NP-MRD: Showing NP-Card for 4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid (NP0208548)

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Record Information

Version

2.0

Created at

2022-09-05 05:35:45 UTC

Updated at

2022-09-05 05:35:45 UTC

NP-MRD ID

NP0208548

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid

Description

4-Amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-C-hydroxycarbonimidoyl}methyl)-C-hydroxycarbonimidoyl]butanoic acid belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. 4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid is found in Phorbas tenacior. 4-Amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-C-hydroxycarbonimidoyl}methyl)-C-hydroxycarbonimidoyl]butanoic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 42  0  0  0  0  0  0  0  0999 V2000
   -5.7307    1.6302    1.7747 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4855    0.9337    1.8382 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5489   -0.4433    1.2158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9243   -0.4099   -0.2281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9569   -1.8057   -0.7367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2563   -1.9993   -1.9497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6735   -2.8762    0.0680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4002    1.7012    1.1791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6984    2.8069    0.6759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0795    1.2040    1.1209 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9930    1.9233    0.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2812    1.1712    0.5721 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2660    0.0607    1.1530 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4800    1.6813    0.0196 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6870    0.9006    0.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3064    0.5131   -0.9633 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5286   -0.2768   -0.8988 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1333   -0.6539   -2.0870 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2891   -1.3999   -2.1098 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8826   -1.7967   -0.9074 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0348   -2.5407   -0.9023 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3057   -1.4377    0.2902 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1353   -0.6818    0.2640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3635    1.3979    2.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5320    2.6601    1.7008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2136    0.8332    2.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2751   -1.0916    1.7568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5631   -0.9325    1.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1625    0.1640   -0.8092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9334    0.0554   -0.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3501   -3.6317    0.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8709    0.2787    1.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8970    2.9478    0.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2426    2.0753   -0.5946 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5112    2.6000   -0.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0062    0.6832    1.1338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8788    0.8001   -1.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6950   -0.3602   -3.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7616   -1.6944   -3.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5133   -2.8402   -1.7392 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7622   -1.7431    1.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6924   -0.4065    1.2071 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  7  1  0
  5  6  2  0
  2  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 23 17  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  1
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  7 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
 18 38  1  0
 19 39  1  0
 21 40  1  0
 22 41  1  0
 23 42  1  0
M  END


  Mrv1533004201500342D          

 23 23  0  0  0  0            999 V2000
    6.4302   -8.6625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -8.6625    0.0000 C   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  2  0  0  0  0
  5  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 17 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208548

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC(CCC(O)=O)C(=O)NCC(=O)NC=CC1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H19N3O5/c16-12(5-6-14(21)22)15(23)18-9-13(20)17-8-7-10-1-3-11(19)4-2-10/h1-4,7-8,12,19H,5-6,9,16H2,(H,17,20)(H,18,23)(H,21,22)

> <INCHI_KEY>
DHVZUWTVYSXYQE-UHFFFAOYSA-N

> <FORMULA>
C15H19N3O5

> <MOLECULAR_WEIGHT>
321.333

> <EXACT_MASS>
321.132470724

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
32.04583149761022

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]carbamoyl}methyl)carbamoyl]butanoic acid

> <ALOGPS_LOGP>
-1.93

> <JCHEM_LOGP>
-3.0801662595475348

> <ALOGPS_LOGS>
-3.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.471449794953212

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8385237180617238

> <JCHEM_PKA_STRONGEST_BASIC>
8.127946667693186

> <JCHEM_POLAR_SURFACE_AREA>
141.75

> <JCHEM_REFRACTIVITY>
82.2517

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.83e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]carbamoyl}methyl)carbamoyl]butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  N   UNK     0      12.003 -16.170   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.668 -14.630   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       8.002 -12.320   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      13.337 -13.860   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      13.337 -12.320   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0      14.670 -14.630   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      16.004 -13.860   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.338 -14.630   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      17.338 -16.170   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      18.672 -13.860   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.673 -14.630   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      24.006 -13.860   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      25.340 -14.630   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.340 -16.170   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      26.674 -16.940   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      24.006 -16.940   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.673 -16.170   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    2    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   17                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Value	Source
4-Amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-C-hydroxycarbonimidoyl}methyl)-C-hydroxycarbonimidoyl]butanoate	Generator

Chemical Formula

C₁₅H₁₉N₃O₅

Average Mass

321.3330 Da

Monoisotopic Mass

321.13247 Da

IUPAC Name

4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]carbamoyl}methyl)carbamoyl]butanoic acid

Traditional Name

4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]carbamoyl}methyl)carbamoyl]butanoic acid

CAS Registry Number

Not Available

SMILES

NC(CCC(O)=O)C(=O)NCC(=O)NC=CC1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C15H19N3O5/c16-12(5-6-14(21)22)15(23)18-9-13(20)17-8-7-10-1-3-11(19)4-2-10/h1-4,7-8,12,19H,5-6,9,16H2,(H,17,20)(H,18,23)(H,21,22)

InChI Key

DHVZUWTVYSXYQE-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

Species Name	Source	Reference
Anchinoe tenacior	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Dipeptides

Alternative Parents

Substituents

Alpha-dipeptide
Glutamic acid or derivatives
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Styrene
1-hydroxy-2-unsubstituted benzenoid
Hydroxy fatty acid
Amino fatty acid
Phenol
Fatty amide
Fatty acyl
Benzenoid
N-acyl-amine
Monocyclic benzene moiety
Amino acid or derivatives
Amino acid
Carboxamide group
Secondary carboxylic acid amide
Monocarboxylic acid or derivatives
Carboxylic acid
Organic nitrogen compound
Primary aliphatic amine
Organonitrogen compound
Organooxygen compound
Carbonyl group
Primary amine
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen compound
Organic oxygen compound
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	-1.9	ALOGPS
logP	-3.1	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	3.84	ChemAxon
pKa (Strongest Basic)	8.13	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	141.75 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	82.25 m³·mol⁻¹	ChemAxon
Polarizability	32.05 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

73117687

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid (NP0208548)

MOL for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

3D MOL for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

3D SDF for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

3D-SDF for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

PDB for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

3D PDB for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

SMILES for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

INCHI for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

Structure for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)

3D Structure for NP0208548 (4-amino-4-[({[2-(4-hydroxyphenyl)ethenyl]-c-hydroxycarbonimidoyl}methyl)-c-hydroxycarbonimidoyl]butanoic acid)