NP-MRD: Showing NP-Card for n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide (NP0285010)

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Record Information

Version

2.0

Created at

2022-09-09 12:59:05 UTC

Updated at

2022-09-09 12:59:05 UTC

NP-MRD ID

NP0285010

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide

Description

N-({2,6a-dihydroxy-1H,3aH,5H,6H,6aH-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1H-pyrrole-2-carboxamide belongs to the class of organic compounds known as 2-heteroaryl carboxamides. 2-Heteroaryl carboxamides are compounds containing a heteroaromatic ring that carries a carboxamide group. n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide is found in Agelas nakamurai. N-({2,6a-dihydroxy-1H,3aH,5H,6H,6aH-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1H-pyrrole-2-carboxamide is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -5.9064    0.3695    0.5578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7015    0.2923    0.1404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2551   -0.6416   -0.8345 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0516   -0.0504   -1.4326 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0888   -1.0009   -1.5685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8730   -0.4593   -1.0658 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1477   -1.5114   -0.9603 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4053   -1.0641   -0.4661 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7166   -0.5872    0.8213 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -0.4965    1.7742 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0887   -0.1418    1.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1552   -0.1415    0.2695 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2588    0.3454    0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9795    0.5316    0.1384 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.8567    0.6345    2.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5692    0.3362    2.2952 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3409    0.2557    0.1448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5975    0.9632   -0.4376 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1847    2.1581   -0.9872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6159    1.0982    0.5575 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6902   -1.5631   -1.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3257    0.4056   -2.4196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6096    0.3289   -1.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3340   -2.0034   -1.9655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2740   -2.3549   -0.3285 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2666   -1.0732   -1.1327 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1518   -0.4641   -0.7720 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5125    1.0344    2.9660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9893    0.4585    3.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6524    1.0685    0.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6452   -0.4095    0.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9890    1.9961   -1.9467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5385    1.6862    1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 19  1  6
 18 17  1  0
 17  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 20  1  0
  4 18  1  0
 20 18  1  0
 16 11  1  0
 19 32  1  0
 17 30  1  0
 17 31  1  0
  6 23  1  6
  7 24  1  0
  7 25  1  0
  8 26  1  0
 12 27  1  0
 15 28  1  0
 16 29  1  0
  4 22  1  6
  3 21  1  0
 20 33  1  0
M  END


  Mrv1533004191522112D          

 20 22  0  0  0  0            999 V2000
    0.7846   -1.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4849   -0.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3099   -0.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7224   -1.3819    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5474   -1.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9599   -0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9599   -2.0964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6244   -2.8501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2375   -3.4021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1512   -4.2226    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.9519   -2.9896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804   -2.1826    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8792   -0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692   -1.3349    0.0000 N   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 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
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  2 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0285010

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC12CC(CNC(=O)C3=CC(Br)=CN3)OC1NC(=O)N2

> <INCHI_IDENTIFIER>
InChI=1S/C11H13BrN4O4/c12-5-1-7(13-3-5)8(17)14-4-6-2-11(19)9(20-6)15-10(18)16-11/h1,3,6,9,13,19H,2,4H2,(H,14,17)(H2,15,16,18)

> <INCHI_KEY>
YLLFBOZQQVYTKE-UHFFFAOYSA-N

> <FORMULA>
C11H13BrN4O4

> <MOLECULAR_WEIGHT>
345.153

> <EXACT_MASS>
344.012018

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
29.365094214680347

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-({6a-hydroxy-2-oxo-hexahydro-1H-furo[2,3-d]imidazolidin-5-yl}methyl)-4-bromo-1H-pyrrole-2-carboxamide

> <ALOGPS_LOGP>
-0.41

> <JCHEM_LOGP>
-0.13580074133333317

> <ALOGPS_LOGS>
-2.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.614630778421803

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.761180903617381

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3031178177816938

> <JCHEM_POLAR_SURFACE_AREA>
115.48000000000002

> <JCHEM_REFRACTIVITY>
70.3618

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.03e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-({6a-hydroxy-2-oxo-tetrahydro-1H-furo[2,3-d]imidazolidin-5-yl}methyl)-4-bromo-1H-pyrrole-2-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  O   UNK     0       1.465  -3.556   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.465  -2.016   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.000  -2.492   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.905  -1.246   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.445  -1.246   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -3.215  -2.580   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -4.755  -2.580   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -5.525  -1.246   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -5.525  -3.913   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.899  -5.320   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.043  -6.351   0.000  0.00  0.00           C+0
HETATM   12 Br   UNK     0      -5.882  -7.882   0.000  0.00  0.00          Br+0
HETATM   13  C   UNK     0      -7.377  -5.581   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -7.057  -4.074   0.000  0.00  0.00           N+0
HETATM   15  O   UNK     0      -0.000  -0.000   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       2.929  -0.000   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       3.834  -1.246   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.374  -1.246   0.000  0.00  0.00           O+0
HETATM   20  N   UNK     0       2.929  -2.492   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   16   20                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    9                                                       
CONECT   15    4   16                                                       
CONECT   16   15    2   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    2                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₃BrN₄O₄

Average Mass

345.1530 Da

Monoisotopic Mass

344.01202 Da

IUPAC Name

N-({6a-hydroxy-2-oxo-hexahydro-1H-furo[2,3-d]imidazolidin-5-yl}methyl)-4-bromo-1H-pyrrole-2-carboxamide

Traditional Name

N-({6a-hydroxy-2-oxo-tetrahydro-1H-furo[2,3-d]imidazolidin-5-yl}methyl)-4-bromo-1H-pyrrole-2-carboxamide

CAS Registry Number

Not Available

SMILES

OC12CC(CNC(=O)C3=CC(Br)=CN3)OC1NC(=O)N2

InChI Identifier

InChI=1S/C11H13BrN4O4/c12-5-1-7(13-3-5)8(17)14-4-6-2-11(19)9(20-6)15-10(18)16-11/h1,3,6,9,13,19H,2,4H2,(H,14,17)(H2,15,16,18)

InChI Key

YLLFBOZQQVYTKE-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
Agelas nakamurai	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-heteroaryl carboxamides. 2-Heteroaryl carboxamides are compounds containing a heteroaromatic ring that carries a carboxamide group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

2-heteroaryl carboxamides

Alternative Parents

Substituents

2-heteroaryl carboxamide
Pyrrole-2-carboxamide
Pyrrole-2-carboxylic acid or derivatives
Aryl bromide
Aryl halide
Substituted pyrrole
2-imidazoline
Heteroaromatic compound
Pyrrole
Tetrahydrofuran
Isourea
Secondary carboxylic acid amide
Alkanolamine
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Organooxygen compound
Organonitrogen compound
Organobromide
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Organohalogen 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	-0.41	ALOGPS
logP	-0.14	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	9.76	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	115.48 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	70.36 m³·mol⁻¹	ChemAxon
Polarizability	29.37 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

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

72820801

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide (NP0285010)

MOL for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

3D MOL for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

3D SDF for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

3D-SDF for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

PDB for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

3D PDB for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

SMILES for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

INCHI for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

Structure for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)

3D Structure for NP0285010 (n-({2,6a-dihydroxy-1h,3ah,5h,6h-furo[2,3-d]imidazol-5-yl}methyl)-4-bromo-1h-pyrrole-2-carboxamide)