NP-MRD: Showing NP-Card for (1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate (NP0321247)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 23:21:31 UTC

Updated at

2022-09-11 23:21:31 UTC

NP-MRD ID

NP0321247

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate

Description

Diacetyldihydroterrein belongs to the class of organic compounds known as alpha-acyloxy ketones. These are ketones that have an acyloxy substituent alpha to the carbonyl group. They have the general structure R4C(=O)OC(R2)(R3)C(R1)=O (R1=organyl, R4=H or organyl; R2,R3 = any atom). (1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate is found in Aspergillus stellatus. Based on a literature review very few articles have been published on Diacetyldihydroterrein.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 33  0  0  0  0  0  0  0  0999 V2000
    3.6261   -1.4315    0.9689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6422   -0.1755    0.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3995    0.6272    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2498   -0.1420   -0.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2812   -1.3565   -0.8678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0752   -1.7651   -1.3139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3798   -2.5758   -2.1884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9320   -0.9142   -0.4014 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2524   -0.8503   -0.8504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3090   -1.3575   -0.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7255   -1.2824   -0.6187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0214   -1.8916    0.9844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1590    0.3316   -0.4738 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4873    1.3522    0.3907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8537    2.6240    0.0869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1699    3.5806    1.1714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9155    2.9591   -1.1158 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0151   -2.3294    0.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6080   -1.6475    1.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2298   -1.2905    1.9233 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4732    0.4779    0.5563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9266   -0.3779   -0.9107 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2148    0.9282    1.2520 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4493    1.5669   -0.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1799   -1.9803   -0.9612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8683   -1.4145    0.5865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7947   -0.5067   -1.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9069   -2.2822   -1.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4210   -1.1795    0.2160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2461    0.7361   -1.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2682    3.7370    1.1627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8094    3.2477    2.1496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7001    4.5825    0.9898 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  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
  8 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 13  4  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  8 26  1  1
 11 27  1  0
 11 28  1  0
 11 29  1  0
 13 30  1  6
 16 31  1  0
 16 32  1  0
 16 33  1  0
M  END


  Mrv1652309122201212D          

 17 17  0  0  1  0            999 V2000
   -0.8612    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   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
    1.4652   -0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 O   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
   -0.4790   -2.2438    0.0000 O   0  0  0  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 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4974    0.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259   -0.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2820    0.5872    0.0000 O   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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0321247

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1=CC(=O)[C@H](OC(C)=O)[C@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H16O5/c1-4-5-9-6-10(15)12(17-8(3)14)11(9)16-7(2)13/h6,11-12H,4-5H2,1-3H3/t11-,12-/m0/s1

> <INCHI_KEY>
WLSDLBZHCOHBHX-RYUDHWBXSA-N

> <FORMULA>
C12H16O5

> <MOLECULAR_WEIGHT>
240.255

> <EXACT_MASS>
240.099773615

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
24.455812985267432

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate

> <JCHEM_LOGP>
1.2661364440000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.98546032325341

> <JCHEM_PKA_STRONGEST_BASIC>
-6.4608253604202

> <JCHEM_POLAR_SURFACE_AREA>
69.67000000000002

> <JCHEM_REFRACTIVITY>
59.226400000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate

> <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      -1.608   3.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.735  -1.536   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.615  -1.536   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.011  -2.943   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.543  -3.104   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.894  -4.188   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.651   1.651   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.795   0.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.475  -0.886   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.260   1.096   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   13                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8    4   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₁₆O₅

Average Mass

240.2550 Da

Monoisotopic Mass

240.09977 Da

IUPAC Name

(1R,2S)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate

Traditional Name

(1R,2S)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

CCCC1=CC(=O)[C@H](OC(C)=O)[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C12H16O5/c1-4-5-9-6-10(15)12(17-8(3)14)11(9)16-7(2)13/h6,11-12H,4-5H2,1-3H3/t11-,12-/m0/s1

InChI Key

WLSDLBZHCOHBHX-RYUDHWBXSA-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
Aspergillus stellatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha-acyloxy ketones. These are ketones that have an acyloxy substituent alpha to the carbonyl group. They have the general structure R4C(=O)OC(R2)(R3)C(R1)=O (R1=organyl, R4=H or organyl; R2,R3 = any atom).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alpha-acyloxy ketones

Alternative Parents

Substituents

Alpha-acyloxy ketone
Dicarboxylic acid or derivatives
Cyclic ketone
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
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	1.27	ChemAxon
pKa (Strongest Acidic)	11.99	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	69.67 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	59.23 m³·mol⁻¹	ChemAxon
Polarizability	24.46 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

9921429

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11746725

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate (NP0321247)

MOL for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

3D MOL for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

3D SDF for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

3D-SDF for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

PDB for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

3D PDB for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

SMILES for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

INCHI for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

Structure for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)

3D Structure for NP0321247 ((1r,2s)-2-(acetyloxy)-5-oxo-3-propylcyclopent-3-en-1-yl acetate)