NP-MRD: Showing NP-Card for 3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate (NP0186870)

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Record Information

Version

2.0

Created at

2022-09-04 02:51:24 UTC

Updated at

2022-09-04 02:51:24 UTC

NP-MRD ID

NP0186870

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate

Description

Rhinacanthin I belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone). 3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate is found in Rhinacanthus nasutus. Based on a literature review very few articles have been published on Rhinacanthin I.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042204512D          

 31 32  0  0  0  0            999 V2000
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5572   -7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7322   -5.8855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
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 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
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 25 27  1  0  0  0  0
 16 27  1  0  0  0  0
 27 28  2  0  0  0  0
  2 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END

     RDKit          3D

 61 62  0  0  0  0  0  0  0  0999 V2000
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    6.7476    0.2520   -0.6314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5305    0.1370    0.1872 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2959    0.4148   -0.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1948    1.2990    0.2845 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6567    0.4552    0.4035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5289   -0.5012    0.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3241   -1.7078    0.9539 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8301   -0.3980   -0.3692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7025   -1.4654   -0.3789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9276   -1.4136   -1.0351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2713   -0.2661   -1.6886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4220    0.8060   -1.6928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2038    0.7468   -1.0371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2836    1.8642   -1.0233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5915    2.9172   -1.6192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0446    1.7139   -0.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2199    2.6873   -0.2951 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9131   -0.6368   -1.7993 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8990   -2.0953   -1.3322 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0619   -0.3504   -2.5056 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5537    1.7956    0.5409 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4481   -0.8771    0.6255 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4823    0.8688    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3874    1.3606   -1.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2810   -0.3956   -1.4384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8004   -0.6238    0.6062 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6491    3.3120   -0.1113 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5959    2.5059   -1.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958    3.0784    0.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6164    0.3210    3.3824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8187   -2.0775    3.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1594   -0.7438    4.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6173   -0.3963    3.1122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -1.6288   -0.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9189   -2.7369    1.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4580   -1.9777    0.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6400    0.7511    0.1623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2908    1.4655    1.6778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0329   -2.0299    1.6221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4611   -2.3843    0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6056   -2.2367   -1.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2306   -0.2004   -2.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6804    1.7317   -2.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0589   -0.5321   -2.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8569   -2.4403   -1.3004 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3161   -2.1142   -0.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5326   -2.6522   -2.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9070    0.2884   -3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
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 29 31  1  0
 29  2  1  0
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 23 56  1  0
M  END


  Mrv1652309042204512D          

 31 32  0  0  0  0            999 V2000
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5572   -7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7322   -5.8855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
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 17 18  1  0  0  0  0
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 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
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 29 30  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0186870

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(O)C(=C)CC\C=C(/C)C(=O)OCC(C)(C)CC1=C(O)C2=CC=CC=C2C(=O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H30O6/c1-15(17(3)26)9-8-10-16(2)24(30)31-14-25(4,5)13-20-21(27)18-11-6-7-12-19(18)22(28)23(20)29/h6-7,10-12,17,26-27H,1,8-9,13-14H2,2-5H3/b16-10+

> <INCHI_KEY>
WSQAPTBHFZVTMV-MHWRWJLKSA-N

> <FORMULA>
C25H30O6

> <MOLECULAR_WEIGHT>
426.509

> <EXACT_MASS>
426.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
47.147937748659785

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(1-hydroxy-3,4-dioxo-3,4-dihydronaphthalen-2-yl)-2,2-dimethylpropyl (2E)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate

> <JCHEM_LOGP>
4.665555523666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.559847583369685

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.618442942187311

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6791196983975136

> <JCHEM_POLAR_SURFACE_AREA>
100.9

> <JCHEM_REFRACTIVITY>
120.56719999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2E)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667 -10.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001 -13.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.668 -13.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.002 -10.780   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.336 -13.090   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -9.336 -14.630   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0     -10.669 -12.320   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0     -12.003 -13.090   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -14.107 -13.654   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -12.567 -10.986   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -16.004 -13.860   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0     -14.670 -14.630   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0     -17.338 -14.630   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -17.338 -16.170   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -18.672 -16.940   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -20.005 -16.170   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -20.005 -11.550   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0     -17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -17.338 -10.010   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.334 -13.090   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -1.334 -14.630   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   16   28                                                  
CONECT   28   27                                                            
CONECT   29    2   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₀O₆

Average Mass

426.5090 Da

Monoisotopic Mass

426.20424 Da

IUPAC Name

3-(1-hydroxy-3,4-dioxo-3,4-dihydronaphthalen-2-yl)-2,2-dimethylpropyl (2E)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate

Traditional Name

3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2E)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate

CAS Registry Number

Not Available

SMILES

CC(O)C(=C)CC\C=C(/C)C(=O)OCC(C)(C)CC1=C(O)C2=CC=CC=C2C(=O)C1=O

InChI Identifier

InChI=1S/C25H30O6/c1-15(17(3)26)9-8-10-16(2)24(30)31-14-25(4,5)13-20-21(27)18-11-6-7-12-19(18)22(28)23(20)29/h6-7,10-12,17,26-27H,1,8-9,13-14H2,2-5H3/b16-10+

InChI Key

WSQAPTBHFZVTMV-MHWRWJLKSA-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
Rhinacanthus nasutus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone).

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Naphthoquinone
1-naphthol
Aromatic monoterpenoid
Bicyclic monoterpenoid
Monoterpenoid
Fatty alcohol
Aryl ketone
Quinone
Fatty acid ester
Fatty acyl
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Ketone
Carboxylic acid ester
Cyclic ketone
Secondary alcohol
Monocarboxylic acid or derivatives
Enol
Carboxylic acid derivative
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
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	4.67	ChemAxon
pKa (Strongest Acidic)	5.62	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	100.9 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	120.57 m³·mol⁻¹	ChemAxon
Polarizability	47.15 Å³	ChemAxon
Number of Rings	2	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

C00041099

Chemspider ID

8940227

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10764908

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate (NP0186870)

MOL for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

3D MOL for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

3D SDF for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

3D-SDF for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

PDB for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

3D PDB for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

SMILES for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

INCHI for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

Structure for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)

3D Structure for NP0186870 (3-(1-hydroxy-3,4-dioxonaphthalen-2-yl)-2,2-dimethylpropyl (2e)-7-hydroxy-2-methyl-6-methylideneoct-2-enoate)