NP-MRD: Showing NP-Card for (3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid (NP0309742)

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Record Information

Version

2.0

Created at

2022-09-11 04:33:07 UTC

Updated at

2022-09-11 04:33:07 UTC

NP-MRD ID

NP0309742

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid

Description

Leu-Asp-Ser, also known as L-D-S or L-leu-L-asp-L-ser, belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. Leu-Asp-Ser is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. (3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid is found in Trypanosoma brucei. (3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid was first documented in 2013 (PMID: 23566958). Based on a literature review very few articles have been published on Leu-Asp-Ser.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 45  0  0  0  0  0  0  0  0999 V2000
   -5.1394    1.9829    0.5333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3412    1.0759   -0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8857   -0.3296   -0.1976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8977    1.1366    0.0588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0197    0.2526   -0.8016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4252   -1.1370   -0.7431 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6271    0.3532   -0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0563    1.5676   -0.3001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0028   -0.6912    0.1203 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3540   -0.6801    0.6116 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5376   -1.6093    1.8178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1919   -2.9836    1.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0450   -3.1828    0.9250 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0608   -4.0608    1.5900 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2923   -1.2153   -0.4199 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0612   -2.5204   -0.8238 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2578   -0.5655   -0.9337 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6582    0.7751   -0.6583 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1701    0.8411   -0.8421 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7772   -0.0430    0.0574 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0143    1.7081   -1.5909 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2307    1.2710   -2.4768 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2352    3.0800   -1.5369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3232    2.9815    0.0452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1325    1.5257    0.8173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5906    2.1003    1.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4315    1.4332   -1.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9707   -0.3374    0.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7557   -0.8648   -1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3342   -0.8292    0.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7647    0.8404    1.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5455    2.1723   -0.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1263    0.5978   -1.8448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9316   -1.6382   -1.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0530   -1.5392    0.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3813    2.3105    0.2228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6000    0.3693    0.8980 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5912   -1.6064    2.1406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9286   -1.2296    2.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7395   -5.0314    1.5817 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8528   -3.0690   -1.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4691    1.1023    0.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5782    1.8509   -0.6997 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4061    0.4750   -1.8788 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1913   -0.1658    0.8364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3803    3.5263   -0.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 14  1  0
 12 13  2  0
 10 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 23  1  0
 21 22  2  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
  6 34  1  0
  6 35  1  0
  8 36  1  0
 10 37  1  1
 11 38  1  0
 11 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  1
 19 43  1  0
 19 44  1  0
 20 45  1  0
 23 46  1  0
M  END


  Mrv1652309112206332D          

 23 22  0  0  1  0            999 V2000
   -4.1763    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4618    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4618    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0329    1.4289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0329    0.6039    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3184    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3184    2.6664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    1.8414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8250    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    2.6664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039    3.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    3.0789    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    3.9039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395    4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    5.1414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    5.1414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039    3.9039    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
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  4  0  0  0
  7  9  2  0  0  0  0
 10  9  1  6  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
 10 15  1  0  0  0  0
 15 16  1  4  0  0  0
 15 17  2  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0309742

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C[C@H](N)C(O)=N[C@@H](CC(O)=O)C(O)=N[C@@H](CO)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H23N3O7/c1-6(2)3-7(14)11(20)15-8(4-10(18)19)12(21)16-9(5-17)13(22)23/h6-9,17H,3-5,14H2,1-2H3,(H,15,20)(H,16,21)(H,18,19)(H,22,23)/t7-,8-,9-/m0/s1

> <INCHI_KEY>
PVMPDMIKUVNOBD-CIUDSAMLSA-N

> <FORMULA>
C13H23N3O7

> <MOLECULAR_WEIGHT>
333.341

> <EXACT_MASS>
333.153600093

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
32.76768053264127

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S)-3-{[(2S)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1S)-1-carboxy-2-hydroxyethyl]-C-hydroxycarbonimidoyl}propanoic acid

