NP-MRD: Showing NP-Card for 5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one (NP0201641)

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Record Information

Version

2.0

Created at

2022-09-04 20:43:28 UTC

Updated at

2022-09-04 20:43:28 UTC

NP-MRD ID

NP0201641

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one

Description

AC1L8BX0 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. 5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one is found in Penicillium canescens. AC1L8BX0 is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
    5.8028    0.0995   -0.7189 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8769    0.3399    0.1955 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4655   -0.1661    0.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0253   -0.5307    1.4742 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5439   -1.3922   -0.7825 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6354    0.9314   -0.4916 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1117    2.1586   -0.8258 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1058    2.9046   -1.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9806    2.1833   -1.2752 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2873    0.9573   -0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3906   -0.1630   -0.6130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7736   -0.2049   -0.0352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4903   -1.4500   -0.0030 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7611   -1.5487    0.6084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3447   -2.6763    0.6898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4605   -0.3898    1.1686 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7693   -0.0777    0.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7212   -1.2256    0.4188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4652    0.5149   -0.8664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6633    0.8074    1.1767 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3971    0.9590    0.5827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7991    2.0914    0.5816 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6396   -0.4811   -1.6327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8279    0.4748   -0.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1763    0.9372    1.0584 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0117   -0.9825    1.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7919   -1.2001    1.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9757    0.3616    2.1309 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7898   -2.1598   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5578   -1.8819   -0.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5366   -1.0375   -1.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1190    2.4867   -0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520    3.9400   -1.6325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7602   -1.1075   -1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0849   -2.3178   -0.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6743   -0.6289    2.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2630    0.7203    1.1090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7121   -0.8310    0.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3301   -1.9838   -0.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7799   -1.6828    1.4455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7514   -0.1545   -1.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9430    1.4647   -0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4042    0.6394   -1.4430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0756    1.6305    1.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 19  1  0
 17 16  1  0
 16 20  1  0
 20 21  1  0
 21 22  2  0
 21 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 12 11  2  0
 11 10  1  0
 10  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  6  3  1  0
  3  4  1  0
  3  5  1  0
  3  2  1  0
  2  1  2  3
 14 16  1  0
  9 10  1  0
 18 38  1  0
 18 39  1  0
 18 40  1  0
 17 37  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 16 36  1  1
 20 44  1  0
 13 35  1  0
 11 34  1  0
  7 32  1  0
  8 33  1  0
  4 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  5 31  1  0
  2 25  1  0
  1 23  1  0
  1 24  1  0
M  END


  Mrv1533004251504552D          

 22 23  0  0  0  0            999 V2000
    2.2501    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2501    6.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9646    5.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5356    5.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5356    4.7652    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    3.5277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    4.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597    3.0428    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203    2.2581    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2752    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0598    3.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8049    4.0823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3148    2.5131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8444    3.5526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4575    3.0006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    5.5902    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    6.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    6.8277    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  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
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  4  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
 10 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0201641

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1NC(=O)C(NC1=O)=CC1=C(NC=N1)C(C)(C)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C16H22N4O2/c1-6-16(4,5)13-10(17-8-18-13)7-11-14(21)20-12(9(2)3)15(22)19-11/h6-9,12H,1H2,2-5H3,(H,17,18)(H,19,22)(H,20,21)

> <INCHI_KEY>
RSGRSUVVCYUKLM-UHFFFAOYSA-N

> <FORMULA>
C16H22N4O2

> <MOLECULAR_WEIGHT>
302.378

> <EXACT_MASS>
302.174275964

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
32.78276358652739

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[5-(2-methylbut-3-en-2-yl)-1H-imidazol-4-yl]methylidene}-6-(propan-2-yl)piperazine-2,5-dione

> <ALOGPS_LOGP>
1.88

> <JCHEM_LOGP>
1.094245367

> <ALOGPS_LOGS>
-3.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.345109761694541

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.339791771420892

> <JCHEM_PKA_STRONGEST_BASIC>
5.745798340736427

> <JCHEM_POLAR_SURFACE_AREA>
86.88

> <JCHEM_REFRACTIVITY>
85.47409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-isopropyl-6-{[5-(2-methylbut-3-en-2-yl)-1H-imidazol-4-yl]methylidene}piperazine-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       4.200  12.745   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.200  11.205   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.534  10.435   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.867  10.435   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       2.867   8.895   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       1.533   8.125   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.533   6.585   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.199   8.895   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.134   8.125   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.134   6.585   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       0.111   5.680   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -0.364   4.215   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -1.904   4.215   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -2.380   5.680   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.845   6.156   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.369   7.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.321   4.691   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.310   6.632   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.454   5.601   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       0.199  10.435   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       1.533  11.205   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.533  12.745   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   20                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   10   15                                                  
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19                                                       
CONECT   19   18                                                            
CONECT   20    8   21                                                       
CONECT   21   20    4   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₂N₄O₂

Average Mass

302.3780 Da

Monoisotopic Mass

302.17428 Da

IUPAC Name

3-{[5-(2-methylbut-3-en-2-yl)-1H-imidazol-4-yl]methylidene}-6-(propan-2-yl)piperazine-2,5-dione

Traditional Name

3-isopropyl-6-{[5-(2-methylbut-3-en-2-yl)-1H-imidazol-4-yl]methylidene}piperazine-2,5-dione

CAS Registry Number

Not Available

SMILES

CC(C)C1NC(=O)C(NC1=O)=CC1=C(NC=N1)C(C)(C)C=C

InChI Identifier

InChI=1S/C16H22N4O2/c1-6-16(4,5)13-10(17-8-18-13)7-11-14(21)20-12(9(2)3)15(22)19-11/h6-9,12H,1H2,2-5H3,(H,17,18)(H,19,22)(H,20,21)

InChI Key

RSGRSUVVCYUKLM-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
Penicillium canescens	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
Dioxopiperazine
2,5-dioxopiperazine
1,4-diazinane
Piperazine
Heteroaromatic compound
Azole
Imidazole
Carboxamide group
Lactam
Secondary carboxylic acid amide
Organoheterocyclic compound
Azacycle
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Carbonyl group
Organopnictogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	1.88	ALOGPS
logP	1.09	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	11.34	ChemAxon
pKa (Strongest Basic)	5.75	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.88 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	85.47 m³·mol⁻¹	ChemAxon
Polarizability	32.78 Å³	ChemAxon
Number of Rings	2	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

375594

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one (NP0201641)

MOL for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

3D MOL for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

3D SDF for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

3D-SDF for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

PDB for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

3D PDB for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

SMILES for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

INCHI for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

Structure for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)

3D Structure for NP0201641 (5-hydroxy-6-isopropyl-3-{[5-(2-methylbut-3-en-2-yl)-1h-imidazol-4-yl]methylidene}-1,6-dihydropyrazin-2-one)