NP-MRD: Showing NP-Card for (-)-Milolide E (NP0080737)

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Record Information

Version

2.0

Created at

2022-04-29 01:43:55 UTC

Updated at

2022-04-29 01:43:55 UTC

NP-MRD ID

NP0080737

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Milolide E

Description

(1R,2R,3R,5R,7S,8R,11R,12S,13R,14S,15R,16R,17S,19R)-2,13-bis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9,18-trioxapentacyclo[12.5.0.0³,⁵.0⁸,¹².0¹⁷,¹⁹]Nonadecan-16-yl hexanoate belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. (-)-Milolide E is found in Braiareum stechei and Briareum stechei. Based on a literature review very few articles have been published on (1R,2R,3R,5R,7S,8R,11R,12S,13R,14S,15R,16R,17S,19R)-2,13-bis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9,18-trioxapentacyclo[12.5.0.0³,⁵.0⁸,¹².0¹⁷,¹⁹]Nonadecan-16-yl hexanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203432D          

 42 46  0  0  1  0            999 V2000
   -3.4633   -3.1354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4557   -2.3105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1663   -1.8914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8845   -2.2972    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8922   -3.1222    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1816   -3.5413    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4710   -3.9604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3833   -3.7851    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1703   -4.0327    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9525   -3.7705    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.4312   -3.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2250   -3.4278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4235   -2.2736    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9324   -1.6107    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1455   -1.3631    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -6.1572    0.3093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  4  3  1  1  0  0  0
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 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
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 41 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292203432D          

 42 46  0  0  1  0            999 V2000
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   -4.7307   -0.9359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2288   -0.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1572    0.3093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6316    0.6195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1378   -0.5381    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9200   -0.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4876    0.3830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4111   -0.9388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6569    0.3259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4339   -0.8499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2639   -2.0928    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -6.7885   -4.5790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1629   -4.6665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2505   -5.5714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7791   -6.3038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0558   -5.8233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7335   -4.0315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1530   -1.0683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6712   -1.9557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9308   -2.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8874   -3.2152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2366   -1.8758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5130   -2.3202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2264   -1.9027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9398   -2.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6815   -1.9710    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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  1  7  1  6  0  0  0
  5  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  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 14 24  1  6  0  0  0
 21 25  1  6  0  0  0
 15 26  1  1  0  0  0
 13 27  1  6  0  0  0
 10 28  1  6  0  0  0
  9 28  1  6  0  0  0
  8 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  5 33  1  1  0  0  0
  3 34  1  1  0  0  0
  2 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080737

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC(=O)O[C@H]1[C@@H]2O[C@@H]2[C@@]2(C)[C@H]([C@H]1C)[C@@H](OC(C)=O)[C@@]1(O)[C@@H](C)C(=O)O[C@H]1[C@@H](Cl)C(=C)[C@H]1O[C@H]1[C@@H]2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H41ClO11/c1-8-9-10-11-17(34)39-20-12(2)18-24(37-15(5)32)30(36)14(4)28(35)42-25(30)19(31)13(3)21-22(40-21)26(38-16(6)33)29(18,7)27-23(20)41-27/h12,14,18-27,36H,3,8-11H2,1-2,4-7H3/t12-,14+,18-,19+,20-,21-,22-,23+,24-,25+,26+,27+,29+,30+/m1/s1

> <INCHI_KEY>
CUHLXAPALODJHT-KWDRBULTSA-N

> <FORMULA>
C30H41ClO11

> <MOLECULAR_WEIGHT>
613.1

> <EXACT_MASS>
612.2337398

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
60.81126800712377

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,5R,7S,8R,11R,12S,13R,14S,15R,16R,17S,19R)-2,13-bis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9,18-trioxapentacyclo[12.5.0.0^{3,5}.0^{8,12}.0^{17,19}]nonadecan-16-yl hexanoate

