NP-MRD: Showing NP-Card for (8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol (NP0282729)

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Record Information

Version

2.0

Created at

2022-09-09 09:40:55 UTC

Updated at

2022-09-09 09:40:55 UTC

NP-MRD ID

NP0282729

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol

Description

CHEMBL481046 belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring. (8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol is found in Tovomita longifolia. Based on a literature review very few articles have been published on CHEMBL481046.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092211402D          

 27 30  0  0  1  0            999 V2000
   -1.2448   -0.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1842   -0.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  1  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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  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  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 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
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
 11 26  1  0  0  0  0
 27 26  1  6  0  0  0
  2 27  1  0  0  0  0
  7 27  1  0  0  0  0
M  END

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -3.3101   -0.5297    2.0605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8625    0.1766    0.7978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9934   -0.0551   -0.2152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8369    1.6494    1.0884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8559    2.4180    0.2893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5024    1.8492    0.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3556    0.4254    0.6478 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0875    0.4875    2.1246 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7589   -0.1489    0.0030 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7722   -1.2919   -0.7668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2880   -2.1620   -0.5800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2866   -3.3010   -1.3497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3097   -4.2281   -1.2270 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7046   -3.5696   -2.2548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7774   -2.6938   -2.4452 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7366   -3.0532   -3.3825 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8041   -1.5440   -1.6880 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8253   -0.5632   -1.8821 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4669   -0.5121   -2.9788 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2498    0.4478   -0.9146 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6095    1.7297   -1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0765    2.6725   -0.4728 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1891    2.3493    0.8652 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8384    1.0901    1.3175 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3696    0.1473    0.4134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3250   -1.8024    0.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5756   -0.3185    0.2369 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7719   -0.2073    2.9686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4170   -0.3817    2.1787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1657   -1.6112    1.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5653   -0.5607   -1.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4131    0.8992   -0.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7893   -0.6946    0.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8552    2.0635    0.8551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7435    1.7850    2.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2820    2.6696   -0.7258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7399    3.4288    0.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2339    1.7770   -0.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3170    2.4753    0.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4130    1.4613    2.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4084   -0.3821    2.6931 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0381    0.5173    2.2543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0508   -4.0851   -0.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7020   -4.4666   -2.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5504   -2.5657   -3.6208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5150    1.9748   -2.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3664    3.6706   -0.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5508    3.0686    1.5747 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9225    0.8277    2.3602 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1362   -0.8294    0.8353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9316   -1.9807    1.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2586   -2.3740    0.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6486   -0.1757   -0.8854 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  1
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 26  1  0
 26 27  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 27  2  1  0
 25 20  1  0
 27  7  1  0
 17 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  8 40  1  0
  8 41  1  0
  8 42  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  6
 13 43  1  0
 14 44  1  0
 16 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
M  END


  Mrv1652309092211402D          

 27 30  0  0  1  0            999 V2000
   -1.2448   -0.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1842   -0.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  1  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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  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  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 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
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
 11 26  1  0  0  0  0
 27 26  1  6  0  0  0
  2 27  1  0  0  0  0
  7 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0282729

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC[C@]2(C)OC3=C(C[C@@H]12)C(O)=CC(O)=C3C(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H26O4/c1-22(2)10-7-11-23(3)18(22)12-15-16(24)13-17(25)19(21(15)27-23)20(26)14-8-5-4-6-9-14/h4-6,8-9,13,18,24-25H,7,10-12H2,1-3H3/t18-,23-/m0/s1

> <INCHI_KEY>
NUBZMOOMCLFMKK-MBSDFSHPSA-N

> <FORMULA>
C23H26O4

> <MOLECULAR_WEIGHT>
366.457

> <EXACT_MASS>
366.183109317

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
39.80900464009489

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4aS,9aS)-5-benzoyl-1,1,4a-trimethyl-2,3,4,4a,9,9a-hexahydro-1H-xanthene-6,8-diol

> <JCHEM_LOGP>
5.9548100086666675

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.018129320546276

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.543860827652212

> <JCHEM_PKA_STRONGEST_BASIC>
-4.942688320312109

> <JCHEM_POLAR_SURFACE_AREA>
66.75999999999999

> <JCHEM_REFRACTIVITY>
104.84420000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(8aS,10aS)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5H-xanthene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.324  -1.130   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.344  -1.130   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   27                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   27                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   26                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   10   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   11   27                                                       
CONECT   27   26    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₆O₄

Average Mass

366.4570 Da

Monoisotopic Mass

366.18311 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)CCC[C@]2(C)OC3=C(C[C@@H]12)C(O)=CC(O)=C3C(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C23H26O4/c1-22(2)10-7-11-23(3)18(22)12-15-16(24)13-17(25)19(21(15)27-23)20(26)14-8-5-4-6-9-14/h4-6,8-9,13,18,24-25H,7,10-12H2,1-3H3/t18-,23-/m0/s1

InChI Key

NUBZMOOMCLFMKK-MBSDFSHPSA-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
Tovomita longifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthenes

Alternative Parents

Substituents

Benzophenone
Xanthene
Aryl-phenylketone
Aryl ketone
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Ketone
Oxacycle
Ether
Organic oxide
Organooxygen compound
Aldehyde
Hydrocarbon derivative
Organic oxygen 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

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

9734435

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11559661

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol (NP0282729)

MOL for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

3D MOL for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

3D SDF for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

3D-SDF for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

PDB for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

3D PDB for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

SMILES for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

INCHI for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

Structure for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)

3D Structure for NP0282729 ((8as,10as)-4-benzoyl-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5h-xanthene-1,3-diol)