NP-MRD: Showing NP-Card for 4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol (NP0240461)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 00:17:10 UTC

Updated at

2022-09-07 00:17:10 UTC

NP-MRD ID

NP0240461

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol

Description

4-(4-Hydroxyphenyl)-3,4-dihydroquinoline-2,3,4-triol belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group. Based on a literature review very few articles have been published on 4-(4-hydroxyphenyl)-3,4-dihydroquinoline-2,3,4-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -2.2250    3.4793    0.3796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8162    2.1466    0.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7111    1.2750    0.3395 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4292   -0.1011    0.0908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4463   -1.0271    0.3988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1650   -2.3520    0.1704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9304   -2.7212   -0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9684   -1.8100   -0.6269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2195   -0.4500   -0.4073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1621    0.5253   -0.7412 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0020    0.4286   -2.1599 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1418    0.0711   -0.1642 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3380   -0.0688    1.1887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5702   -0.4912    1.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6055   -0.7735    0.7732 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8576   -1.2010    1.2181 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4182   -0.6370   -0.5728 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1749   -0.2127   -1.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4713    1.9149   -0.4459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2325    2.7371   -1.5772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7608    3.9175   -0.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3987   -0.7028    0.7950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8923   -3.1425    0.3790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7558   -3.7929   -0.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0145   -2.0670   -1.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6898    0.9378   -2.6263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5025    0.1622    1.8464 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167   -0.5988    2.7240 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5537   -0.4858    1.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2170   -0.8538   -1.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -0.1230   -2.1018 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2522    2.3363    0.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1756    3.6807   -1.2770 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 10 19  1  0
 18 12  1  0
  9  4  1  0
 20 33  1  0
 19 32  1  1
  1 21  1  0
  5 22  1  0
  6 23  1  0
  7 24  1  0
  8 25  1  0
 11 26  1  0
 13 27  1  0
 14 28  1  0
 16 29  1  0
 17 30  1  0
 18 31  1  0
M  END


  Mrv1652309072202172D          

 20 22  0  0  0  0            999 V2000
    0.0000    0.0000    0.0000 O   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 N   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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -2.2820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808   -3.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6505   -3.6892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1620   -3.5460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6923   -4.1779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4441   -2.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0862   -2.1387    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
    0.0000   -1.6500    0.0000 O   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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 10 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240461

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1C(O)=NC2=CC=CC=C2C1(O)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H13NO4/c17-10-7-5-9(6-8-10)15(20)11-3-1-2-4-12(11)16-14(19)13(15)18/h1-8,13,17-18,20H,(H,16,19)

> <INCHI_KEY>
KCCQWQGKTHFIKZ-UHFFFAOYSA-N

> <FORMULA>
C15H13NO4

> <MOLECULAR_WEIGHT>
271.272

> <EXACT_MASS>
271.084457903

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.862085529007494

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(4-hydroxyphenyl)-3,4-dihydroquinoline-2,3,4-triol

> <JCHEM_LOGP>
1.659970358666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.461725332357663

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.6594490427970805

> <JCHEM_PKA_STRONGEST_BASIC>
-0.26873850671994604

> <JCHEM_POLAR_SURFACE_AREA>
93.28000000000002

> <JCHEM_REFRACTIVITY>
74.3248

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-(4-hydroxyphenyl)-3H-quinoline-2,3,4-triol

> <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  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       2.667   0.000   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.657  -4.260   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.677  -4.260   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.204  -5.707   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.214  -6.887   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.302  -6.619   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.292  -7.799   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.829  -5.172   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.161  -3.992   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9   11   12   19                                             
CONECT   11   10                                                            
CONECT   12   10   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   12                                                       
CONECT   19   10    2   20                                                  
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₃NO₄

Average Mass

271.2720 Da

Monoisotopic Mass

271.08446 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1C(O)=NC2=CC=CC=C2C1(O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C15H13NO4/c17-10-7-5-9(6-8-10)15(20)11-3-1-2-4-12(11)16-14(19)13(15)18/h1-8,13,17-18,20H,(H,16,19)

InChI Key

KCCQWQGKTHFIKZ-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Phenylquinolines

Direct Parent

Phenylquinolines

Alternative Parents

Substituents

Phenylquinoline
Dihydroquinoline
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Cyclic carboximidic acid
Tertiary alcohol
1,2-diol
Secondary alcohol
Azacycle
Polyol
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic nitrogen compound
Alcohol
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

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

162842220

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol (NP0240461)

MOL for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

3D MOL for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

3D SDF for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

3D-SDF for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

PDB for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

3D PDB for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

SMILES for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

INCHI for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

Structure for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)

3D Structure for NP0240461 (4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol)