NP-MRD: Showing NP-Card for 9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one (NP0240094)

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Record Information

Version

2.0

Created at

2022-09-06 23:49:31 UTC

Updated at

2022-09-06 23:49:32 UTC

NP-MRD ID

NP0240094

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one

Description

ZINC14650630 belongs to the class of organic compounds known as 5-methoxypsoralens. These are psoralens containing a methoxy group attached at the C5 position of the psoralen group. Based on a literature review very few articles have been published on ZINC14650630.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    5.1453    1.6764    0.7131 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4920    0.5795    0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0586   -0.2998   -0.7019 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2334    0.2243    1.0234 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2719   -0.9819    1.7150 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0633    0.1343    0.0366 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9143   -0.0707    0.8245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3555   -0.2079    0.3495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8360   -1.4580    0.0327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3210   -2.6705    0.0803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1680   -3.5800   -0.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3482   -2.9675   -0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1380   -1.6255   -0.4574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9160   -0.4887   -0.6087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2100   -0.6875   -1.0995 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2648   -0.9181   -0.1746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4630    0.7806   -0.2997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2858    1.8718   -0.4724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8003    3.1366   -0.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5045    3.1797    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0282    4.3217    0.6244 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7550    2.1154    0.4708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544    0.8967    0.1870 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0812    1.9949    0.2678 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7275    2.3037    1.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6073    0.3580   -1.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7203   -1.0794   -0.2852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1956   -0.7959   -1.1908 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9360    1.0001    1.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3271   -1.7625    1.0927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2431   -0.7645   -0.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0092    1.0032   -0.6181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9338   -4.6545   -0.3683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2339   -3.4461   -1.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9197   -0.6303    0.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5502   -1.9790   -0.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1473   -0.3239   -0.4715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3010    1.7811   -0.8500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3914    4.0343   -0.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  8 23  1  0
 23 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 17 14  1  0
  9 13  1  0
 22 23  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 12 34  1  0
 11 33  1  0
  6 31  1  0
  6 32  1  0
  4 29  1  1
  5 30  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  1 24  1  0
  1 25  1  0
 18 38  1  0
 19 39  1  0
M  END


  Mrv1652309072201492D          

 23 25  0  0  1  0            999 V2000
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6018    2.0445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4222    2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7578    1.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
  8 23  1  0  0  0  0
 17 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0240094

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C=COC2=C(OC[C@@H](O)C(C)=C)C2=C1C=CC(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O6/c1-9(2)12(18)8-22-17-15-11(6-7-21-15)14(20-3)10-4-5-13(19)23-16(10)17/h4-7,12,18H,1,8H2,2-3H3/t12-/m1/s1

> <INCHI_KEY>
UBAMGTKSOKGECF-GFCCVEGCSA-N

> <FORMULA>
C17H16O6

> <MOLECULAR_WEIGHT>
316.309

> <EXACT_MASS>
316.094688235

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.943056573573955

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-{[(2S)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxy-7H-furo[3,2-g]chromen-7-one

> <JCHEM_LOGP>
1.971416637666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.838799406843645

> <JCHEM_PKA_STRONGEST_BASIC>
-2.86533944741498

> <JCHEM_POLAR_SURFACE_AREA>
78.13000000000001

> <JCHEM_REFRACTIVITY>
82.7233

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
9-{[(2S)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-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       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      12.323   3.816   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      13.855   3.977   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.481   2.570   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.670  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      16.004   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22    8   17                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₆O₆

Average Mass

316.3090 Da

Monoisotopic Mass

316.09469 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=C2C=COC2=C(OC[C@@H](O)C(C)=C)C2=C1C=CC(=O)O2

InChI Identifier

InChI=1S/C17H16O6/c1-9(2)12(18)8-22-17-15-11(6-7-21-15)14(20-3)10-4-5-13(19)23-16(10)17/h4-7,12,18H,1,8H2,2-3H3/t12-/m1/s1

InChI Key

UBAMGTKSOKGECF-GFCCVEGCSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 5-methoxypsoralens. These are psoralens containing a methoxy group attached at the C5 position of the psoralen group.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Furanocoumarins

Direct Parent

5-methoxypsoralens

Alternative Parents

Substituents

5-methoxypsoralen
Benzopyran
1-benzopyran
Benzofuran
Anisole
Phenol ether
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Furan
Lactone
Secondary alcohol
Organoheterocyclic compound
Ether
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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

28424414

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

92468407

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one (NP0240094)

MOL for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

3D MOL for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

3D SDF for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

3D-SDF for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

PDB for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

3D PDB for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

SMILES for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

INCHI for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

Structure for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)

3D Structure for NP0240094 (9-{[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]oxy}-4-methoxyfuro[3,2-g]chromen-7-one)