NP-MRD: Showing NP-Card for (2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one (NP0244838)

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Record Information

Version

2.0

Created at

2022-09-07 05:43:23 UTC

Updated at

2022-09-07 05:43:24 UTC

NP-MRD ID

NP0244838

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one

Description

Isousnic acid, also known as isousnate, belongs to the class of organic compounds known as acetophenones. These are organic compounds containing the acetophenone structure. (2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one is found in Parmotrema reticulatum, Ramalina hierrensis and Xanthoparmelia vagans. (2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one was first documented in 2011 (PMID: 21351753). Based on a literature review a small amount of articles have been published on Isousnic acid (PMID: 34323187) (PMID: 33749458).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072207432D          

 25 27  0  0  1  0            999 V2000
    0.6159   -2.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4229   -2.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6778   -3.2303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9749   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9130   -0.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7464   -0.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4139   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2208   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4758    0.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7729   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5798   -0.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5179   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0700   -2.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8150   -3.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8769   -2.2741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4560   -2.7887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1589   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3339   -1.3910    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6695   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7819   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0368   -2.7887    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  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
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
  4 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 41 43  0  0  0  0  0  0  0  0999 V2000
    5.5211    0.6933   -0.9865 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1206    1.1044   -0.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8461    2.3497   -0.8620 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1017    0.1536   -0.4820 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3481   -1.1334   -0.3842 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -1.6628   -0.5370 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2477   -2.0761   -0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9679   -1.6862   -0.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2191   -2.3081    0.2279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2217   -1.3202    0.4062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5500   -1.4688    0.7287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0773   -2.8551    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4059   -0.4172    0.9011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7553   -0.6261    1.2316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9034    0.8438    0.7408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7874    1.9795    0.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3447    3.3776    0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0044    1.7670    1.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5441    1.0514    0.4041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1457    2.3184    0.2626 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6963   -0.0579    0.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6382   -0.2412   -0.2836 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4604   -0.3135   -1.8898 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7378    0.6215   -0.0428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7165    1.7260    0.4936 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5868   -0.0187   -1.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1747    1.5904   -1.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9184    0.1923   -0.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8959   -2.3775    0.1446 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4570   -3.1223   -0.0166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5850   -2.9603    1.8864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3186   -3.6229    0.7215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8700   -2.9854    0.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0510   -1.5864    1.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5542    3.6374    1.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9919    3.6080   -0.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2043    4.0722    0.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4414    2.9045    0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4266   -0.7288   -2.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3120   -1.0884   -1.9992 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1926    0.6664   -2.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 15 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  2  0
 24  4  1  0
 22  8  1  0
 21 10  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
 14 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 20 38  1  0
 23 39  1  0
 23 40  1  0
 23 41  1  0
M  END


  Mrv1652309072207432D          

 25 27  0  0  1  0            999 V2000
    0.6159   -2.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4229   -2.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6778   -3.2303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9749   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9130   -0.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7464   -0.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4139   -0.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2208   -0.4349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4758    0.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7729   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5798   -0.8764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5179   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0700   -2.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8150   -3.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8769   -2.2741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4560   -2.7887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1589   -1.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3339   -1.3910    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6695   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7819   -2.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0368   -2.7887    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  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
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
  4 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0244838

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C1=C(O)C=C2OC3=C(C)C(O)=C(C(C)=O)C(O)=C3[C@@]2(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H16O7/c1-6-14(22)12(8(3)20)15(23)13-16(6)25-10-5-9(21)11(7(2)19)17(24)18(10,13)4/h5,21-23H,1-4H3/t18-/m0/s1

