NP-MRD: Showing NP-Card for (2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one (NP0240670)

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Record Information

Version

2.0

Created at

2022-09-07 00:33:13 UTC

Updated at

2022-09-07 00:33:13 UTC

NP-MRD ID

NP0240670

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one

Description

(2R,3R)-2-[(4E)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-2H,3H,4H-furo[2,3-b]chromen-4-one belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one). (2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one is found in Ferula fukanensis. Based on a literature review very few articles have been published on (2R,3R)-2-[(4E)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-2H,3H,4H-furo[2,3-b]chromen-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202332D          

 29 31  0  0  1  0            999 V2000
    3.6236    1.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390    1.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    0.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2259    2.0994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4413    1.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8282    2.3965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2698    1.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4851    0.7826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1280    1.3346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3136   -0.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9267   -0.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7552   -1.3834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7552   -2.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -1.1104    0.0000 O   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
    4.7812   -2.7604    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   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 O   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
    1.8532   -2.6029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5983   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 28 29  1  1  0  0  0
M  END

     RDKit          3D

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    3.3228    1.0090    1.4136 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309072202332D          

 29 31  0  0  1  0            999 V2000
    3.6236    1.8023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390    1.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    0.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2259    2.0994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4413    1.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8282    2.3965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2698    1.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4851    0.7826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1280    1.3346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3136   -0.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9267   -0.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7552   -1.3834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7552   -2.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -1.1104    0.0000 O   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
    4.7812   -2.7604    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
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  1  2  1  0  0  0  0
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  8  9  1  0  0  0  0
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 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
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M  END
> <DATABASE_ID>
NP0240670

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C2=C(O[C@]1(C)CCC\C(C)=C\C(=O)C=C(C)C)OC1=CC(O)=CC=C1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O5/c1-14(2)11-18(26)12-15(3)7-6-10-24(5)16(4)21-22(27)19-9-8-17(25)13-20(19)28-23(21)29-24/h8-9,11-13,16,25H,6-7,10H2,1-5H3/b15-12+/t16-,24-/m1/s1

> <INCHI_KEY>
NKADAHGDGPLCME-NDIQIQBTSA-N

> <FORMULA>
C24H28O5

> <MOLECULAR_WEIGHT>
396.483

> <EXACT_MASS>
396.193674002

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.7151270162535

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R)-2-[(4E)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-2H,3H,4H-furo[2,3-b]chromen-4-one

> <JCHEM_LOGP>
5.536521167333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.408271488389375

> <JCHEM_PKA_STRONGEST_BASIC>
-3.757161546385482

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
123.57579999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R)-2-[(4E)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       6.764   3.364   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.299   2.888   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.979   1.382   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.155   3.919   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.690   3.443   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.546   4.473   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.370   1.937   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.906   1.461   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.239   2.491   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.585  -0.046   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.730  -1.076   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.410  -2.582   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.554  -3.613   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.410  -4.643   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.459  -2.367   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.258  -2.073   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.591  -2.843   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.925  -2.073   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.259  -2.843   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.592  -2.073   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.259  -4.383   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.925  -5.153   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.591  -4.383   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.258  -5.153   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.258  -6.693   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.924  -4.383   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.459  -4.859   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.983  -6.323   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   28                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   18   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   16   28                                                  
CONECT   28   27   13   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈O₅

Average Mass

396.4830 Da

Monoisotopic Mass

396.19367 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1C2=C(O[C@]1(C)CCC\C(C)=C\C(=O)C=C(C)C)OC1=CC(O)=CC=C1C2=O

InChI Identifier

InChI=1S/C24H28O5/c1-14(2)11-18(26)12-15(3)7-6-10-24(5)16(4)21-22(27)19-9-8-17(25)13-20(19)28-23(21)29-24/h8-9,11-13,16,25H,6-7,10H2,1-5H3/b15-12+/t16-,24-/m1/s1

InChI Key

NKADAHGDGPLCME-NDIQIQBTSA-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
Ferula fukanensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarins and derivatives. These are polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Not Available

Direct Parent

Coumarins and derivatives

Alternative Parents

Substituents

Chromone
Coumarin
Aromatic monoterpenoid
Benzopyran
Monoterpenoid
1-benzopyran
Furopyran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Pyranone
Benzenoid
Pyran
Acryloyl-group
Heteroaromatic compound
Enone
Furan
Vinylogous ester
Alpha,beta-unsaturated ketone
Ketone
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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

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

13082519

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15939571

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one (NP0240670)

MOL for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

3D MOL for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

3D SDF for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

3D-SDF for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

PDB for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

3D PDB for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

SMILES for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

INCHI for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

Structure for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)

3D Structure for NP0240670 ((2r,3r)-2-[(4e)-4,8-dimethyl-6-oxonona-4,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-3h-furo[2,3-b]chromen-4-one)