NP-MRD: Showing NP-Card for (2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one (NP0228949)

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Record Information

Version

2.0

Created at

2022-09-06 08:48:35 UTC

Updated at

2022-09-06 08:48:35 UTC

NP-MRD ID

NP0228949

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

Description

Goniolactone F belongs to the class of organic compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. (2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one is found in Goniothalamus cheliensis. Based on a literature review very few articles have been published on Goniolactone F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062210482D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309062210482D          

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 17 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 12 24  1  0  0  0  0
 24 25  2  0  0  0  0
  6 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
  5 32  1  0  0  0  0
 33 32  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 38 37  1  6  0  0  0
  4 38  1  0  0  0  0
 33 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0228949

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)[C@H]1[C@H](O[C@@H]2CC(=O)O[C@H]12)[C@@H](OC1=CC(O)=C2C(=O)C[C@H](OC2=C1)C1=CC=CC=C1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H26O8/c1-16(31)26-29-24(15-25(34)38-29)37-30(26)28(18-10-6-3-7-11-18)35-19-12-20(32)27-21(33)14-22(36-23(27)13-19)17-8-4-2-5-9-17/h2-13,22,24,26,28-30,32H,14-15H2,1H3/t22-,24+,26+,28-,29-,30-/m0/s1

> <INCHI_KEY>
UBRQHXUVYDXHOP-FPZHPECOSA-N

> <FORMULA>
C30H26O8

> <MOLECULAR_WEIGHT>
514.53

> <EXACT_MASS>
514.162767797

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
52.09034695032739

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-7-[(S)-[(2S,3S,3aR,6aR)-3-acetyl-5-oxo-hexahydrofuro[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

> <JCHEM_LOGP>
4.715912232

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.06591518052642

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.671125704804254

> <JCHEM_PKA_STRONGEST_BASIC>
-4.0752289713534005

> <JCHEM_POLAR_SURFACE_AREA>
108.36000000000003

> <JCHEM_REFRACTIVITY>
134.13520000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-7-[(S)-[(2S,3S,3aR,6aR)-3-acetyl-5-oxo-tetrahydro-2H-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.986  -9.900   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.016  -8.756   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -7.523  -9.076   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -5.540  -7.291   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.446  -6.045   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.986  -6.045   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -8.756  -7.379   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0     -10.296  -7.379   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -11.066  -6.045   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -12.606  -6.045   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0     -13.376  -4.711   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0     -13.376  -7.379   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -12.606  -8.712   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -11.066  -8.712   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0     -13.376 -10.046   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0     -14.916 -10.046   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -15.686 -11.380   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -14.916 -12.713   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -15.686 -14.047   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -17.226 -14.047   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -17.996 -12.713   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -17.226 -11.380   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -15.686  -8.712   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -14.916  -7.379   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0     -15.686  -6.045   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -8.756  -4.711   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -10.296  -4.711   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -11.066  -3.378   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -10.296  -2.044   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.756  -2.044   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.986  -3.378   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -5.540  -4.799   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -4.076  -5.275   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.611  -4.799   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.706  -6.045   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.166  -6.045   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -2.611  -7.291   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -4.076  -6.815   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   38                                                  
CONECT    5    4    6   32                                                  
CONECT    6    5    7   26                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   24                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    8                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   16   24                                                       
CONECT   24   23   12   25                                                  
CONECT   25   24                                                            
CONECT   26    6   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
CONECT   32    5   33                                                       
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37    4   33                                                  
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₂₆O₈

Average Mass

514.5300 Da

Monoisotopic Mass

514.16277 Da

IUPAC Name

(2S)-7-[(S)-[(2S,3S,3aR,6aR)-3-acetyl-5-oxo-hexahydrofuro[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

(2S)-7-[(S)-[(2S,3S,3aR,6aR)-3-acetyl-5-oxo-tetrahydro-2H-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

CAS Registry Number

Not Available

SMILES

CC(=O)[C@H]1[C@H](O[C@@H]2CC(=O)O[C@H]12)[C@@H](OC1=CC(O)=C2C(=O)C[C@H](OC2=C1)C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C30H26O8/c1-16(31)26-29-24(15-25(34)38-29)37-30(26)28(18-10-6-3-7-11-18)35-19-12-20(32)27-21(33)14-22(36-23(27)13-19)17-8-4-2-5-9-17/h2-13,22,24,26,28-30,32H,14-15H2,1H3/t22-,24+,26+,28-,29-,30-/m0/s1

InChI Key

UBRQHXUVYDXHOP-FPZHPECOSA-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
Goniothalamus cheliensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

Flavanones

Alternative Parents

Substituents

5-hydroxyflavonoid
Hydroxyflavonoid
Flavanone
Chromone
Chromane
Benzopyran
1-benzopyran
Furofuran
Aryl alkyl ketone
Aryl ketone
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Gamma butyrolactone
Benzenoid
Vinylogous acid
Oxolane
Carboxylic acid ester
Lactone
Ketone
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Organooxygen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
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	4.72	ChemAxon
pKa (Strongest Acidic)	8.67	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	108.36 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	134.14 m³·mol⁻¹	ChemAxon
Polarizability	52.09 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00045979

Chemspider ID

8521841

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10346383

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one (NP0228949)

MOL for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D MOL for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D SDF for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D-SDF for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

PDB for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D PDB for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

SMILES for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

INCHI for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

Structure for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D Structure for NP0228949 ((2s)-7-[(s)-[(2s,3s,3ar,6ar)-3-acetyl-5-oxo-tetrahydro-2h-furo[3,2-b]furan-2-yl](phenyl)methoxy]-5-hydroxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)