NP-MRD: Showing NP-Card for acetylcordiaquinol I (NP0033452)

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Record Information

Version

2.0

Created at

2021-06-19 23:59:32 UTC

Updated at

2021-06-30 00:03:14 UTC

NP-MRD ID

NP0033452

Secondary Accession Numbers

None

Natural Product Identification

Common Name

acetylcordiaquinol I

Provided By

JEOL Database JEOL Logo

Description

acetylcordiaquinol I is found in Cordia fragrantissima. acetylcordiaquinol I was first documented in 2008 (Mori, K., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202101593D          

 46 48  0  0  0  0            999 V2000
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   -0.0256   -1.0864    3.7105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7211   -0.1219    3.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3361   -1.5014    2.4334 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2562   -0.7352    1.4220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5048   -1.1472    0.9520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0995   -0.4539   -0.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1611    4.5030   -2.7898 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
M  END

     RDKit          3D

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   -0.0256   -1.0864    3.7105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7211   -0.1219    3.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3361   -1.5014    2.4334 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652306202101593D          

 46 48  0  0  0  0            999 V2000
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   -0.0256   -1.0864    3.7105 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0033452

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C([H])C(OC(=O)C([H])([H])[H])=C2C(=C1OC(=O)C([H])([H])[H])C(=O)C1=C(C(=O)C([H])([H])C([H])([H])[C@]1(C([H])([H])[H])C2([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O6/c1-10-14(23)7-8-20(4)9-13-15(25-11(2)21)5-6-16(26-12(3)22)17(13)19(24)18(10)20/h5-6H,7-9H2,1-4H3/t20-/m1/s1

> <INCHI_KEY>
ROMNSZXJDGCIMH-HXUWFJFHSA-N

> <FORMULA>
C20H20O6

> <MOLECULAR_WEIGHT>
356.374

> <EXACT_MASS>
356.125988364

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
36.73114612229003

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(10aR)-4-(acetyloxy)-8,10a-dimethyl-7,9-dioxo-5,6,7,9,10,10a-hexahydroanthracen-1-yl acetate

> <ALOGPS_LOGP>
2.79

> <JCHEM_LOGP>
2.4775761500000004

> <ALOGPS_LOGS>
-4.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.595623092363358

