NP-MRD: Showing NP-Card for 2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid (NP0167515)

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Record Information

Version

2.0

Created at

2022-09-03 03:06:23 UTC

Updated at

2022-09-03 03:06:23 UTC

NP-MRD ID

NP0167515

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid

Description

2-(2-{2-[(2-{2-[N,3-dimethyl-2-(N-methyl-1-phenylformamido)butanamido]-N,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-N,3-dimethylbutanamido}-N,3-dimethylpentanamido)-3-methylbutanoic 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-(2-{2-[(2-{2-[N,3-dimethyl-2-(N-methyl-1-phenylformamido)butanamido]-N,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-N,3-dimethylbutanamido}-N,3-dimethylpentanamido)-3-methylbutanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261513522D          

 57 57  0  0  0  0            999 V2000
   11.1673   -4.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2509   -3.5549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5819   -3.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8293   -3.4101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6655   -2.2514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9966   -1.7686    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0802   -0.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2440   -2.1065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1603   -2.9273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5750   -1.6237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8224   -1.9617    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1534   -1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2370   -0.6581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4008   -1.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3172   -2.6376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5646   -2.9756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9862   -3.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7318   -1.3341    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8154   -0.5133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9792   -1.6720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8956   -2.4928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3102   -1.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3939   -0.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7249    0.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1465   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5576   -1.5272    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4740   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8887   -1.0444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9723   -0.2236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1361   -1.3823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0524   -2.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2998   -2.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7214   -2.6859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4671   -0.8995    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5507   -0.0788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6308   -2.0583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0455   -0.7547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7071   -1.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3761   -0.6099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2925    0.2109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5399    0.5488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1291    0.0660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6586   -0.8030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9896   -0.3202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4112   -0.4650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4182   -1.9134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5018   -1.0927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0871   -2.3962    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.0035   -3.2170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8397   -2.0583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5087   -2.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2613   -2.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4251   -3.3618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9234   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2544   -0.7547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6760   -0.8995    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  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
 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
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 30 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 38 43  1  0  0  0  0
 10 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
  5 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
 51 55  1  0  0  0  0
 55 56  2  0  0  0  0
 55 57  1  0  0  0  0
M  END

     RDKit          3D

129129  0  0  0  0  0  0  0  0999 V2000
   -6.2267   -0.3547   -3.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6074    0.9928   -2.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6870    0.5429   -0.2592 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9774    0.5506    0.3850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1173    1.4564    1.3298 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1673   -0.1971    0.2413 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2328   -1.2871   -0.6776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2843    0.2225    1.0801 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.3337    0.8452    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4269    1.2647    0.7074 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1148    0.9725   -1.1210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8380   -0.7197    2.0499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8730   -1.2390    3.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6558    1.0408    0.6557 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0116    2.0966    1.6072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3156    0.5735    0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7181    1.0317    1.8088 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5365   -0.2811   -0.1111 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1381    0.0225    0.1022 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1451    0.2732    0.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6879    2.0069    2.0665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4426    2.9956    1.9442 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4074    1.1867    3.3175 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7847   -1.9683   -1.1785 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4017   -1.7412   -1.7203 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.1126   -1.3558   -0.8249 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.0147   -1.1581   -1.9186 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4102   -1.9441    0.3950 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.6969   -0.9689   -1.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2768   -1.7454   -0.9227 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3974    0.9558   -1.8316 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8043    2.8492   -2.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9195    4.9197   -1.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004261513522D          

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M  END
> <DATABASE_ID>
NP0167515

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(N(C)C(=O)C(NC(=O)C(C(C)C)N(C)C(=O)C(C(C)C)N(C)C(=O)C(C(C)C)N(C)C(=O)C1=CC=CC=C1)C(C)C)C(=O)N(C)C(C(C)C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C43H72N6O8/c1-18-29(12)36(42(55)48(16)35(28(10)11)43(56)57)49(17)39(52)31(24(2)3)44-37(50)32(25(4)5)45(13)40(53)34(27(8)9)47(15)41(54)33(26(6)7)46(14)38(51)30-22-20-19-21-23-30/h19-29,31-36H,18H2,1-17H3,(H,44,50)(H,56,57)

> <INCHI_KEY>
OJXSCBQWQXUTTR-UHFFFAOYSA-N

> <FORMULA>
C43H72N6O8

> <MOLECULAR_WEIGHT>
801.083

> <EXACT_MASS>
800.541163302

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
129

> <JCHEM_AVERAGE_POLARIZABILITY>
88.39630227513206

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{2-[2-(2-{2-[N,3-dimethyl-2-(N-methyl-1-phenylformamido)butanamido]-N,3-dimethylbutanamido}-3-methylbutanamido)-N,3-dimethylbutanamido]-N,3-dimethylpentanamido}-3-methylbutanoic acid

> <ALOGPS_LOGP>
4.32

> <JCHEM_LOGP>
5.299635061333333

> <ALOGPS_LOGS>
-5.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.570497415325185

