NP-MRD: Showing NP-Card for Quinoline-2-methanol (NP0023934)

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Record Information

Version

2.0

Created at

2021-01-06 08:57:24 UTC

Updated at

2021-07-15 17:43:05 UTC

NP-MRD ID

NP0023934

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Quinoline-2-methanol

Provided By

NPAtlas

Description

2-Quinolinylmethanol belongs to the class of organic compounds known as quinolines and derivatives. Quinolines and derivatives are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. Quinoline-2-methanol is found in Streptomyces. Quinoline-2-methanol was first documented in 1976 (PMID: 993116). Based on a literature review very few articles have been published on 2-Quinolinylmethanol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242121043D          

 21 22  0  0  0  0            999 V2000
    3.7619    0.9328    0.3668 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0383    0.6888   -0.7981 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6628    0.1704   -0.4745 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4834   -1.1922   -0.3575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2108   -1.6336   -0.0603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8481   -0.7673    0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1229   -1.2024    0.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1320   -0.2748    0.5748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9292    1.0844    0.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6494    1.5042    0.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6232    0.5938   -0.0109 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6368    1.0099   -0.3040 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2778    0.5958    1.1586 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5625   -0.0821   -1.3950 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9242    1.6313   -1.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3227   -1.8855   -0.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0666   -2.6890    0.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3136   -2.2616    0.5149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1395   -0.6150    0.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7306    1.8087    0.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4594    2.5837    0.0526 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
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  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
 12  3  1  0  0  0  0
 11  6  1  0  0  0  0
  1 13  1  0  0  0  0
  2 14  1  0  0  0  0
  2 15  1  0  0  0  0
  4 16  1  0  0  0  0
  5 17  1  0  0  0  0
  7 18  1  0  0  0  0
  8 19  1  0  0  0  0
  9 20  1  0  0  0  0
 10 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0023934

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])C1=C([H])C([H])=C2C([H])=C([H])C([H])=C([H])C2=N1

> <INCHI_IDENTIFIER>
InChI=1S/C10H9NO/c12-7-9-6-5-8-3-1-2-4-10(8)11-9/h1-6,12H,7H2

> <INCHI_KEY>
HREHOXSRYOZKNT-UHFFFAOYSA-N

> <FORMULA>
C10H9NO

> <MOLECULAR_WEIGHT>
159.188

> <EXACT_MASS>
159.068413914

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
21

> <JCHEM_AVERAGE_POLARIZABILITY>
17.105415111322383

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(quinolin-2-yl)methanol

> <ALOGPS_LOGP>
1.63

> <JCHEM_LOGP>
1.445022594333333

> <ALOGPS_LOGS>
-1.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.24755444456384

> <JCHEM_PKA_STRONGEST_BASIC>
4.094978300704355

> <JCHEM_POLAR_SURFACE_AREA>
33.120000000000005

> <JCHEM_REFRACTIVITY>
46.272999999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.96e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
quinolin-2-ylmethanol

> <JCHEM_VEBER_RULE>
1

$$$$

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  O   UNK     0       3.762   0.933   0.367  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.038   0.689  -0.798  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.663   0.170  -0.475  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.483  -1.192  -0.358  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.211  -1.634  -0.060  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.848  -0.767   0.116  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.123  -1.202   0.413  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.132  -0.275   0.575  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.929   1.084   0.453  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.649   1.504   0.156  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.623   0.594  -0.011  0.00  0.00           C+0
HETATM   12  N   UNK     0       0.637   1.010  -0.304  0.00  0.00           N+0
HETATM   13  H   UNK     0       3.278   0.596   1.159  0.00  0.00           H+0
HETATM   14  H   UNK     0       3.563  -0.082  -1.395  0.00  0.00           H+0
HETATM   15  H   UNK     0       2.924   1.631  -1.331  0.00  0.00           H+0
HETATM   16  H   UNK     0       2.323  -1.886  -0.497  0.00  0.00           H+0
HETATM   17  H   UNK     0       0.067  -2.689   0.032  0.00  0.00           H+0
HETATM   18  H   UNK     0      -2.314  -2.262   0.515  0.00  0.00           H+0
HETATM   19  H   UNK     0      -4.139  -0.615   0.810  0.00  0.00           H+0
HETATM   20  H   UNK     0      -3.731   1.809   0.582  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.459   2.584   0.053  0.00  0.00           H+0
CONECT    1    2   13                                                       
CONECT    2    1    3   14   15                                             
CONECT    3    2    4   12                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9   19                                                  
CONECT    9    8   10   20                                                  
CONECT   10    9   11   21                                                  
CONECT   11   10   12    6                                                  
CONECT   12   11    3                                                       
CONECT   13    1                                                            
CONECT   14    2                                                            
CONECT   15    2                                                            
CONECT   16    4                                                            
CONECT   17    5                                                            
CONECT   18    7                                                            
CONECT   19    8                                                            
CONECT   20    9                                                            
CONECT   21   10                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol View NMR Assignments

Synonyms

Value	Source
2-Hydroxymethylquinoline	HMDB

Chemical Formula

C₁₀H₉NO

Average Mass

159.1880 Da

Monoisotopic Mass

159.06841 Da

IUPAC Name

(quinolin-2-yl)methanol

Traditional Name

quinolin-2-ylmethanol

CAS Registry Number

Not Available

SMILES

OCC1=NC2=CC=CC=C2C=C1

InChI Identifier

InChI=1S/C10H9NO/c12-7-9-6-5-8-3-1-2-4-10(8)11-9/h1-6,12H,7H2

InChI Key

HREHOXSRYOZKNT-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
Streptomyces	NPAtlas	993116

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolines and derivatives. Quinolines and derivatives are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Not Available

Direct Parent

Quinolines and derivatives

Alternative Parents

Not Available

Substituents

Not Available

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	1.63	ALOGPS
logP	1.45	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	14.25	ChemAxon
pKa (Strongest Basic)	4.09	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	33.12 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	46.27 m³·mol⁻¹	ChemAxon
Polarizability	17.11 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA021438

HMDB ID

HMDB0245312

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

65957

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73196

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Omura S, Iwai Y, Suzuki Y, Awaya J, Konda Y: Production of quinoline-2-methanol and quinoline-2-methanol acetate by a new species of Kitasatoa Kitasato griseophaeus. J Antibiot (Tokyo). 1976 Aug;29(8):797-803. doi: 10.7164/antibiotics.29.797. [PubMed:993116 ]

Showing NP-Card for Quinoline-2-methanol (NP0023934)

MOL for NP0023934 (Quinoline-2-methanol)

3D MOL for NP0023934 (Quinoline-2-methanol)

3D SDF for NP0023934 (Quinoline-2-methanol)

3D-SDF for NP0023934 (Quinoline-2-methanol)

PDB for NP0023934 (Quinoline-2-methanol)

3D PDB for NP0023934 (Quinoline-2-methanol)

SMILES for NP0023934 (Quinoline-2-methanol)

INCHI for NP0023934 (Quinoline-2-methanol)

Structure for NP0023934 (Quinoline-2-methanol)

3D Structure for NP0023934 (Quinoline-2-methanol)