NP-MRD: Showing NP-Card for 4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one (NP0222659)

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Record Information

Version

2.0

Created at

2022-09-06 00:33:02 UTC

Updated at

2022-09-06 00:33:02 UTC

NP-MRD ID

NP0222659

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

Description

(S)-Angelicain belongs to the class of organic compounds known as furanochromones. These are polycyclic aromatic compounds containing a furan ring fused to a 1-benzopyran-4-one ring system (S)-Angelicain is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, (S)-Angelicain has been detected, but not quantified in, a few different foods, such as fats and oils, green vegetables, and herbs and spices. 4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one is found in Actaea cimicifuga. This could make (S)-angelicain a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
   -4.4946    1.6934    0.3160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9132    0.3184    0.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2715   -0.3488   -1.0054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4950   -0.4243    1.3264 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4350    0.3610    0.5560 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7905   -0.9839    0.5503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3524   -0.6305    0.2763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3923    0.6230   -0.3001 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8261    1.2073   -0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0293    0.5650   -0.4594 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1819    1.0842   -0.7879 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3364    0.4900   -0.6020 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5756    1.2185   -1.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6717    0.4052   -0.7425 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3895   -0.7484   -0.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2254   -1.3668    0.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2345   -2.5026    0.8661 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0465   -0.6899    0.1195 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8467   -1.2674    0.4786 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8698   -2.5223    1.0570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7049    1.0718   -0.4067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5831    1.6934    0.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0585    2.2124    1.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2763    2.2610   -0.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208   -1.4670   -0.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6326   -0.0341   -1.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3296   -0.0436   -1.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8917   -1.1958    1.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2893    0.8692    1.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1548   -1.6100   -0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8663   -1.5041    1.5117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8658    2.1909   -1.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5551    1.4411   -2.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6345    2.1888   -0.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6182   -0.3662   -1.3726 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3450   -1.2310    0.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0004   -2.9578    1.3250 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7 19  2  0
 19 20  1  0
 19 18  1  0
 18 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  2  0
 15 16  1  0
 16 17  2  0
 10  9  1  0
  9  8  2  0
  8 21  1  0
 21  5  1  0
  8  7  1  0
 16 18  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  0
  6 31  1  0
 20 37  1  0
 13 33  1  0
 13 34  1  0
 14 35  1  0
 15 36  1  0
  9 32  1  0
M  END


  Mrv0541 02241218202D          

 21 23  0  0  0  0            999 V2000
   -1.4846   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7421    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0004   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6596    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4846   -0.2471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9796    0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4846    1.0721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6596    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0004    1.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7421    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4846    1.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2271    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8871    1.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6296    0.8246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6296    0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8046    0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8046   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2271    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4846   -1.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0004   -1.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8046    1.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  2  0  0  0  0
  2  3  1  0  0  0  0
  2 10  2  0  0  0  0
  3  4  2  0  0  0  0
  3 20  1  0  0  0  0
  4  5  1  0  0  0  0
  4  8  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6 16  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  1  0  0  0  0
 12 13  1  0  0  0  0
 12 18  2  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0222659

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)C1CC2=C(O)C3=C(OC(CO)=CC3=O)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C15H16O6/c1-15(2,19)12-4-8-10(21-12)5-11-13(14(8)18)9(17)3-7(6-16)20-11/h3,5,12,16,18-19H,4,6H2,1-2H3

> <INCHI_KEY>
FHCHSXPHLRBEBR-UHFFFAOYSA-N

> <FORMULA>
C15H16O6

> <MOLECULAR_WEIGHT>
292.2839

> <EXACT_MASS>
292.094688244

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
30.024818102338457

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one

> <ALOGPS_LOGP>
1.33

> <JCHEM_LOGP>
1.1201119726666668

> <ALOGPS_LOGS>
-2.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.887851963501571

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.73913593325781

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0834446583868402

> <JCHEM_POLAR_SURFACE_AREA>
96.22

> <JCHEM_REFRACTIVITY>
75.4241

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.63e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2H,3H-furo[3,2-g]chromen-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -2.771  -0.769   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.385   0.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.001  -0.769   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.231   0.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.771  -0.461   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.695   0.769   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.771   2.001   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.231   1.539   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.001   2.309   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.385   1.539   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.771   2.309   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.157   1.539   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.389   2.309   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.775   1.539   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.775   0.769   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.235   0.769   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.235  -0.769   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.157   0.001   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.771  -2.309   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.001  -2.309   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.235   2.309   0.000  0.00  0.00           O+0
CONECT    1    2   18   19                                                  
CONECT    2    1    3   10                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   16                                                  
CONECT    7    6    8                                                       
CONECT    8    4    7    9                                                  
CONECT    9    8   10                                                       
CONECT   10    2    9   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   16                                                            
CONECT   16    6   15   17   21                                             
CONECT   17   16                                                            
CONECT   18    1   12                                                       
CONECT   19    1                                                            
CONECT   20    3                                                            
CONECT   21   16                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₆O₆

Average Mass

292.2839 Da

Monoisotopic Mass

292.09469 Da

IUPAC Name

4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one

Traditional Name

4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2H,3H-furo[3,2-g]chromen-5-one

CAS Registry Number

Not Available

SMILES

CC(C)(O)C1CC2=C(O)C3=C(OC(CO)=CC3=O)C=C2O1

InChI Identifier

InChI=1S/C15H16O6/c1-15(2,19)12-4-8-10(21-12)5-11-13(14(8)18)9(17)3-7(6-16)20-11/h3,5,12,16,18-19H,4,6H2,1-2H3

InChI Key

FHCHSXPHLRBEBR-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
Actaea cimicifuga	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanochromones. These are polycyclic aromatic compounds containing a furan ring fused to a 1-benzopyran-4-one ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Furanochromones

Alternative Parents

Substituents

Furanochromone
Coumaran
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Tertiary alcohol
Ether
Oxacycle
Alcohol
Aromatic alcohol
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	1.33	ALOGPS
logP	1.12	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	8.74	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	75.42 m³·mol⁻¹	ChemAxon
Polarizability	30.02 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

HMDB ID

HMDB0030120

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB001921

KNApSAcK ID

Not Available

Chemspider ID

9197863

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11022681

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one (NP0222659)

MOL for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D MOL for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D SDF for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D-SDF for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

PDB for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D PDB for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

SMILES for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

INCHI for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

Structure for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D Structure for NP0222659 (4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)