NP-MRD: Showing NP-Card for 2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate (NP0281971)

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Record Information

Version

2.0

Created at

2022-09-09 08:37:17 UTC

Updated at

2022-09-09 08:37:18 UTC

NP-MRD ID

NP0281971

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate

Description

2-{8-Formyl-6-hydroxy-3a,5a-dimethyl-2H,3H,3aH,4H,5H,5aH,6H,7H-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate is found in Sarcodon scabrosus. Based on a literature review very few articles have been published on 2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2H,3H,3aH,4H,5H,5aH,6H,7H-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210372D          

 42 44  0  0  0  0            999 V2000
  -15.3559   -1.3546    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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 36 90  1  0
 36 91  1  0
 37 92  1  0
 37 93  1  0
 38 94  1  0
 38 95  1  0
 40 96  1  0
 40 97  1  0
 40 98  1  0
 41 99  1  0
 41100  1  0
 42101  1  0
 42102  1  0
 30 84  1  0
M  END


  Mrv1652309092210372D          

 42 44  0  0  0  0            999 V2000
  -15.3559   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.6414   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9270   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2125   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4980   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7836   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0691   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3546   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6401   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9257   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2112   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4967   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7823   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0678   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3533   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6389   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9244   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2099   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2099   -2.5921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4954   -1.3546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7810   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0665   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0665   -0.5296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3520   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4017   -1.4316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6566   -0.6470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0193   -0.1230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0317    0.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6843    1.2066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5128    2.0136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2718    2.2685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4858    1.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8326    0.2624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6575    0.2501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4636   -0.4754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2811   -0.3647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0156   -1.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7607   -1.8731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9537   -2.0447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4386   -2.7121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5412   -2.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2658   -2.5876    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 25 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 24 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281971

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCC=CCCCCCCCC(=O)OCC(C)C1=C2C3=CC=C(CC(O)C3(C)CCC2(C)CC1)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C38H60O4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-35(41)42-29-30(2)32-23-24-37(3)25-26-38(4)33(36(32)37)22-21-31(28-39)27-34(38)40/h12-13,21-22,28,30,34,40H,5-11,14-20,23-27,29H2,1-4H3

> <INCHI_KEY>
MSIVJNMEKJEZGC-UHFFFAOYSA-N

> <FORMULA>
C38H60O4

> <MOLECULAR_WEIGHT>
580.894

> <EXACT_MASS>
580.449160412

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
72.29874905112763

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2H,3H,3aH,4H,5H,5aH,6H,7H-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate

> <JCHEM_LOGP>
9.203445124000002

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.548378389136381

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9963392925917463

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
178.1494

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2H,3H,4H,5H,6H,7H-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0     -28.664  -2.529   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -27.331  -3.299   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -25.997  -2.529   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -24.663  -3.299   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -23.330  -2.529   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -21.996  -3.299   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -20.662  -2.529   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -19.329  -3.299   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -17.995  -2.529   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -16.661  -3.299   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -15.328  -2.529   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -13.994  -3.299   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -12.660  -2.529   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -11.327  -3.299   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.993  -2.529   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.659  -3.299   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.326  -2.529   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.992  -3.299   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -5.992  -4.839   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -4.658  -2.529   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.324  -3.299   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.991  -2.529   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.991  -0.989   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.657  -3.299   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.750  -2.672   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.226  -1.208   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.036  -0.230   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.059   1.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.277   2.252   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.957   3.759   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.507   4.235   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.773   1.887   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.421   0.490   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.961   0.467   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.732  -0.887   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.258  -0.681   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.762  -2.032   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.287  -3.497   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.780  -3.817   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.685  -5.063   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.010  -5.150   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.496  -4.830   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   42                                                  
CONECT   25   24   26   39                                                  
CONECT   26   25   27   35                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   26   36   37                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   25   40   41                                             
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   24                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

View in JSmol

Synonyms

Value	Source
2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2H,3H,3ah,4H,5H,5ah,6H,7H-cyclohepta[e]inden-1-yl}propyl octadec-9-enoic acid	Generator

Chemical Formula

C₃₈H₆₀O₄

Average Mass

580.8940 Da

Monoisotopic Mass

580.44916 Da

IUPAC Name

2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2H,3H,3aH,4H,5H,5aH,6H,7H-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate

Traditional Name

2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2H,3H,4H,5H,6H,7H-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCC=CCCCCCCCC(=O)OCC(C)C1=C2C3=CC=C(CC(O)C3(C)CCC2(C)CC1)C=O

InChI Identifier

InChI=1S/C38H60O4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-35(41)42-29-30(2)32-23-24-37(3)25-26-38(4)33(36(32)37)22-21-31(28-39)27-34(38)40/h12-13,21-22,28,30,34,40H,5-11,14-20,23-27,29H2,1-4H3

InChI Key

MSIVJNMEKJEZGC-UHFFFAOYSA-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
Sarcodon scabrosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Fatty acid ester
Fatty acyl
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
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	9.2	ChemAxon
pKa (Strongest Acidic)	14.55	ChemAxon
pKa (Strongest Basic)	-3	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	20	ChemAxon
Refractivity	178.15 m³·mol⁻¹	ChemAxon
Polarizability	72.3 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162943780

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate (NP0281971)

MOL for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

3D MOL for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

3D SDF for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

3D-SDF for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

PDB for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

3D PDB for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

SMILES for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

INCHI for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

Structure for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)

3D Structure for NP0281971 (2-{8-formyl-6-hydroxy-3a,5a-dimethyl-2h,3h,4h,5h,6h,7h-cyclohepta[e]inden-1-yl}propyl octadec-9-enoate)