NP-MRD: Showing NP-Card for desacetylplectranthone (NP0029349)

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Record Information

Version

2.0

Created at

2021-06-19 21:00:05 UTC

Updated at

2021-06-29 23:56:39 UTC

NP-MRD ID

NP0029349

Secondary Accession Numbers

None

Natural Product Identification

Common Name

desacetylplectranthone

Provided By

JEOL Database JEOL Logo

Description

desacetylplectranthone is found in Plectranthus cylindraceus. desacetylplectranthone was first documented in 2000 (PMID: 11141110). Based on a literature review very few articles have been published on desacetylplectranthone.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123003D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306192123003D          

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 13 39  1  0  0  0  0
  7 27  1  6  0  0  0
  8 28  1  0  0  0  0
  8 29  1  0  0  0  0
  8 30  1  0  0  0  0
  9 31  1  0  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
 14 40  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0029349

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]12C([H])([H])C(=O)C([H])=C(C([H])([H])[H])[C@@]1([H])[C@]([H])(OC(=O)C([H])([H])[H])[C@@]([H])(C([H])([H])C2([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O4/c1-10(2)14-5-6-17(9-18)8-13(20)7-11(3)15(17)16(14)21-12(4)19/h7,10,14-16,18H,5-6,8-9H2,1-4H3/t14-,15-,16+,17-/m0/s1

> <INCHI_KEY>
OAASJLOTHOKQQN-NXOAAHMSSA-N

> <FORMULA>
C17H26O4

> <MOLECULAR_WEIGHT>
294.391

> <EXACT_MASS>
294.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.33759273175623

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,4aR,8aR)-4a-(hydroxymethyl)-8-methyl-6-oxo-2-(propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl acetate

> <ALOGPS_LOGP>
1.67

> <JCHEM_LOGP>
1.9770258103333325

> <ALOGPS_LOGS>
-3.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.573360873717277

