NP-MRD: Showing NP-Card for (2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one (NP0219646)

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Record Information

Version

2.0

Created at

2022-09-05 20:42:44 UTC

Updated at

2022-09-05 20:42:44 UTC

NP-MRD ID

NP0219646

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

Description

(2Z,4E,6E,8E,10E,12E,14E,16E,18E)-3-hydroxy-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one is found in Agelas schmidtii. Based on a literature review very few articles have been published on (2Z,4E,6E,8E,10E,12E,14E,16E,18E)-3-hydroxy-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052222422D          

 43 44  0  0  1  0            999 V2000
    3.4856  -17.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0376  -17.0636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.1614  -18.9759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.9413  -19.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7483  -19.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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 43 95  1  0
M  END


  Mrv1652309052222422D          

 43 44  0  0  1  0            999 V2000
    3.4856  -17.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0376  -17.0636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8446  -17.2351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0995  -18.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9065  -18.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1614  -18.9759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6094  -19.5890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9684  -19.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5204  -18.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3274  -18.7059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8794  -18.0928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6864  -18.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9413  -19.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7483  -19.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3893  -19.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6442  -20.4466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5823  -19.4905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0303  -20.1036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7827  -16.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9757  -16.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7207  -15.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9138  -15.1513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6588  -14.3667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2109  -13.7536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8519  -14.1952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5969  -13.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2100  -13.2390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4650  -12.4544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0870  -11.8413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2720  -12.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8240  -12.8960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269  -11.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3339  -11.3267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5888  -10.5421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8859  -11.9398    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4379  -11.3267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2185  -12.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4734  -13.2093    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9885  -13.8768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2984  -13.2093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5533  -12.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3621  -12.5878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1118  -11.8174    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
  3  4  2  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
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 35 33  1  1  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219646

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\C=C(/C)\C=C\C1=CC=C(C)C(C)=C1C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C(/O)=C/C(=O)[C@@]1(C)C[C@H](O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H52O3/c1-28(17-13-18-30(3)21-23-35-24-22-31(4)33(6)34(35)7)15-11-12-16-29(2)19-14-20-32(5)37(42)25-38(43)40(10)27-36(41)26-39(40,8)9/h11-25,36,41-42H,26-27H2,1-10H3/b12-11+,17-13+,19-14+,23-21+,28-15+,29-16+,30-18+,32-20+,37-25-/t36-,40-/m1/s1

> <INCHI_KEY>
JCNLLLQYNIILBJ-VCHZWVHSSA-N

> <FORMULA>
C40H52O3

> <MOLECULAR_WEIGHT>
580.853

> <EXACT_MASS>
580.391645534

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
73.05079429304902

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z,4E,6E,8E,10E,12E,14E,16E,18E)-3-hydroxy-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

> <JCHEM_LOGP>
9.951595069

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.224102475734792

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.877533825613744

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7081493216005583

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
195.09910000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,4E,6E,8E,10E,12E,14E,16E,18E)-3-hydroxy-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       6.506 -32.996   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.537 -31.852   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.043 -32.172   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.519 -33.637   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.025 -33.957   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.501 -35.422   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.471 -36.566   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.008 -35.742   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.038 -34.597   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.544 -34.918   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.575 -33.773   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.081 -34.093   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.557 -35.558   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.064 -35.878   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.527 -36.702   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      18.003 -38.167   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.020 -36.382   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.990 -37.527   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.061 -30.387   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.555 -30.067   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.079 -28.603   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.572 -28.282   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.096 -26.818   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.127 -25.673   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.590 -26.498   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.114 -25.033   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.392 -24.713   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.868 -23.248   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.162 -22.104   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.374 -22.928   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -3.405 -24.072   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -2.850 -21.463   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.357 -21.143   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -4.832 -19.679   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -5.387 -22.288   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -6.417 -21.143   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -4.141 -23.193   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -4.617 -24.657   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -3.712 -25.903   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -6.157 -24.657   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -6.633 -23.193   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -8.143 -23.497   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -7.675 -22.059   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   10   18                                                  
CONECT   18   17                                                            
CONECT   19    2   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37   41                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   35   42   43                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   88    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₅₂O₃

Average Mass

580.8530 Da

Monoisotopic Mass

580.39165 Da

IUPAC Name

(2Z,4E,6E,8E,10E,12E,14E,16E,18E)-3-hydroxy-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

Traditional Name

(2Z,4E,6E,8E,10E,12E,14E,16E,18E)-3-hydroxy-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

CAS Registry Number

Not Available

SMILES

C\C(\C=C\C=C(/C)\C=C\C1=CC=C(C)C(C)=C1C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C(/O)=C/C(=O)[C@@]1(C)C[C@H](O)CC1(C)C

InChI Identifier

InChI=1S/C40H52O3/c1-28(17-13-18-30(3)21-23-35-24-22-31(4)33(6)34(35)7)15-11-12-16-29(2)19-14-20-32(5)37(42)25-38(43)40(10)27-36(41)26-39(40,8)9/h11-25,36,41-42H,26-27H2,1-10H3/b12-11+,17-13+,19-14+,23-21+,28-15+,29-16+,30-18+,32-20+,37-25-/t36-,40-/m1/s1

InChI Key

JCNLLLQYNIILBJ-VCHZWVHSSA-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
Agelas schmidti	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Styrene
Monocyclic benzene moiety
Cyclopentanol
Benzenoid
Acryloyl-group
Cyclic alcohol
Enone
Vinylogous acid
Alpha,beta-unsaturated ketone
Ketone
Secondary alcohol
Enol
Organic oxide
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	9.95	ChemAxon
pKa (Strongest Acidic)	9.88	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	195.1 m³·mol⁻¹	ChemAxon
Polarizability	73.05 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

163185391

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one (NP0219646)

MOL for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D MOL for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D SDF for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D-SDF for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

PDB for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D PDB for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

SMILES for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

INCHI for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

Structure for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D Structure for NP0219646 ((2z,4e,6e,8e,10e,12e,14e,16e,18e)-3-hydroxy-1-[(1s,4r)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)