> <JCHEM_LOGP>
-3.0034618346208415

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.489619602167431

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.9442183100244925

> <JCHEM_PKA_STRONGEST_BASIC>
9.60540452111018

> <JCHEM_POLAR_SURFACE_AREA>
186.02999999999997

> <JCHEM_REFRACTIVITY>
77.3882

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-{[(2S)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1S)-1-carboxy-2-hydroxyethyl]-C-hydroxycarbonimidoyl}propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.796   3.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.462   2.667   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.462   1.127   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.128   3.437   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.795   2.667   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -3.795   1.127   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -2.461   3.437   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.461   4.977   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0      -1.127   2.667   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       0.206   3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.540   2.667   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.874   4.977   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       4.207   2.667   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.206   4.977   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.127   5.747   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       1.540   5.747   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       1.540   7.287   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.874   8.057   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.874   9.597   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.206   8.057   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.206   9.597   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -1.127   7.287   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   44    0
END

View in JSmol

Synonyms

Value	Source
L-D-S	ChEBI
L-Leu-L-asp-L-ser	ChEBI
LDS	ChEBI

Chemical Formula

C₁₃H₂₃N₃O₇

Average Mass

333.3410 Da

Monoisotopic Mass

333.15360 Da

IUPAC Name

(3S)-3-{[(2S)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1S)-1-carboxy-2-hydroxyethyl]-C-hydroxycarbonimidoyl}propanoic acid

Traditional Name

(3S)-3-{[(2S)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1S)-1-carboxy-2-hydroxyethyl]-C-hydroxycarbonimidoyl}propanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)C[C@H](N)C(O)=N[C@@H](CC(O)=O)C(O)=N[C@@H](CO)C(O)=O

InChI Identifier

InChI=1S/C13H23N3O7/c1-6(2)3-7(14)11(20)15-8(4-10(18)19)12(21)16-9(5-17)13(22)23/h6-9,17H,3-5,14H2,1-2H3,(H,15,20)(H,16,21)(H,18,19)(H,22,23)/t7-,8-,9-/m0/s1

InChI Key

PVMPDMIKUVNOBD-CIUDSAMLSA-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
Trypanosoma brucei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Leucine or derivatives
Aspartic acid or derivatives
N-acyl-alpha-amino acid
N-acyl-l-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Serine or derivatives
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Hydroxy fatty acid
Beta-hydroxy acid
Branched fatty acid
Hydroxy acid
Fatty amide
N-acyl-amine
Fatty acyl
Dicarboxylic acid or derivatives
Fatty acid
Amino acid
Carboxamide group
Amino acid or derivatives
Secondary carboxylic acid amide
Carboxylic acid
Alcohol
Primary aliphatic amine
Organonitrogen compound
Organooxygen compound
Primary alcohol
Carbonyl group
Primary amine
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

tripeptide (CHEBI:73563 )

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	ChemAxon
pKa (Strongest Acidic)	2.94	ChemAxon
pKa (Strongest Basic)	9.61	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	186.03 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	77.39 m³·mol⁻¹	ChemAxon
Polarizability	32.77 Å³	ChemAxon
Number of Rings	0	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

28639367

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71464621

PDB ID

Not Available

ChEBI ID

73563

Good Scents ID

Not Available

References

General References

Himaya SW, Dewapriya P, Kim SK: EGFR tyrosine kinase inhibitory peptide attenuates Helicobacter pylori-mediated hyper-proliferation in AGS enteric epithelial cells. Toxicol Appl Pharmacol. 2013 Jun 15;269(3):205-14. doi: 10.1016/j.taap.2013.03.020. Epub 2013 Apr 6. [PubMed:23566958 ]
LOTUS database [Link]

Showing NP-Card for (3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid (NP0309742)

MOL for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

3D MOL for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

3D SDF for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

3D-SDF for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

PDB for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

3D PDB for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

SMILES for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

INCHI for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

Structure for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)

3D Structure for NP0309742 ((3s)-3-{[(2s)-2-amino-1-hydroxy-4-methylpentylidene]amino}-3-{[(1s)-1-carboxy-2-hydroxyethyl]-c-hydroxycarbonimidoyl}propanoic acid)