NP-MRD: Showing NP-Card for yunngnin A (NP0028067)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-06-19 20:03:21 UTC

Updated at

2021-06-29 23:54:36 UTC

NP-MRD ID

NP0028067

Secondary Accession Numbers

None

Natural Product Identification

Common Name

yunngnin A

Provided By

JEOL Database JEOL Logo

Description

yunngnin A is found in Heracleum yunngningense. yunngnin A was first documented in 2005 (Taniguchi, M., et al.). Based on a literature review very few articles have been published on 7-hydroxy-5,6-dimethoxy-2-oxo-2H-chromene-8-carbaldehyde.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192122033D          

 28 29  0  0  0  0            999 V2000
   -1.1295   -0.5118   -5.3017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2214   -0.5094   -4.3812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7748   -0.2178   -3.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2387   -1.2382   -2.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1796   -2.5057   -2.8415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7789   -0.9470   -1.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2064   -2.0049   -0.1705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1276   -3.1605   -0.5798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8624    0.3670   -0.5526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3790    0.6476    0.7471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4198    1.9204    1.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0005    2.1573    2.4262 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9965    2.9795    0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4612    2.7398   -0.7668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4104    1.3928   -1.3308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8994    1.0895   -2.6132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4176    2.1285   -3.3492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7120    1.8580   -3.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4343   -1.3328   -5.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5989    0.4470   -5.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5403   -0.6579   -6.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8009   -3.1127   -2.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447   -1.7301    0.8374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0224    3.9703    0.8998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8800    3.5427   -1.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6238    1.4960   -4.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2903    1.1569   -3.2761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2612    2.8043   -3.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15  9  1  0  0  0  0
 11 12  2  0  0  0  0
 16 17  1  0  0  0  0
  4  6  1  0  0  0  0
 17 18  1  0  0  0  0
  6  9  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  2  0  0  0  0
  2  1  1  0  0  0  0
 15 16  2  0  0  0  0
  4  5  1  0  0  0  0
 16  3  1  0  0  0  0
  6  7  1  0  0  0  0
 15 14  1  0  0  0  0
  7 23  1  0  0  0  0
  9 10  1  0  0  0  0
  7  8  2  0  0  0  0
 13 24  1  0  0  0  0
 14 25  1  0  0  0  0
 18 26  1  0  0  0  0
 18 27  1  0  0  0  0
 18 28  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
M  END


  Mrv1652306192122033D          

 28 29  0  0  0  0            999 V2000
   -1.1295   -0.5118   -5.3017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2214   -0.5094   -4.3812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7748   -0.2178   -3.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2387   -1.2382   -2.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1796   -2.5057   -2.8415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7789   -0.9470   -1.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2064   -2.0049   -0.1705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1276   -3.1605   -0.5798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8624    0.3670   -0.5526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3790    0.6476    0.7471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4198    1.9204    1.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0005    2.1573    2.4262 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9965    2.9795    0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4612    2.7398   -0.7668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4104    1.3928   -1.3308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8994    1.0895   -2.6132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4176    2.1285   -3.3492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7120    1.8580   -3.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4343   -1.3328   -5.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5989    0.4470   -5.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5403   -0.6579   -6.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8009   -3.1127   -2.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447   -1.7301    0.8374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0224    3.9703    0.8998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8800    3.5427   -1.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6238    1.4960   -4.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2903    1.1569   -3.2761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2612    2.8043   -3.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15  9  1  0  0  0  0
 11 12  2  0  0  0  0
 16 17  1  0  0  0  0
  4  6  1  0  0  0  0
 17 18  1  0  0  0  0
  6  9  2  0  0  0  0
  3  2  1  0  0  0  0
  3  4  2  0  0  0  0
  2  1  1  0  0  0  0
 15 16  2  0  0  0  0
  4  5  1  0  0  0  0
 16  3  1  0  0  0  0
  6  7  1  0  0  0  0
 15 14  1  0  0  0  0
  7 23  1  0  0  0  0
  9 10  1  0  0  0  0
  7  8  2  0  0  0  0
 13 24  1  0  0  0  0
 14 25  1  0  0  0  0
 18 26  1  0  0  0  0
 18 27  1  0  0  0  0
 18 28  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0028067

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C2C([H])=C([H])C(=O)OC2=C1C([H])=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H10O6/c1-16-11-6-3-4-8(14)18-10(6)7(5-13)9(15)12(11)17-2/h3-5,15H,1-2H3

> <INCHI_KEY>
IVKYXTYKRIADDE-UHFFFAOYSA-N

> <FORMULA>
C12H10O6

> <MOLECULAR_WEIGHT>
250.206

> <EXACT_MASS>
250.047738042

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
23.409580651554666

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-hydroxy-5,6-dimethoxy-2-oxo-2H-chromene-8-carbaldehyde

