NP-MRD: Showing NP-Card for (2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid (NP0159035)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-02 16:43:11 UTC

Updated at

2022-09-02 16:43:11 UTC

NP-MRD ID

NP0159035

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid

Description

(2S)-2-{[(6-bromo-1H-indol-3-yl)(hydroxy)methylidene]amino}-3-(1H-imidazol-5-yl)propanoic acid belongs to the class of organic compounds known as histidine and derivatives. Histidine and derivatives are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine 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 (2S)-2-{[(6-bromo-1H-indol-3-yl)(hydroxy)methylidene]amino}-3-(1H-imidazol-5-yl)propanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    1.4603   -2.4763   -0.1630 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1192   -1.4699   -0.5384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4694   -1.6728   -0.7879 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.1453   -0.7069 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1432    0.8727    0.1799 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5746    1.0818   -0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1380    1.9628   -0.9182 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4752    1.8723   -0.8331 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7504    0.9430    0.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5936    0.4587    0.5691 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0847   -0.1740   -0.4150 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4521   -0.5662    0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3529   -1.0197    1.6965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -0.5660    0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5833   -0.9663    2.0161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8910   -0.8131    1.8289 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1123   -0.3168    0.5999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2719    0.0221   -0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2218    0.5240   -1.3682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8483    0.9787   -2.2737 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.9873    0.6838   -1.9667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8402    0.3409   -1.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8830   -0.1554   -0.0016 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0688   -2.2198   -0.1772 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6105    0.1898   -1.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9540    0.5762    1.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5594    1.8375    0.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6442    2.6470   -1.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7221    0.6170    0.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5220   -0.2706    1.2964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0231   -1.8117    2.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1207   -1.3556    2.9354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6544   -1.0308    2.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2257   -0.1114    0.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9192    1.0727   -2.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8550    0.4608   -1.7299 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  4 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  2  0
 10  6  1  0
 23 14  1  0
 23 17  1  0
  3 24  1  0
  4 25  1  6
  5 26  1  0
  5 27  1  0
  7 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  0
 15 32  1  0
 16 33  1  0
 18 34  1  0
 21 35  1  0
 22 36  1  0
M  END


  Mrv1652309022218432D          

 23 25  0  0  1  0            999 V2000
   -1.2400   -4.0623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371   -2.6646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3739   -3.7192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1190   -4.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6657   -4.7588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6657   -5.5838    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1190   -5.8387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -5.1713    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  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  2  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
  4 11  1  1  0  0  0
 11 12  2  0  0  0  0
 12 13  1  4  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  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  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 14 23  1  0  0  0  0
 17 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0159035

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)[C@H](CC1=CN=CN1)N=C(O)C1=CNC2=CC(Br)=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C15H13BrN4O3/c16-8-1-2-10-11(6-18-12(10)3-8)14(21)20-13(15(22)23)4-9-5-17-7-19-9/h1-3,5-7,13,18H,4H2,(H,17,19)(H,20,21)(H,22,23)/t13-/m0/s1

> <INCHI_KEY>
FZDXEGZWBPGVQB-ZDUSSCGKSA-N

> <FORMULA>
C15H13BrN4O3

> <MOLECULAR_WEIGHT>
377.198

> <EXACT_MASS>
376.017103

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
32.88718430520264

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-{[(6-bromo-1H-indol-3-yl)(hydroxy)methylidene]amino}-3-(1H-imidazol-5-yl)propanoic acid

> <ALOGPS_LOGP>
1.79

> <JCHEM_LOGP>
1.1851889447266248

> <ALOGPS_LOGS>
-3.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.593320336363072

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.11780715039747

> <JCHEM_PKA_STRONGEST_BASIC>
6.624717103284681

> <JCHEM_POLAR_SURFACE_AREA>
114.35999999999999

> <JCHEM_REFRACTIVITY>
87.4043

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.25e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-{[(6-bromo-1H-indol-3-yl)(hydroxy)methylidene]amino}-3-(3H-imidazol-4-yl)propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0      -2.315  -7.583   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.839  -6.118   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.869  -4.974   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -0.333  -5.798   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.698  -6.943   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.222  -8.407   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.243  -8.883   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -1.243 -10.423   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       0.222 -10.899   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       1.127  -9.653   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0       0.143  -4.334   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.680  -5.158   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   20 Br   UNK     0       7.591   0.237   0.000  0.00  0.00          Br+0
HETATM   21  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6                                                       
CONECT   11    4   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   14   17                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
(2S)-2-{[(6-bromo-1H-indol-3-yl)(hydroxy)methylidene]amino}-3-(1H-imidazol-5-yl)propanoate	Generator

Chemical Formula

C₁₅H₁₃BrN₄O₃

Average Mass

377.1980 Da

Monoisotopic Mass

376.01710 Da

IUPAC Name

(2S)-2-{[(6-bromo-1H-indol-3-yl)(hydroxy)methylidene]amino}-3-(1H-imidazol-5-yl)propanoic acid

Traditional Name

(2S)-2-{[(6-bromo-1H-indol-3-yl)(hydroxy)methylidene]amino}-3-(3H-imidazol-4-yl)propanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)[C@H](CC1=CN=CN1)N=C(O)C1=CNC2=CC(Br)=CC=C12

InChI Identifier

InChI=1S/C15H13BrN4O3/c16-8-1-2-10-11(6-18-12(10)3-8)14(21)20-13(15(22)23)4-9-5-17-7-19-9/h1-3,5-7,13,18H,4H2,(H,17,19)(H,20,21)(H,22,23)/t13-/m0/s1

InChI Key

FZDXEGZWBPGVQB-ZDUSSCGKSA-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 histidine and derivatives. Histidine and derivatives are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine 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

Histidine and derivatives

Alternative Parents

Substituents

Histidine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Indolecarboxamide derivative
Indolecarboxylic acid derivative
Indole
Indole or derivatives
Imidazolyl carboxylic acid derivative
Pyrrole-3-carboxamide
Pyrrole-3-carboxylic acid or derivatives
Aryl bromide
Aryl halide
Benzenoid
Substituted pyrrole
Vinylogous amide
Azole
Pyrrole
Imidazole
Heteroaromatic compound
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid
Organoheterocyclic compound
Azacycle
Monocarboxylic acid or derivatives
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organohalogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organobromide
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
logP	1.79	ALOGPS
logP	1.19	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	3.12	ChemAxon
pKa (Strongest Basic)	6.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	114.36 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	87.4 m³·mol⁻¹	ChemAxon
Polarizability	32.89 Å³	ChemAxon
Number of Rings	3	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

8699014

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10523618

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid (NP0159035)

MOL for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

3D MOL for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

3D SDF for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

3D-SDF for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

PDB for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

3D PDB for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

SMILES for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

INCHI for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

Structure for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)

3D Structure for NP0159035 ((2s)-2-{[(6-bromo-1h-indol-3-yl)(hydroxy)methylidene]amino}-3-(3h-imidazol-4-yl)propanoic acid)