NP-MRD: Showing NP-Card for (2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid (NP0148843)

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Record Information

Version

2.0

Created at

2022-09-02 04:39:11 UTC

Updated at

2022-09-02 04:39:11 UTC

NP-MRD ID

NP0148843

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid

Description

(2E)-3-(4-{[(2S,3S,4S,5S)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-N-[(4R,5R,6S,7R)-4,6,7-trihydroxy-hexahydro-2H-1,3-benzodioxol-5-yl]prop-2-enimidic acid belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. (2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid is found in Streptomyces hygroscopicus. Based on a literature review very few articles have been published on (2E)-3-(4-{[(2S,3S,4S,5S)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-N-[(4R,5R,6S,7R)-4,6,7-trihydroxy-hexahydro-2H-1,3-benzodioxol-5-yl]prop-2-enimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022206392D          

 36 39  0  0  1  0            999 V2000
    7.7917    8.3386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309022206392D          

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 27 28  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  1  6  0  0  0
 11 30  1  0  0  0  0
 30 31  2  0  0  0  0
  8 31  1  0  0  0  0
 31 32  1  0  0  0  0
  6 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
  4 35  1  0  0  0  0
 35 36  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0148843

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)[C@H]1O[C@@H](OC2=CC=C(\C=C(/C)C(O)=N[C@H]3[C@@H](O)C4OCOC4[C@H](O)[C@H]3O)C=C2O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H29NO12/c1-8(22(32)24-13-14(27)16(29)21-20(15(13)28)33-7-34-21)5-10-3-4-12(11(26)6-10)35-23-18(31)17(30)19(36-23)9(2)25/h3-6,13-21,23,26-31H,7H2,1-2H3,(H,24,32)/b8-5+/t13-,14+,15-,16-,17+,18+,19-,20?,21?,23-/m1/s1

> <INCHI_KEY>
YQYJSBFKSSDGFO-KFNANMTRSA-N

> <FORMULA>
C23H29NO12

> <MOLECULAR_WEIGHT>
511.48

> <EXACT_MASS>
511.168975378

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
50.59219933179506

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-3-(4-{[(2S,3S,4S,5S)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-N-[(4R,5R,6S,7R)-4,6,7-trihydroxy-hexahydro-2H-1,3-benzodioxol-5-yl]prop-2-enimidic acid

> <ALOGPS_LOGP>
-0.42

> <JCHEM_LOGP>
-0.8655929826666668

> <ALOGPS_LOGS>
-2.33

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.690241466462705

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.475665084718228

> <JCHEM_PKA_STRONGEST_BASIC>
2.130199191519818

> <JCHEM_POLAR_SURFACE_AREA>
207.95999999999998

> <JCHEM_REFRACTIVITY>
118.07640000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.41e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-(4-{[(2S,3S,4S,5S)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-N-[(4R,5R,6S,7R)-4,6,7-trihydroxy-hexahydro-2H-1,3-benzodioxol-5-yl]prop-2-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      14.545  15.565   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.918  14.159   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      12.387  13.998   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      14.823  12.913   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      14.347  11.448   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      15.593  10.543   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      15.593   9.003   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      14.260   8.233   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.260   6.693   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.926   5.923   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.592   6.693   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.259   5.923   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.925   6.693   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.925   8.233   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.591   5.923   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.258   6.693   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       7.591   4.383   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       6.258   3.613   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  O   UNK     0       7.591   1.303   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.924  -0.237   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.924   5.923   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.592   8.233   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.926   9.003   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      12.926  10.543   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      16.839  11.448   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      18.304  10.972   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      16.363  12.913   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      17.269  14.159   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   35                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   33                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   31                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   28                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23   28                                                  
CONECT   28   27   18   29                                                  
CONECT   29   28                                                            
CONECT   30   11   31                                                       
CONECT   31   30    8   32                                                  
CONECT   32   31                                                            
CONECT   33    6   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33    4   36                                                  
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Value	Source
(2E)-3-(4-{[(2S,3S,4S,5S)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-N-[(4R,5R,6S,7R)-4,6,7-trihydroxy-hexahydro-2H-1,3-benzodioxol-5-yl]prop-2-enimidate	Generator

Chemical Formula

C₂₃H₂₉NO₁₂

Average Mass

511.4800 Da

Monoisotopic Mass

511.16898 Da

IUPAC Name

(2E)-3-(4-{[(2S,3S,4S,5S)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-N-[(4R,5R,6S,7R)-4,6,7-trihydroxy-hexahydro-2H-1,3-benzodioxol-5-yl]prop-2-enimidic acid

Traditional Name

(2E)-3-(4-{[(2S,3S,4S,5S)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-N-[(4R,5R,6S,7R)-4,6,7-trihydroxy-hexahydro-2H-1,3-benzodioxol-5-yl]prop-2-enimidic acid

CAS Registry Number

Not Available

SMILES

CC(=O)[C@H]1O[C@@H](OC2=CC=C(\C=C(/C)C(O)=N[C@H]3[C@@H](O)C4OCOC4[C@H](O)[C@H]3O)C=C2O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C23H29NO12/c1-8(22(32)24-13-14(27)16(29)21-20(15(13)28)33-7-34-21)5-10-3-4-12(11(26)6-10)35-23-18(31)17(30)19(36-23)9(2)25/h3-6,13-21,23,26-31H,7H2,1-2H3,(H,24,32)/b8-5+/t13-,14+,15-,16-,17+,18+,19-,20?,21?,23-/m1/s1

InChI Key

YQYJSBFKSSDGFO-KFNANMTRSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces hygroscopicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
O-glycosyl compound
Pentose monosaccharide
Phenoxy compound
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monosaccharide
Monocyclic benzene moiety
Cyclitol or derivatives
Tetrahydrofuran
Cyclic alcohol
Meta-dioxolane
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Carboximidic acid derivative
Carboximidic acid
Acetal
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Carbonyl group
Alcohol
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	-0.42	ALOGPS
logP	-0.87	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	5.48	ChemAxon
pKa (Strongest Basic)	2.13	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	207.96 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	118.08 m³·mol⁻¹	ChemAxon
Polarizability	50.59 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

163009212

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid (NP0148843)

MOL for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

3D MOL for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

3D SDF for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

3D-SDF for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

PDB for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

3D PDB for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

SMILES for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

INCHI for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

Structure for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)

3D Structure for NP0148843 ((2e)-3-(4-{[(2s,3s,4s,5s)-5-acetyl-3,4-dihydroxyoxolan-2-yl]oxy}-3-hydroxyphenyl)-2-methyl-n-[(4r,5r,6s,7r)-4,6,7-trihydroxy-hexahydro-2h-1,3-benzodioxol-5-yl]prop-2-enimidic acid)