NP-MRD: Showing NP-Card for n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid (NP0141930)

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Record Information

Version

2.0

Created at

2022-09-01 20:21:26 UTC

Updated at

2022-09-01 20:21:26 UTC

NP-MRD ID

NP0141930

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid

Description

2,3-Dihydroxybenzoylputrescine belongs to the class of organic compounds known as salicylamides. These are carboxamide derivatives of salicylic acid. Salicylic acid is the ortho-hydroxylated derivative of benzoic acid. 2,3-Dihydroxybenzoylputrescine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
    5.4902   -0.6621   -0.3887 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0480   -0.5072   -0.4574 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5929    0.0974    0.8360 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0947    0.3073    0.8807 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3340   -0.9669    0.7237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1247   -0.7355    0.7756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7049    0.0521   -0.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0652    0.5232   -1.1376 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1262    0.3591   -0.2662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5747    1.1665   -1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9069    1.4774   -1.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7895    1.0158   -0.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3848    0.2238    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3120   -0.2149    1.4964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0215   -0.0974    0.6656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6683   -0.8829    1.7262 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9334    0.2055   -0.7665 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7771   -0.7333    0.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5624   -1.5156   -0.5808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8368    0.1414   -1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0825    1.0724    0.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8648   -0.6222    1.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8475    0.7181    1.9070 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7726    1.0481    0.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5948   -1.7160    1.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4811   -1.3958   -0.3011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6297   -1.1941    1.5813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8469    1.5119   -2.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2277    2.1104   -2.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8328    1.2791   -0.5637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0548   -0.7872    2.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1726   -1.2782    2.4554 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 15  9  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 14 31  1  0
 16 32  1  0
M  END


  Mrv1533004171508312D          

 16 16  0  0  0  0            999 V2000
    0.7145   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0141930

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NCCCCNC(=O)C1=CC=CC(O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C11H16N2O3/c12-6-1-2-7-13-11(16)8-4-3-5-9(14)10(8)15/h3-5,14-15H,1-2,6-7,12H2,(H,13,16)

> <INCHI_KEY>
FZYQWMMQZJYKMY-UHFFFAOYSA-N

> <FORMULA>
C11H16N2O3

> <MOLECULAR_WEIGHT>
224.26

> <EXACT_MASS>
224.116092383

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
24.120835843971477

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-(4-aminobutyl)-2,3-dihydroxybenzamide

> <ALOGPS_LOGP>
-0.34

> <JCHEM_LOGP>
-0.03170427777422858

> <ALOGPS_LOGS>
-2.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
11.924443365375538

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.298653373102592

> <JCHEM_PKA_STRONGEST_BASIC>
9.910820317160363

> <JCHEM_POLAR_SURFACE_AREA>
95.58

> <JCHEM_REFRACTIVITY>
61.45470000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.21e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-(4-aminobutyl)-2,3-dihydroxybenzamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  N   UNK     0       1.334  -6.930   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       8.002  -7.700   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.336 -10.010   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    9   16                                                  
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₆N₂O₃

Average Mass

224.2600 Da

Monoisotopic Mass

224.11609 Da

IUPAC Name

N-(4-aminobutyl)-2,3-dihydroxybenzamide

Traditional Name

N-(4-aminobutyl)-2,3-dihydroxybenzamide

CAS Registry Number

Not Available

SMILES

NCCCCNC(=O)C1=CC=CC(O)=C1O

InChI Identifier

InChI=1S/C11H16N2O3/c12-6-1-2-7-13-11(16)8-4-3-5-9(14)10(8)15/h3-5,14-15H,1-2,6-7,12H2,(H,13,16)

InChI Key

FZYQWMMQZJYKMY-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 salicylamides. These are carboxamide derivatives of salicylic acid. Salicylic acid is the ortho-hydroxylated derivative of benzoic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Salicylamides

Alternative Parents

Substituents

Salicylamide
Benzamide
Benzoyl
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Vinylogous acid
Amino acid or derivatives
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Organic oxide
Amine
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Primary amine
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	-0.34	ALOGPS
logP	-0.032	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	8.3	ChemAxon
pKa (Strongest Basic)	9.91	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	95.58 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	61.45 m³·mol⁻¹	ChemAxon
Polarizability	24.12 Å³	ChemAxon
Number of Rings	1	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

85550078

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid (NP0141930)

MOL for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

3D MOL for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

3D SDF for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

3D-SDF for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

PDB for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

3D PDB for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

SMILES for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

INCHI for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

Structure for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)

3D Structure for NP0141930 (n-(4-aminobutyl)-2,3-dihydroxybenzenecarboximidic acid)