NP-MRD: Showing NP-Card for (3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol (NP0146910)

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Record Information

Version

2.0

Created at

2022-09-02 02:24:25 UTC

Updated at

2022-09-02 02:24:25 UTC

NP-MRD ID

NP0146910

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol

Description

Remijinine belongs to the class of organic compounds known as indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole. (3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol is found in Ciliosemina pedunculata. (3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol was first documented in 2004 (PMID: 15497937). Based on a literature review very few articles have been published on Remijinine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -4.9630    1.3300    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0514    1.4663   -0.6125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6099    1.1256   -0.5026 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2718    0.0623   -1.5132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2116   -0.8067   -0.9605 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8500   -1.6906    0.0192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9107   -0.8812    0.7910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3496    0.5412    0.8577 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8263    0.3564    1.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2582    0.0719   -0.2612 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1229   -0.4285   -0.3903 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4645   -1.7265    0.2431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9448   -2.0801    0.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2448   -3.3007    0.6153 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4228   -0.4735   -1.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8339   -1.2465   -2.8359 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3685    0.3485   -2.1221 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8160    1.0226   -0.9768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8091    1.9940   -0.7757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0485    2.4954    0.4799 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3293    2.0663    1.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3628    1.1156    1.3544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0939    0.5866    0.0980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9891    1.6069    0.1336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7304    0.9504    1.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4289    1.8880   -1.5811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9809    2.0420   -0.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8305    0.5741   -2.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1308   -0.5130   -1.8572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1662   -2.0417    0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3761   -2.4653   -0.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8319   -0.8554    0.1541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1406   -1.3091    1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7771    1.1430    1.6567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4054    1.3337    1.4442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7299   -0.3690    1.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2884    1.0329   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3330   -1.6599    1.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9305   -2.6075   -0.1099 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6152   -1.3293    0.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1628   -2.1837   -1.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9953   -3.7612    0.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841   -2.2367   -2.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3612    2.3128   -1.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8335    3.2559    0.6050 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5403    2.4797    2.5522 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7910    0.7639    2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 11 12  1  1
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
 11 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 11  1  0
  5 10  1  0
 23 18  1  0
  3  8  1  0
 14 42  1  0
 13 40  1  0
 13 41  1  0
 12 38  1  0
 12 39  1  0
 10 37  1  6
  9 35  1  0
  9 36  1  0
  8 34  1  1
  7 32  1  0
  7 33  1  0
  6 30  1  0
  6 31  1  0
  4 28  1  0
  4 29  1  0
  3 27  1  6
  2 26  1  0
  1 24  1  0
  1 25  1  0
 16 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
M  END


  Mrv1652309022204242D          

 23 26  0  0  1  0            999 V2000
    2.3305   -3.1936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3305   -2.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450   -1.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450   -1.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7595   -0.7186    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8970   -1.2686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8970   -1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7595   -2.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4739   -1.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4739   -1.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1884   -0.7186    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5240   -1.4723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3444   -1.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6800   -2.3122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7035   -0.0512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8785   -0.0512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1884    0.6163    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9730    0.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6875    0.7738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4020    0.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4020   -0.4637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6875   -0.8762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9730   -0.4637    0.0000 C   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  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 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
 18 23  1  0  0  0  0
 11 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146910

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC[C@]1(C2CC3CCN2CC3C=C)C(O)=NC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H24N2O2/c1-2-13-12-21-9-7-14(13)11-17(21)19(8-10-22)15-5-3-4-6-16(15)20-18(19)23/h2-6,13-14,17,22H,1,7-12H2,(H,20,23)/t13?,14?,17?,19-/m0/s1

> <INCHI_KEY>
MUTOOCDUQXGEEC-SVUWXIQYSA-N

> <FORMULA>
C19H24N2O2

> <MOLECULAR_WEIGHT>
312.413

> <EXACT_MASS>
312.183778021

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.429899257819145

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)-3H-indol-2-ol

> <ALOGPS_LOGP>
2.10

> <JCHEM_LOGP>
-0.1670706392762607

> <ALOGPS_LOGS>
-3.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.949847243744212

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7925111559384397

> <JCHEM_PKA_STRONGEST_BASIC>
10.006733625039486

> <JCHEM_POLAR_SURFACE_AREA>
56.06

> <JCHEM_REFRACTIVITY>
93.19260000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.78e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       4.350  -5.961   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.350  -4.421   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.684  -3.651   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.684  -2.111   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       7.018  -1.341   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       7.274  -2.368   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.274  -3.395   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.018  -4.421   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.351  -3.651   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.351  -2.111   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.685  -1.341   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.311  -2.748   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.843  -2.909   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.469  -4.316   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.780  -0.095   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.240  -0.095   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       9.685   1.150   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0      11.150   0.675   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.483   1.445   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.817   0.675   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.817  -0.865   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.483  -1.635   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.150  -0.865   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10   12   15   23                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   11   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18   11                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄N₂O₂

Average Mass

312.4130 Da

Monoisotopic Mass

312.18378 Da

IUPAC Name

(3S)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)-3H-indol-2-ol

Traditional Name

(3S)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol

CAS Registry Number

Not Available

SMILES

OCC[C@]1(C2CC3CCN2CC3C=C)C(O)=NC2=CC=CC=C12

InChI Identifier

InChI=1S/C19H24N2O2/c1-2-13-12-21-9-7-14(13)11-17(21)19(8-10-22)15-5-3-4-6-16(15)20-18(19)23/h2-6,13-14,17,22H,1,7-12H2,(H,20,23)/t13?,14?,17?,19-/m0/s1

InChI Key

MUTOOCDUQXGEEC-SVUWXIQYSA-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
Ciliosemina pedunculata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolines. Indolines are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolines

Direct Parent

Indolines

Alternative Parents

Substituents

Dihydroindole
Quinuclidine
Aralkylamine
Piperidine
Benzenoid
Amino acid or derivatives
Carboxamide group
Lactam
Tertiary aliphatic amine
Tertiary amine
Secondary carboxylic acid amide
Carboxylic acid derivative
Azacycle
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Amine
Primary 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	2.1	ALOGPS
logP	-0.17	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	3.79	ChemAxon
pKa (Strongest Basic)	10.01	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	56.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	93.19 m³·mol⁻¹	ChemAxon
Polarizability	34.43 Å³	ChemAxon
Number of Rings	4	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

C00026579

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

101358425

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Diaz JG, Sazatornil JG, Rodriguez ML, Mesia LR, Arana GV: Five new alkaloids from the leaves of Remijia peruviana. J Nat Prod. 2004 Oct;67(10):1667-71. doi: 10.1021/np040053k. [PubMed:15497937 ]
LOTUS database [Link]

Showing NP-Card for (3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol (NP0146910)

MOL for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

3D MOL for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

3D SDF for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

3D-SDF for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

PDB for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

3D PDB for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

SMILES for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

INCHI for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

Structure for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)

3D Structure for NP0146910 ((3s)-3-{5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-3-(2-hydroxyethyl)indol-2-ol)