NP-MRD: Showing NP-Card for 1-Cinnamoyl-3-hydroxypyrrolidine (NP0140007)

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Record Information

Version

2.0

Created at

2022-06-29 20:20:45 UTC

Updated at

2022-06-29 20:20:45 UTC

NP-MRD ID

NP0140007

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-Cinnamoyl-3-hydroxypyrrolidine

Description

1-Cinnamoyl-3-hydroxypyrrolidine belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid. Based on a literature review very few articles have been published on 1-Cinnamoyl-3-hydroxypyrrolidine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 32  0  0  0  0  0  0  0  0999 V2000
   -0.8525    0.4117   -2.4245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8805    0.1767   -1.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3967    0.0191   -0.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5297    0.1222   -1.1586 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8311   -0.0235   -0.5327 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9731    0.1068   -1.3315 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2475   -0.0167   -0.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4540   -0.2766    0.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3451   -0.4084    1.3213 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0514   -0.2820    0.7951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1145    0.0683   -0.4998 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2336   -0.2013    0.9203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7241   -0.2223    1.1912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2428    0.6954    0.1087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5876    0.4825   -0.1616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4256    0.2083   -1.0951 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4393   -0.1864    0.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4661    0.3309   -2.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8250    0.3133   -2.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1335    0.0834   -1.4327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4335   -0.3798    0.9553 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4812   -0.6135    2.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2009   -0.3895    1.4445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7405    0.5903    1.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7561   -1.1712    1.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1084   -1.2475    1.0250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9675    0.1423    2.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9938    1.7442    0.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9186   -0.1783    0.4683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7971   -0.8034   -1.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4652    0.9051   -1.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 16  1  0
 11  2  1  0
  2  1  2  0
  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
 16 14  1  0
 10  5  1  0
 15 29  1  0
 14 28  1  1
 13 26  1  0
 13 27  1  0
 12 24  1  0
 12 25  1  0
 16 30  1  0
 16 31  1  0
  3 17  1  0
  4 18  1  0
  6 19  1  0
  7 20  1  0
  8 21  1  0
  9 22  1  0
 10 23  1  0
M  END


  Mrv1652306292222202D          

 16 17  0  0  0  0            999 V2000
    3.4186   -3.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1637   -3.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -3.8062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0837   -3.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -2.5366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -1.7116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8538   -4.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1893   -5.2273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0333   -4.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5484   -5.0548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2721   -4.9686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7571   -5.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5775   -5.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9131   -4.7961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4282   -4.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6077   -4.2149    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
  1  5  1  0  0  0  0
  5  6  1  0  0  0  0
  3  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0140007

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1CCN(C1)C(=O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H15NO2/c15-12-8-9-14(10-12)13(16)7-6-11-4-2-1-3-5-11/h1-7,12,15H,8-10H2/b7-6+

> <INCHI_KEY>
FHARWVZPAKTDJR-VOTSOKGWSA-N

> <FORMULA>
C13H15NO2

> <MOLECULAR_WEIGHT>
217.268

> <EXACT_MASS>
217.110278727

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
24.05195566258915

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-1-(3-hydroxypyrrolidin-1-yl)-3-phenylprop-2-en-1-one

> <ALOGPS_LOGP>
1.32

> <JCHEM_LOGP>
1.034595631333333

> <ALOGPS_LOGS>
-1.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.826910249615317

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4268950252093905

> <JCHEM_POLAR_SURFACE_AREA>
40.54

> <JCHEM_REFRACTIVITY>
63.53440000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.98e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-1-(3-hydroxypyrrolidin-1-yl)-3-phenylprop-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0       6.381  -5.640   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.906  -7.105   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       4.366  -7.105   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       3.890  -5.640   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.136  -4.735   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.136  -3.195   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.460  -8.351   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.087  -9.758   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.929  -8.190   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.024  -9.436   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.508  -9.275   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.413 -10.521   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.945 -10.360   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.571  -8.953   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.666  -7.707   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.134  -7.868   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    1    6                                                  
CONECT    6    5                                                            
CONECT    7    3    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₅NO₂

Average Mass

217.2680 Da

Monoisotopic Mass

217.11028 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1CCN(C1)C(=O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1S/C13H15NO2/c15-12-8-9-14(10-12)13(16)7-6-11-4-2-1-3-5-11/h1-7,12,15H,8-10H2/b7-6+

InChI Key

FHARWVZPAKTDJR-VOTSOKGWSA-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 cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Not Available

Direct Parent

Cinnamic acids and derivatives

Alternative Parents

Substituents

Cinnamic acid or derivatives
N-acylpyrrolidine
Styrene
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Secondary alcohol
Tertiary amine
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Amine
Carbonyl group
Organic nitrogen compound
Alcohol
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

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

29365183

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

62917426

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 1-Cinnamoyl-3-hydroxypyrrolidine (NP0140007)

MOL for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

3D MOL for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

3D SDF for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

3D-SDF for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

PDB for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

3D PDB for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

SMILES for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

INCHI for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

Structure for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)

3D Structure for NP0140007 (1-Cinnamoyl-3-hydroxypyrrolidine)