NP-MRD: Showing NP-Card for (2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one (NP0246583)

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Record Information

Version

2.0

Created at

2022-09-07 08:06:25 UTC

Updated at

2022-09-07 08:06:25 UTC

NP-MRD ID

NP0246583

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

DTXSID90964182 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. (2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one is found in Ammi visnaga and Angelica japonica. Based on a literature review very few articles have been published on DTXSID90964182.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    5.7422    1.6144    0.1715 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4810    0.7998    0.1230 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5804   -0.5673    0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4178   -1.3419   -0.0459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4874   -2.5859   -0.1566 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2185   -0.6847    0.0339 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0294   -1.4060   -0.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9459   -2.7575   -0.1251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2095   -0.7396    0.0736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2157    0.6278    0.1940 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729    1.3240    0.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    0.6871    0.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3189    1.3876    0.1960 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5672    1.0240    0.2538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3410    0.0310   -0.3500 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7812    0.0532    0.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3878    1.3405   -0.4715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0488   -0.1037    1.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4208   -0.9880   -0.6517 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6252   -1.2320    0.0553 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0353    1.9074   -0.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5581    1.0675    0.6758 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5671    2.5572    0.7447 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5573   -1.0703   -0.0613 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5545   -3.5024   -0.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9871    2.4054    0.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2679    0.1537   -1.4500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1219    1.1836   -1.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5963    2.0509   -0.8462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9219    1.9033    0.3275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3313    0.4303    2.1279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0970   -1.1832    1.7618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0967    0.2767    1.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9504   -1.0813   -1.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7453   -1.9638   -0.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9363   -1.6181    1.0335 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 14  1  0
 14 15  1  0
 15 20  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 16 19  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13  2  1  0
 12  6  1  0
 20  9  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  3 24  1  0
  8 25  1  0
 15 27  1  6
 20 35  1  0
 20 36  1  0
 17 28  1  0
 17 29  1  0
 17 30  1  0
 18 31  1  0
 18 32  1  0
 18 33  1  0
 19 34  1  0
 11 26  1  0
M  END


  Mrv1652309072210062D          

 20 22  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -1.4924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8419   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6669   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4919   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6669   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6669   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -0.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 15 20  1  0  0  0  0
  9 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246583

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(=O)C2=C(O)C3=C(O[C@@H](C3)C(C)(C)O)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C15H16O5/c1-7-4-9(16)13-11(19-7)6-10-8(14(13)17)5-12(20-10)15(2,3)18/h4,6,12,17-18H,5H2,1-3H3/t12-/m0/s1

> <INCHI_KEY>
LJSWMDKKEBOERP-LBPRGKRZSA-N

> <FORMULA>
C15H16O5

> <MOLECULAR_WEIGHT>
276.288

> <EXACT_MASS>
276.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
29.13127119116809

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <JCHEM_LOGP>
2.1670219393333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.290081461378694

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.548995299994135

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1064372190017364

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
73.88040000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2H,3H-furo[3,2-g]chromen-5-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       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       8.133  -2.786   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.038  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.578  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.118  -1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.578  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.578  -0.000   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.133  -0.294   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   12                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   20                                                  
CONECT   10    9   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12    2                                                       
CONECT   14   10   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16                                                            
CONECT   20   15    9                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₆O₅

Average Mass

276.2880 Da

Monoisotopic Mass

276.09977 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)C2=C(O)C3=C(O[C@@H](C3)C(C)(C)O)C=C2O1

InChI Identifier

InChI=1S/C15H16O5/c1-7-4-9(16)13-11(19-7)6-10-8(14(13)17)5-12(20-10)15(2,3)18/h4,6,12,17-18H,5H2,1-3H3/t12-/m0/s1

InChI Key

LJSWMDKKEBOERP-LBPRGKRZSA-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
Ammi visnaga	LOTUS Database	35616633
Angelica japonica	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
Pyran
Benzenoid
Vinylogous acid
Tertiary alcohol
Heteroaromatic compound
Ether
Oxacycle
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organooxygen compound
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	2.17	ChemAxon
pKa (Strongest Acidic)	7.55	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	73.88 m³·mol⁻¹	ChemAxon
Polarizability	29.13 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

2340775

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3083595

PDB ID

Not Available

ChEBI ID

182467

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one (NP0246583)

MOL for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

3D MOL for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

3D SDF for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

3D-SDF for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

PDB for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

3D PDB for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

SMILES for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

INCHI for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

Structure for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)

3D Structure for NP0246583 ((2s)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methyl-2h,3h-furo[3,2-g]chromen-5-one)