  0  0  0
 10 13  1  6  0  0  0
  3 14  1  1  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  1  0  0  0
 19 22  1  1  0  0  0
 18 23  1  6  0  0  0
 17 24  1  1  0  0  0
 24 25  1  0  0  0  0
  1 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0057482

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@H](O[C@@H]2O[C@@H]3C[C@H]4[C@H](O)[C@@H](Cl)[C@@](O)(CO3)[C@@H]24)[C@@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H23ClO10/c16-12-8(18)4-1-6-23-3-15(12,22)7(4)13(25-6)26-14-11(21)10(20)9(19)5(2-17)24-14/h4-14,17-22H,1-3H2/t4-,5-,6-,7-,8+,9-,10+,11+,12-,13+,14+,15-/m1/s1

> <INCHI_KEY>
JWOORQMSHBLSDU-CEABKSKNSA-N

> <FORMULA>
C15H23ClO10

> <MOLECULAR_WEIGHT>
398.79

> <EXACT_MASS>
398.0979746

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
36.97472056739128

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5S,6R)-2-{[(1R,4S,5R,6S,7R,8S,9S)-5-chloro-4,6-dihydroxy-2,10-dioxatricyclo[5.3.1.0^{4,8}]undecan-9-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-1.98

> <JCHEM_LOGP>
-2.6821162063333333

> <ALOGPS_LOGS>
-0.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.649780640304328

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.063076703223924

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847587232825

> <JCHEM_POLAR_SURFACE_AREA>
158.3

> <JCHEM_REFRACTIVITY>
81.2897

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.39e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5S,6R)-2-{[(1R,4S,5R,6S,7R,8S,9S)-5-chloro-4,6-dihydroxy-2,10-dioxatricyclo[5.3.1.0^{4,8}]undecan-9-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       2.293   0.806   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.343  -0.416   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.814  -1.444   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.146  -0.549   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.388   0.868   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.534   2.255   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.937   2.255   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.410  -0.414   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.251  -1.787   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.644  -1.588   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.003  -0.133   0.000  0.00  0.00           C+0
HETATM   12 Cl   UNK     0      -0.484   0.268   0.000  0.00  0.00          Cl+0
HETATM   13  O   UNK     0       0.725  -2.823   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       4.799  -2.984   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.459  -3.741   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.132  -2.959   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.791  -3.717   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.777  -5.257   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.104  -6.039   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.444  -5.281   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.771  -6.064   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       2.089  -7.579   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -0.564  -6.014   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.535  -2.935   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.876  -3.692   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       1.095   1.774   0.000  0.00  0.00           O+0
CONECT    1    2    7   11   26                                             
CONECT    2    1    3    9                                                  
CONECT    3    2    4   14                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6    1                                                       
CONECT    8    5    9                                                       
CONECT    9    8    2   10                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10    1   12                                                  
CONECT   12   11                                                            
CONECT   13   10                                                            
CONECT   14    3   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   24                                                  
CONECT   18   17   19   23                                                  
CONECT   19   18   20   22                                                  
CONECT   20   19   15   21                                                  
CONECT   21   20                                                            
CONECT   22   19                                                            
CONECT   23   18                                                            
CONECT   24   17   25                                                       
CONECT   25   24                                                            
CONECT   26    1                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₃ClO₁₀

Average Mass

398.7900 Da

Monoisotopic Mass

398.09797 Da

IUPAC Name

(2S,3S,4S,5S,6R)-2-{[(1R,4S,5R,6S,7R,8S,9S)-5-chloro-4,6-dihydroxy-2,10-dioxatricyclo[5.3.1.0^{4,8}]undecan-9-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,3S,4S,5S,6R)-2-{[(1R,4S,5R,6S,7R,8S,9S)-5-chloro-4,6-dihydroxy-2,10-dioxatricyclo[5.3.1.0^{4,8}]undecan-9-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H](O[C@@H]2O[C@@H]3C[C@H]4[C@H](O)[C@@H](Cl)[C@@](O)(CO3)[C@@H]24)[C@@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C15H23ClO10/c16-12-8(18)4-1-6-23-3-15(12,22)7(4)13(25-6)26-14-11(21)10(20)9(19)5(2-17)24-14/h4-14,17-22H,1-3H2/t4-,5-,6-,7-,8+,9-,10+,11+,12-,13+,14+,15-/m1/s1

InChI Key

JWOORQMSHBLSDU-CEABKSKNSA-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
Rehmannia glutinosa	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
Oxepane
Dioxepane
1,3-dioxepane
Oxane
Monosaccharide
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Halohydrin
Chlorohydrin
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Organochloride
Organohalogen compound
Alkyl halide
Alkyl chloride
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	-2.7	ChemAxon
logS	-0.22	ALOGPS
pKa (Strongest Acidic)	12.06	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	158.3 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	81.29 m³·mol⁻¹	ChemAxon
Polarizability	36.97 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

154496679

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Glutinoside (NP0057482)

MOL for NP0057482 (Glutinoside)

3D MOL for NP0057482 (Glutinoside)

3D SDF for NP0057482 (Glutinoside)

3D-SDF for NP0057482 (Glutinoside)

PDB for NP0057482 (Glutinoside)

3D PDB for NP0057482 (Glutinoside)

SMILES for NP0057482 (Glutinoside)

INCHI for NP0057482 (Glutinoside)

Structure for NP0057482 (Glutinoside)

3D Structure for NP0057482 (Glutinoside)