NP-MRD: Showing NP-Card for 2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one (NP0162638)

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Record Information

Version

2.0

Created at

2022-09-02 21:04:45 UTC

Updated at

2022-09-02 21:04:45 UTC

NP-MRD ID

NP0162638

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one

Description

2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one is found in Peperomia alata.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
   -2.8073   -1.2378   -1.9052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0332   -0.7611   -0.7538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3436   -1.0141   -0.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7070   -0.0634    0.9591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5493    0.1708    1.9149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3026    0.4342    1.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2982    1.1768    1.8312 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0328    0.0199   -0.0529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7427    0.3663   -0.6508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0751    1.0543    0.0473 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2859   -0.0038   -1.9945 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8177   -1.0325   -1.9172 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9674   -0.4186   -1.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8692    0.3466   -1.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9464    0.9175   -1.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1849    0.7676    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2856    0.0063    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1941   -0.5775    0.1561 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7268   -0.0071    2.1080 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0893    0.4458    2.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1875    1.2324    0.9363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3850   -2.0674    0.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1003   -0.9179   -0.9373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5946   -0.4812    1.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9749    0.9163    0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7837    1.0897    2.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5418   -0.6958    2.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3734    1.4654    2.7997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0469   -0.2524   -2.7311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1641    0.9788   -2.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4985   -1.8973   -1.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0984   -1.4744   -2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    0.4778   -2.9856 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6530    1.5176   -1.8575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4911   -1.1806    0.7535 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2017    1.1152    2.9749 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7594   -0.4163    2.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 21  1  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  2  0
  8  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
 18 13  1  0
 17 16  1  0
  7 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  0
 20 36  1  0
 20 37  1  0
 18 35  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
M  END


  Mrv1652309022223042D          

 21 23  0  0  0  0            999 V2000
    6.9246    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  6  8  2  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0162638

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=C(C(=O)CCC2=CC=C3OCOC3=C2)C(=O)CCC1

> <INCHI_IDENTIFIER>
InChI=1S/C16H16O5/c17-11-2-1-3-12(18)16(11)13(19)6-4-10-5-7-14-15(8-10)21-9-20-14/h5,7-8,17H,1-4,6,9H2

> <INCHI_KEY>
AKVWKQWXOKLWDY-UHFFFAOYSA-N

> <FORMULA>
C16H16O5

> <MOLECULAR_WEIGHT>
288.299

> <EXACT_MASS>
288.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
29.89105448979666

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[3-(2H-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one

> <ALOGPS_LOGP>
1.57

> <JCHEM_LOGP>
2.4782739586666667

> <ALOGPS_LOGS>
-3.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.4782878253636325

> <JCHEM_PKA_STRONGEST_BASIC>
-4.740970617932946

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
76.10220000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[3-(2H-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0      12.926   5.923   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      12.926   4.383   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.260   3.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.260   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.926   1.303   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.592   2.073   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      10.259   1.303   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      11.592   3.613   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.259   4.383   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.259   5.923   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.925   3.613   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    2    9                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   13                                                       
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₆O₅

Average Mass

288.2990 Da

Monoisotopic Mass

288.09977 Da

IUPAC Name

2-[3-(2H-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one

Traditional Name

2-[3-(2H-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one

CAS Registry Number

Not Available

SMILES

OC1=C(C(=O)CCC2=CC=C3OCOC3=C2)C(=O)CCC1

InChI Identifier

InChI=1S/C16H16O5/c17-11-2-1-3-12(18)16(11)13(19)6-4-10-5-7-14-15(8-10)21-9-20-14/h5,7-8,17H,1-4,6,9H2

InChI Key

AKVWKQWXOKLWDY-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

Species Name	Source	Reference
Peperomia alata	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	1.57	ALOGPS
logP	2.48	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	4.48	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	76.1 m³·mol⁻¹	ChemAxon
Polarizability	29.89 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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one (NP0162638)

MOL for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

3D MOL for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

3D SDF for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

3D-SDF for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

PDB for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

3D PDB for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

SMILES for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

INCHI for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

Structure for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)

3D Structure for NP0162638 (2-[3-(2h-1,3-benzodioxol-5-yl)propanoyl]-3-hydroxycyclohex-2-en-1-one)