NP-MRD: Showing NP-Card for 2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone (NP0190741)

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Record Information

Version

2.0

Created at

2022-09-04 07:28:11 UTC

Updated at

2022-09-04 07:28:11 UTC

NP-MRD ID

NP0190741

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone

Description

2,2,2-Trifluoro-1-(5-methyl-4-undecyl-2,3-dihydro-1H-pyrrol-1-yl)ethan-1-one belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms. Based on a literature review very few articles have been published on 2,2,2-trifluoro-1-(5-methyl-4-undecyl-2,3-dihydro-1H-pyrrol-1-yl)ethan-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 53  0  0  0  0  0  0  0  0999 V2000
   -6.6546   -1.9706   -1.6368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0333   -0.6359   -1.9403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2673   -0.0852   -0.7486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1602   -0.9900   -0.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3898   -0.4738    0.8620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7807    0.8457    0.5290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9774    1.4302    1.6704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8425    0.5433    2.0857 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1351    0.3017    0.9421 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7424    1.5509    0.4341 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6433    1.3036   -0.7261 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7854    0.3979   -0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    0.8414   -0.4589 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4274    2.2537   -0.5821 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9578   -0.2269   -0.2448 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3593   -0.2078   -0.4273 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9208    0.8523   -0.8243 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1964   -1.4088   -0.1634 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0333   -1.7508    1.1566 F   0  0  0  0  0  0  0  0  0  0  0  0
    6.8338   -2.4586   -1.0174 F   0  0  0  0  0  0  0  0  0  0  0  0
    8.5215   -1.1418   -0.4296 F   0  0  0  0  0  0  0  0  0  0  0  0
    4.2011   -1.3853    0.2069 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8577   -1.0704   -0.4383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8786   -2.0349   -0.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0205   -2.8256   -1.8797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5794   -2.0635   -2.2527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4071   -0.6316   -2.8443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8744    0.0775   -2.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8503    0.8937   -1.1118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9374    0.1210    0.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5887   -2.0128   -0.1214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4693   -1.1651   -1.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6464   -1.2511    1.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0914   -0.4150    1.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2001    0.7863   -0.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6332    1.5601    0.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6684    1.5069    2.5345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6386    2.4340    1.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1931   -0.4273    2.4304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2840    1.0357    2.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2376   -0.3094    0.1385 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9767   -0.2599    1.4648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0313    2.2893    0.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.0920    1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9734    0.8376   -1.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9622    2.2630   -1.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6665    2.5067   -1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3654    2.4208   -0.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6124    2.9170   -0.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1224   -1.4098    1.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6258   -2.3377   -0.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0732   -1.5984    0.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9379   -1.5144   -1.4813 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
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 22  1  0
 22 23  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 23 12  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  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 14 47  1  0
 14 48  1  0
 14 49  1  0
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
M  END


  Mrv1652309042209282D          

 23 23  0  0  0  0            999 V2000
    3.8583   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5727   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2872   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0017   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7161   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4306   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1451   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8596   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5740   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2885   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0030   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7174   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4711   -4.9411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6426   -4.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0232   -5.5542    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.8436   -5.4680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3286   -6.1354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1792   -4.7143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5147   -3.9606    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   14.9329   -5.0498    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   13.4255   -4.3787    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   12.6107   -6.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8037   -6.0971    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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 12 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190741

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC1=C(C)N(CC1)C(=O)C(F)(F)F

> <INCHI_IDENTIFIER>
InChI=1S/C18H30F3NO/c1-3-4-5-6-7-8-9-10-11-12-16-13-14-22(15(16)2)17(23)18(19,20)21/h3-14H2,1-2H3

> <INCHI_KEY>
DSNMBYIZKSVKBM-UHFFFAOYSA-N

> <FORMULA>
C18H30F3NO

> <MOLECULAR_WEIGHT>
333.439

> <EXACT_MASS>
333.227949079

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.34995141232926

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,2,2-trifluoro-1-(5-methyl-4-undecyl-2,3-dihydro-1H-pyrrol-1-yl)ethan-1-one

> <JCHEM_LOGP>
5.728556251666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
20.310000000000002

> <JCHEM_REFRACTIVITY>
89.0147

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone

> <JCHEM_VEBER_RULE>
0

$$$$

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       7.202  -9.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.536  -9.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.869  -9.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.203  -9.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.537  -9.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.870  -9.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.204  -9.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.538  -9.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.872  -9.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.205  -9.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.539  -9.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.873  -9.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      23.279  -9.223   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      23.600  -7.717   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      24.310 -10.368   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      25.841 -10.207   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      26.747 -11.453   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      26.468  -8.800   0.000  0.00  0.00           C+0
HETATM   19  F   UNK     0      27.094  -7.393   0.000  0.00  0.00           F+0
HETATM   20  F   UNK     0      27.875  -9.426   0.000  0.00  0.00           F+0
HETATM   21  F   UNK     0      25.061  -8.174   0.000  0.00  0.00           F+0
HETATM   22  C   UNK     0      23.540 -11.702   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.034 -11.381   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   23                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   22                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   15   23                                                       
CONECT   23   22   12                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₃₀F₃NO

Average Mass

333.4390 Da

Monoisotopic Mass

333.22795 Da

IUPAC Name

2,2,2-trifluoro-1-(5-methyl-4-undecyl-2,3-dihydro-1H-pyrrol-1-yl)ethan-1-one

Traditional Name

2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC1=C(C)N(CC1)C(=O)C(F)(F)F

InChI Identifier

InChI=1S/C18H30F3NO/c1-3-4-5-6-7-8-9-10-11-12-16-13-14-22(15(16)2)17(23)18(19,20)21/h3-14H2,1-2H3

InChI Key

DSNMBYIZKSVKBM-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolines

Sub Class

Not Available

Direct Parent

Pyrrolines

Alternative Parents

Substituents

Pyrroline
Tertiary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Azacycle
Alkyl fluoride
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organofluoride
Organohalogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Alkyl halide
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	5.73	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	20.31 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	89.01 m³·mol⁻¹	ChemAxon
Polarizability	37.35 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

162879345

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone (NP0190741)

MOL for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

3D MOL for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

3D SDF for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

3D-SDF for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

PDB for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

3D PDB for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

SMILES for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

INCHI for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

Structure for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)

3D Structure for NP0190741 (2,2,2-trifluoro-1-(2-methyl-3-undecyl-4,5-dihydropyrrol-1-yl)ethanone)