> <ALOGPS_LOGP>
3.58

> <JCHEM_LOGP>
2.948471476666669

> <ALOGPS_LOGS>
-4.00

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.372845591244946

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9377626964176486

> <JCHEM_POLAR_SURFACE_AREA>
150.48999999999998

> <JCHEM_REFRACTIVITY>
143.2969

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.20e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,5R,7S,8R,11R,12S,13R,14S,15R,16R,17S,19R)-2,13-bis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9,18-trioxapentacyclo[12.5.0.0^{3,5}.0^{8,12}.0^{17,19}]nonadecan-16-yl hexanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -6.465  -5.853   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.451  -4.313   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.777  -3.531   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.118  -4.288   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.132  -5.828   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.806  -6.610   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -6.479  -7.393   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0     -10.049  -7.065   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -11.518  -7.528   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -12.978  -7.038   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -13.872  -5.784   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -15.353  -6.399   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -13.857  -4.244   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -12.941  -3.007   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -11.472  -2.544   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.011  -3.034   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -8.831  -1.747   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -9.761  -0.124   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0     -11.494   0.577   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -8.646   1.156   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -11.457  -1.004   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -12.917  -0.515   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -13.977   0.715   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0     -13.834  -1.752   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0     -10.560   0.608   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -10.143  -1.586   0.000  0.00  0.00           O+0
HETATM   27 Cl   UNK     0     -15.426  -3.907   0.000  0.00  0.00          Cl+0
HETATM   28  O   UNK     0     -12.672  -8.547   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -9.637  -8.711   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -9.801 -10.400   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -8.921 -11.767   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0     -11.304 -10.870   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -8.836  -7.526   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -7.752  -1.994   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -4.986  -3.651   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -3.604  -4.421   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -3.523  -6.002   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -2.308  -3.502   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -0.958  -4.331   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.423  -3.552   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.754  -4.421   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.139  -3.679   0.000  0.00  0.00           C+0
CONECT    1    2    6    7                                                  
CONECT    2    1    3   35                                                  
CONECT    3    2    4   34                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6    8   33                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    1                                                       
CONECT    8    5    9   29                                                  
CONECT    9    8   10   28                                                  
CONECT   10    9   11   28                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   27                                                  
CONECT   14   13   15   24                                                  
CONECT   15   14   16   21   26                                             
CONECT   16   15    4   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   15   22   25                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   14                                                       
CONECT   25   21                                                            
CONECT   26   15                                                            
CONECT   27   13                                                            
CONECT   28   10    9                                                       
CONECT   29    8   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33    5                                                            
CONECT   34    3                                                            
CONECT   35    2   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,3R,5R,7S,8R,11R,12S,13R,14S,15R,16R,17S,19R)-2,13-Bis(acetyloxy)-7-chloro-12-hydroxy-1,11,15-trimethyl-6-methylidene-10-oxo-4,9,18-trioxapentacyclo[12.5.0.0,.0,.0,]nonadecan-16-yl hexanoic acid	Generator

Chemical Formula

C₃₀H₄₁ClO₁₁

Average Mass

613.1000 Da

Monoisotopic Mass

612.23374 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CCCCCC(=O)O[C@H]1[C@@H]2O[C@@H]2[C@@]2(C)[C@H]([C@H]1C)[C@@H](OC(C)=O)[C@@]1(O)[C@@H](C)C(=O)O[C@H]1[C@@H](Cl)C(=C)[C@H]1O[C@H]1[C@@H]2OC(C)=O

InChI Identifier

InChI=1S/C30H41ClO11/c1-8-9-10-11-17(34)39-20-12(2)18-24(37-15(5)32)30(36)14(4)28(35)42-25(30)19(31)13(3)21-22(40-21)26(38-16(6)33)29(18,7)27-23(20)41-27/h12,14,18-27,36H,3,8-11H2,1-2,4-7H3/t12-,14+,18-,19+,20-,21-,22-,23+,24-,25+,26+,27+,29+,30+/m1/s1

InChI Key

CUHLXAPALODJHT-KWDRBULTSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Braiareum stechei	-	KNApSAcK
Briareum stechei	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Oxepane
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
Alkyl halide
Alkyl chloride
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.58	ALOGPS
logP	2.95	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	12.37	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	150.49 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	143.3 m³·mol⁻¹	ChemAxon
Polarizability	60.81 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163013775

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Milolide E (NP0080737)

MOL for NP0080737 ((-)-Milolide E)

3D MOL for NP0080737 ((-)-Milolide E)

3D SDF for NP0080737 ((-)-Milolide E)

3D-SDF for NP0080737 ((-)-Milolide E)

PDB for NP0080737 ((-)-Milolide E)

3D PDB for NP0080737 ((-)-Milolide E)

SMILES for NP0080737 ((-)-Milolide E)

INCHI for NP0080737 ((-)-Milolide E)

Structure for NP0080737 ((-)-Milolide E)

3D Structure for NP0080737 ((-)-Milolide E)