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.016140712306582

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2049962300053885

> <JCHEM_POLAR_SURFACE_AREA>
167.95

> <JCHEM_REFRACTIVITY>
220.15670000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{2-[2-(2-{2-[N,3-dimethyl-2-(N-methyl-1-phenylformamido)butanamido]-N,3-dimethylbutanamido}-3-methylbutanamido)-N,3-dimethylbutanamido]-N,3-dimethylpentanamido}-3-methylbutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      20.846  -8.168   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.002  -6.636   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.753  -5.735   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.348  -6.365   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      19.909  -4.203   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      18.660  -3.301   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      18.816  -1.769   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.255  -3.932   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      17.099  -5.464   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      16.007  -3.031   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      14.602  -3.662   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      13.353  -2.761   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.509  -1.229   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.948  -3.391   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.792  -4.924   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.387  -5.554   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.041  -5.825   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      10.699  -2.490   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      10.855  -0.958   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.295  -3.121   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.138  -4.653   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.046  -2.220   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.202  -0.688   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.953   0.213   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.607  -0.057   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       6.641  -2.851   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       6.485  -4.383   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.392  -1.950   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.548  -0.417   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.987  -2.580   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.831  -4.112   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.426  -4.743   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.080  -5.014   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0       2.739  -1.679   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0       2.895  -0.147   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       1.178  -3.842   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       0.085  -1.409   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.320  -2.040   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.569  -1.138   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.413   0.394   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.008   1.025   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.241   0.123   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      16.163  -1.499   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      14.914  -0.598   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      17.568  -0.868   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      21.314  -3.572   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      21.470  -2.040   0.000  0.00  0.00           O+0
HETATM   49  N   UNK     0      22.563  -4.473   0.000  0.00  0.00           N+0
HETATM   50  C   UNK     0      22.407  -6.005   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      23.968  -3.842   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      25.216  -4.743   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      26.621  -4.112   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      25.060  -6.275   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      24.124  -2.310   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      22.875  -1.409   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      25.528  -1.679   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   47                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   44                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   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   26                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   22   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   34                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   30   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   43                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   38                                                       
CONECT   44   10   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47    5   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52   55                                                  
CONECT   52   51   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52                                                            
CONECT   55   51   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  114    0
END

View in JSmol

Synonyms

Value	Source
2-(2-{2-[(2-{2-[N,3-dimethyl-2-(N-methyl-1-phenylformamido)butanamido]-N,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-N,3-dimethylbutanamido}-N,3-dimethylpentanamido)-3-methylbutanoate	Generator

Chemical Formula

C₄₃H₇₂N₆O₈

Average Mass

801.0830 Da

Monoisotopic Mass

800.54116 Da

IUPAC Name

2-{2-[2-(2-{2-[N,3-dimethyl-2-(N-methyl-1-phenylformamido)butanamido]-N,3-dimethylbutanamido}-3-methylbutanamido)-N,3-dimethylbutanamido]-N,3-dimethylpentanamido}-3-methylbutanoic acid

Traditional Name

2-{2-[2-(2-{2-[N,3-dimethyl-2-(N-methyl-1-phenylformamido)butanamido]-N,3-dimethylbutanamido}-3-methylbutanamido)-N,3-dimethylbutanamido]-N,3-dimethylpentanamido}-3-methylbutanoic acid

CAS Registry Number

Not Available

SMILES

CCC(C)C(N(C)C(=O)C(NC(=O)C(C(C)C)N(C)C(=O)C(C(C)C)N(C)C(=O)C(C(C)C)N(C)C(=O)C1=CC=CC=C1)C(C)C)C(=O)N(C)C(C(C)C)C(O)=O

InChI Identifier

InChI=1S/C43H72N6O8/c1-18-29(12)36(42(55)48(16)35(28(10)11)43(56)57)49(17)39(52)31(24(2)3)44-37(50)32(25(4)5)45(13)40(53)34(27(8)9)47(15)41(54)33(26(6)7)46(14)38(51)30-22-20-19-21-23-30/h19-29,31-36H,18H2,1-17H3,(H,44,50)(H,56,57)

InChI Key

OJXSCBQWQXUTTR-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

Not Available

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
Isoleucine or derivatives
Valine or derivatives
Hippuric acid or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Alpha-amino acid amide
Alpha-amino acid or derivatives
Benzamide
Benzoic acid or derivatives
Benzoyl
Monocyclic benzene moiety
Benzenoid
N-acyl-amine
Tertiary carboxylic acid amide
Carboxamide group
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxygen compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organic nitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	4.32	ALOGPS
logP	5.3	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	4.02	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	167.95 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	220.16 m³·mol⁻¹	ChemAxon
Polarizability	88.4 Å³	ChemAxon
Number of Rings	1	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

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

73240744

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-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid (NP0167515)

MOL for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

3D MOL for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

3D SDF for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

3D-SDF for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

PDB for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

3D PDB for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

SMILES for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

INCHI for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

Structure for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)

3D Structure for NP0167515 (2-(2-{2-[(2-{2-[n,3-dimethyl-2-(n-methyl-1-phenylformamido)butanamido]-n,3-dimethylbutanamido}-1-hydroxy-3-methylbutylidene)amino]-n,3-dimethylbutanamido}-n,3-dimethylpentanamido)-3-methylbutanoic acid)