NP-MRD: Showing NP-Card for Erigerenone A (NP0072082)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 17:27:38 UTC

Updated at

2022-04-28 17:27:38 UTC

NP-MRD ID

NP0072082

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Erigerenone A

Description

(1R)-2-Oxo-4-methoxy-5alpha-[(Z)-1-propenyl]-3-cyclopentene-1beta-acetic acid methyl ester belongs to the class of organic compounds known as vinylogous esters. These are organic compounds containing an ester group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety. Erigerenone A is found in Erigeron philadelphicus L. Based on a literature review very few articles have been published on (1R)-2-Oxo-4-methoxy-5alpha-[(Z)-1-propenyl]-3-cyclopentene-1beta-acetic acid methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
   -2.9791    2.3150   -0.0653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9806    2.6090    0.9778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0260    1.7600    1.2034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7504    0.5128    0.5844 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5155   -0.0794   -0.4622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7835   -0.6117   -0.4186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0753   -1.9723   -0.2058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8058   -0.0679   -1.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4928    0.5500   -1.3519 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3106    1.0252   -2.1754 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    0.5297    0.1147 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4316   -0.7267    0.5292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8307   -0.7507    0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3571    0.2050   -0.5534 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6674   -1.8200    0.3822 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0090   -1.8801   -0.0101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8440    1.7297    0.3286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6079    2.0338   -1.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4858    3.3262   -0.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0520    3.5661    1.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3136    2.0671    2.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7198   -0.2705    1.4287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6631   -2.2769    0.7884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1857   -2.0616   -0.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6319   -2.5544   -1.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0861   -0.4353   -2.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2672    1.3959    0.4843 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9113   -1.6421    0.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4202   -0.7659    1.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6043   -2.2266    0.8491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3782   -0.8988   -0.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1137   -2.5844   -0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 13  1  0
 13 14  2  0
 13 12  1  0
 12 11  1  0
 11  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
 12 28  1  0
 12 29  1  0
 11 27  1  1
  4 22  1  1
  3 21  1  0
  2 20  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
M  END


  Mrv1652304282219272D          

 16 16  0  0  1  0            999 V2000
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0558    1.6913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4427    2.2433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8405    1.9462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0120    2.7532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0059   -1.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8264   -1.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2857   -0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 12  1  6  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0072082

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@@H]1[C@@H](\C=C/C)C(OC)=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H16O4/c1-4-5-8-9(6-12(14)16-3)10(13)7-11(8)15-2/h4-5,7-9H,6H2,1-3H3/b5-4-/t8-,9-/m1/s1

> <INCHI_KEY>
WEXBONOFEQOHQL-UVSMVFJQSA-N

> <FORMULA>
C12H16O4

> <MOLECULAR_WEIGHT>
224.256

> <EXACT_MASS>
224.104858995

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
23.289557355231032

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[(1R,2R)-3-methoxy-5-oxo-2-[(1Z)-prop-1-en-1-yl]cyclopent-3-en-1-yl]acetate

> <ALOGPS_LOGP>
1.66

> <JCHEM_LOGP>
1.0329178536666666

> <ALOGPS_LOGS>
-2.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.55897755677938

> <JCHEM_PKA_STRONGEST_BASIC>
-4.767974352110747

> <JCHEM_POLAR_SURFACE_AREA>
52.60000000000001

> <JCHEM_REFRACTIVITY>
61.937400000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.18e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1R,2R)-3-methoxy-5-oxo-2-[(1Z)-prop-1-en-1-yl]cyclopent-3-en-1-yl]acetate

> <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       1.060   2.080   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.060   3.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.651   1.651   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.971   3.157   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.826   4.188   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -3.436   3.633   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.756   5.139   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.615  -1.536   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.011  -2.943   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.543  -3.104   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.735  -1.536   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.267  -1.375   0.000  0.00  0.00           C+0
CONECT    1    2    3    6                                                  
CONECT    2    1                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6   12                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10                                                            
CONECT   12    5   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15    4   16                                                       
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

View in JSmol

Synonyms

Value	Source
(1R)-2-oxo-4-Methoxy-5a-[(Z)-1-propenyl]-3-cyclopentene-1b-acetate methyl ester	Generator
(1R)-2-oxo-4-Methoxy-5a-[(Z)-1-propenyl]-3-cyclopentene-1b-acetic acid methyl ester	Generator
(1R)-2-oxo-4-Methoxy-5alpha-[(Z)-1-propenyl]-3-cyclopentene-1beta-acetate methyl ester	Generator
(1R)-2-oxo-4-Methoxy-5α-[(Z)-1-propenyl]-3-cyclopentene-1β-acetate methyl ester	Generator
(1R)-2-oxo-4-Methoxy-5α-[(Z)-1-propenyl]-3-cyclopentene-1β-acetic acid methyl ester	Generator

Chemical Formula

C₁₂H₁₆O₄

Average Mass

224.2560 Da

Monoisotopic Mass

224.10486 Da

IUPAC Name

methyl 2-[(1R,2R)-3-methoxy-5-oxo-2-[(1Z)-prop-1-en-1-yl]cyclopent-3-en-1-yl]acetate

Traditional Name

methyl [(1R,2R)-3-methoxy-5-oxo-2-[(1Z)-prop-1-en-1-yl]cyclopent-3-en-1-yl]acetate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@@H]1[C@@H](\C=C/C)C(OC)=CC1=O

InChI Identifier

InChI=1S/C12H16O4/c1-4-5-8-9(6-12(14)16-3)10(13)7-11(8)15-2/h4-5,7-9H,6H2,1-3H3/b5-4-/t8-,9-/m1/s1

InChI Key

WEXBONOFEQOHQL-UVSMVFJQSA-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
Erigeron philadelphicus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as vinylogous esters. These are organic compounds containing an ester group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Vinylogous esters

Sub Class

Not Available

Direct Parent

Vinylogous esters

Alternative Parents

Substituents

Vinylogous ester
Methyl ester
Cyclic ketone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	1.66	ALOGPS
logP	1.03	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	16.56	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	61.94 m³·mol⁻¹	ChemAxon
Polarizability	23.29 Å³	ChemAxon
Number of Rings	1	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

9260583

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11085437

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Erigerenone A (NP0072082)

MOL for NP0072082 (Erigerenone A)

3D MOL for NP0072082 (Erigerenone A)

3D SDF for NP0072082 (Erigerenone A)

3D-SDF for NP0072082 (Erigerenone A)

PDB for NP0072082 (Erigerenone A)

3D PDB for NP0072082 (Erigerenone A)

SMILES for NP0072082 (Erigerenone A)

INCHI for NP0072082 (Erigerenone A)

Structure for NP0072082 (Erigerenone A)

3D Structure for NP0072082 (Erigerenone A)