NP-MRD: Showing NP-Card for Feretoside (NP0138775)

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Record Information

Version

2.0

Created at

2022-06-29 18:35:37 UTC

Updated at

2022-06-29 18:35:37 UTC

NP-MRD ID

NP0138775

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Feretoside

Description

Feretoside belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton. Feretoside is found in Alibertia macrophylla, Eucommia ulmoides, Feretia apodanthera, Galium mollugo, Gardenia jasminoides, Genipa americana, Oldenlandia corymbosa, Oldenlandia herbacea, Paederia foetida, Catunaregam spinosa, Rhododendron latoucheae and Rosenbergiodendron formosum. It was first documented in 2005 (PMID: 16276972). Based on a literature review very few articles have been published on Feretoside (PMID: 23847077).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292220352D          

 28 30  0  0  1  0            999 V2000
    2.5645    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769   -1.6527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10  5  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  9 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 16  1  1  0  0  0
  8 17  1  1  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 21 26  1  6  0  0  0
 20 27  1  1  0  0  0
 19 28  1  6  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -6.2671    2.1140    2.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0548    1.4898    1.7923 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8606    2.1747    1.9114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8539    3.3231    2.4055 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5957    1.5965    1.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4860    2.2806    1.6078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3067    1.7315    1.1974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1817    0.6449    0.3180 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9464   -0.0809    0.7563 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9893   -0.0289   -0.1663 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2894   -1.3013   -0.6486 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4957   -1.3386   -1.3121 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6512   -2.6943   -1.9710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6131   -2.9199   -2.8870 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6578   -1.1817   -0.3501 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5870   -0.3561   -0.9610 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1220   -0.5090    0.9061 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4094   -1.4180    1.6878 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1709    0.6026    0.5264 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8171    1.5372   -0.2795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3952   -0.1934    0.1818 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7825   -0.4494   -1.2352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610   -0.8919   -2.3106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5292   -1.0451   -3.5307 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0794   -0.2244   -1.4001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7259    0.2040   -0.1445 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7555   -0.6312    0.2187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6033    0.2409    0.8919 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.0793    1.3596    2.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2005    2.3992    3.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4558    2.9486    1.5361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4763    3.2766    2.0361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0896    1.0623   -0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    0.5874   -1.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5482   -0.5849   -2.1483 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5902   -2.6547   -2.5653 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7637   -3.5133   -1.2537 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9743   -2.1613   -2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1073   -2.1632   -0.1104 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2140   -0.0247   -0.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9867   -0.1622    1.4849 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9828   -2.2088    1.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8461    1.1320    1.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3301    2.1616    0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1197   -1.2169    0.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0978   -0.0825   -2.5032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3904   -1.8561   -2.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5157   -0.2062   -4.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6014   -0.3405   -2.3410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1332    1.2285   -0.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5332   -1.1915    0.9961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9251   -0.4646    1.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  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
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  8 21  1  0
 21 28  1  0
 28 26  1  0
 26 27  1  0
 26 25  1  0
 25 22  2  0
 22 23  1  0
 23 24  1  0
 28  5  1  0
 19 10  1  0
 22 21  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  6 32  1  0
  8 33  1  6
 10 34  1  6
 12 35  1  6
 13 36  1  0
 13 37  1  0
 14 38  1  0
 15 39  1  1
 16 40  1  0
 17 41  1  1
 18 42  1  0
 19 43  1  1
 20 44  1  0
 21 45  1  1
 28 52  1  1
 26 50  1  6
 27 51  1  0
 25 49  1  0
 23 46  1  0
 23 47  1  0
 24 48  1  0
M  END


  Mrv1652306292220352D          

 28 30  0  0  1  0            999 V2000
    2.5645    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769   -1.6527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10  5  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  9 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 16  1  1  0  0  0
  8 17  1  1  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 21 26  1  6  0  0  0
 20 27  1  1  0  0  0
 19 28  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0138775

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]2[C@@H]1[C@H](O)C=C2CO

> <INCHI_IDENTIFIER>
InChI=1S/C17H24O11/c1-25-15(24)7-5-26-16(10-6(3-18)2-8(20)11(7)10)28-17-14(23)13(22)12(21)9(4-19)27-17/h2,5,8-14,16-23H,3-4H2,1H3/t8-,9-,10-,11+,12-,13+,14-,16+,17+/m1/s1

