NP-MRD: Showing NP-Card for methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate (NP0186940)

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Record Information

Version

2.0

Created at

2022-09-04 02:56:58 UTC

Updated at

2022-09-04 02:56:58 UTC

NP-MRD ID

NP0186940

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate

Description

Methyl (2S)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]Tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate belongs to the class of organic compounds known as p-phthalate esters. These are ester derivatives of p-phthalic acids, which are based on a benzene 1,4-dicarboxylic acid skeleton. methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate is found in Graphis proserpens. Based on a literature review very few articles have been published on methyl (2S)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]Tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042204562D          

 24 26  0  0  1  0            999 V2000
    3.6497    3.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9163    3.2644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    2.4403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5707    1.9941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0740    1.3394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783    1.1558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2362    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0612    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783   -0.3308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0740   -0.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8904   -1.3187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
    4.5070    2.5142    0.2951 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6667    1.3707    0.1285 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2968    1.4437    0.2775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7867    2.5495    0.5672 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4081    0.2901    0.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9428   -0.9449   -0.2064 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1179   -2.0463   -0.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6124   -3.2997   -0.6859 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0118   -3.4322   -0.8509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470   -1.9087   -0.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8308   -0.7025    0.1175 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508    0.3845    0.2663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2890    1.7151    0.5847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4662    2.3636    0.1805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3984    3.8283   -0.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6591    1.7820    0.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0693    0.4012    0.2633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4256    0.2007    0.4631 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2803   -0.6824    0.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0215   -1.9283    0.5402 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3950   -1.7541    0.3535 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5077   -2.9479   -0.2806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1392   -3.0689   -0.4056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6143   -4.1729   -0.6963 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0946    3.1055    1.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5000    3.0815   -0.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5221    2.1880    0.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9988   -1.0492   -0.3315 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5580   -3.0351    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3304   -2.7524   -1.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3083   -4.4635   -1.0795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5078    4.0317   -0.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3999    4.4485    0.7779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2787    4.0777   -0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4265    2.4624   -0.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0464    0.6699   -0.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8500   -2.2909    1.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8604   -2.4289    0.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  2  0
 10 23  1  0
 23 24  2  0
 23 22  1  0
 22 20  1  0
 20 21  1  0
 20 19  1  0
 19 17  2  0
 17 18  1  0
 17 16  1  0
 16 14  2  0
 14 15  1  0
 14 13  1  0
 13 12  1  0
 12 11  2  0
 12  5  1  0
 11 10  1  0
 11 19  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  6 28  1  0
  9 29  1  0
  9 30  1  0
  9 31  1  0
 20 37  1  1
 21 38  1  0
 18 36  1  0
 16 35  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
M  END


  Mrv1652309042204562D          

 24 26  0  0  1  0            999 V2000
    3.6497    3.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9163    3.2644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    2.4403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5707    1.9941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0740    1.3394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783    1.1558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2362    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0612    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783   -0.3308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0740   -0.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8904   -1.3187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0186940

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC(OC)=C2C(=O)O[C@H](O)C3=C(O)C=C(C)OC1=C23

> <INCHI_IDENTIFIER>
InChI=1S/C16H14O8/c1-6-4-8(17)10-12-11(16(20)24-15(10)19)9(21-2)5-7(13(12)23-6)14(18)22-3/h4-5,15,17,19H,1-3H3/t15-/m0/s1

> <INCHI_KEY>
SZQCDAMPRNWLHM-HNNXBMFYSA-N

> <FORMULA>
C16H14O8

> <MOLECULAR_WEIGHT>
334.28

> <EXACT_MASS>
334.068867411

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
31.609042697416275

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2S)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0^{5,14}]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate

> <JCHEM_LOGP>
0.7011094903333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.78446099729156

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.842326937072492

> <JCHEM_PKA_STRONGEST_BASIC>
-4.417246785584433

> <JCHEM_POLAR_SURFACE_AREA>
111.52000000000001

> <JCHEM_REFRACTIVITY>
83.29299999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0^{5,14}]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       6.813   6.799   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.444   6.094   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.370   4.555   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.665   3.722   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.000   4.620   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.871   2.500   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.373   2.157   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.041   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.581   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.373  -0.617   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.871  -0.960   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.529  -2.462   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.000  -0.000   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   23                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11    5   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   11   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   10   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0,]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylic acid	Generator

Chemical Formula

C₁₆H₁₄O₈

Average Mass

334.2800 Da

Monoisotopic Mass

334.06887 Da

IUPAC Name

methyl (2S)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0^{5,14}]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate

Traditional Name

methyl (2S)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0^{5,14}]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC(OC)=C2C(=O)O[C@H](O)C3=C(O)C=C(C)OC1=C23

InChI Identifier

InChI=1S/C16H14O8/c1-6-4-8(17)10-12-11(16(20)24-15(10)19)9(21-2)5-7(13(12)23-6)14(18)22-3/h4-5,15,17,19H,1-3H3/t15-/m0/s1

InChI Key

SZQCDAMPRNWLHM-HNNXBMFYSA-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
Graphis proserpens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-phthalate esters. These are ester derivatives of p-phthalic acids, which are based on a benzene 1,4-dicarboxylic acid skeleton.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

p-Phthalate esters

Alternative Parents

Substituents

Para-phthalic acid ester
Para_phthalic_acid
M-methoxybenzoic acid or derivatives
Benzopyran
Isochromane
2-benzopyran
Anisole
Alkyl aryl ether
Dicarboxylic acid or derivatives
Methyl ester
Carboxylic acid ester
Hemiacetal
Lactone
Ether
Enol
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen 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
logP	0.7	ChemAxon
pKa (Strongest Acidic)	6.84	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	111.52 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	83.29 m³·mol⁻¹	ChemAxon
Polarizability	31.61 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

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

163014044

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate (NP0186940)

MOL for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

3D MOL for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

3D SDF for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

3D-SDF for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

PDB for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

3D PDB for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

SMILES for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

INCHI for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

Structure for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)

3D Structure for NP0186940 (methyl (2s)-2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate)