NP-MRD: Showing NP-Card for (3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol (NP0328258)

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Record Information

Version

2.0

Created at

2022-09-12 11:34:30 UTC

Updated at

2022-09-12 11:34:30 UTC

NP-MRD ID

NP0328258

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol

Description

3-{2-[(3S,4Z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxy-3H-indol-2-ol belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. (3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol is found in Neolaugeria resinosa. Based on a literature review very few articles have been published on 3-{2-[(3S,4Z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxy-3H-indol-2-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -1.5877   -0.5998   -2.2261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6823   -0.8787   -1.2485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3606   -0.6057    0.1831 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6191   -0.9503    0.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6302    0.0227    0.9449 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9693   -0.4302    0.8531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3535    1.3192    0.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9731    1.7591    0.8809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9617    0.7486    0.5222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6963    1.1339    0.5462 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3741    0.2308    0.2381 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6448    0.5962    0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2126    1.8958    0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5112    3.0535    0.9132 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5045    1.7984    0.4525 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9066    0.4933    0.0807 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1239   -0.1174   -0.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2761    0.6185   -0.0384 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5523    0.0834   -0.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2067   -1.4429   -0.5160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0891   -2.2275   -0.6522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8719   -1.6239   -0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7586   -0.2909   -0.0534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7539   -1.3283   -2.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2131    0.4417   -2.1770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0141   -0.7131   -3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8775   -1.9996   -1.3210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6298   -0.4384   -1.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6188   -1.3879    0.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2706   -1.0762    2.0428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9592   -1.9415    0.6008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0517   -1.5224    0.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5253   -0.0703   -0.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5446   -0.0442    1.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0435    2.0702    1.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4588    1.5099   -0.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7214    2.7669    0.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9863    1.7783    2.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4605    2.1752    0.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1954   -0.8047   -0.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6786    3.5149    1.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3018    0.9039   -0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5992   -0.5472   -1.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8938   -0.4800    0.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1665   -1.9422   -0.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1445   -3.2730   -0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9508   -2.1781   -0.5017 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
  9  3  1  0
 23 12  1  0
 23 16  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  1
  4 30  1  0
  4 31  1  0
  6 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
 10 39  1  0
 11 40  1  0
 14 41  1  0
 19 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
M  END


  Mrv1652309122213342D          

 23 25  0  0  1  0            999 V2000
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -3.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.7192    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1190   -4.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6880   -4.6754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9429   -5.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    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  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  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
   -0.1712   -0.6979    0.0000 O   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
    2.6378    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    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  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 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
 16 23  1  0  0  0  0
 12 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328258

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1CN(C)CC\C1=C\C=C1/C(O)=NC2=C(OC)C=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H24N2O2/c1-4-13-12-21(2)11-10-14(13)8-9-16-15-6-5-7-17(23-3)18(15)20-19(16)22/h5-9,13H,4,10-12H2,1-3H3,(H,20,22)/b14-8-,16-9-/t13-/m1/s1

> <INCHI_KEY>
YEGCSPZRLCQFJL-YJZBBDNSSA-N

> <FORMULA>
C19H24N2O2

> <MOLECULAR_WEIGHT>
312.413

> <EXACT_MASS>
312.183778021

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.365861827156905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3Z)-3-{2-[(3S,4Z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxy-3H-indol-2-ol

> <JCHEM_LOGP>
2.3285224654124477

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.7522073353389382

> <JCHEM_PKA_STRONGEST_BASIC>
15.000000390376954

> <JCHEM_POLAR_SURFACE_AREA>
45.06

> <JCHEM_REFRACTIVITY>
97.05270000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3Z)-3-{2-[(3S,4Z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.204  -6.622   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.698  -6.943   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.222  -8.407   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      -1.284  -8.727   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -1.760 -10.192   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.315  -7.583   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.839  -6.118   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.333  -5.798   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.143  -4.334   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  O   UNK     0      -0.320  -1.303   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.924   1.777   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.590   2.547   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   16   12                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄N₂O₂

Average Mass

312.4130 Da

Monoisotopic Mass

312.18378 Da

IUPAC Name

(3Z)-3-{2-[(3S,4Z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxy-3H-indol-2-ol

Traditional Name

(3Z)-3-{2-[(3S,4Z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol

CAS Registry Number

Not Available

SMILES

CC[C@@H]1CN(C)CC\C1=C\C=C1/C(O)=NC2=C(OC)C=CC=C12

InChI Identifier

InChI=1S/C19H24N2O2/c1-4-13-12-21(2)11-10-14(13)8-9-16-15-6-5-7-17(23-3)18(15)20-19(16)22/h5-9,13H,4,10-12H2,1-3H3,(H,20,22)/b14-8-,16-9-/t13-/m1/s1

InChI Key

YEGCSPZRLCQFJL-YJZBBDNSSA-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
Neolaugeria resinosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Not Available

Direct Parent

Indoles and derivatives

Alternative Parents

Substituents

Indole or derivatives
Anisole
Alkyl aryl ether
Piperidine
Benzenoid
Cyclic carboximidic acid
Tertiary amine
Tertiary aliphatic amine
Azacycle
Ether
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Amine
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen 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	2.33	ChemAxon
pKa (Strongest Acidic)	-2.8	ChemAxon
pKa (Strongest Basic)	15	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	45.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	97.05 m³·mol⁻¹	ChemAxon
Polarizability	36.37 Å³	ChemAxon
Number of Rings	3	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

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

163193907

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol (NP0328258)

MOL for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

3D MOL for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

3D SDF for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

3D-SDF for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

PDB for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

3D PDB for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

SMILES for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

INCHI for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

Structure for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)

3D Structure for NP0328258 ((3z)-3-{2-[(3s,4z)-3-ethyl-1-methylpiperidin-4-ylidene]ethylidene}-7-methoxyindol-2-ol)