NP-MRD: Showing NP-Card for IL 11 (NP0062095)

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Record Information

Version

2.0

Created at

2022-04-28 06:45:58 UTC

Updated at

2022-04-28 06:45:58 UTC

NP-MRD ID

NP0062095

Secondary Accession Numbers

None

Natural Product Identification

Common Name

IL 11

Description

(3S)-3-(4-chlorophenyl)-1-(3-methylpyridin-2-yl)pyrrolidine-2,5-dione belongs to the class of organic compounds known as phenylpyrrolidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms. IL 11 is found in Strain I-11. Based on a literature review very few articles have been published on (3S)-3-(4-chlorophenyl)-1-(3-methylpyridin-2-yl)pyrrolidine-2,5-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
   -1.9636   -1.3444    1.3268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8985   -0.6586    0.4298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2318   -1.0510    0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1112   -0.3994   -0.3733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6706    0.5973   -1.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3654    0.9323   -1.2181 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4649    0.3337   -0.4165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0836    0.6955   -0.4214 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5413    1.9534   -0.0321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1279    2.8426    0.6722 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349    2.1045   -0.5662 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2171    0.7801   -1.0900 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4553    0.1980   -0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7709    0.0221    0.6919 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9801   -0.5502    1.0696 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9023   -0.9602    0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4102   -1.6774    0.6368 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.6011   -0.7913   -1.2036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958   -0.2216   -1.5542 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0359   -0.0868   -0.8065 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0185   -1.3368   -0.8923 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0492   -0.7816    1.5789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7583   -2.3825    0.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4932   -1.5191    2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5782   -1.8322    1.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1547   -0.6784   -0.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3864    1.1030   -1.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5073    2.5401    0.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7643    2.8712   -1.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2340    0.8385   -2.2193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0210    0.3563    1.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1579   -0.6554    2.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3292   -1.1150   -1.9501 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2429   -0.1271   -2.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  7  2  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 20  1  0
 20 21  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
  3  2  1  0
 20  8  1  0
 19 13  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 27  1  0
  4 26  1  0
  3 25  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  6
 14 31  1  0
 15 32  1  0
 18 33  1  0
 19 34  1  0
M  END


  Mrv1652304282208452D          

 21 23  0  0  1  0            999 V2000
    1.3819   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1830   -3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3507   -2.0195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -1.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3068   -0.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6937   -0.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9091   -0.6605    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1792   -2.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4324   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9173   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5817   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7613   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -5.1768    0.0000 Cl  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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  9 14  1  0  0  0  0
  2 15  1  1  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
 15 20  1  0  0  0  0
 18 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0062095

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C(N=CC=C1)N1C(=O)C[C@H](C1=O)C1=CC=C(Cl)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H13ClN2O2/c1-10-3-2-8-18-15(10)19-14(20)9-13(16(19)21)11-4-6-12(17)7-5-11/h2-8,13H,9H2,1H3/t13-/m0/s1

> <INCHI_KEY>
CPDUOSJMCFQXID-ZDUSSCGKSA-N

> <FORMULA>
C16H13ClN2O2

> <MOLECULAR_WEIGHT>
300.74

> <EXACT_MASS>
300.0665554

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
30.486599631847373

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S)-3-(4-chlorophenyl)-1-(3-methylpyridin-2-yl)pyrrolidine-2,5-dione

> <ALOGPS_LOGP>
2.04

> <JCHEM_LOGP>
3.059204373

> <ALOGPS_LOGS>
-3.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.894796864352244

> <JCHEM_PKA_STRONGEST_BASIC>
2.0083674194624987

> <JCHEM_POLAR_SURFACE_AREA>
50.27

> <JCHEM_REFRACTIVITY>
79.62780000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.94e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-(4-chlorophenyl)-1-(3-methylpyridin-2-yl)pyrrolidine-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.580  -3.215   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.104  -4.680   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.564  -4.680   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.342  -5.926   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       0.088  -3.215   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.377  -2.739   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.521  -3.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.986  -3.294   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.306  -1.788   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.162  -0.757   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -1.697  -1.233   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -2.201  -5.276   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.009  -5.926   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.540  -5.765   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.446  -7.011   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.819  -8.417   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.288  -8.578   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.382  -7.333   0.000  0.00  0.00           C+0
HETATM   21 Cl   UNK     0       5.724  -9.663   0.000  0.00  0.00          Cl+0
CONECT    1    2    6                                                       
CONECT    2    1    3   15                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   13                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14    9                                                            
CONECT   15    2   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   18                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₃ClN₂O₂

Average Mass

300.7400 Da

Monoisotopic Mass

300.06656 Da

IUPAC Name

(3S)-3-(4-chlorophenyl)-1-(3-methylpyridin-2-yl)pyrrolidine-2,5-dione

Traditional Name

(3S)-3-(4-chlorophenyl)-1-(3-methylpyridin-2-yl)pyrrolidine-2,5-dione

CAS Registry Number

Not Available

SMILES

CC1=C(N=CC=C1)N1C(=O)C[C@H](C1=O)C1=CC=C(Cl)C=C1

InChI Identifier

InChI=1S/C16H13ClN2O2/c1-10-3-2-8-18-15(10)19-14(20)9-13(16(19)21)11-4-6-12(17)7-5-11/h2-8,13H,9H2,1H3/t13-/m0/s1

InChI Key

CPDUOSJMCFQXID-ZDUSSCGKSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Strain I-11	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpyrrolidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolidines

Sub Class

Phenylpyrrolidines

Direct Parent

Phenylpyrrolidines

Alternative Parents

Substituents

3-phenylpyrrolidine
Methylpyridine
Halobenzene
Chlorobenzene
Imidolactam
Benzenoid
2-pyrrolidone
Pyrrolidone
Pyridine
Carboxylic acid imide, n-substituted
Monocyclic benzene moiety
Aryl halide
Aryl chloride
Heteroaromatic compound
Pyrrole
Dicarboximide
Carboxylic acid imide
Lactam
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	2.04	ALOGPS
logP	3.06	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	15.89	ChemAxon
pKa (Strongest Basic)	2.01	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	50.27 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	79.63 m³·mol⁻¹	ChemAxon
Polarizability	30.49 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

162865721

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for IL 11 (NP0062095)

MOL for NP0062095 (IL 11)

3D MOL for NP0062095 (IL 11)

3D SDF for NP0062095 (IL 11)

3D-SDF for NP0062095 (IL 11)

PDB for NP0062095 (IL 11)

3D PDB for NP0062095 (IL 11)

SMILES for NP0062095 (IL 11)

INCHI for NP0062095 (IL 11)

Structure for NP0062095 (IL 11)

3D Structure for NP0062095 (IL 11)