NP-MRD: Showing NP-Card for (7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid (NP0258296)

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Record Information

Version

2.0

Created at

2022-09-07 23:41:04 UTC

Updated at

2022-09-07 23:41:04 UTC

NP-MRD ID

NP0258296

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid

Description

SCHEMBL3267428 belongs to the class of organic compounds known as 7-hydroxycoumarins. These are coumarins that contain one or more hydroxyl groups attached to the C7 position the coumarin skeleton. (7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid is found in Pelargonium sidoides. Based on a literature review very few articles have been published on SCHEMBL3267428.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 32  0  0  0  0  0  0  0  0999 V2000
   -2.5660    2.8679   -0.7503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8877    1.7565   -1.2425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9245    1.0334   -0.5778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4162    1.3311   -0.6501 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8186    2.3959   -1.4181 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3656    0.5762    0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7085    0.8778   -0.0378 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7501    0.2261   -1.2084 S   0  0  0  0  0  6  0  0  0  0  0  0
    3.1673   -1.0445   -1.7839 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0227    1.1649   -2.3244 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2080   -0.1345   -0.4541 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9699   -0.4908    0.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8087   -1.2431    1.4804 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4437   -2.2616    2.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2966   -2.9657    2.8548 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1239   -2.6206    2.3390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8123   -1.8740    1.6593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3915   -0.8081    0.8927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3094   -0.0330    0.1934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6425   -0.3588    0.2881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1504   -1.2826   -0.6755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4958    2.5650   -0.2074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9140    3.3594    0.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8367    3.6067   -1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1494    2.9577   -1.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4652    0.5639    0.2057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1786   -3.4641    2.9492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8734   -2.0840    1.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3163   -1.9460   -1.0484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9093   -1.9463   -0.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5058   -0.7247   -1.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8 11  1  0
  8  9  2  0
  8 10  2  0
  6 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 19  3  1  0
 18 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 25  1  0
 11 26  1  0
 16 27  1  0
 17 28  1  0
 21 29  1  0
 21 30  1  0
 21 31  1  0
M  END


  Mrv1652309082201412D          

 21 22  0  0  0  0            999 V2000
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   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
    0.0000    0.0000    0.0000 O   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    1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    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 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
    4.2868   -0.0000    0.0000 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  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
  8 10  2  0  0  0  0
  8 11  1  0  0  0  0
  6 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258296

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C(OS(O)(=O)=O)=C2OC(=O)C=CC2=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C11H10O9S/c1-17-8-5-3-4-6(12)19-9(5)11(20-21(14,15)16)7(13)10(8)18-2/h3-4,13H,1-2H3,(H,14,15,16)

> <INCHI_KEY>
LAMLWTMHNFDLFG-UHFFFAOYSA-N

> <FORMULA>
C11H10O9S

> <MOLECULAR_WEIGHT>
318.25

> <EXACT_MASS>
318.004553076

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
27.276038832085483

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(7-hydroxy-5,6-dimethoxy-2-oxo-2H-chromen-8-yl)oxidanesulfonic acid

> <JCHEM_LOGP>
1.0355730943333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.348735523147258

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.529739237890456

> <JCHEM_PKA_STRONGEST_BASIC>
-4.537759340835712

> <JCHEM_POLAR_SURFACE_AREA>
128.59

> <JCHEM_REFRACTIVITY>
68.42860000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM    8  S   UNK     0       4.001   2.310   0.000  0.00  0.00           S+0
HETATM    9  O   UNK     0       4.771   0.976   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       3.231   3.644   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       5.335   3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8                                                            
CONECT   12    6   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12   19                                                  
CONECT   19   18    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₀O₉S

Average Mass

318.2500 Da

Monoisotopic Mass

318.00455 Da

IUPAC Name

(7-hydroxy-5,6-dimethoxy-2-oxo-2H-chromen-8-yl)oxidanesulfonic acid

Traditional Name

(7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(OS(O)(=O)=O)=C2OC(=O)C=CC2=C1OC

InChI Identifier

InChI=1S/C11H10O9S/c1-17-8-5-3-4-6(12)19-9(5)11(20-21(14,15)16)7(13)10(8)18-2/h3-4,13H,1-2H3,(H,14,15,16)

InChI Key

LAMLWTMHNFDLFG-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
Pelargonium sidoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-hydroxycoumarins. These are coumarins that contain one or more hydroxyl groups attached to the C7 position the coumarin skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Hydroxycoumarins

Direct Parent

7-hydroxycoumarins

Alternative Parents

Substituents

7-hydroxycoumarin
Arylsulfate
Benzopyran
1-benzopyran
Anisole
Phenol ether
Alkyl aryl ether
Pyranone
Phenol
Benzenoid
Sulfuric acid ester
Sulfate-ester
Sulfuric acid monoester
Pyran
Heteroaromatic compound
Organic sulfuric acid or derivatives
Lactone
Organoheterocyclic compound
Ether
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen 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	1.04	ChemAxon
pKa (Strongest Acidic)	-2.5	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	128.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	68.43 m³·mol⁻¹	ChemAxon
Polarizability	27.28 Å³	ChemAxon
Number of Rings	2	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25051520

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid (NP0258296)

MOL for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

3D MOL for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

3D SDF for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

3D-SDF for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

PDB for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

3D PDB for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

SMILES for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

INCHI for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

Structure for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)

3D Structure for NP0258296 ((7-hydroxy-5,6-dimethoxy-2-oxochromen-8-yl)oxidanesulfonic acid)