NP-MRD: Showing NP-Card for 1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one (NP0144841)

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Record Information

Version

2.0

Created at

2022-09-01 23:54:51 UTC

Updated at

2022-09-01 23:54:52 UTC

NP-MRD ID

NP0144841

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one

Description

1-[6-Hydroxy-4-methoxy-4'-(propan-2-yl)-3H-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl]-3-phenylpropan-1-one belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position. 1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one is found in Piper aduncum. Based on a literature review very few articles have been published on 1-[6-hydroxy-4-methoxy-4'-(propan-2-yl)-3H-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl]-3-phenylpropan-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201542D          

 30 33  0  0  0  0            999 V2000
    5.6180    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7614   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6180   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7614   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4759   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1904   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1904   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4759   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7614   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6180    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6180    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8334    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3485    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9360   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1110   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6985    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8735    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4610   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4610    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1110    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9360    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8334   -0.2549    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
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  4  5  1  0  0  0  0
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M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
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   -0.6026   -2.3915    0.0572 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2549    2.4073   -0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309022201542D          

 30 33  0  0  0  0            999 V2000
    5.6180    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7614   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6180   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7614   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4759   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0144841

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C(C(=O)CCC2=CC=CC=C2)C2=C1CC1(CCC(C=C1)C(C)C)O2

> <INCHI_IDENTIFIER>
InChI=1S/C26H30O4/c1-17(2)19-11-13-26(14-12-19)16-20-23(29-3)15-22(28)24(25(20)30-26)21(27)10-9-18-7-5-4-6-8-18/h4-8,11,13,15,17,19,28H,9-10,12,14,16H2,1-3H3

> <INCHI_KEY>
NVHLTNASIPVGQS-UHFFFAOYSA-N

> <FORMULA>
C26H30O4

> <MOLECULAR_WEIGHT>
406.522

> <EXACT_MASS>
406.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.766696435594625

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[6-hydroxy-4-methoxy-4'-(propan-2-yl)-3H-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl]-3-phenylpropan-1-one

> <ALOGPS_LOGP>
5.52

> <JCHEM_LOGP>
6.416414379000001

> <ALOGPS_LOGS>
-5.89

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.866709572933207

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.40141426054014

> <JCHEM_PKA_STRONGEST_BASIC>
-4.608375949082197

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
119.56519999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.24e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-{6-hydroxy-4'-isopropyl-4-methoxy-3H-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-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  C   UNK     0      10.487   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.821   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.821   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.154   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.154   0.000   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      14.488  -0.770   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      11.821  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.821  -2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.487  -3.080   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      13.154  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.154  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.488  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.822  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.155  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.155  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.822  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.488  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.487   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.487   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.022   2.016   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.117   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.347  -0.564   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.807  -0.564   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.037   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.497   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.727  -0.564   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.727   2.104   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.807   2.104   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.347   2.104   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.022  -0.476   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   18                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    7   19   30                                                  
CONECT   19   18    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   29   30                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   24   29                                                       
CONECT   29   28   21                                                       
CONECT   30   21   18                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₀O₄

Average Mass

406.5220 Da

Monoisotopic Mass

406.21441 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C(C(=O)CCC2=CC=CC=C2)C2=C1CC1(CCC(C=C1)C(C)C)O2

InChI Identifier

InChI=1S/C26H30O4/c1-17(2)19-11-13-26(14-12-19)16-20-23(29-3)15-22(28)24(25(20)30-26)21(27)10-9-18-7-5-4-6-8-18/h4-8,11,13,15,17,19,28H,9-10,12,14,16H2,1-3H3

InChI Key

NVHLTNASIPVGQS-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
Piper aduncum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

2'-Hydroxy-dihydrochalcones

Alternative Parents

Substituents

2'-hydroxy-dihydrochalcone
Butyrophenone
Coumaran
Benzofuran
Anisole
Phenol ether
Aryl ketone
Aryl alkyl ketone
Alkyl aryl ether
Phenol
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Ketone
Oxacycle
Ether
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	5.52	ALOGPS
logS	-5.9	ALOGPS

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

74819289

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one (NP0144841)

MOL for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

3D MOL for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

3D SDF for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

3D-SDF for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

PDB for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

3D PDB for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

SMILES for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

INCHI for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

Structure for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)

3D Structure for NP0144841 (1-{6-hydroxy-4'-isopropyl-4-methoxy-3h-spiro[1-benzofuran-2,1'-cyclohexan]-2'-en-7-yl}-3-phenylpropan-1-one)