> <ALOGPS_LOGP>
1.74

> <JCHEM_LOGP>
1.526954107

> <ALOGPS_LOGS>
-2.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.491619620031245

> <JCHEM_PKA_STRONGEST_BASIC>
-4.646893799072106

> <JCHEM_POLAR_SURFACE_AREA>
82.06000000000002

> <JCHEM_REFRACTIVITY>
63.03990000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-5,6-dimethoxy-2-oxochromene-8-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.129  -0.512  -5.302  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.221  -0.509  -4.381  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.775  -0.218  -3.115  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.239  -1.238  -2.316  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.180  -2.506  -2.841  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.779  -0.947  -1.026  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.206  -2.005  -0.171  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.128  -3.160  -0.580  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.862   0.367  -0.553  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.379   0.648   0.747  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.420   1.920   1.301  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.001   2.157   2.426  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.997   2.979   0.462  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.461   2.740  -0.767  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.410   1.393  -1.331  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.899   1.089  -2.613  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.418   2.128  -3.349  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.712   1.858  -3.889  0.00  0.00           C+0
HETATM   19  H   UNK     0      -0.434  -1.333  -5.099  0.00  0.00           H+0
HETATM   20  H   UNK     0      -0.599   0.447  -5.291  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.540  -0.658  -6.305  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.801  -3.113  -2.166  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.145  -1.730   0.837  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.022   3.970   0.900  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.880   3.543  -1.366  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.624   1.496  -4.917  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.290   1.157  -3.276  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.261   2.804  -3.918  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    3    1                                                       
CONECT    3    2    4   16                                                  
CONECT    4    6    3    5                                                  
CONECT    5    4   22                                                       
CONECT    6    4    9    7                                                  
CONECT    7    6   23    8                                                  
CONECT    8    7                                                            
CONECT    9   15    6   10                                                  
CONECT   10   11    9                                                       
CONECT   11   10   13   12                                                  
CONECT   12   11                                                            
CONECT   13   11   14   24                                                  
CONECT   14   13   15   25                                                  
CONECT   15    9   16   14                                                  
CONECT   16   17   15    3                                                  
CONECT   17   16   18                                                       
CONECT   18   17   26   27   28                                             
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    5                                                            
CONECT   23    7                                                            
CONECT   24   13                                                            
CONECT   25   14                                                            
CONECT   26   18                                                            
CONECT   27   18                                                            
CONECT   28   18                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₂H₁₀O₆

Average Mass

250.2060 Da

Monoisotopic Mass

250.04774 Da

IUPAC Name

7-hydroxy-5,6-dimethoxy-2-oxo-2H-chromene-8-carbaldehyde

Traditional Name

7-hydroxy-5,6-dimethoxy-2-oxochromene-8-carbaldehyde

CAS Registry Number

Not Available

SMILES

[H]OC1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C2C([H])=C([H])C(=O)OC2=C1C([H])=O

InChI Identifier

InChI=1S/C12H10O6/c1-16-11-6-3-4-8(14)18-10(6)7(5-13)9(15)12(11)17-2/h3-5,15H,1-2H3

InChI Key

IVKYXTYKRIADDE-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Heracleum yungningense	KNApSAcK Database	22123792
Heracleum yunngningense	JEOL database	Taniguchi, M., et al, Chem. Pharm. Bull. 53, 701 (2005)

Chemical Taxonomy

Description

This compound 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
Benzopyran
1-benzopyran
Anisole
Alkyl aryl ether
Pyranone
Aryl-aldehyde
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Lactone
Organoheterocyclic compound
Oxacycle
Ether
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aldehyde
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	1.74	ALOGPS
logP	1.53	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	7.49	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	63.04 m³·mol⁻¹	ChemAxon
Polarizability	23.41 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

C00031438

Chemspider ID

9520629

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11345691

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Taniguchi, M., et al. (2005). Taniguchi, M., et al, Chem. Pharm. Bull. 53, 701 (2005). Chem. Pharm. Bull..

Showing NP-Card for yunngnin A (NP0028067)

MOL for NP0028067 (yunngnin A)

3D MOL for NP0028067 (yunngnin A)

3D SDF for NP0028067 (yunngnin A)

3D-SDF for NP0028067 (yunngnin A)

PDB for NP0028067 (yunngnin A)

3D PDB for NP0028067 (yunngnin A)

SMILES for NP0028067 (yunngnin A)

INCHI for NP0028067 (yunngnin A)

Structure for NP0028067 (yunngnin A)

3D Structure for NP0028067 (yunngnin A)