NP-MRD: Showing NP-Card for (11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione (NP0228819)

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Record Information

Version

2.0

Created at

2022-09-06 08:37:32 UTC

Updated at

2022-09-06 08:37:32 UTC

NP-MRD ID

NP0228819

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione

Description

Teuvincenone E belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. (11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione is found in Teucrium fruticans. (11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione was first documented in 2020 (PMID: 33065407). Based on a literature review very few articles have been published on Teuvincenone E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062210372D          

 25 28  0  0  1  0            999 V2000
    1.2336   -1.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7942    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185    0.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2306    0.8721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5109    1.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8548    1.1625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336   -1.9412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2018   -1.3105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2973   -2.3768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -1.5264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9362   -1.3437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  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  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 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
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 12 25  1  0  0  0  0
M  END

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
   -5.4207    0.8660   -0.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730    0.6833   -0.1851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4750   -0.5313   -0.4718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3602   -1.7185   -0.6322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0319   -0.7247   -0.6458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6087   -1.7209   -1.4266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1884   -1.9679   -1.6439 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2189   -2.9124   -2.3836 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391   -1.0708   -0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1052   -1.2999   -1.1644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4850   -2.3361   -1.9750 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0648   -0.4953   -0.5545 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6331    0.5181    0.2394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2895    0.7438    0.4356 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8745    1.7823    1.2499 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2989   -0.0437   -0.1608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1249    0.2100    0.0619 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4856    0.2091    1.5388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5525    1.6014   -0.4353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9949    1.7592   -0.0700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4003    2.8677    0.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7696    1.1813    0.7368 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8724    0.9011   -0.1125 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1728    0.9062    0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5509   -0.5024   -0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8257    0.3247    0.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6156    1.9762    0.0332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9219    0.4315   -0.9222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3921   -1.4360   -0.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3286   -2.0106   -1.6951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9941   -2.5915   -0.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3288   -2.3688   -1.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4586   -2.5455   -2.1528 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5664    2.3682    1.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8622   -0.5063    2.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4658    1.2310    1.9709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5311   -0.1490    1.6285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9864    2.4063    0.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4517    1.5702   -1.5353 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9105    1.6302   -0.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1484    1.7481    1.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2452   -0.0678    1.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9894    1.0012   -0.0585 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9441   -0.7102   -1.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9831   -1.2079    0.1596 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  1  0
 25 12  1  0
 12 13  2  0
 13 22  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16  9  1  0
  9  7  1  0
  7  8  2  0
  7  6  1  0
  6  5  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  2 20  1  0
 20 21  2  0
 20 19  1  0
 19 17  1  0
 17 18  1  1
  9 10  2  0
 10 11  1  0
 22 23  1  0
 17 16  1  0
 10 12  1  0
 17  5  1  0
 24 41  1  0
 24 42  1  0
 24 43  1  0
 23 40  1  6
 25 44  1  0
 25 45  1  0
 15 34  1  0
  6 32  1  0
  4 29  1  0
  4 30  1  0
  4 31  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 19 38  1  0
 19 39  1  0
 18 35  1  0
 18 36  1  0
 18 37  1  0
 11 33  1  0
M  END


  Mrv1652309062210372D          

 25 28  0  0  1  0            999 V2000
    1.2336   -1.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7942    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185    0.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2306    0.8721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5109    1.6480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8548    1.1625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336   -1.9412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2018   -1.3105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2973   -2.3768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -1.5264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9362   -1.3437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  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  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 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
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 12 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0228819

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2=C(O1)C(O)=C1C(C(=O)C=C3C(C)=C(C)C(=O)C[C@]13C)=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O5/c1-8-5-11-17(23)15-13(21)6-12-9(2)10(3)14(22)7-20(12,4)16(15)18(24)19(11)25-8/h6,8,23-24H,5,7H2,1-4H3/t8?,20-/m0/s1

> <INCHI_KEY>
CEFJBQPEKNGIIU-YTPZWRSRSA-N

> <FORMULA>
C20H20O5

> <MOLECULAR_WEIGHT>
340.375

> <EXACT_MASS>
340.131073744

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
36.487261191206755

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-11,17-dihydroxy-2,5,6,14-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaene-4,9-dione

> <JCHEM_LOGP>
3.3339662206666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.824011136496988

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.028289908906856

> <JCHEM_PKA_STRONGEST_BASIC>
-4.614810903998695

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
94.65270000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-11,17-dihydroxy-2,5,6,14-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaene-4,9-dione

> <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       2.303  -2.082   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.819  -1.811   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.342  -0.363   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.349   0.815   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.858  -0.092   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.381   1.357   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.897   1.628   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.420   3.076   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.890   0.451   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.406   0.722   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.929   2.170   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.399  -0.456   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.875  -1.904   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.359  -2.175   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.836  -3.624   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.367  -0.998   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.851  -1.269   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.843  -2.446   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.327  -2.717   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.811  -2.988   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.288  -4.437   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.091  -2.849   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      13.366  -1.985   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.814  -2.508   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.938  -0.506   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   16                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   25                                                  
CONECT   13   12   14   22                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    9   17                                                  
CONECT   17   16    5   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19    2   21                                                  
CONECT   21   20                                                            
CONECT   22   13   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   12                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

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Synonyms

Not Available

Chemical Formula

C₂₀H₂₀O₅

Average Mass

340.3750 Da

Monoisotopic Mass

340.13107 Da

IUPAC Name

(2S)-11,17-dihydroxy-2,5,6,14-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaene-4,9-dione

Traditional Name

(2S)-11,17-dihydroxy-2,5,6,14-tetramethyl-15-oxatetracyclo[8.7.0.0^{2,7}.0^{12,16}]heptadeca-1(17),5,7,10,12(16)-pentaene-4,9-dione

CAS Registry Number

Not Available

SMILES

CC1CC2=C(O1)C(O)=C1C(C(=O)C=C3C(C)=C(C)C(=O)C[C@]13C)=C2O

InChI Identifier

InChI=1S/C20H20O5/c1-8-5-11-17(23)15-13(21)6-12-9(2)10(3)14(22)7-20(12,4)16(15)18(24)19(11)25-8/h6,8,23-24H,5,7H2,1-4H3/t8?,20-/m0/s1

InChI Key

CEFJBQPEKNGIIU-YTPZWRSRSA-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
Teucrium fruticans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
Naphthofuran
Naphthalene
Coumaran
Aryl ketone
Cyclohexenone
Alkyl aryl ether
Vinylogous acid
Cyclic ketone
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.33	ChemAxon
pKa (Strongest Acidic)	9.03	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	94.65 m³·mol⁻¹	ChemAxon
Polarizability	36.49 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

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

132556482

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang X, Peng T, Shi X, Fang D, Tang L, Chen F, Wang F, Zhang G, Luo Y: Diterpenoids caryopterisoids D - Q and iridoid glucoside derivatives caryopterisides F - H from Caryopteris glutinosa. Phytochemistry. 2020 Dec;180:112534. doi: 10.1016/j.phytochem.2020.112534. Epub 2020 Oct 13. [PubMed:33065407 ]
LOTUS database [Link]

Showing NP-Card for (11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione (NP0228819)

MOL for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

3D MOL for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

3D SDF for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

3D-SDF for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

PDB for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

3D PDB for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

SMILES for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

INCHI for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

Structure for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)

3D Structure for NP0228819 ((11bs)-7,11-dihydroxy-3,4,9,11b-tetramethyl-1h,8h,9h-phenanthro[3,2-b]furan-2,6-dione)