NP-MRD: Showing NP-Card for methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate (NP0147462)

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Record Information

Version

2.0

Created at

2022-09-02 03:04:30 UTC

Updated at

2022-09-02 03:04:30 UTC

NP-MRD ID

NP0147462

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate

Description

Methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propyl-5,6,9,10-tetrahydroanthracene-2-carboxylate belongs to the class of organic compounds known as anthracenecarboxylic acids. These are organic compounds containing a carboxylic acid group attached to an anthracene ring system. methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate is found in Garveia annulata. Methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propyl-5,6,9,10-tetrahydroanthracene-2-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241502572D          

 30 32  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   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  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   -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
   -2.8579   -1.6500    0.0000 O   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   -0.0000    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
   -2.1434   -2.8875    0.0000 O   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
   -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  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
    0.7145   -3.7125    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
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    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
    2.5307   -3.6159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7561   -3.6159    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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 19 27  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
  4 30  1  0  0  0  0
 14 30  2  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -1.7244   -2.8041    1.2056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6645   -2.6612    0.0299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1047   -1.7925   -1.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7622   -0.4411   -0.6524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8130    0.4642   -0.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1821    0.1142   -0.8377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5379    0.2658   -2.0402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1438   -0.3571    0.0184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4398   -0.6409   -0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5066    1.7461   -0.1223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5605    2.6478   -0.0015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3334    3.9714    0.4091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2318    2.1376    0.1579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2026    1.2306    0.0313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4542   -0.0909   -0.3819 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6711   -0.9979   -0.5161 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5288   -2.1709   -0.8777 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0416   -0.5463   -0.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3113    0.6755    0.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1749    1.6131    0.3048 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3967    2.7922    0.6748 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6730    1.1249    0.4586 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0413    2.3462   -0.3811 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021    1.4888    1.9410 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6904    0.0971    0.2675 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9233    0.4036    0.4923 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3607   -1.2367   -0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4340   -2.2597   -0.3371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1053   -1.5522   -0.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8475   -2.8526   -0.8074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2634   -1.8204    1.4143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2648   -3.1904    2.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9005   -3.5154    0.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7428   -3.7180   -0.3964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6171   -2.3629    0.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9557   -1.7034   -1.8643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3332   -2.3733   -1.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7035    0.1531   -1.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4596   -1.5930   -1.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1946   -0.6900    0.3450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9133    4.0312    1.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7290    4.5488   -0.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3248    4.4936    0.4609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9766    3.1364    0.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5831    2.2268   -1.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7686    3.2794    0.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1425    2.3235   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8997    0.9374    2.5016 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5332    2.5651    2.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6540    1.1856    2.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1945   -2.1784    0.4540 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8447   -2.1416   -1.3552 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9841   -3.2726   -0.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5337   -3.0366   -1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  5 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 19 22  1  0
 22 23  1  0
 22 24  1  0
 22 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 15  4  1  0
 29 18  1  0
 20 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  9 38  1  0
  9 39  1  0
  9 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
 28 51  1  0
 28 52  1  0
 28 53  1  0
 30 54  1  0
M  END


  Mrv1533004241502572D          

 30 32  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   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  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   -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
   -2.8579   -1.6500    0.0000 O   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   -0.0000    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
   -2.1434   -2.8875    0.0000 O   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
   -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  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
    0.7145   -3.7125    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
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    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
    2.5307   -3.6159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7561   -3.6159    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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 19 27  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
  4 30  1  0  0  0  0
 14 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0147462

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1=C(C(=O)OC)C(OC)=CC2=C1C(=O)C1=C(C2=O)C(C)(C)C(=O)C(C)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O7/c1-7-8-11-14-12(9-13(29-5)15(11)22(28)30-6)19(25)17-16(20(14)26)18(24)10(2)21(27)23(17,3)4/h9,24H,7-8H2,1-6H3

> <INCHI_KEY>
VGYJVPPIYDSYPC-UHFFFAOYSA-N

> <FORMULA>
C23H24O7

> <MOLECULAR_WEIGHT>
412.438

> <EXACT_MASS>
412.152203113

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
43.59351555006783

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propyl-5,6,9,10-tetrahydroanthracene-2-carboxylate

> <ALOGPS_LOGP>
3.14

> <JCHEM_LOGP>
3.6015047093333328

> <ALOGPS_LOGS>
-4.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6422675236294055

> <JCHEM_PKA_STRONGEST_BASIC>
-4.90457020237855

> <JCHEM_POLAR_SURFACE_AREA>
106.97

> <JCHEM_REFRACTIVITY>
112.0885

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.21e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.724  -6.750   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.278  -6.750   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   30                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8                                                            
CONECT   10    5   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15   30                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   24                                                  
CONECT   18   17   19   28                                                  
CONECT   19   18   20   27                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   17   25   26                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   19                                                            
CONECT   28   18   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    4   14                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
Methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propyl-5,6,9,10-tetrahydroanthracene-2-carboxylic acid	Generator

Chemical Formula

C₂₃H₂₄O₇

Average Mass

412.4380 Da

Monoisotopic Mass

412.15220 Da

IUPAC Name

methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propyl-5,6,9,10-tetrahydroanthracene-2-carboxylate

Traditional Name

methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate

CAS Registry Number

Not Available

SMILES

CCCC1=C(C(=O)OC)C(OC)=CC2=C1C(=O)C1=C(C2=O)C(C)(C)C(=O)C(C)=C1O

InChI Identifier

InChI=1S/C23H24O7/c1-7-8-11-14-12(9-13(29-5)15(11)22(28)30-6)19(25)17-16(20(14)26)18(24)10(2)21(27)23(17,3)4/h9,24H,7-8H2,1-6H3

InChI Key

VGYJVPPIYDSYPC-UHFFFAOYSA-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
Garveia annulata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenecarboxylic acids. These are organic compounds containing a carboxylic acid group attached to an anthracene ring system.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Anthracenecarboxylic acids and derivatives

Direct Parent

Anthracenecarboxylic acids

Alternative Parents

Substituents

Anthracene carboxylic acid
9,10-anthraquinone
Anthraquinone
2-naphthalenecarboxylic acid
2-naphthalenecarboxylic acid or derivatives
O-methoxybenzoic acid or derivatives
Anisole
Aryl ketone
Quinone
Phenol ether
Alkyl aryl ether
Vinylogous acid
Methyl ester
Ketone
Carboxylic acid ester
Cyclic ketone
Ether
Enol
Carboxylic acid derivative
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.14	ALOGPS
logP	3.6	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	3.64	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	106.97 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112.09 m³·mol⁻¹	ChemAxon
Polarizability	43.59 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

23425673

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate (NP0147462)

MOL for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

3D MOL for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

3D SDF for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

3D-SDF for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

PDB for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

3D PDB for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

SMILES for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

INCHI for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

Structure for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)

3D Structure for NP0147462 (methyl 8-hydroxy-3-methoxy-5,5,7-trimethyl-6,9,10-trioxo-1-propylanthracene-2-carboxylate)