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.062331249452345

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7680229867562822

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
80.7347

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4aR,8aR)-4a-(hydroxymethyl)-2-isopropyl-8-methyl-6-oxo-1,2,3,4,5,8a-hexahydronaphthalen-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
    0.3138   -2.9671   -2.8994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2852   -3.0143   -1.5277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2330   -3.9824   -0.7833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8979   -1.8293   -1.2500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4870   -1.7132    0.0640 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6619   -0.7009   -0.0078 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7243   -1.0866   -1.0896 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9168   -0.1198   -1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2624   -2.5106   -0.8953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1281    0.7247   -0.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0777    1.1308    0.7916 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1164    0.1471    0.8952 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9866    0.2927   -0.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0488   -0.6518   -0.3883 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0178    0.5663    2.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3341    0.3985    3.4128 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5285    1.1621    4.3550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5432   -0.7751    3.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8579   -1.5805    2.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6169   -2.8522    2.8500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3998   -1.3209    1.1180 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4745   -2.8243   -3.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8223   -3.9132   -3.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0477   -2.1593   -2.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9063   -2.6892    0.3250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1667   -0.7073    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2573   -1.0407   -2.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3674   -0.0346   -0.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6924   -0.4634   -1.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6214    0.8793   -1.4344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0770   -2.7209   -1.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4894   -3.2619   -1.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6467   -2.6530    0.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7230    0.8186   -1.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9451    1.4510   -0.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5844    1.2274    1.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7130    2.1370    0.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4304    1.2950   -0.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4177    0.1639   -1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6296   -0.4294   -1.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9392   -0.0276    2.1169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3054    1.6204    1.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8616   -0.9638    4.6136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6364   -2.7938    2.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1068   -3.7095    2.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6943   -3.0537    3.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4541   -1.9970    0.9734 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 21  1  0
 16 17  2  0
 19 20  1  0
 16 18  1  0
 12 13  1  6
 16 15  1  0
 21 47  1  6
 18 19  2  0
  5  4  1  0
 19 21  1  0
  6  7  1  0
 12 15  1  0
  7  8  1  0
 12 11  1  0
  7  9  1  0
 21  5  1  0
 13 14  1  0
  5  6  1  0
  4  2  1  0
  6 10  1  0
  2  1  1  0
 10 11  1  0
  2  3  2  0
 18 43  1  0
 15 41  1  0
 15 42  1  0
  5 25  1  1
  6 26  1  1
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 13 38  1  0
 13 39  1  0
  7 27  1  6
  8 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
  9 32  1  0
  9 33  1  0
 14 40  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       0.314  -2.967  -2.899  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.285  -3.014  -1.528  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.233  -3.982  -0.783  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.898  -1.829  -1.250  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.487  -1.713   0.064  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.662  -0.701  -0.008  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.724  -1.087  -1.090  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.917  -0.120  -1.101  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.262  -2.511  -0.895  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.128   0.725  -0.240  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.078   1.131   0.792  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.116   0.147   0.895  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.987   0.293  -0.384  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.049  -0.652  -0.388  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.018   0.566   2.082  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.334   0.399   3.413  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.529   1.162   4.355  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.543  -0.775   3.594  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.858  -1.581   2.565  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.617  -2.852   2.850  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.400  -1.321   1.118  0.00  0.00           C+0
HETATM   22  H   UNK     0      -0.475  -2.824  -3.643  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.822  -3.913  -3.106  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.048  -2.159  -2.956  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.906  -2.689   0.325  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.167  -0.707   0.968  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.257  -1.041  -2.082  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.367  -0.035  -0.107  0.00  0.00           H+0
HETATM   29  H   UNK     0      -5.692  -0.463  -1.795  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.621   0.879  -1.434  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.077  -2.721  -1.597  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.489  -3.262  -1.081  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.647  -2.653   0.120  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.723   0.819  -1.254  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.945   1.451  -0.168  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.584   1.227   1.760  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.713   2.137   0.547  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.430   1.295  -0.426  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.418   0.164  -1.306  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.630  -0.429  -1.137  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.939  -0.028   2.117  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.305   1.620   1.982  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.862  -0.964   4.614  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.636  -2.794   2.457  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.107  -3.709   2.398  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.694  -3.054   3.924  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.454  -1.997   0.973  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    5    2                                                       
CONECT    5    4   21    6   25                                             
CONECT    6    7    5   10   26                                             
CONECT    7    6    8    9   27                                             
CONECT    8    7   28   29   30                                             
CONECT    9    7   31   32   33                                             
CONECT   10    6   11   34   35                                             
CONECT   11   12   10   36   37                                             
CONECT   12   21   13   15   11                                             
CONECT   13   12   14   38   39                                             
CONECT   14   13   40                                                       
CONECT   15   16   12   41   42                                             
CONECT   16   17   18   15                                                  
CONECT   17   16                                                            
CONECT   18   16   19   43                                                  
CONECT   19   20   18   21                                                  
CONECT   20   19   44   45   46                                             
CONECT   21   12   47   19    5                                             
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    5                                                            
CONECT   26    6                                                            
CONECT   27    7                                                            
CONECT   28    8                                                            
CONECT   29    8                                                            
CONECT   30    8                                                            
CONECT   31    9                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34   10                                                            
CONECT   35   10                                                            
CONECT   36   11                                                            
CONECT   37   11                                                            
CONECT   38   13                                                            
CONECT   39   13                                                            
CONECT   40   14                                                            
CONECT   41   15                                                            
CONECT   42   15                                                            
CONECT   43   18                                                            
CONECT   44   20                                                            
CONECT   45   20                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   96    0
END

