NP-MRD: Showing NP-Card for 2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one (NP0171227)

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Record Information

Version

2.0

Created at

2022-09-03 07:39:32 UTC

Updated at

2022-09-03 07:39:33 UTC

NP-MRD ID

NP0171227

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one

Description

Rutarin belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety. 2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one is found in Atalantia racemosa, Peucedanum praeruptorum and Seseli grandivittatum. Based on a literature review very few articles have been published on Rutarin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032209392D          

 30 33  0  0  1  0            999 V2000
   -0.2817   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -3.9979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -3.9979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4944   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4944   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -5.2354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233   -6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -2.6029    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
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
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  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  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  1  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  6  0  0  0
 16 29  1  0  0  0  0
  7 29  2  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -2.5553   -2.9721    2.3561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2838   -2.3260    1.2229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7642   -2.3996    1.5030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0238   -3.0037    0.0515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9221   -0.8719    1.0660 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5609   -0.3290   -0.1962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6491    0.7944   -0.5353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8427    1.9371   -1.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8121    2.8504   -1.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0110    3.9962   -2.2016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9582    4.8706   -2.3431 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2275    4.5348   -1.7212 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2046    5.3477   -1.8533 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4085    1.4149   -0.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8596    0.4425   -0.1111 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0789   -0.6835    0.6809 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9926   -1.5592    0.1572 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6654   -2.2692    1.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6495   -2.9350    2.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0045   -0.9317   -0.7434 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4735   -0.8063   -2.0243 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3558    0.4527   -0.2461 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8480    0.4403    1.0477 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0901    1.2820   -0.2737 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0764    1.9965   -1.4878 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4376    0.5144    0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5359   -0.7110    0.7526 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9158   -4.0344    2.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8295   -2.5169    3.3317 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1523   -2.7229   -0.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2338   -0.2494    1.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6004   -0.0030   -0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7805    2.1805   -1.7591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9722    4.1898   -2.6592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0631    5.7819   -2.9196 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4959    0.1475   -1.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4908   -2.3816   -0.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0917   -1.5337    2.0456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4420   -2.9713    0.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0216   -3.4961    2.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9024   -1.5973   -0.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7166   -1.5512   -2.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1049    0.9009   -0.9604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6707    1.2924    1.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1679    2.0241    0.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5390    1.5443   -2.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 11 10  2  0
 10  9  1  0
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 30  5  1  0
 27 18  1  0
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  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
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 11 43  1  0
 10 42  1  0
  8 41  1  0
M  END


  Mrv1652309032209392D          

 30 33  0  0  1  0            999 V2000
   -0.2817   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -3.9979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -3.9979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4944   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2201   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4944   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -5.2354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233   -6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -2.6029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
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 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  6  0  0  0
 16 29  1  0  0  0  0
  7 29  2  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171227

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)C1CC2=C(O1)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C1OC(=O)C=CC1=C2

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O10/c1-20(2,26)11-6-9-5-8-3-4-12(22)29-16(8)18(17(9)28-11)30-19-15(25)14(24)13(23)10(7-21)27-19/h3-5,10-11,13-15,19,21,23-26H,6-7H2,1-2H3/t10-,11?,13-,14+,15-,19+/m1/s1

> <INCHI_KEY>
JWWFVRMFYKPZNE-RINUOYIASA-N

> <FORMULA>
C20H24O10

> <MOLECULAR_WEIGHT>
424.402

> <EXACT_MASS>
424.136946973

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
41.46800119949076

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(2-hydroxypropan-2-yl)-9-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H,7H-furo[3,2-g]chromen-7-one

> <ALOGPS_LOGP>
-0.51

> <JCHEM_LOGP>
-0.8392398079999998

> <ALOGPS_LOGS>
-2.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.166307770672653

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.196424191849431

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923662274575

> <JCHEM_POLAR_SURFACE_AREA>
155.14000000000001

> <JCHEM_REFRACTIVITY>
100.46620000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.81e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2-hydroxypropan-2-yl)-9-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H-furo[3,2-g]chromen-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.526  -3.613   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.014  -3.613   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.014  -5.153   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.014  -2.073   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.554  -3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.459  -2.367   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.591  -2.843   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.925  -2.073   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.259  -2.843   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.259  -4.383   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.592  -5.153   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       8.925  -5.153   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.591  -4.383   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.258  -5.153   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.258  -6.693   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.924  -7.463   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.590  -6.693   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.257  -7.463   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.923  -6.693   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.411  -7.463   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.257  -9.003   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.923  -9.773   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.590  -9.773   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.590 -11.313   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.924  -9.003   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.258  -9.773   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.924  -4.383   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.459  -4.859   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6   30                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   29                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9   16                                                  
CONECT   16   15   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18   28                                                  
CONECT   28   27                                                            
CONECT   29   16    7   30                                                  
CONECT   30   29    5                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₄O₁₀

Average Mass

424.4020 Da

Monoisotopic Mass

424.13695 Da

IUPAC Name

2-(2-hydroxypropan-2-yl)-9-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H,7H-furo[3,2-g]chromen-7-one

Traditional Name

2-(2-hydroxypropan-2-yl)-9-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,3H-furo[3,2-g]chromen-7-one

CAS Registry Number

Not Available

SMILES

CC(C)(O)C1CC2=C(O1)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C1OC(=O)C=CC1=C2

InChI Identifier

InChI=1S/C20H24O10/c1-20(2,26)11-6-9-5-8-3-4-12(22)29-16(8)18(17(9)28-11)30-19-15(25)14(24)13(23)10(7-21)27-19/h3-5,10-11,13-15,19,21,23-26H,6-7H2,1-2H3/t10-,11?,13-,14+,15-,19+/m1/s1

InChI Key

JWWFVRMFYKPZNE-RINUOYIASA-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
Atalantia racemosa	LOTUS Database	35616633
Peucedanum praeruptorum	LOTUS Database	35616633
Seseli grandivittatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Coumarin glycosides

Direct Parent

Coumarin glycosides

Alternative Parents

Substituents

Coumarin o-glycoside
Coumarin-8-o-glycoside
Phenolic glycoside
Furanocoumarin
Linear furanocoumarin
Psoralen
Glycosyl compound
O-glycosyl compound
Benzopyran
1-benzopyran
Coumaran
Alkyl aryl ether
Pyranone
Benzenoid
Monosaccharide
Oxane
Pyran
Tertiary alcohol
Heteroaromatic compound
Lactone
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Ether
Polyol
Organic oxygen compound
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Primary alcohol
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	-0.51	ALOGPS
logP	-0.84	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	155.14 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	100.47 m³·mol⁻¹	ChemAxon
Polarizability	41.47 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00002496

Chemspider ID

10259273

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12315119

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one (NP0171227)

MOL for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

3D MOL for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

3D SDF for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

3D-SDF for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

PDB for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

3D PDB for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

SMILES for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

INCHI for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

Structure for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)

3D Structure for NP0171227 (2-(2-hydroxypropan-2-yl)-9-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2h,3h-furo[3,2-g]chromen-7-one)