NP-MRD: Showing NP-Card for n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid (NP0258700)

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Record Information

Version

2.0

Created at

2022-09-08 00:17:20 UTC

Updated at

2022-09-08 00:17:21 UTC

NP-MRD ID

NP0258700

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid

Description

Kikumycin A, also known as tan 868 b, 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. Based on a literature review very few articles have been published on Kikumycin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    7.4917   -2.7973   -0.3672 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8762   -1.8444   -0.4988 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1269   -0.8269   -0.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7014    0.4722   -0.4692 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7516   -0.9866    0.1613 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0067    0.0971    0.3841 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6710   -0.0362    0.8065 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5769    0.4778    0.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8297    1.0673   -1.0171 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1936    0.3258    0.5177 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508    0.7698   -0.1029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0464    0.4186    0.6694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4009    0.6761    0.4067 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9094    0.7983   -0.7602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0739    0.6696   -1.8596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3323    1.0674   -0.9818 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0119   -0.0195   -1.7899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5359   -0.9507   -0.6924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0025    0.0296    0.3218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0360   -0.0991    1.1055 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6254   -0.9571    1.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0922    1.1189    0.2523 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5190   -0.2514    1.7744 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8079   -0.2843    1.6458 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4190    1.0342   -1.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3931    0.7703    0.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3569   -1.9634    0.2964 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4749    1.0520    0.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4913   -0.5336    1.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0236    1.3104   -1.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4554    0.1991   -2.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4439    2.0494   -1.4811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3305   -0.5898   -2.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8726    0.4283   -2.3173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3332   -1.6104   -1.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6695   -1.5421   -0.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9905    1.8514    0.9922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0603   -0.6715    2.5898 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4986   -0.7196    2.3148 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
  3  2  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 23  2  0
 23 24  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 22  1  0
 24 10  1  0
 22 16  1  0
  4 25  1  0
  4 26  1  0
  2  1  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
 11 30  1  0
 23 38  1  0
 24 39  1  0
 15 31  1  0
 16 32  1  6
 17 33  1  0
 17 34  1  0
 18 35  1  0
 18 36  1  0
 20 21  1  0
 22 37  1  0
M  END


  Mrv1652309082202172D          

 22 23  0  0  0  0            999 V2000
    1.6738    1.3096    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9593    0.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2449    1.3096    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9593    0.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2449   -0.3404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2449   -1.1654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9593   -1.5779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6738   -1.1654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9593   -2.4029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6268   -2.8879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3718   -3.6725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8568   -4.3399    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5212   -5.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7007   -5.1798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0061   -5.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8311   -5.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0861   -6.5456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4186   -7.0306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4186   -7.8556    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7512   -6.5456    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5468   -3.6725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2919   -2.8879    0.0000 N   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  2  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
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 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
 15 20  1  0  0  0  0
 11 21  2  0  0  0  0
 21 22  1  0  0  0  0
  9 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258700

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC(=N)\C=C\NC(=O)C1=CC(=CN1)N=C(O)C1CCC(=N)N1

> <INCHI_IDENTIFIER>
InChI=1S/C13H17N7O2/c14-10(15)3-4-17-12(21)9-5-7(6-18-9)19-13(22)8-1-2-11(16)20-8/h3-6,8,18H,1-2H2,(H3,14,15)(H2,16,20)(H,17,21)(H,19,22)/b4-3+

> <INCHI_KEY>
LQPIARFCQJVRNW-ONEGZZNKSA-N

> <FORMULA>
C13H17N7O2

> <MOLECULAR_WEIGHT>
303.326

> <EXACT_MASS>
303.144372815

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.29830484399186

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-(5-{[(1E)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1H-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid

> <JCHEM_LOGP>
-3.5967244886413066

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
11.075024277903687

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.417066857789131

> <JCHEM_PKA_STRONGEST_BASIC>
16.58915495607348

> <JCHEM_POLAR_SURFACE_AREA>
163.23

> <JCHEM_REFRACTIVITY>
103.62769999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-(5-{[(1E)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1H-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  N   UNK     0       3.124   2.445   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       1.791   1.675   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       0.457   2.445   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       1.791   0.135   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.457  -0.635   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       0.457  -2.175   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       1.791  -2.945   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.124  -2.175   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.791  -4.485   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.037  -5.391   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.561  -6.855   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       3.466  -8.101   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       2.840  -9.508   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.308  -9.669   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.745 -10.754   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.285 -10.754   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.761 -12.219   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.515 -13.124   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       4.515 -14.664   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0       3.269 -12.219   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       1.021  -6.855   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       0.545  -5.391   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   21                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   15                                                       
CONECT   21   11   22                                                       
CONECT   22   21    9                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
TAN 868 b	MeSH
TAN-868b	MeSH

Chemical Formula

C₁₃H₁₇N₇O₂

Average Mass

303.3260 Da

Monoisotopic Mass

303.14437 Da

IUPAC Name

N-(5-{[(1E)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1H-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid

Traditional Name

N-(5-{[(1E)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1H-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid

CAS Registry Number

Not Available

SMILES

NC(=N)\C=C\NC(=O)C1=CC(=CN1)N=C(O)C1CCC(=N)N1

InChI Identifier

InChI=1S/C13H17N7O2/c14-10(15)3-4-17-12(21)9-5-7(6-18-9)19-13(22)8-1-2-11(16)20-8/h3-6,8,18H,1-2H2,(H3,14,15)(H2,16,20)(H,17,21)(H,19,22)/b4-3+

InChI Key

LQPIARFCQJVRNW-ONEGZZNKSA-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 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
Substituted pyrrole
Imidolactam
Pyrrole
Pyrrolidine
Heteroaromatic compound
Secondary carboxylic acid amide
Amidine
Carboxylic acid amidine
Carboximidic acid
Carboximidic acid derivative
Azacycle
Carboximidamide
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organoheterocyclic compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen 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	-3.6	ChemAxon
pKa (Strongest Acidic)	3.42	ChemAxon
pKa (Strongest Basic)	16.59	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	163.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	103.63 m³·mol⁻¹	ChemAxon
Polarizability	31.3 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

C00018728

Chemspider ID

19990876

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

135616733

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid (NP0258700)

MOL for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

3D MOL for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

3D SDF for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

3D-SDF for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

PDB for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

3D PDB for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

SMILES for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

INCHI for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

Structure for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)

3D Structure for NP0258700 (n-(5-{[(1e)-2-carbamimidoyleth-1-en-1-yl]carbamoyl}-1h-pyrrol-3-yl)-5-iminopyrrolidine-2-carboximidic acid)