RDKit          3D

47 48  0  0  0  0  0  0  0  0999 V2000
    0.3138   -2.9671   -2.8994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2852   -3.0143   -1.5277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2330   -3.9824   -0.7833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8979   -1.8293   -1.2500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4870   -1.7132    0.0640 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6619   -0.7009   -0.0078 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7243   -1.0866   -1.0896 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9168   -0.1198   -1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2624   -2.5106   -0.8953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1281    0.7247   -0.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0777    1.1308    0.7916 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1164    0.1471    0.8952 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9866    0.2927   -0.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0488   -0.6518   -0.3883 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0178    0.5663    2.0821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3341    0.3985    3.4128 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5285    1.1621    4.3550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5432   -0.7751    3.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8579   -1.5805    2.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6169   -2.8522    2.8500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3998   -1.3209    1.1180 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4745   -2.8243   -3.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8223   -3.9132   -3.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0477   -2.1593   -2.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9063   -2.6892    0.3250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1667   -0.7073    0.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2573   -1.0407   -2.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3674   -0.0346   -0.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6924   -0.4634   -1.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6214    0.8793   -1.4344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0770   -2.7209   -1.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4894   -3.2619   -1.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6467   -2.6530    0.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7230    0.8186   -1.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9451    1.4510   -0.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5844    1.2274    1.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7130    2.1370    0.5467 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4304    1.2950   -0.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4177    0.1639   -1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6296   -0.4294   -1.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9392   -0.0276    2.1169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3054    1.6204    1.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8616   -0.9638    4.6136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6364   -2.7938    2.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1068   -3.7095    2.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6943   -3.0537    3.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4541   -1.9970    0.9734 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 21  1  0
 16 17  2  0
 19 20  1  0
 16 18  1  0
 12 13  1  6
 16 15  1  0
 21 47  1  6
 18 19  2  0
  5  4  1  0
 19 21  1  0
  6  7  1  0
 12 15  1  0
  7  8  1  0
 12 11  1  0
  7  9  1  0
 21  5  1  0
 13 14  1  0
  5  6  1  0
  4  2  1  0
  6 10  1  0
  2  1  1  0
 10 11  1  0
  2  3  2  0
 18 43  1  0
 15 41  1  0
 15 42  1  0
  5 25  1  1
  6 26  1  1
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 13 38  1  0
 13 39  1  0
  7 27  1  6
  8 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
  9 32  1  0
  9 33  1  0
 14 40  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₆O₄

Average Mass

294.3910 Da

Monoisotopic Mass

294.18311 Da

IUPAC Name

(1R,2S,4aR,8aR)-4a-(hydroxymethyl)-8-methyl-6-oxo-2-(propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl acetate

Traditional Name

(1R,2S,4aR,8aR)-4a-(hydroxymethyl)-2-isopropyl-8-methyl-6-oxo-1,2,3,4,5,8a-hexahydronaphthalen-1-yl acetate

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]12C([H])([H])C(=O)C([H])=C(C([H])([H])[H])[C@@]1([H])[C@]([H])(OC(=O)C([H])([H])[H])[C@@]([H])(C([H])([H])C2([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C17H26O4/c1-10(2)14-5-6-17(9-18)8-13(20)7-11(3)15(17)16(14)21-12(4)19/h7,10,14-16,18H,5-6,8-9H2,1-4H3/t14-,15-,16+,17-/m0/s1

InChI Key

OAASJLOTHOKQQN-NXOAAHMSSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, 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
Plectranthus cylindraceus	JEOL database	Orabi, K. Y., et al, J. Nat. Prod. 63, 1665 (2000)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids

Alternative Parents

Substituents

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid
Cyclohexenone
Cyclic ketone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	1.67	ALOGPS
logP	1.98	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	15.06	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	80.73 m³·mol⁻¹	ChemAxon
Polarizability	32.34 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

Not Available

Chemspider ID

8955462

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10780149

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Orabi KY, Mossa JS, Muhammed I, Alloush MH, Galal AM, El-Feraly FS, McPhail AT: New eudesmane sesquiterpenes from Plectranthus cylindraceus. J Nat Prod. 2000 Dec;63(12):1665-8. doi: 10.1021/np000124p. [PubMed:11141110 ]
Orabi, K. Y., et al. (2000). Orabi, K. Y., et al, J. Nat. Prod. 63, 1665 (2000). J. Nat. Prod..

Showing NP-Card for desacetylplectranthone (NP0029349)

MOL for NP0029349 (desacetylplectranthone)

3D MOL for NP0029349 (desacetylplectranthone)

3D SDF for NP0029349 (desacetylplectranthone)

3D-SDF for NP0029349 (desacetylplectranthone)

PDB for NP0029349 (desacetylplectranthone)

3D PDB for NP0029349 (desacetylplectranthone)

SMILES for NP0029349 (desacetylplectranthone)

INCHI for NP0029349 (desacetylplectranthone)

Structure for NP0029349 (desacetylplectranthone)

3D Structure for NP0029349 (desacetylplectranthone)