> <JCHEM_PKA_STRONGEST_BASIC>
-6.447200847470098

> <JCHEM_POLAR_SURFACE_AREA>
86.74000000000001

> <JCHEM_REFRACTIVITY>
93.44059999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.13e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(10aR)-4-(acetyloxy)-8,10a-dimethyl-7,9-dioxo-6,10-dihydro-5H-anthracen-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
    0.6046   -2.0052    4.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0256   -1.0864    3.7105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7211   -0.1219    3.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3361   -1.5014    2.4334 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2562   -0.7352    1.4220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5048   -1.1472    0.9520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0995   -0.4539   -0.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4276    0.6274   -0.6707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0895    1.2676   -1.7239 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5613    0.9314   -2.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2427    1.7480   -4.0223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6988    0.0900   -3.1878 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1739    1.0591   -0.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4314    0.3592    0.8660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8108    0.7193    1.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2216    2.1871    1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4703    3.1320    2.0547 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7433    2.2876    1.3541 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3443    3.5643    0.7984 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0623    3.6731   -0.6797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8743    4.2092   -1.4320 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7404    3.1862   -1.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    3.4706   -2.6547 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8985    2.5586   -0.3457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4988    2.2490   -0.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938    2.9995   -1.5567 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6929   -1.9253    4.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2826   -3.0332    4.5296 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2839   -1.7176    5.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0076   -2.0028    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0713   -0.7607   -0.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1213    2.8124   -3.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3016    1.4826   -4.0692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7832    1.5394   -4.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9021    0.5207    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5049    0.0354    0.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3824    3.0357    1.9678 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7308    2.9145    3.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7139    4.1831    1.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9528    2.2177    2.4288 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2609    1.4389    0.8850 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4303    3.5407    0.9433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9560    4.4566    1.2986 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124    3.3275   -3.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7619    2.7956   -3.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1611    4.5030   -2.7898 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 18  1  0
 24 22  2  0
 22 20  1  0
 20 19  1  0
 19 18  1  0
  6  7  2  0
  5  4  1  0
 14 15  1  0
  8  9  1  0
 13 25  1  0
 25 26  2  0
 25 24  1  0
 16 17  1  0
 16 15  1  0
 22 23  1  0
 16 24  1  0
 20 21  2  0
 14  5  2  0
  4  2  1  0
  5  6  1  0
  9 10  1  0
 14 13  1  0
 10 12  2  0
 10 11  1  0
  7  8  1  0
  2  1  1  0
  8 13  2  0
  2  3  2  0
  6 30  1  0
  7 31  1  0
 15 35  1  0
 15 36  1  0
 19 42  1  0
 19 43  1  0
 18 40  1  0
 18 41  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
 23 44  1  0
 23 45  1  0
 23 46  1  0
 11 32  1  0
 11 33  1  0
 11 34  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       0.605  -2.005   4.714  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.026  -1.086   3.711  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.721  -0.122   3.998  0.00  0.00           O+0
HETATM    4  O   UNK     0       0.336  -1.501   2.433  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.256  -0.735   1.422  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.505  -1.147   0.952  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.099  -0.454  -0.094  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.428   0.627  -0.671  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.090   1.268  -1.724  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.561   0.931  -2.966  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.243   1.748  -4.022  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.699   0.090  -3.188  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.174   1.059  -0.193  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.431   0.359   0.866  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.811   0.719   1.351  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.222   2.187   1.089  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.470   3.132   2.055  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.743   2.288   1.354  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.344   3.564   0.798  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.062   3.673  -0.680  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.874   4.209  -1.432  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.740   3.186  -1.197  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.498   3.471  -2.655  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.899   2.559  -0.346  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.499   2.249  -0.789  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.094   2.999  -1.557  0.00  0.00           O+0
HETATM   27  H   UNK     0       1.693  -1.925   4.656  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.283  -3.033   4.530  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.284  -1.718   5.719  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.008  -2.003   1.394  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.071  -0.761  -0.470  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.121   2.812  -3.806  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.302   1.483  -4.069  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.783   1.539  -4.993  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.902   0.521   2.426  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.505   0.035   0.842  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.382   3.036   1.968  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.731   2.914   3.097  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.714   4.183   1.865  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.953   2.218   2.429  0.00  0.00           H+0
HETATM   41  H   UNK     0       4.261   1.439   0.885  0.00  0.00           H+0
HETATM   42  H   UNK     0       5.430   3.541   0.943  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.956   4.457   1.299  0.00  0.00           H+0
HETATM   44  H   UNK     0       3.412   3.328  -3.241  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.762   2.796  -3.100  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.161   4.503  -2.790  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    5    2                                                       
CONECT    5    4   14    6                                                  
CONECT    6    7    5   30                                                  
CONECT    7    6    8   31                                                  
CONECT    8    9    7   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   12   11                                                  
CONECT   11   10   32   33   34                                             
CONECT   12   10                                                            
CONECT   13   25   14    8                                                  
CONECT   14   15    5   13                                                  
CONECT   15   14   16   35   36                                             
CONECT   16   18   17   15   24                                             
CONECT   17   16   37   38   39                                             
CONECT   18   16   19   40   41                                             
CONECT   19   20   18   42   43                                             
CONECT   20   22   19   21                                                  
CONECT   21   20                                                            
CONECT   22   24   20   23                                                  
CONECT   23   22   44   45   46                                             
CONECT   24   22   25   16                                                  
CONECT   25   13   26   24                                                  
CONECT   26   25                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    6                                                            
CONECT   31    7                                                            
CONECT   32   11                                                            
CONECT   33   11                                                            
CONECT   34   11                                                            
CONECT   35   15                                                            
CONECT   36   15                                                            
CONECT   37   17                                                            
CONECT   38   17                                                            
CONECT   39   17                                                            
CONECT   40   18                                                            
CONECT   41   18                                                            
CONECT   42   19                                                            
CONECT   43   19                                                            
CONECT   44   23                                                            
CONECT   45   23                                                            
CONECT   46   23                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   96    0
END