> <INCHI_KEY>
WSGPLSDARZNMCW-LPGRTNKPSA-N

> <FORMULA>
C17H24O11

> <MOLECULAR_WEIGHT>
404.368

> <EXACT_MASS>
404.131861593

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.69057657881727

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,4aS,5R,7aS)-5-hydroxy-7-(hydroxymethyl)-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,7aH-cyclopenta[c]pyran-4-carboxylate

> <ALOGPS_LOGP>
-1.82

> <JCHEM_LOGP>
-3.3675886423333328

> <ALOGPS_LOGS>
-1.14

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.172709930674518

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.20396636831982

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7414609030598482

> <JCHEM_POLAR_SURFACE_AREA>
175.37

> <JCHEM_REFRACTIVITY>
89.9451

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.92e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
scandoside methyl ester

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0       4.787   6.160   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.787   4.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.454   4.620   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.454   0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.846  -1.941   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.877  -3.085   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       2.846   3.481   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.454  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.788  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.122  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.122  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.788  -5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.454  -4.620   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.788  -6.930   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.122  -7.700   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      11.455  -5.390   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      11.455  -2.310   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       8.788  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   11                                                            
CONECT   17    8   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20   28                                                  
CONECT   20   19   21   27                                                  
CONECT   21   20   22   26                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22   18                                                       
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   21                                                            
CONECT   27   20                                                            
CONECT   28   19                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₄O₁₁

Average Mass

404.3680 Da

Monoisotopic Mass

404.13186 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

27530-67-2

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]2[C@@H]1[C@H](O)C=C2CO

InChI Identifier

InChI=1S/C17H24O11/c1-25-15(24)7-5-26-16(10-6(3-18)2-8(20)11(7)10)28-17-14(23)13(22)12(21)9(4-19)27-17/h2,5,8-14,16-23H,3-4H2,1H3/t8-,9-,10-,11+,12-,13+,14-,16+,17+/m1/s1

InChI Key

WSGPLSDARZNMCW-LPGRTNKPSA-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
Alibertia macrophylla	LOTUS Database	35616633
Eucommia ulmoides	LOTUS Database	35616633
Feretia apodanthera	LOTUS Database	35616633
Galium mollugo	LOTUS Database	35616633
Gardenia jasminoides	LOTUS Database	35616633
Genipa americana	LOTUS Database	35616633
Oldenlandia corymbosa	LOTUS Database	35616633
Oldenlandia herbacea	LOTUS Database	35616633
Paederia foetida	LOTUS Database	35616633
Randia dumetorum	LOTUS Database	35616633
Rhododendron latoucheae	LOTUS Database	35616633
Rosenbergiodendron formosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Iridoid O-glycosides

Alternative Parents

Substituents

Iridoid o-glycoside
Hexose monosaccharide
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Bicyclic monoterpenoid
Monoterpenoid
Monosaccharide
Oxane
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Carboxylic acid ester
Secondary alcohol
Acetal
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Polyol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Primary alcohol
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

terpene glycoside (CHEBI:9046 )
Iridoids (C09798 )

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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00003097

Chemspider ID

390873

KEGG Compound ID

C09798

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

442433

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Nam JW, Kim SY, Yoon T, Lee YJ, Kil YS, Lee YS, Seo EK: Heat shock factor 1 inducers from the bark of Eucommia ulmoides as cytoprotective agents. Chem Biodivers. 2013 Jul;10(7):1322-7. doi: 10.1002/cbdv.201200401. [PubMed:23847077 ]
Kim DH, Lee HJ, Oh YJ, Kim MJ, Kim SH, Jeong TS, Baek NI: Iridoid glycosides isolated from Oldenlandia diffusa inhibit LDL-oxidation. Arch Pharm Res. 2005 Oct;28(10):1156-60. doi: 10.1007/BF02972979. [PubMed:16276972 ]

Showing NP-Card for Feretoside (NP0138775)

MOL for NP0138775 (Feretoside)

3D MOL for NP0138775 (Feretoside)

3D SDF for NP0138775 (Feretoside)

3D-SDF for NP0138775 (Feretoside)

PDB for NP0138775 (Feretoside)

3D PDB for NP0138775 (Feretoside)

SMILES for NP0138775 (Feretoside)

INCHI for NP0138775 (Feretoside)

Structure for NP0138775 (Feretoside)

3D Structure for NP0138775 (Feretoside)