NP-MRD: Showing NP-Card for (s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid (NP0291916)

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Record Information

Version

2.0

Created at

2022-09-09 23:11:43 UTC

Updated at

2022-09-09 23:11:44 UTC

NP-MRD ID

NP0291916

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid

Description

Giganticine 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. (s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid is found in Calotropis gigantea. (s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid was first documented in 1998 (PMID: 9548837). Based on a literature review very few articles have been published on giganticine (PMID: 11520243).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
    6.0963    1.2109    0.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9393    1.1815   -0.6597 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9499    0.2706   -1.0812 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6054    0.3930   -0.6717 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3861    1.3662    0.0837 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392   -0.5142   -1.0963 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2817   -0.4930   -0.7570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4234   -1.4790   -1.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9178   -1.5426   -0.9877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4984   -0.6094   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9394   -0.6132    0.1534 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1146   -0.4622    1.5904 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1337    0.1728    2.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1321    0.7524    1.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3282    0.3333    3.4045 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6436   -1.7929   -0.3344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1721   -2.5924    0.5039 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7853   -2.1133   -1.6628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6869    0.3812    0.3409 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6890    0.4406    0.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8606    2.2106    1.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3677    0.4481    1.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1054    0.8677    1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8967    0.8304   -1.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6552    2.1965   -1.0272 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9677   -1.2915   -1.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8593   -2.2334   -1.9081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5432   -2.3485   -1.4119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3662    0.2989   -0.3594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2997    0.0628    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7731    1.7217    0.7133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0836    0.8929    1.6514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1249    1.2345    3.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3303   -1.5540   -2.3188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1156    1.1343    0.9847 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2660    1.2389    0.4924 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 19  1  0
 19 20  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 11 16  1  0
 16 18  1  0
 16 17  2  0
 20  7  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 19 35  1  0
 20 36  1  0
 11 29  1  6
 14 30  1  0
 14 31  1  0
 14 32  1  0
 15 33  1  0
 18 34  1  0
M  END


  Mrv1652309102201112D          

 20 20  0  0  1  0            999 V2000
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  2  0  0  0  0
 13 14  1  4  0  0  0
 13 15  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  2  0  0  0  0
  7 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0291916

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=O)NC1=CC=C(C=C1)[C@H](N=C(C)O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H16N2O5/c1-3-20-13(19)15-10-6-4-9(5-7-10)11(12(17)18)14-8(2)16/h4-7,11H,3H2,1-2H3,(H,14,16)(H,15,19)(H,17,18)/t11-/m0/s1

> <INCHI_KEY>
LXZCEJOKBHKJLM-NSHDSACASA-N

> <FORMULA>
C13H16N2O5

> <MOLECULAR_WEIGHT>
280.28

> <EXACT_MASS>
280.105921623

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.485776912213566

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-{4-[(ethoxycarbonyl)amino]phenyl}-2-[(1-hydroxyethylidene)amino]acetic acid

> <JCHEM_LOGP>
1.6412140359999996

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.6203386947064065

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3243542716170777

> <JCHEM_PKA_STRONGEST_BASIC>
0.05473289486744348

> <JCHEM_POLAR_SURFACE_AREA>
108.22000000000001

> <JCHEM_REFRACTIVITY>
71.56200000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(S)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0       5.335  -4.620   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      12.003  -6.930   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.337  -9.240   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.003 -10.010   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   20                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   11   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   10   20                                                       
CONECT   20   19    7                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₆N₂O₅

Average Mass

280.2800 Da

Monoisotopic Mass

280.10592 Da

IUPAC Name

(2S)-2-{4-[(ethoxycarbonyl)amino]phenyl}-2-[(1-hydroxyethylidene)amino]acetic acid

Traditional Name

(S)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid

CAS Registry Number

Not Available

SMILES

CCOC(=O)NC1=CC=C(C=C1)[C@H](N=C(C)O)C(O)=O

InChI Identifier

InChI=1S/C13H16N2O5/c1-3-20-13(19)15-10-6-4-9(5-7-10)11(12(17)18)14-8(2)16/h4-7,11H,3H2,1-2H3,(H,14,16)(H,15,19)(H,17,18)/t11-/m0/s1

InChI Key

LXZCEJOKBHKJLM-NSHDSACASA-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
Calotropis gigantea	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
Phenylcarbamic acid ester
Monocyclic benzene moiety
Benzenoid
Carbamic acid ester
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid
Monocarboxylic acid or derivatives
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	1.64	ChemAxon
pKa (Strongest Acidic)	3.32	ChemAxon
pKa (Strongest Basic)	0.055	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	108.22 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	71.56 m³·mol⁻¹	ChemAxon
Polarizability	28.49 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

9025626

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10850332

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Suparpprom C, Vilaivan T: Synthesis of 2-[4'-(ethylcarbamoyl)phenyl]-N-acetylglycine, the proposed structure for giganticine. J Nat Prod. 2001 Aug;64(8):1114-6. doi: 10.1021/np010046l. [PubMed:11520243 ]
Pari K, Rao PJ, Devakumar C, Rastogi JN: A Novel Insect Antifeedant Nonprotein Amino Acid from Calotropis gigantea J Nat Prod. 1998 Jan 23;61(1):102-4. doi: 10.1021/np970255z. [PubMed:9548837 ]
LOTUS database [Link]

Showing NP-Card for (s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid (NP0291916)

MOL for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

3D MOL for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

3D SDF for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

3D-SDF for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

PDB for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

3D PDB for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

SMILES for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

INCHI for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

Structure for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)

3D Structure for NP0291916 ((s)-{4-[(ethoxycarbonyl)amino]phenyl}[(1-hydroxyethylidene)amino]acetic acid)