NP-MRD: Showing NP-Card for (2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid (NP0188169)

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Record Information

Version

2.0

Created at

2022-09-04 04:27:07 UTC

Updated at

2022-09-04 04:27:07 UTC

NP-MRD ID

NP0188169

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid

Description

(2S)-2-{[(2E)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1H-indol-3-yl)propanoic acid belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. (2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid is found in Fuligo aurea. Based on a literature review very few articles have been published on (2S)-2-{[(2E)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1H-indol-3-yl)propanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042206272D          

 26 28  0  0  1  0            999 V2000
   -3.0668   -7.3723    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8118   -6.5877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3639   -5.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1089   -5.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3020   -5.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0470   -4.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371   -2.6646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752   -1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203   -0.9238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822   -1.8800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7499   -5.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0049   -6.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  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  1  4  0  0  0
  8 10  2  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 13 21  1  0  0  0  0
 16 21  1  0  0  0  0
 11 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  2  0  0  0  0
  2 26  1  0  0  0  0
M  END

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
    8.6014   -0.6485   -1.0553 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1854   -0.6491   -0.9488 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4069   -1.7531   -1.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0364   -1.7062   -1.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3654   -0.5361   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9126   -0.5476   -0.6001 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2093    0.4973   -0.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7546    0.3740   -0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1319   -0.8294   -0.4694 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0102    1.3715    0.1458 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4166    1.3126    0.2364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8811    0.5775    1.4751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3746    0.5730    1.4737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2127    1.3687    2.2631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4884    1.0683    1.9689 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5432    0.1143    1.0250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6195   -0.5094    0.4096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3510   -1.4592   -0.5316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0542   -1.8163   -0.8882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9971   -1.1681   -0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2344   -0.1942    0.7165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9457    2.6964    0.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1686    3.7045    0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3013    3.0006    0.2296 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1457    0.5678   -0.4592 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5413    0.5104   -0.5799 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1677   -1.2482   -0.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0340   -0.0338   -1.7749 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9156   -2.6657   -1.4861 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4523   -2.5846   -1.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3827   -1.4904   -0.8201 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6801    1.4369   -0.0356 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4889   -1.6734   -0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7858    0.7125   -0.6388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5355    1.0407    2.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5436   -0.4590    1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8261    2.0797    2.9658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3069    1.5225    2.4207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6502   -0.2780    0.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1708   -1.9630   -1.0292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8879   -2.5719   -1.6374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9820   -1.3982   -0.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9220    2.9737   -0.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6759    1.4901   -0.1688 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1008    1.4193   -0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 11 22  1  0
 22 24  1  0
 22 23  2  0
  5 25  1  0
 25 26  2  0
 26  2  1  0
 21 13  1  0
 21 16  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  4 30  1  0
  6 31  1  0
  7 32  1  0
  9 33  1  0
 11 34  1  6
 12 35  1  0
 12 36  1  0
 14 37  1  0
 15 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 24 43  1  0
 25 44  1  0
 26 45  1  0
M  END


  Mrv1652309042206272D          

 26 28  0  0  1  0            999 V2000
   -3.0668   -7.3723    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8118   -6.5877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3639   -5.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1089   -5.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3020   -5.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0470   -4.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371   -2.6646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752   -1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203   -0.9238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822   -1.8800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7499   -5.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0049   -6.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  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  1  4  0  0  0
  8 10  2  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 13 21  1  0  0  0  0
 16 21  1  0  0  0  0
 11 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  2  0  0  0  0
  2 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0188169

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC1=CC=C(\C=C\C(O)=N[C@@H](CC2=CNC3=CC=CC=C23)C(O)=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H19N3O3/c21-15-8-5-13(6-9-15)7-10-19(24)23-18(20(25)26)11-14-12-22-17-4-2-1-3-16(14)17/h1-10,12,18,22H,11,21H2,(H,23,24)(H,25,26)/b10-7+/t18-/m0/s1

> <INCHI_KEY>
TZFPHPZWQAKWNP-HKMNZKMDSA-N

> <FORMULA>
C20H19N3O3

> <MOLECULAR_WEIGHT>
349.39

> <EXACT_MASS>
349.142641484

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.03106460560906

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-{[(2E)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1H-indol-3-yl)propanoic acid

> <JCHEM_LOGP>
2.749926530756612

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
6.40960715158116

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6716369275326164

> <JCHEM_PKA_STRONGEST_BASIC>
4.53418081968055

> <JCHEM_POLAR_SURFACE_AREA>
111.7

> <JCHEM_REFRACTIVITY>
101.28490000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-{[(2E)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1H-indol-3-yl)propanoic 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  N   UNK     0      -5.725 -13.762   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      -5.249 -12.297   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.279 -11.153   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.803  -9.688   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.297  -9.368   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.821  -7.903   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.315  -7.583   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.839  -6.118   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.869  -4.974   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0      -0.333  -5.798   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.887  -3.189   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.411  -1.724   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -2.393  -3.509   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -3.267 -10.512   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.742 -11.977   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   13   16                                                  
CONECT   22   11   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    5   26                                                       
CONECT   26   25    2                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
(2S)-2-{[(2E)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1H-indol-3-yl)propanoate	Generator

Chemical Formula

C₂₀H₁₉N₃O₃

Average Mass

349.3900 Da

Monoisotopic Mass

349.14264 Da

IUPAC Name

(2S)-2-{[(2E)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1H-indol-3-yl)propanoic acid

Traditional Name

(2S)-2-{[(2E)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1H-indol-3-yl)propanoic acid

CAS Registry Number

Not Available

SMILES

NC1=CC=C(\C=C\C(O)=N[C@@H](CC2=CNC3=CC=CC=C23)C(O)=O)C=C1

InChI Identifier

InChI=1S/C20H19N3O3/c21-15-8-5-13(6-9-15)7-10-19(24)23-18(20(25)26)11-14-12-22-17-4-2-1-3-16(14)17/h1-10,12,18,22H,11,21H2,(H,23,24)(H,25,26)/b10-7+/t18-/m0/s1

InChI Key

TZFPHPZWQAKWNP-HKMNZKMDSA-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
Fuligo aurea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-L-alpha-amino acids

Alternative Parents

Substituents

N-acyl-l-alpha-amino acid
Cinnamic acid amide
Cinnamic acid or derivatives
Indolyl carboxylic acid derivative
3-alkylindole
Indole
Indole or derivatives
Styrene
Aniline or substituted anilines
Monocyclic benzene moiety
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Carboxamide group
Secondary carboxylic acid amide
Amino acid
Azacycle
Organoheterocyclic compound
Carboxylic acid
Monocarboxylic acid or derivatives
Primary amine
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Amine
Hydrocarbon derivative
Carbonyl group
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.75	ChemAxon
pKa (Strongest Acidic)	3.67	ChemAxon
pKa (Strongest Basic)	4.53	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	111.7 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	101.28 m³·mol⁻¹	ChemAxon
Polarizability	37.03 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

17262109

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16104254

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid (NP0188169)

MOL for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

3D MOL for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

3D SDF for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

3D-SDF for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

PDB for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

3D PDB for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

SMILES for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

INCHI for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

Structure for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)

3D Structure for NP0188169 ((2s)-2-{[(2e)-3-(4-aminophenyl)-1-hydroxyprop-2-en-1-ylidene]amino}-3-(1h-indol-3-yl)propanoic acid)