NP-MRD: Showing NP-Card for (3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol (NP0166596)

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Record Information

Version

2.0

Created at

2022-09-03 02:00:46 UTC

Updated at

2022-09-03 02:00:46 UTC

NP-MRD ID

NP0166596

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol

Description

CHEMBL4759212 belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. (3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol is found in Huperzia serrata. Based on a literature review very few articles have been published on CHEMBL4759212.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 42  0  0  0  0  0  0  0  0999 V2000
   -3.5863   -1.3902    0.4649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3585   -0.6973    0.5954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3477   -1.2872    1.0596 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0515   -0.7049    1.2302 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9719   -1.5933    0.5529 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3471   -1.1599    0.7598 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1656   -1.4778    1.8648 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3459   -0.8936    1.7741 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3400   -0.1890    0.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4014    0.5663    0.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2155    1.1949   -1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9996    1.0617   -1.7539 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779    0.3077   -1.2200 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458   -0.3277   -0.0103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0171    0.6843    0.8193 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2198    1.3834    0.9586 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0265    1.3058    0.3443 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3019    0.6976    0.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3185    1.3329   -0.3521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6345    0.7752   -0.5402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5308    0.2921    0.3744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6036   -0.1317   -0.3224 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3927    0.0766   -1.6233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1914    0.6301   -1.7565 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7128   -1.9574   -0.3468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2416   -0.7249    2.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8143   -2.6261    0.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7162   -1.7395   -0.5294 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8014   -2.1272    2.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1015   -0.9949    2.4861 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3413    0.6499    0.6733 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0316    1.7775   -1.4766 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8748    1.5652   -2.7042 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0114    0.1804   -1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3617    2.1583    0.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0923    2.3778   -0.6597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4384    0.2519    1.4641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0595   -0.1510   -2.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7623    0.9039   -2.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 18  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  4 15  1  0
 14  6  1  0
 24 20  1  0
 14  9  1  0
 16 35  1  0
 19 36  1  0
 21 37  1  0
 23 38  1  0
 24 39  1  0
  1 25  1  0
  4 26  1  1
  5 27  1  0
  5 28  1  0
  7 29  1  0
  8 30  1  0
 10 31  1  0
 11 32  1  0
 12 33  1  0
 13 34  1  0
M  END


  Mrv1652309032204002D          

 24 27  0  0  1  0            999 V2000
    3.6018   -3.0331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7948   -3.2047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2428   -2.5916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  1  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
    1.1387   -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
    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
    1.1809   -3.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.7192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329   -4.1608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399   -3.9893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0919   -4.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8989   -4.4309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2344   -3.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0549   -3.7634    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2265   -4.5704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5120   -4.9829    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  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  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  2  0  0  0  0
  6 14  1  0  0  0  0
  9 14  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
  2 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0166596

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=N\C(=C\C2=CN=CN2)C(O)=N[C@H]1CC1=CNC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C17H15N5O2/c23-16-14(5-10-7-19-13-4-2-1-3-12(10)13)21-17(24)15(22-16)6-11-8-18-9-20-11/h1-4,6-9,14,19H,5H2,(H,18,20)(H,21,24)(H,22,23)/b15-6+/t14-/m0/s1

> <INCHI_KEY>
ITXQTTPWGBFRNK-ULIPXBITSA-N

> <FORMULA>
C17H15N5O2

> <MOLECULAR_WEIGHT>
321.34

> <EXACT_MASS>
321.122574743

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
32.56517831565071

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E,6S)-3-[(1H-imidazol-5-yl)methylidene]-6-[(1H-indol-3-yl)methyl]-3,6-dihydropyrazine-2,5-diol

> <ALOGPS_LOGP>
1.32

> <JCHEM_LOGP>
0.8536016947104813

> <ALOGPS_LOGS>
-3.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
7.094696444011322

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.527776381822376

> <JCHEM_PKA_STRONGEST_BASIC>
7.823644119591817

> <JCHEM_POLAR_SURFACE_AREA>
109.65

> <JCHEM_REFRACTIVITY>
90.36350000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.22e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,6S)-3-(3H-imidazol-4-ylmethylidene)-6-(1H-indol-3-ylmethyl)-6H-pyrazine-2,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  O   UNK     0       6.723  -5.662   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.217  -5.982   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       4.187  -4.838   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.204  -6.622   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.698  -6.943   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       3.235  -7.767   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.741  -7.447   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.772  -8.591   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.278  -8.271   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.904  -6.864   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       9.436  -7.025   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       9.756  -8.531   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       8.422  -9.301   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    6    9                                                  
CONECT   15    4   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    2   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₅N₅O₂

Average Mass

321.3400 Da

Monoisotopic Mass

321.12257 Da

IUPAC Name

(3E,6S)-3-[(1H-imidazol-5-yl)methylidene]-6-[(1H-indol-3-yl)methyl]-3,6-dihydropyrazine-2,5-diol

Traditional Name

(3E,6S)-3-(3H-imidazol-4-ylmethylidene)-6-(1H-indol-3-ylmethyl)-6H-pyrazine-2,5-diol

CAS Registry Number

Not Available

SMILES

OC1=N\C(=C\C2=CN=CN2)C(O)=N[C@H]1CC1=CNC2=CC=CC=C12

InChI Identifier

InChI=1S/C17H15N5O2/c23-16-14(5-10-7-19-13-4-2-1-3-12(10)13)21-17(24)15(22-16)6-11-8-18-9-20-11/h1-4,6-9,14,19H,5H2,(H,18,20)(H,21,24)(H,22,23)/b15-6+/t14-/m0/s1

InChI Key

ITXQTTPWGBFRNK-ULIPXBITSA-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
Huperzia serrata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
3-alkylindole
Indole
Indole or derivatives
Dioxopiperazine
2,5-dioxopiperazine
Benzenoid
1,4-diazinane
Substituted pyrrole
Piperazine
Heteroaromatic compound
Azole
Imidazole
Pyrrole
Carboxamide group
Secondary carboxylic acid amide
Lactam
Azacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organonitrogen compound
Organooxygen compound
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	1.32	ALOGPS
logP	0.85	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	2.53	ChemAxon
pKa (Strongest Basic)	7.82	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	109.65 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	90.36 m³·mol⁻¹	ChemAxon
Polarizability	32.57 Å³	ChemAxon
Number of Rings	4	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

98789527

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol (NP0166596)

MOL for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

3D MOL for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

3D SDF for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

3D-SDF for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

PDB for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

3D PDB for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

SMILES for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

INCHI for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

Structure for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)

3D Structure for NP0166596 ((3e,6s)-3-(3h-imidazol-4-ylmethylidene)-6-(1h-indol-3-ylmethyl)-6h-pyrazine-2,5-diol)