NP-MRD: Showing NP-Card for 2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid (NP0184417)

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Record Information

Version

2.0

Created at

2022-09-03 23:32:30 UTC

Updated at

2022-09-03 23:32:31 UTC

NP-MRD ID

NP0184417

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid

Description

SCHEMBL16431143 belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review very few articles have been published on SCHEMBL16431143.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 37  0  0  0  0  0  0  0  0999 V2000
   -2.8207    1.7009    1.0033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0240    0.9555   -0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6660    1.6092   -1.4076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6369   -0.2981   -0.3504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9917   -0.9421    0.8237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155   -1.3993    0.4679 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4802   -0.6494    0.8816 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7729   -1.0183    0.5729 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.2297    1.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3640    0.8194    0.0162 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7175    0.3662   -1.2603 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3615    1.9101   -0.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9273    2.4492    0.9803 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962    2.3448   -1.3144 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9295   -2.1740   -0.1705 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8429   -2.9190   -0.5814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4587   -2.5501   -0.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5415   -3.3233   -0.6994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7444    1.8043    1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3325    1.2504    1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2013    2.7427    0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3970    1.0931   -2.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4389    2.6956   -1.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7685    1.4612   -1.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7773   -0.8769   -1.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9101   -0.1982    1.6391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6188   -1.8078    1.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3479    0.2554    1.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6505    0.3162    1.9443 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7964   -0.8786    1.3175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2763    1.3127    0.4711 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3841   -0.3798   -1.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4780    0.9357   -2.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3531    3.0256   -1.8927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9456   -2.4733   -0.4196 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9661   -3.8248   -1.1654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5004   -3.1057   -0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 14  1  0
 12 13  2  0
  8 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17  6  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  7 28  1  0
  9 29  1  0
  9 30  1  0
 10 31  1  1
 11 32  1  0
 11 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 18 37  1  0
M  END


  Mrv1652309042201322D          

 18 18  0  0  0  0            999 V2000
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   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
    2.8579    0.8250    0.0000 N   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
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    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
  2  4  2  0  0  0  0
  4  5  1  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  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
 12 14  1  0  0  0  0
  8 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184417

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=CC(CC(N)C(O)=O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C14H19NO3/c1-9(2)3-5-11-7-10(4-6-13(11)16)8-12(15)14(17)18/h3-4,6-7,12,16H,5,8,15H2,1-2H3,(H,17,18)

> <INCHI_KEY>
UFFPHPAGEHMRFF-UHFFFAOYSA-N

> <FORMULA>
C14H19NO3

> <MOLECULAR_WEIGHT>
249.31

> <EXACT_MASS>
249.136493476

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
27.709392851306962

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid

> <JCHEM_LOGP>
0.23990990307770094

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.073775295830483

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9098525878049406

> <JCHEM_PKA_STRONGEST_BASIC>
9.697002029160535

> <JCHEM_POLAR_SURFACE_AREA>
83.55000000000001

> <JCHEM_REFRACTIVITY>
71.34

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       5.335   1.540   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    8   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    6   18                                                  
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₉NO₃

Average Mass

249.3100 Da

Monoisotopic Mass

249.13649 Da

IUPAC Name

2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid

Traditional Name

2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=CC(CC(N)C(O)=O)=CC=C1O

InChI Identifier

InChI=1S/C14H19NO3/c1-9(2)3-5-11-7-10(4-6-13(11)16)8-12(15)14(17)18/h3-4,6-7,12,16H,5,8,15H2,1-2H3,(H,17,18)

InChI Key

UFFPHPAGEHMRFF-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 tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Tyrosine and derivatives

Alternative Parents

Substituents

Tyrosine or derivatives
Phenylalanine or derivatives
3-phenylpropanoic-acid
Amphetamine or derivatives
Alpha-amino acid
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Phenol
Monocyclic benzene moiety
Benzenoid
Amino acid
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Primary amine
Primary aliphatic amine
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Organic oxide
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	0.24	ChemAxon
pKa (Strongest Acidic)	1.91	ChemAxon
pKa (Strongest Basic)	9.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	83.55 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	71.34 m³·mol⁻¹	ChemAxon
Polarizability	27.71 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

29814027

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23760112

PDB ID

Not Available

ChEBI ID

182673

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid (NP0184417)

MOL for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

3D MOL for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

3D SDF for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

3D-SDF for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

PDB for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

3D PDB for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

SMILES for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

INCHI for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

Structure for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)

3D Structure for NP0184417 (2-amino-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]propanoic acid)