NP-MRD: Showing NP-Card for Hanabiratakelide C (NP0009387)

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Record Information

Version

2.0

Created at

2020-12-09 06:47:06 UTC

Updated at

2021-07-15 17:03:07 UTC

NP-MRD ID

NP0009387

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Hanabiratakelide C

Provided By

NPAtlas

Description

4,5,6-Trihydroxy-7-methoxy-1,3-dihydro-2-benzofuran-1-one belongs to the class of organic compounds known as gallic acid and derivatives. Gallic acid and derivatives are compounds containing a 3,4,5-trihydroxybenzoic acid moiety. Hanabiratakelide C is found in Sparassis crispa. Based on a literature review very few articles have been published on 4,5,6-trihydroxy-7-methoxy-1,3-dihydro-2-benzofuran-1-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106353D          

 23 24  0  0  0  0            999 V2000
    3.2571   -0.5901    0.3345 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725   -0.5398   -0.6545 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9638   -0.1090   -0.4418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6120    1.2096   -0.5944 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5682    2.1529   -0.9693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6863    1.6650   -0.3882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0152    3.0031   -0.5492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6325    0.7423   -0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9399    1.1060    0.2052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3345   -0.6053    0.1505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0415   -1.0032   -0.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0370   -2.4310    0.1672 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1021   -3.1428    0.0570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2219   -2.8677    0.5204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1292   -1.7946    0.5328 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9817    0.2464    0.1140 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8466   -0.4150    1.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8208   -1.5637    0.2653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3413    3.1302   -1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9479    3.3485   -0.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3468    2.0142    0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5593   -1.6153    1.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9481   -1.9409   -0.1993 H   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
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11  3  1  0  0  0  0
 15 10  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  5 19  1  0  0  0  0
  7 20  1  0  0  0  0
  9 21  1  0  0  0  0
 15 22  1  0  0  0  0
 15 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0009387

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(O[H])C(O[H])=C(OC([H])([H])[H])C2=C1C([H])([H])OC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C9H8O6/c1-14-8-4-3(2-15-9(4)13)5(10)6(11)7(8)12/h10-12H,2H2,1H3

> <INCHI_KEY>
QLTQFCMMGBXFCE-UHFFFAOYSA-N

> <FORMULA>
C9H8O6

> <MOLECULAR_WEIGHT>
212.157

> <EXACT_MASS>
212.032087978

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
23

> <JCHEM_AVERAGE_POLARIZABILITY>
18.87036559423911

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,5,6-trihydroxy-7-methoxy-1,3-dihydro-2-benzofuran-1-one

> <ALOGPS_LOGP>
0.72

> <JCHEM_LOGP>
0.45958285066666665

> <ALOGPS_LOGS>
-1.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.058743542868607

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.035241470513053

> <JCHEM_PKA_STRONGEST_BASIC>
-4.953972629987898

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
49.043800000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.16e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5,6-trihydroxy-7-methoxy-3H-2-benzofuran-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       3.257  -0.590   0.335  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.272  -0.540  -0.655  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.964  -0.109  -0.442  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.612   1.210  -0.594  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.568   2.153  -0.969  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.686   1.665  -0.388  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.015   3.003  -0.549  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.633   0.742  -0.019  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.940   1.106   0.205  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.335  -0.605   0.151  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.042  -1.003  -0.065  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.037  -2.431   0.167  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.102  -3.143   0.057  0.00  0.00           O+0
HETATM   14  O   UNK     0      -1.222  -2.868   0.520  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.129  -1.795   0.533  0.00  0.00           C+0
HETATM   16  H   UNK     0       3.982   0.246   0.114  0.00  0.00           H+0
HETATM   17  H   UNK     0       2.847  -0.415   1.335  0.00  0.00           H+0
HETATM   18  H   UNK     0       3.821  -1.564   0.265  0.00  0.00           H+0
HETATM   19  H   UNK     0       1.341   3.130  -1.090  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.948   3.349  -0.404  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.347   2.014   0.136  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.559  -1.615   1.556  0.00  0.00           H+0
HETATM   23  H   UNK     0      -2.948  -1.941  -0.199  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4   19                                                       
CONECT    6    4    7    8                                                  
CONECT    7    6   20                                                       
CONECT    8    6    9   10                                                  
CONECT    9    8   21                                                       
CONECT   10    8   11   15                                                  
CONECT   11   10   12    3                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   10   22   23                                             
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    5                                                            
CONECT   20    7                                                            
CONECT   21    9                                                            
CONECT   22   15                                                            
CONECT   23   15                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₉H₈O₆

Average Mass

212.1570 Da

Monoisotopic Mass

212.03209 Da

IUPAC Name

4,5,6-trihydroxy-7-methoxy-1,3-dihydro-2-benzofuran-1-one

Traditional Name

4,5,6-trihydroxy-7-methoxy-3H-2-benzofuran-1-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(O)=C(O)C2=C1C(=O)OC2

InChI Identifier

InChI=1S/C9H8O6/c1-14-8-4-3(2-15-9(4)13)5(10)6(11)7(8)12/h10-12H,2H2,1H3

InChI Key

QLTQFCMMGBXFCE-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Sparassis crispa	NPAtlas	20686231

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gallic acid and derivatives. Gallic acid and derivatives are compounds containing a 3,4,5-trihydroxybenzoic acid moiety.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Gallic acid and derivatives

Alternative Parents

Substituents

Gallic acid or derivatives
Isobenzofuranone
Phthalide
Isocoumaran
Anisole
Phenol ether
Alkyl aryl ether
Phenol
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
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	0.72	ALOGPS
logP	0.46	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	8.04	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	49.04 m³·mol⁻¹	ChemAxon
Polarizability	18.87 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

NPAtlas ID

NPA010831

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78434875

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46927894

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Hanabiratakelide C (NP0009387)

MOL for NP0009387 (Hanabiratakelide C)

3D MOL for NP0009387 (Hanabiratakelide C)

3D SDF for NP0009387 (Hanabiratakelide C)

3D-SDF for NP0009387 (Hanabiratakelide C)

PDB for NP0009387 (Hanabiratakelide C)

3D PDB for NP0009387 (Hanabiratakelide C)

SMILES for NP0009387 (Hanabiratakelide C)

INCHI for NP0009387 (Hanabiratakelide C)

Structure for NP0009387 (Hanabiratakelide C)

3D Structure for NP0009387 (Hanabiratakelide C)