RDKit          3D

46 48  0  0  0  0  0  0  0  0999 V2000
    0.6046   -2.0052    4.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0256   -1.0864    3.7105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7211   -0.1219    3.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3361   -1.5014    2.4334 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2562   -0.7352    1.4220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5048   -1.1472    0.9520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0995   -0.4539   -0.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4276    0.6274   -0.6707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0895    1.2676   -1.7239 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5613    0.9314   -2.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2427    1.7480   -4.0223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6988    0.0900   -3.1878 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1739    1.0591   -0.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4314    0.3592    0.8660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8108    0.7193    1.3506 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2216    2.1871    1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4703    3.1320    2.0547 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7433    2.2876    1.3541 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3443    3.5643    0.7984 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0623    3.6731   -0.6797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8743    4.2092   -1.4320 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7404    3.1862   -1.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    3.4706   -2.6547 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8985    2.5586   -0.3457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4988    2.2490   -0.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938    2.9995   -1.5567 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6929   -1.9253    4.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2826   -3.0332    4.5296 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2839   -1.7176    5.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0076   -2.0028    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0713   -0.7607   -0.4702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1213    2.8124   -3.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3016    1.4826   -4.0692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7832    1.5394   -4.9926 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9021    0.5207    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5049    0.0354    0.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3824    3.0357    1.9678 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7308    2.9145    3.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7139    4.1831    1.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9528    2.2177    2.4288 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2609    1.4389    0.8850 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4303    3.5407    0.9433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9560    4.4566    1.2986 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124    3.3275   -3.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7619    2.7956   -3.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1611    4.5030   -2.7898 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 18  1  0
 24 22  2  0
 22 20  1  0
 20 19  1  0
 19 18  1  0
  6  7  2  0
  5  4  1  0
 14 15  1  0
  8  9  1  0
 13 25  1  0
 25 26  2  0
 25 24  1  0
 16 17  1  0
 16 15  1  0
 22 23  1  0
 16 24  1  0
 20 21  2  0
 14  5  2  0
  4  2  1  0
  5  6  1  0
  9 10  1  0
 14 13  1  0
 10 12  2  0
 10 11  1  0
  7  8  1  0
  2  1  1  0
  8 13  2  0
  2  3  2  0
  6 30  1  0
  7 31  1  0
 15 35  1  0
 15 36  1  0
 19 42  1  0
 19 43  1  0
 18 40  1  0
 18 41  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
 23 44  1  0
 23 45  1  0
 23 46  1  0
 11 32  1  0
 11 33  1  0
 11 34  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₀O₆

Average Mass

356.3740 Da

Monoisotopic Mass

356.12599 Da

IUPAC Name

(10aR)-4-(acetyloxy)-8,10a-dimethyl-7,9-dioxo-5,6,7,9,10,10a-hexahydroanthracen-1-yl acetate

Traditional Name

(10aR)-4-(acetyloxy)-8,10a-dimethyl-7,9-dioxo-6,10-dihydro-5H-anthracen-1-yl acetate

CAS Registry Number

Not Available

SMILES

[H]C1=C([H])C(OC(=O)C([H])([H])[H])=C2C(=C1OC(=O)C([H])([H])[H])C(=O)C1=C(C(=O)C([H])([H])C([H])([H])[C@]1(C([H])([H])[H])C2([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H20O6/c1-10-14(23)7-8-20(4)9-13-15(25-11(2)21)5-6-16(26-12(3)22)17(13)19(24)18(10)20/h5-6H,7-9H2,1-4H3/t20-/m1/s1

InChI Key

ROMNSZXJDGCIMH-HXUWFJFHSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cordia fragrantissima	JEOL database	Mori, K., et al, J. Nat. Prod. 71, 18 (2008)

Chemical Taxonomy

Classification

Not classified

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	2.79	ALOGPS
logP	2.48	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	19.6	ChemAxon
pKa (Strongest Basic)	-6.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	86.74 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	93.44 m³·mol⁻¹	ChemAxon
Polarizability	36.73 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

Not Available

References

General References

Mori, K., et al. (2008). Mori, K., et al, J. Nat. Prod. 71, 18 (2008). J. Nat. Prod..

Showing NP-Card for acetylcordiaquinol I (NP0033452)

MOL for NP0033452 (acetylcordiaquinol I)

3D MOL for NP0033452 (acetylcordiaquinol I)

3D SDF for NP0033452 (acetylcordiaquinol I)

3D-SDF for NP0033452 (acetylcordiaquinol I)

PDB for NP0033452 (acetylcordiaquinol I)

3D PDB for NP0033452 (acetylcordiaquinol I)

SMILES for NP0033452 (acetylcordiaquinol I)

INCHI for NP0033452 (acetylcordiaquinol I)

Structure for NP0033452 (acetylcordiaquinol I)

3D Structure for NP0033452 (acetylcordiaquinol I)