NP-MRD: Showing NP-Card for 2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol (NP0193496)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 10:57:03 UTC

Updated at

2022-09-04 10:57:04 UTC

NP-MRD ID

NP0193496

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol

Description

2-[(3E,4R)-4-[1-(1H-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethan-1-ol belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. 2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol is found in Alstonia scholaris. Based on a literature review very few articles have been published on 2-[(3E,4R)-4-[1-(1H-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethan-1-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
   -0.3912    0.1129   -1.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0582    0.2786   -0.5446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3309    0.0435   -0.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9123    0.2816    1.0499 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2618   -0.0826    1.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -0.0441    1.9682 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5227   -0.4829    1.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7462   -0.9577    0.3668 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7360   -0.9933   -0.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4613   -0.5534   -0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3109   -0.4700   -0.9367 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0629    0.7082    0.4986 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2573   -0.5013    1.4262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7718   -1.6607    0.6054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0612   -1.4158    0.0334 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0669   -2.3449    0.4197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4762   -0.0458    0.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3909    0.9234   -0.1146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5409    2.0563   -0.8321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5058    3.0660   -1.0430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2580    3.1870   -2.4214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4043    0.2827   -2.1026 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3304   -0.1914   -2.5199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4826    0.6931    1.9492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0636    0.3293    2.9527 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3204   -0.4563    2.3781 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7426   -1.3040    0.1148 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9687   -1.3735   -1.5470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1967   -0.7609   -1.9248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6268    1.5614    1.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0134   -0.2745    2.1903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3216   -0.8320    1.8835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0632   -1.9767   -0.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8700   -2.5210    1.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8649   -2.7507    1.4483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0913   -1.8886    0.4687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0841   -3.2172   -0.2733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2451    0.0941   -0.7348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0350    0.1053    1.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5125    2.2107   -1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9534    4.0622   -0.7516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5955    2.9643   -0.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1293    4.1386   -2.6893 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 12 18  1  0
 18 17  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 17 15  1  0
 11  3  1  0
 10  5  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 14 33  1  0
 14 34  1  0
 13 31  1  0
 13 32  1  0
 12 30  1  1
  1 22  1  0
  1 23  1  0
  4 24  1  0
  6 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 17 38  1  0
 17 39  1  0
 19 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  0
M  END


  Mrv1652309042212572D          

 21 23  0  0  1  0            999 V2000
   -0.5837   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    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 C   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
    1.1387   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1712    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    1.4455    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -2.1269    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  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
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  3 11  1  0  0  0  0
 12  2  1  1  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193496

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CC[C@@H](C(=C)C2=CC3=CC=CC=C3N2)\C(C1)=C/CO

> <INCHI_IDENTIFIER>
InChI=1S/C18H22N2O/c1-13(16-7-9-20(2)12-15(16)8-10-21)18-11-14-5-3-4-6-17(14)19-18/h3-6,8,11,16,19,21H,1,7,9-10,12H2,2H3/b15-8-/t16-/m0/s1

> <INCHI_KEY>
NBQBLPKOVYSSJR-YMDFIQGPSA-N

> <FORMULA>
C18H22N2O

> <MOLECULAR_WEIGHT>
282.387

> <EXACT_MASS>
282.173213336

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
32.54857571550906

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(3E,4R)-4-[1-(1H-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethan-1-ol

> <JCHEM_LOGP>
2.2039416499999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.78466848778454

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.116594205852252

> <JCHEM_PKA_STRONGEST_BASIC>
8.335987650935493

> <JCHEM_POLAR_SURFACE_AREA>
39.260000000000005

> <JCHEM_REFRACTIVITY>
88.28509999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(3E,4R)-4-[1-(1H-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol

> <JCHEM_VEBER_RULE>
1

$$$$

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      -1.090  -2.637   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.320  -1.303   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       2.126  -2.549   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -1.090   0.031   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.320   1.365   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.090   2.698   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -2.630   2.698   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -3.400   4.032   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.400   1.365   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.630   0.031   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.400  -1.303   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.630  -2.637   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -3.400  -3.970   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10    3                                                       
CONECT   12    2   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   12   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₂N₂O

Average Mass

282.3870 Da

Monoisotopic Mass

282.17321 Da

IUPAC Name

2-[(3E,4R)-4-[1-(1H-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethan-1-ol

Traditional Name

2-[(3E,4R)-4-[1-(1H-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol

CAS Registry Number

Not Available

SMILES

CN1CC[C@@H](C(=C)C2=CC3=CC=CC=C3N2)\C(C1)=C/CO

InChI Identifier

InChI=1S/C18H22N2O/c1-13(16-7-9-20(2)12-15(16)8-10-21)18-11-14-5-3-4-6-17(14)19-18/h3-6,8,11,16,19,21H,1,7,9-10,12H2,2H3/b15-8-/t16-/m0/s1

InChI Key

NBQBLPKOVYSSJR-YMDFIQGPSA-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
Alstonia Alstonia scholaris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

Indoles

Alternative Parents

Substituents

Indole
Benzenoid
Substituted pyrrole
Piperidine
Heteroaromatic compound
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Azacycle
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
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	2.2	ChemAxon
pKa (Strongest Acidic)	15.12	ChemAxon
pKa (Strongest Basic)	8.34	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	39.26 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	88.29 m³·mol⁻¹	ChemAxon
Polarizability	32.55 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

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

163185509

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol (NP0193496)

MOL for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

3D MOL for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

3D SDF for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

3D-SDF for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

PDB for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

3D PDB for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

SMILES for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

INCHI for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

Structure for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)

3D Structure for NP0193496 (2-[(3e,4r)-4-[1-(1h-indol-2-yl)ethenyl]-1-methylpiperidin-3-ylidene]ethanol)