NP-MRD: Showing NP-Card for 5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione (NP0327423)

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Record Information

Version

2.0

Created at

2022-09-12 09:59:12 UTC

Updated at

2022-09-12 09:59:13 UTC

NP-MRD ID

NP0327423

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione

Description

5-Hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. Based on a literature review very few articles have been published on 5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122211592D          

 49 51  0  0  0  0            999 V2000
    1.0606    1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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  3 55  1  0
  2 53  1  6
  1 50  1  0
  1 51  1  0
  1 52  1  0
 46 93  1  0
 45 92  1  0
 43 90  1  1
 44 91  1  0
 41 86  1  6
 42 87  1  0
 42 88  1  0
 42 89  1  0
M  END


  Mrv1652309122211592D          

 49 51  0  0  0  0            999 V2000
    1.0606    1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8731    1.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1552    0.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6249   -0.2865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8125   -0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2822   -0.7752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3428    0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6249    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4374   -0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7196   -0.9185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9677    0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6855    1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2158    1.8960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0283    1.7527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9337    2.6712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1212    2.8145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6515    3.4465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8390    3.5897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0266    3.7330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5918    3.1679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3162    3.2442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7784    2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5909    2.1825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2481    1.6938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303    0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2927    0.9761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -0.2692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125   -1.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -1.0942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -0.2692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2414    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5643    1.5505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3768    1.6938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0340    2.1825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3162    2.9577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1287    3.1010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2141    3.5897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0681    4.3650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0266    3.4465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3087    2.6712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1212    2.5279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6515    3.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4034    1.7527    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 21 19  1  4  0  0  0
 21 22  2  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
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  2  0  0  0  0
  9 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
  9 36  1  0  0  0  0
 36 37  2  0  0  0  0
  8 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 45 43  1  4  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
  2 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0327423

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(=O)C(C2CC(=O)CCC(C)OC(=O)C=CC(O)C(C)OC2=O)(C2CC(=O)CCC(C)OC(=O)C=CC(O)C(C)OC2=O)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C34H44O15/c1-17-6-8-22(35)15-24(31(42)48-20(4)26(37)10-12-29(40)45-17)34(28(39)14-19(3)47-33(34)44)25-16-23(36)9-7-18(2)46-30(41)13-11-27(38)21(5)49-32(25)43/h10-13,17-21,24-27,37-38H,6-9,14-16H2,1-5H3

> <INCHI_KEY>
WPPOFQTZLGPDIZ-UHFFFAOYSA-N

> <FORMULA>
C34H44O15

> <MOLECULAR_WEIGHT>
692.711

> <EXACT_MASS>
692.268020717

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
67.89531595765864

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione

> <JCHEM_LOGP>
2.0655063083333323

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.850722940782372

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.355217378115267

> <JCHEM_PKA_STRONGEST_BASIC>
-3.345915879895643

> <JCHEM_POLAR_SURFACE_AREA>
223.16999999999993

> <JCHEM_REFRACTIVITY>
167.68320000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       1.980   2.359   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.496   2.092   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.023   0.645   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.033  -0.535   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.517  -0.267   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.527  -1.447   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.990   1.180   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.527   1.447   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.517   0.267   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.506   1.447   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.033   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.550  -0.267   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -5.077  -1.715   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -5.540   0.912   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.013   2.359   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.003   3.539   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.519   3.272   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.476   4.986   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.960   5.254   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.949   6.433   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.433   6.701   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.916   6.968   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.105   5.913   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.590   6.056   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.453   4.341   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.970   4.074   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.463   3.162   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.990   1.715   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.546   1.822   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -0.183  -0.503   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.151   0.267   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.183  -2.043   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.517  -2.813   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.517  -4.353   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.850  -2.043   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -2.850  -0.503   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -4.184   0.267   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.053   2.894   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -2.570   3.162   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -0.064   4.074   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -0.590   5.521   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.107   5.789   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.400   6.701   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -0.127   8.148   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       1.916   6.433   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.443   4.986   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.960   4.719   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       4.949   5.899   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       4.486   3.272   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   49                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   38                                                  
CONECT    9    8   10   30   36                                             
CONECT   10    9   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   10   29                                                  
CONECT   29   28                                                            
CONECT   30    9   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35    9   37                                                  
CONECT   37   36                                                            
CONECT   38    8   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47    2                                                       
MASTER        0    0    0    0    0    0    0    0   49    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₄O₁₅

Average Mass

692.7110 Da

Monoisotopic Mass

692.26802 Da

IUPAC Name

5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione

Traditional Name

5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione

CAS Registry Number

Not Available

SMILES

CC1CC(=O)C(C2CC(=O)CCC(C)OC(=O)C=CC(O)C(C)OC2=O)(C2CC(=O)CCC(C)OC(=O)C=CC(O)C(C)OC2=O)C(=O)O1

InChI Identifier

InChI=1S/C34H44O15/c1-17-6-8-22(35)15-24(31(42)48-20(4)26(37)10-12-29(40)45-17)34(28(39)14-19(3)47-33(34)44)25-16-23(36)9-7-18(2)46-30(41)13-11-27(38)21(5)49-32(25)43/h10-13,17-21,24-27,37-38H,6-9,14-16H2,1-5H3

InChI Key

WPPOFQTZLGPDIZ-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Macrolide
Delta_valerolactone
Delta valerolactone
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	2.07	ChemAxon
pKa (Strongest Acidic)	13.36	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	223.17 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	167.68 m³·mol⁻¹	ChemAxon
Polarizability	67.9 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

162822126

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione (NP0327423)

MOL for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

3D MOL for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

3D SDF for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

3D-SDF for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

PDB for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

3D PDB for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

SMILES for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

INCHI for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

Structure for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)

3D Structure for NP0327423 (5-hydroxy-9-[3-(5-hydroxy-6,14-dimethyl-2,8,11-trioxo-1,7-dioxacyclotetradec-3-en-9-yl)-6-methyl-2,4-dioxooxan-3-yl]-6,14-dimethyl-1,7-dioxacyclotetradec-3-ene-2,8,11-trione)