NP-MRD: Showing NP-Card for 2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid (NP0188931)

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Record Information

Version

2.0

Created at

2022-09-04 05:20:35 UTC

Updated at

2022-09-04 05:20:35 UTC

NP-MRD ID

NP0188931

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid

Description

DTXSID50976741 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-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid is found in Streptomyces ficellus. Based on a literature review very few articles have been published on DTXSID50976741.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042207202D          

 29 30  0  0  0  0            999 V2000
    6.9714   -3.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1696   -3.0088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5751   -2.4368    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7825   -2.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1880   -2.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3953   -2.3224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1146   -3.0981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2900   -3.0708    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0612   -2.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7443   -1.8156    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5843   -3.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1788   -4.0385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7917   -3.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9622   -2.7800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1604   -1.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9530   -1.7503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5659   -1.4071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5567   -3.3520    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.3585   -4.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3493   -3.1232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5475   -2.3224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9438   -3.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7456   -4.4961    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7364   -3.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3309   -4.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1431   -3.8938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5317   -4.6215    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.9597   -5.2160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2175   -4.8556    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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 25 29  1  0  0  0  0
M  END

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
    0.8539   -0.2391    2.3302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6950   -0.5901    0.9005 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0971    0.2938   -0.0926 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4189    0.7295   -0.2645 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3990   -0.3887   -0.5149 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7903    0.0049   -0.6932 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7445    0.0844    0.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8749    0.4777   -0.2741 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6913    0.6570   -1.6084 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4166    0.3618   -1.8294 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8936    1.8655    0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2373    2.5455    1.3455 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2073    2.2842    0.3415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7691   -1.0463    0.7088 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0618   -2.1984    1.5664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0864   -2.1601    2.8213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3466   -3.4761    1.0240 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0039   -1.4033   -0.6763 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2484   -2.4921   -1.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9302   -0.7699   -1.5340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0179   -1.1634   -2.7191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8113    0.3443   -1.1055 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4660    0.8798   -2.3012 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9810   -0.2139   -0.2712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8118    0.9302    0.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8729    1.4310   -0.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3634    2.4637    0.0926 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6470    2.6176    1.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6968    1.6873    1.2416 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0047    0.2918    2.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9400   -1.1991    2.9394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8354    0.2405    2.5775 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2736   -1.5558    0.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3774    0.8459   -0.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3767    1.2106   -1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1196   -0.9478   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2769   -1.2015    0.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6096   -0.1308    1.3583 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4119    0.9704   -2.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9618    0.4062   -2.7866 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4091    3.2664    0.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4248   -0.2034    0.9737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0100   -4.3102    1.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9356   -3.3567   -1.3672 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1006   -2.1294   -2.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6320   -2.8043   -0.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3089    1.1643   -0.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9224    1.6245   -2.7469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6449    0.0762   -2.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6469   -0.8608    0.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6072   -0.8799   -0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2283    1.0540   -1.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8186    3.3783    1.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9774    1.5335    1.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  4 11  1  0
 11 13  1  0
 11 12  2  0
  2 14  1  0
 14 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 14 15  1  0
 15 17  1  0
 15 16  2  0
 10  6  1  0
 29 25  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  1
  3 34  1  0
  4 35  1  6
  5 36  1  0
  5 37  1  0
  7 38  1  0
  9 39  1  0
 10 40  1  0
 13 41  1  0
 14 42  1  1
 19 44  1  0
 19 45  1  0
 19 46  1  0
 22 47  1  1
 23 48  1  0
 23 49  1  0
 24 50  1  0
 24 51  1  0
 26 52  1  0
 28 53  1  0
 29 54  1  0
 17 43  1  0
M  END


  Mrv1652309042207202D          

 29 30  0  0  0  0            999 V2000
    6.9714   -3.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1696   -3.0088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5751   -2.4368    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7825   -2.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1880   -2.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3953   -2.3224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1146   -3.0981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2900   -3.0708    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0612   -2.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7443   -1.8156    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5843   -3.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1788   -4.0385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7917   -3.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9622   -2.7800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1604   -1.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9530   -1.7503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5659   -1.4071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5567   -3.3520    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.3585   -4.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3493   -3.1232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5475   -2.3224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9438   -3.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7456   -4.4961    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7364   -3.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3309   -4.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1431   -3.8938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5317   -4.6215    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.9597   -5.2160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2175   -4.8556    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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 25 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0188931

