NP-MRD: Showing NP-Card for (5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one (NP0237936)

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Record Information

Version

2.0

Created at

2022-09-06 21:13:07 UTC

Updated at

2022-09-06 21:13:07 UTC

NP-MRD ID

NP0237936

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one

Description

(5R)-5-[(2R)-2-hydroxy-2-[(2R)-9-oxo-2H,3H,9H-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as p-dioxolo[2,3-h]coumarins. These are organic aromatic compounds that contain a p-dioxole ring that is angularly fused to the benzene ring of a coumarin. In p-dioxolo[2,3-h]coumarins, the coumarin ring system shares its C7-C8 bond with the p-dioxole ring. (5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one is found in Clausena excavata. Based on a literature review very few articles have been published on (5R)-5-[(2R)-2-hydroxy-2-[(2R)-9-oxo-2H,3H,9H-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-2,5-dihydrofuran-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062223132D          

 27 30  0  0  1  0            999 V2000
    2.7474   -2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3184   -1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -2.9684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3105   -3.6359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4742   -3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1416   -3.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8953   -3.5303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4742   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1416   -2.0710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3105   -2.3010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  5 12  1  0  0  0  0
 13  2  1  1  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  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  2  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 13 27  1  0  0  0  0
M  END

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
   -0.4896   -2.7096    1.6963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8046   -1.9209    0.3747 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3575   -2.8935   -0.4366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7339   -0.8342    0.7275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2081    0.0582   -0.3870 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2386    1.0281    0.1112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3678    0.8798   -0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6493    1.6516   -0.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0130    2.2993   -1.5013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1891   -0.1882   -1.4871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0943   -0.6102   -2.2914 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8968   -0.6431   -1.3696 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737   -1.5170   -0.0918 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5835   -1.3405   -1.5685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0400   -0.0472   -1.9056 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1422    0.4562   -1.2475 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    1.1618   -1.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2388    1.6373   -1.1124 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2686    1.3851    0.2420 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3483    1.8628    0.9676 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3534    1.5966    2.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3157    0.8881    2.8791 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3330    0.6542    4.1055 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2988    0.4414    2.1789 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2722    0.6825    0.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2103    0.2200    0.1388 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1411   -0.4994    0.6648 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0298   -2.0089    2.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4684   -3.0575    2.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1982   -3.5131    1.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3466   -2.8666   -0.4479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3790   -0.2059    1.5775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6793   -1.3296    1.1150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3448    0.6348   -0.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0580    1.7491    0.8925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4743    0.9837   -0.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4709    2.3673    0.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7820    1.6891   -2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2687   -2.4223    0.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2787   -2.0874   -2.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4440   -1.5260   -1.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0965    1.3391   -2.9103 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0342    2.1871   -1.5732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111    2.4028    0.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1933    1.9649    2.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  6
  2  4  1  0
  4  5  1  0
  5 12  1  0
 12 10  1  0
 10 11  2  0
 10  7  1  0
  7  8  1  0
  8  9  1  0
  7  6  2  0
  2 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
  6  5  1  0
 27 13  1  0
 26 16  1  0
 25 19  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  8 36  1  0
  8 37  1  0
  9 38  1  0
  6 35  1  0
 13 39  1  6
 14 40  1  0
 14 41  1  0
 17 42  1  0
 18 43  1  0
 20 44  1  0
 21 45  1  0
M  END


  Mrv1652309062223132D          

 27 30  0  0  1  0            999 V2000
    2.7474   -2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3184   -1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -2.9684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3105   -3.6359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4742   -3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1416   -3.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8953   -3.5303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4742   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1416   -2.0710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3105   -2.3010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  5 12  1  0  0  0  0
 13  2  1  1  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  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  2  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 13 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237936

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@](O)(C[C@H]1OC(=O)C(CO)=C1)[C@H]1COC2=CC=C3C=CC(=O)OC3=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O8/c1-19(23,7-12-6-11(8-20)18(22)25-12)14-9-24-13-4-2-10-3-5-15(21)27-16(10)17(13)26-14/h2-6,12,14,20,23H,7-9H2,1H3/t12-,14+,19+/m0/s1

> <INCHI_KEY>
GDPHCYVELMTBIG-BBEJJTJUSA-N

> <FORMULA>
C19H18O8

> <MOLECULAR_WEIGHT>
374.345

> <EXACT_MASS>
374.10016754

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.035623909232655

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R)-5-[(2R)-2-hydroxy-2-[(2R)-9-oxo-2H,3H,9H-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
0.6060977240000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.133950914281328

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.300579624623058

> <JCHEM_PKA_STRONGEST_BASIC>
-2.854316837964854

> <JCHEM_POLAR_SURFACE_AREA>
111.52000000000001

> <JCHEM_REFRACTIVITY>
92.72269999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5R)-5-[(2R)-2-hydroxy-2-[(2R)-9-oxo-2H,3H-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       5.128  -4.977   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.795  -4.207   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.461  -3.437   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.025  -5.541   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.485  -5.541   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.580  -6.787   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.885  -6.311   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.131  -7.216   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.538  -6.590   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.885  -4.771   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.131  -3.866   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       0.580  -4.295   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.565  -0.206   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.495  -4.207   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       9.185  -2.874   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.105  -2.874   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   13                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    5                                                       
CONECT   13    2   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   19   26                                                  
CONECT   26   25   16   27                                                  
CONECT   27   26   13                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₈O₈

Average Mass

374.3450 Da

Monoisotopic Mass

374.10017 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@](O)(C[C@H]1OC(=O)C(CO)=C1)[C@H]1COC2=CC=C3C=CC(=O)OC3=C2O1

InChI Identifier

InChI=1S/C19H18O8/c1-19(23,7-12-6-11(8-20)18(22)25-12)14-9-24-13-4-2-10-3-5-15(21)27-16(10)17(13)26-14/h2-6,12,14,20,23H,7-9H2,1H3/t12-,14+,19+/m0/s1

InChI Key

GDPHCYVELMTBIG-BBEJJTJUSA-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
Clausena excavata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-dioxolo[2,3-h]coumarins. These are organic aromatic compounds that contain a p-dioxole ring that is angularly fused to the benzene ring of a coumarin. In p-dioxolo[2,3-h]coumarins, the coumarin ring system shares its C7-C8 bond with the p-dioxole ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

p-Dioxolo[2,3-h]coumarins

Direct Parent

p-Dioxolo[2,3-h]coumarins

Alternative Parents

Substituents

P-dioxolo[2,3-h]coumarin
Benzo-1,4-dioxane
Benzodioxane
Benzopyran
1-benzopyran
Alkyl aryl ether
Pyranone
2-furanone
Para-dioxin
Benzenoid
Pyran
Heteroaromatic compound
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Lactone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Carbonyl group
Alcohol
Primary alcohol
Organic oxide
Hydrocarbon derivative
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

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

162972427

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one (NP0237936)

MOL for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

3D MOL for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

3D SDF for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

3D-SDF for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

PDB for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

3D PDB for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

SMILES for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

INCHI for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

Structure for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)

3D Structure for NP0237936 ((5r)-5-[(2r)-2-hydroxy-2-[(2r)-9-oxo-2h,3h-[1,4]dioxino[2,3-h]chromen-2-yl]propyl]-3-(hydroxymethyl)-5h-furan-2-one)