> <INCHI_KEY>
GRIDHCOCFJSWSY-SFHVURJKSA-N

> <FORMULA>
C18H16O7

> <MOLECULAR_WEIGHT>
344.319

> <EXACT_MASS>
344.089602855

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
34.227009089218264

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(13),4,6,9,11-pentaen-3-one

> <JCHEM_LOGP>
2.526620417

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.2878105654826

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.619274464558313

> <JCHEM_PKA_STRONGEST_BASIC>
-5.344184610686841

> <JCHEM_POLAR_SURFACE_AREA>
121.13000000000002

> <JCHEM_REFRACTIVITY>
90.64549999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(13),4,6,9,11-pentaen-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       1.150  -4.245   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.656  -4.565   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.132  -6.030   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.687  -3.421   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.211  -1.956   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.704  -1.636   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.241  -0.812   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.747  -1.132   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.993  -0.227   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.239  -1.132   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.746  -0.812   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.221   0.653   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.776  -1.956   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.282  -1.636   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.300  -3.421   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.331  -4.565   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.855  -6.030   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.837  -4.245   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.794  -3.741   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.318  -5.206   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.763  -2.597   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.223  -2.597   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.850  -4.003   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.193  -3.741   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.669  -5.206   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   24                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   21                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   15   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   10   22                                                  
CONECT   22   21    8   23   24                                             
CONECT   23   22                                                            
CONECT   24   22    4   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
Isousnate	Generator

Chemical Formula

C₁₈H₁₆O₇

Average Mass

344.3190 Da

Monoisotopic Mass

344.08960 Da

IUPAC Name

(2R)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(13),4,6,9,11-pentaen-3-one

Traditional Name

(2R)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(13),4,6,9,11-pentaen-3-one

CAS Registry Number

Not Available

SMILES

CC(=O)C1=C(O)C=C2OC3=C(C)C(O)=C(C(C)=O)C(O)=C3[C@@]2(C)C1=O

InChI Identifier

InChI=1S/C18H16O7/c1-6-14(22)12(8(3)20)15(23)13-16(6)25-10-5-9(21)11(7(2)19)17(24)18(10,13)4/h5,21-23H,1-4H3/t18-/m0/s1

InChI Key

GRIDHCOCFJSWSY-SFHVURJKSA-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
Parmotrema reticulatum	LOTUS Database	35616633
Ramalina hierrensis	LOTUS Database	35616633
Xanthoparmelia vagans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acetophenones. These are organic compounds containing the acetophenone structure.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Acetophenones

Direct Parent

Acetophenones

Alternative Parents

Substituents

Acetophenone
Coumaran
Aryl ketone
Aryl alkyl ketone
Phenol
Vinylogous acid
Ketone
Oxacycle
Polyol
Enol
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen 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	2.53	ChemAxon
pKa (Strongest Acidic)	3.62	ChemAxon
pKa (Strongest Basic)	-5.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	121.13 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	90.65 m³·mol⁻¹	ChemAxon
Polarizability	34.23 Å³	ChemAxon
Number of Rings	3	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

68023996

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91739360

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Urena-Vacas I, Burgos EG, Divakar PK, Gomez-Serranillos MP: Dibenzofurans from Lichens - A Pharmacological Overview. Curr Top Med Chem. 2021;21(26):2397-2408. doi: 10.2174/1568026621666210728095214. [PubMed:34323187 ]
Bui VM, Huynh BLC, Pham NKT, Nguyen TAT, Nguyen TTT, Nguyen KPP, Nguyen TP: Usneaceratins A and B, two new secondary metabolites from the lichen Usnea ceratina. Nat Prod Res. 2022 Aug;36(15):3945-3950. doi: 10.1080/14786419.2021.1901288. Epub 2021 Mar 22. [PubMed:33749458 ]
Goel M, Dureja P, Rani A, Uniyal PL, Laatsch H: Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. J Agric Food Chem. 2011 Mar 23;59(6):2299-307. doi: 10.1021/jf1049613. Epub 2011 Feb 25. [PubMed:21351753 ]
LOTUS database [Link]

Showing NP-Card for (2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one (NP0244838)

MOL for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

3D MOL for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

3D SDF for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

3D-SDF for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

PDB for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

3D PDB for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

SMILES for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

INCHI for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

Structure for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)

3D Structure for NP0244838 ((2r)-4,12-diacetyl-5,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),4,6,9,11-pentaen-3-one)