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(NC(CC1=CN=CN1)C(O)=O)C(N(C)C(=O)C(N)CC1=CN=CN1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H25N7O5/c1-9(23-13(16(26)27)4-11-6-20-8-22-11)14(17(28)29)24(2)15(25)12(18)3-10-5-19-7-21-10/h5-9,12-14,23H,3-4,18H2,1-2H3,(H,19,21)(H,20,22)(H,26,27)(H,28,29)

> <INCHI_KEY>
LMUHIYQHLMCRNZ-UHFFFAOYSA-N

> <FORMULA>
C17H25N7O5

> <MOLECULAR_WEIGHT>
407.431

> <EXACT_MASS>
407.191716933

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.79250519022585

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[2-amino-3-(1H-imidazol-5-yl)-N-methylpropanamido]-3-{[1-carboxy-2-(1H-imidazol-5-yl)ethyl]amino}butanoic acid

> <JCHEM_LOGP>
-7.711962089098446

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
2.806489713315608

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.4881455776468302

> <JCHEM_PKA_STRONGEST_BASIC>
9.70064985914795

> <JCHEM_POLAR_SURFACE_AREA>
190.32000000000002

> <JCHEM_REFRACTIVITY>
100.7879

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[2-amino-3-(3H-imidazol-4-yl)-N-methylpropanamido]-3-{[1-carboxy-2-(3H-imidazol-4-yl)ethyl]amino}butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      13.013  -7.111   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.383  -5.616   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      12.274  -4.549   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      10.794  -4.976   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.684  -3.908   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.205  -4.335   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.681  -5.783   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       6.141  -5.732   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       5.714  -4.253   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       6.989  -3.389   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      10.424  -6.471   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.534  -7.538   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       8.944  -6.898   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.863  -5.189   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.233  -3.694   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      16.712  -3.267   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      14.123  -2.627   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      15.972  -6.257   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      15.603  -7.752   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.452  -5.830   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      17.822  -4.335   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      18.562  -6.898   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      18.192  -8.393   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      20.041  -6.471   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      21.151  -7.538   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      22.667  -7.268   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0      23.393  -8.627   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      22.325  -9.737   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      20.939  -9.064   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6                                                       
CONECT   11    4   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    2   15   18                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   14   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   25                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₅N₇O₅

Average Mass

407.4310 Da

Monoisotopic Mass

407.19172 Da

IUPAC Name

2-[2-amino-3-(1H-imidazol-5-yl)-N-methylpropanamido]-3-{[1-carboxy-2-(1H-imidazol-5-yl)ethyl]amino}butanoic acid

Traditional Name

2-[2-amino-3-(3H-imidazol-4-yl)-N-methylpropanamido]-3-{[1-carboxy-2-(3H-imidazol-4-yl)ethyl]amino}butanoic acid

CAS Registry Number

Not Available

SMILES

CC(NC(CC1=CN=CN1)C(O)=O)C(N(C)C(=O)C(N)CC1=CN=CN1)C(O)=O

InChI Identifier

InChI=1S/C17H25N7O5/c1-9(23-13(16(26)27)4-11-6-20-8-22-11)14(17(28)29)24(2)15(25)12(18)3-10-5-19-7-21-10/h5-9,12-14,23H,3-4,18H2,1-2H3,(H,19,21)(H,20,22)(H,26,27)(H,28,29)

InChI Key

LMUHIYQHLMCRNZ-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
Histidine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Alpha-amino acid
Alpha-amino acid or derivatives
Imidazolyl carboxylic acid derivative
Aralkylamine
Dicarboxylic acid or derivatives
Azole
Imidazole
Heteroaromatic compound
Tertiary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Amino acid
Secondary amine
Organoheterocyclic compound
Carboxylic acid
Azacycle
Secondary aliphatic amine
Primary amine
Organopnictogen compound
Hydrocarbon derivative
Primary aliphatic amine
Organic oxygen compound
Carbonyl group
Organic oxide
Organic nitrogen compound
Amine
Organonitrogen compound
Organooxygen 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	-7.7	ChemAxon
pKa (Strongest Acidic)	1.49	ChemAxon
pKa (Strongest Basic)	9.7	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	190.32 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	100.79 m³·mol⁻¹	ChemAxon
Polarizability	39.79 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	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

39729

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

43588

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid (NP0188931)

MOL for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

3D MOL for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

3D SDF for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

3D-SDF for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

PDB for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

3D PDB for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

SMILES for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

INCHI for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

Structure for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)

3D Structure for NP0188931 (2-[2-amino-3-(3h-imidazol-4-yl)-n-methylpropanamido]-3-{[1-carboxy-2-(3h-imidazol-4-yl)ethyl]amino}butanoic acid)