NP-MRD: Showing NP-Card for 3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole (NP0305930)

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Record Information

Version

2.0

Created at

2022-09-10 22:06:29 UTC

Updated at

2022-09-10 22:06:29 UTC

NP-MRD ID

NP0305930

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole

Description

(-)-Hapalindole D belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. 3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole was first documented in 2016 (PMID: 30155122). Based on a literature review a small amount of articles have been published on (-)-Hapalindole D.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
   -2.2045   -3.7559   -1.6842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3049   -2.4555   -1.6310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8432   -1.5528   -0.5728 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3249   -2.3315    0.6076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9242   -0.6198   -0.0594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3989    0.4025    0.8798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1322    1.0939    0.3119 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8925    2.3727    0.9352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610    2.7789    2.0328 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0652    3.3975    0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376    0.0229    0.1512 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2302    0.3529   -0.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6661    1.0334   -1.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0102    1.1666   -1.2637 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4576    0.6086   -0.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7513    0.4595    0.3616 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9515   -0.2407    1.5428 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8407   -0.7700    2.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5655   -0.6040    1.7067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3592    0.1021    0.5107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6990   -0.7238   -1.1455 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9904    0.2313   -2.0991 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.1182   -3.2691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2205    0.1003   -4.6595 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7304   -4.3362   -0.8907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5827   -4.2959   -2.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7959   -1.9725   -2.5045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5438   -1.8256    1.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8542   -3.3393    0.7516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2688   -2.6204    0.4883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6511   -1.2405    0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5028   -0.1725   -0.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1369    0.0328    1.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1862    1.1940    1.0223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4958    1.3650   -0.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2861    2.1147    2.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627    3.7682    2.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4003    4.4252    0.5553 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0824    3.3124    0.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0322    3.2839   -0.7661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1107   -0.6527    0.9947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0439    1.4066   -2.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5722    1.6657   -2.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5889    0.8515   -0.1500 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9514   -0.3742    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0691   -1.3214    3.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7508   -1.0191    2.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0628   -1.4370   -1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  8  1  0
  8  9  2  3
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  6
  2  1  2  3
  3 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  2  0
 21 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 11  7  1  0
 20 12  1  0
 20 15  1  0
 10 38  1  0
 10 39  1  0
 10 40  1  0
  9 36  1  0
  9 37  1  0
  7 35  1  6
  6 33  1  0
  6 34  1  0
  5 31  1  0
  5 32  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  2 27  1  0
  1 25  1  0
  1 26  1  0
 21 48  1  6
 11 41  1  1
 13 42  1  0
 14 43  1  0
 16 44  1  0
 17 45  1  0
 18 46  1  0
 19 47  1  0
M  END


  Mrv1652309112200062D          

 24 26  0  0  1  0            999 V2000
    1.9381   -4.7595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2097   -4.3722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -3.5477    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9978   -3.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.7192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4752   -1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203   -0.9238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822   -1.8800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2428   -2.5916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7948   -3.2047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3469   -3.8178    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 12 20  1  0  0  0  0
 15 20  1  0  0  0  0
 11 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  2  0  0  0  0
 23 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0305930

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)[C@@H]1CC[C@@](C)(C=C)[C@@H](N=C=S)[C@H]1C1=CNC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C21H24N2S/c1-5-21(4)11-10-15(14(2)3)19(20(21)23-13-24)17-12-22-18-9-7-6-8-16(17)18/h5-9,12,15,19-20,22H,1-2,10-11H2,3-4H3/t15-,19+,20-,21+/m0/s1

> <INCHI_KEY>
PPHWDUZMWNUINO-PSMQTCRGSA-N

> <FORMULA>
C21H24N2S

> <MOLECULAR_WEIGHT>
336.5

> <EXACT_MASS>
336.166019955

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
38.2516113036501

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(1R,2S,3S,6R)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1H-indole

> <JCHEM_LOGP>
6.020974779333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.875289082214856

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.774772710287277

> <JCHEM_PKA_STRONGEST_BASIC>
-3.727095234723967

> <JCHEM_POLAR_SURFACE_AREA>
28.15

> <JCHEM_REFRACTIVITY>
104.9869

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-[(1R,2S,3S,6R)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1H-indole

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       3.618  -8.884   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.258  -8.161   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.204  -6.622   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.729  -6.837   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.698  -6.943   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.333  -5.798   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.887  -3.189   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.411  -1.724   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.393  -3.509   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       4.187  -4.838   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       5.217  -5.982   0.000  0.00  0.00           C+0
HETATM   24  S   UNK     0       6.247  -7.126   0.000  0.00  0.00           S+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   21                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12   21                                                  
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   12   15                                                  
CONECT   21   11    3   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₄N₂S

Average Mass

336.5000 Da

Monoisotopic Mass

336.16602 Da

IUPAC Name

3-[(1R,2S,3S,6R)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1H-indole

Traditional Name

3-[(1R,2S,3S,6R)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1H-indole

CAS Registry Number

Not Available

SMILES

CC(=C)[C@@H]1CC[C@@](C)(C=C)[C@@H](N=C=S)[C@H]1C1=CNC2=CC=CC=C12

InChI Identifier

InChI=1S/C21H24N2S/c1-5-21(4)11-10-15(14(2)3)19(20(21)23-13-24)17-12-22-18-9-7-6-8-16(17)18/h5-9,12,15,19-20,22H,1-2,10-11H2,3-4H3/t15-,19+,20-,21+/m0/s1

InChI Key

PPHWDUZMWNUINO-PSMQTCRGSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Aromatic monoterpenoid
Bicyclic monoterpenoid
3-alkylindole
P-menthane monoterpenoid
Indole
Indole or derivatives
Substituted pyrrole
Benzenoid
Heteroaromatic compound
Pyrrole
Isothiocyanate
Organic 1,3-dipolar compound
Organoheterocyclic compound
Azacycle
Propargyl-type 1,3-dipolar organic compound
Organosulfur compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	6.02	ChemAxon
pKa (Strongest Acidic)	16.77	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	28.15 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	104.99 m³·mol⁻¹	ChemAxon
Polarizability	38.25 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

78442493

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

132519929

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Liu Y, Cheng LJ, Yue HT, Che W, Xie JH, Zhou QL: Divergent enantioselective synthesis of hapalindole-type alkaloids using catalytic asymmetric hydrogenation of a ketone to construct the chiral core structure. Chem Sci. 2016 Jul 1;7(7):4725-4729. doi: 10.1039/c6sc00686h. Epub 2016 Apr 12. [PubMed:30155122 ]
LOTUS database [Link]

Showing NP-Card for 3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole (NP0305930)

MOL for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

3D MOL for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

3D SDF for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

3D-SDF for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

PDB for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

3D PDB for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

SMILES for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

INCHI for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

Structure for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)

3D Structure for NP0305930 (3-[(1r,2s,3s,6r)-3-ethenyl-2-isothiocyanato-3-methyl-6-(prop-1-en-2-yl)cyclohexyl]-1h-indole)