NP-MRD: Showing NP-Card for 3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside (NP0083764)

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Record Information

Version

2.0

Created at

2022-04-29 04:42:26 UTC

Updated at

2022-04-29 04:42:26 UTC

NP-MRD ID

NP0083764

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside

Description

(2S,3R,4S,5S,6R)-2-{[3-(2-hydroxyethyl)-1H-indol-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. 3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside is found in Tetracentron sinense . Based on a literature review very few articles have been published on (2S,3R,4S,5S,6R)-2-{[3-(2-hydroxyethyl)-1H-indol-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
    5.7570    0.5494   -1.5306 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9960    1.3572   -0.6921 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0014    0.8670    0.7432 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4450   -0.5020    0.8023 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0969   -1.7001    0.9541 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1959   -2.7029    0.9549 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9552   -2.1929    0.8061 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6922   -2.7445    0.7399 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5828   -1.9222    0.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7163   -0.5654    0.4824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3454    0.3022    0.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6970   -0.0340    0.2311 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2021    0.5732   -0.9086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5280    0.2627   -1.1535 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9858    1.1536   -2.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8343    2.4734   -1.8705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4297    0.5440    0.0192 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6912    0.0486   -0.2500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8548    0.0334    1.3203 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6584    0.4161    2.3646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4504    0.5945    1.4155 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8408    0.2475    2.6168 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9895   -0.0178    0.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0958   -0.8179    0.7095 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2223    1.1393   -2.1778 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3299    2.4094   -0.7679 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9328    1.3455   -1.0572 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0680    0.8437    1.0825 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4162    1.6041    1.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1692   -1.7915    1.0551 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3783   -3.7224    1.0516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6153   -3.8207    0.8184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4091   -2.3933    0.5293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9287   -1.1027    0.2953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6990   -0.7792   -1.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0449    0.9660   -2.5546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3089    1.0063   -3.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8668    3.1121   -2.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5202    1.6447    0.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1879    0.6655   -0.8210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7310   -1.0857    1.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5123   -0.0776    2.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5043    1.6662    1.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5403    1.1114    3.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1150    1.0356    0.4770 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  2  0
  5  6  1  0
  6  7  1  0
  7 24  2  0
 24 23  1  0
 23 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 10  9  1  0
  9  8  2  0
 24  4  1  0
 21 12  1  0
  8  7  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
 23 45  1  0
 12 34  1  6
 14 35  1  6
 15 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  1
 18 40  1  0
 19 41  1  6
 20 42  1  0
 21 43  1  6
 22 44  1  0
  9 33  1  0
  8 32  1  0
M  END


  Mrv1652304292206422D          

 24 26  0  0  1  0            999 V2000
    4.9279    3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9279    1.9354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6424    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6424    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2135   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2054   -0.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4604   -0.8853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 19  2  0  0  0  0
 19 20  1  0  0  0  0
 14 21  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 12 23  1  0  0  0  0
 10 24  1  0  0  0  0
  3 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0083764

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCCC1=CNC2=C1C=C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C16H21NO7/c18-4-3-8-6-17-11-2-1-9(5-10(8)11)23-16-15(22)14(21)13(20)12(7-19)24-16/h1-2,5-6,12-22H,3-4,7H2/t12-,13-,14+,15-,16-/m1/s1

> <INCHI_KEY>
MYNVMBICAGQOMG-IBEHDNSVSA-N

> <FORMULA>
C16H21NO7

> <MOLECULAR_WEIGHT>
339.344

> <EXACT_MASS>
339.13180202

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.36193983653202

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-2-{[3-(2-hydroxyethyl)-1H-indol-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.52

> <JCHEM_LOGP>
-0.9783141683333337

> <ALOGPS_LOGS>
-1.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.19517607104024

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.200038358303017

> <JCHEM_PKA_STRONGEST_BASIC>
-2.4305488307638896

> <JCHEM_POLAR_SURFACE_AREA>
135.4

> <JCHEM_REFRACTIVITY>
82.84070000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.05e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-2-{[3-(2-hydroxyethyl)-1H-indol-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0       9.199   6.693   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       7.865   5.923   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.865   4.383   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.199   3.613   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.533   4.383   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.199   2.073   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      10.533   1.303   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.865   1.303   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.865  -0.237   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.531   2.073   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.198   1.303   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.864   2.073   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.530   1.303   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.197   2.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.268   1.597   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.744   0.132   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.250  -0.188   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.726  -1.652   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.173   2.843   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0      -0.268   4.089   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       1.197   3.613   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.530   4.383   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.864   3.613   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.531   3.613   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   24                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   15   20                                                       
CONECT   20   19   21                                                       
CONECT   21   14   20   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   12                                                       
CONECT   24   10    3                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₁NO₇

Average Mass

339.3440 Da

Monoisotopic Mass

339.13180 Da

IUPAC Name

(2S,3R,4S,5S,6R)-2-{[3-(2-hydroxyethyl)-1H-indol-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,3R,4S,5S,6R)-2-{[3-(2-hydroxyethyl)-1H-indol-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

OCCC1=CNC2=C1C=C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C=C2

InChI Identifier

InChI=1S/C16H21NO7/c18-4-3-8-6-17-11-2-1-9(5-10(8)11)23-16-15(22)14(21)13(20)12(7-19)24-16/h1-2,5-6,12-22H,3-4,7H2/t12-,13-,14+,15-,16-/m1/s1

InChI Key

MYNVMBICAGQOMG-IBEHDNSVSA-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
Tetracentron sinense	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Hexose monosaccharide
O-glycosyl compound
3-alkylindole
Indole
Indole or derivatives
Monosaccharide
Oxane
Substituted pyrrole
Benzenoid
Heteroaromatic compound
Pyrrole
Secondary alcohol
Polyol
Azacycle
Oxacycle
Acetal
Organoheterocyclic compound
Alcohol
Primary alcohol
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	-0.52	ALOGPS
logP	-0.98	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	135.4 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	82.84 m³·mol⁻¹	ChemAxon
Polarizability	33.36 Å³	ChemAxon
Number of Rings	3	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

C00052662

Chemspider ID

17283572

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16126713

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside (NP0083764)

MOL for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

3D MOL for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

3D SDF for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

3D-SDF for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

PDB for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

3D PDB for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

SMILES for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

INCHI for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

Structure for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)

3D Structure for NP0083764 (3-(2-hydroxyethyl)-1H-indole-5-O-beta-D-glucopyranoside)