NP-MRD: Showing NP-Card for [(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid (NP0265409)

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Record Information

Version

2.0

Created at

2022-09-08 09:22:31 UTC

Updated at

2022-09-08 09:22:31 UTC

NP-MRD ID

NP0265409

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid

Description

2-[(2-Amino-1-hydroxy-3-methylbutylidene)amino]-2-{4-carbamimidamido-1-azabicyclo[3.1.0]Hexan-2-yl}acetic acid belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. [(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid is found in Streptomyces ficellus. 2-[(2-Amino-1-hydroxy-3-methylbutylidene)amino]-2-{4-carbamimidamido-1-azabicyclo[3.1.0]Hexan-2-yl}acetic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -7.1527   -0.1431   -0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6954    0.6886   -0.2597 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4363    0.7396   -0.0936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8408    1.8888    0.4731 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6164   -0.3486   -0.4722 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1712   -0.2665   -0.3948 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6581   -0.0072    0.9934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2918   -0.5478    0.9722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1727    0.3873    0.6444 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1174   -0.2681    0.6549 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235   -0.2280   -0.5022 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5061    0.3767   -1.5162 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2578   -0.8655   -0.6016 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6724   -1.5361    0.5845 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2428    0.1737   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4649    1.2458   -0.0449 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5409   -0.5046   -1.4237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0765    1.5512    1.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0122    1.8059    2.1718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0886    2.4486    1.8115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3476   -1.6933    0.1280 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1962   -1.6494   -1.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5413   -1.6415   -0.6583 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9428    2.1153    1.5024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2925    2.5162   -0.1504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0585   -1.2260   -0.8132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8305    0.4367   -1.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2726   -0.6793    1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8254    0.9949    1.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0659   -0.9466    2.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3401    0.7801   -0.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4428   -0.7710    1.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1805   -1.6302   -1.4149 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4705   -1.0354    1.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3068   -2.5034    0.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8368    0.6389   -2.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4105    1.0788    0.5293 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5961    2.2155   -0.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6225    1.3685    0.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3818    0.1454   -1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6579   -0.5874   -2.5134 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6092   -1.5097   -0.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3187    2.8349    2.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9573   -0.7525   -1.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8676   -2.5897   -1.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1958   -2.5005   -0.7968 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 17  1  0
 15 13  1  0
 13 14  1  0
 13 11  1  0
 11 12  2  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  6 23  1  0
 23 22  1  0
 22 21  1  0
  9 18  1  0
 18 20  1  0
 18 19  2  0
 21  8  1  0
 21 23  1  0
 16 37  1  0
 16 38  1  0
 16 39  1  0
 15 36  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 13 33  1  6
 14 34  1  0
 14 35  1  0
 10 32  1  0
  9 31  1  6
  8 30  1  1
  7 28  1  0
  7 29  1  0
  6 27  1  6
  5 26  1  0
  4 24  1  0
  4 25  1  0
  2  1  1  0
 23 46  1  6
 22 44  1  0
 22 45  1  0
 20 43  1  0
M  END


  Mrv1533004151518462D          

 22 23  0  0  0  0            999 V2000
    1.6709   -1.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4959   -1.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9084   -0.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9084   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4959   -2.8817    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7334   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1459   -1.4528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1459   -2.8817    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9709   -2.8817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3834   -3.5962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2039   -3.6824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3755   -4.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1291   -4.8249    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2154   -5.6454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9690   -5.9810    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5479   -6.1303    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6610   -4.9019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8764   -5.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0479   -4.3499    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3834   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9709   -1.4528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2084   -2.1672    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
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 10 19  1  0  0  0  0
 17 19  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0265409

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(N)C(=O)NC(C1CC(NC(N)=N)C2CN12)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H24N6O3/c1-5(2)9(14)11(20)18-10(12(21)22)7-3-6(17-13(15)16)8-4-19(7)8/h5-10H,3-4,14H2,1-2H3,(H,18,20)(H,21,22)(H4,15,16,17)

> <INCHI_KEY>
DGIHWRUPUISVIZ-UHFFFAOYSA-N

> <FORMULA>
C13H24N6O3

> <MOLECULAR_WEIGHT>
312.374

> <EXACT_MASS>
312.190988657

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
31.39027516895758

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(2-amino-3-methylbutanamido)-2-{4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl}acetic acid

> <ALOGPS_LOGP>
-3.29

> <JCHEM_LOGP>
-3.4632989839299313

> <ALOGPS_LOGS>
-2.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.167492092426674

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7992321276838155

> <JCHEM_PKA_STRONGEST_BASIC>
11.927787453178055

> <JCHEM_POLAR_SURFACE_AREA>
157.32999999999998

> <JCHEM_REFRACTIVITY>
88.66319999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.90e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-amino-3-methylbutanamido)({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       3.119  -2.712   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.659  -2.712   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.429  -1.378   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.429  -4.046   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       4.659  -5.379   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       6.969  -4.046   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.739  -2.712   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       7.739  -5.379   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       9.279  -5.379   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.049  -6.713   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.581  -6.874   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.901  -8.380   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      13.308  -9.007   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      13.469 -10.538   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      14.876 -11.165   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0      12.223 -11.443   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      10.567  -9.150   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.103  -9.626   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       9.423  -8.120   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      10.049  -4.046   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.279  -2.712   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      11.589  -4.046   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12   18   19                                                  
CONECT   18   17   19                                                       
CONECT   19   18   10   17                                                  
CONECT   20    9   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
2-[(2-Amino-1-hydroxy-3-methylbutylidene)amino]-2-{4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl}acetate	Generator

Chemical Formula

C₁₃H₂₄N₆O₃

Average Mass

312.3740 Da

Monoisotopic Mass

312.19099 Da

IUPAC Name

2-(2-amino-3-methylbutanamido)-2-{4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl}acetic acid

Traditional Name

(2-amino-3-methylbutanamido)({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid

CAS Registry Number

Not Available

SMILES

CC(C)C(N)C(=O)NC(C1CC(NC(N)=N)C2CN12)C(O)=O

InChI Identifier

InChI=1S/C13H24N6O3/c1-5(2)9(14)11(20)18-10(12(21)22)7-3-6(17-13(15)16)8-4-19(7)8/h5-10H,3-4,14H2,1-2H3,(H,18,20)(H,21,22)(H4,15,16,17)

InChI Key

DGIHWRUPUISVIZ-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
Streptomyces ficellus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Dipeptides

Alternative Parents

Substituents

Alpha-dipeptide
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Valine or derivatives
Alpha-amino acid amide
Alpha-amino acid or derivatives
Piperidine
N-alkylpyrrolidine
N-acyl-amine
Fatty acyl
Fatty amide
Pyrrolidine
Carboxamide group
Amino acid or derivatives
Secondary carboxylic acid amide
Tertiary amine
Tertiary aliphatic amine
Guanidine
Amino acid
Aziridine
Carboxylic acid
Azacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Primary aliphatic amine
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Amine
Organopnictogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic oxide
Primary amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-3.3	ALOGPS
logP	-3.5	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	3.8	ChemAxon
pKa (Strongest Basic)	11.93	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	157.33 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	88.66 m³·mol⁻¹	ChemAxon
Polarizability	31.39 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

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

151592

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid (NP0265409)

MOL for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

3D MOL for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

3D SDF for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

3D-SDF for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

PDB for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

3D PDB for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

SMILES for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

INCHI for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

Structure for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)

3D Structure for NP0265409 ([(2-amino-1-hydroxy-3-methylbutylidene)amino]({4-carbamimidamido-1-azabicyclo[3.1.0]hexan-2-yl})acetic acid)