NP-MRD: Showing NP-Card for (2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide (NP0310572)

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Record Information

Version

2.0

Created at

2022-09-11 05:58:48 UTC

Updated at

2022-09-11 05:58:49 UTC

NP-MRD ID

NP0310572

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide

Description

(2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide is found in Fragaria ananassa.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112207582D          

 45 47  0  0  0  0            999 V2000
    3.6142    0.8943    0.0000 N   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


  Mrv1652309112207582D          

 45 47  0  0  0  0            999 V2000
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    5.5958    4.7841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5866    3.7545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9553    2.0383    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.5497    2.6104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3516    3.4112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3424    2.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9368    2.9536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7295    2.7248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3240    3.2968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1166    3.0680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3148    2.2672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1074    2.0383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7203    1.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9276    1.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1534    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9461    1.0087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5589    0.6655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7571   -0.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1626   -0.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3608   -1.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7663   -2.0803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9737   -1.8515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3792   -2.4235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7755   -1.0506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -0.8218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3700   -0.4786    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 27 33  1  0  0  0  0
 22 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 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
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 38 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0310572

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NCCCNCCCC(N(C(=O)\C=C\C1=CC=C(O)C=C1)C(=O)\C=C\C1=CC=C(O)C(O)=C1)C(=O)\C=C\C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C34H37N3O8/c35-18-2-20-36-19-1-3-27(28(39)13-6-24-7-14-29(40)31(42)21-24)37(33(44)16-9-23-4-11-26(38)12-5-23)34(45)17-10-25-8-15-30(41)32(43)22-25/h4-17,21-22,27,36,38,40-43H,1-3,18-20,35H2/b13-6+,16-9+,17-10+

> <INCHI_KEY>
NKPFJFCCGJLPQU-FXYGUIBDSA-N

> <FORMULA>
C34H37N3O8

> <MOLECULAR_WEIGHT>
615.683

> <EXACT_MASS>
615.258065163

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
66.2594577634576

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-N-[(1E)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-N-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide

> <JCHEM_LOGP>
2.9272312611675777

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
9.196031208621243

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.832904489394421

> <JCHEM_PKA_STRONGEST_BASIC>
9.638497492700045

> <JCHEM_POLAR_SURFACE_AREA>
193.64999999999995

> <JCHEM_REFRACTIVITY>
174.5122

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-N-[(1E)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-N-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide

> <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  N   UNK     0       6.746   1.669   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       8.226   1.242   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.815   1.883   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      11.925   2.951   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      13.405   2.524   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.514   3.591   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.994   3.164   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.104   4.232   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.734   5.727   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      17.843   6.795   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      15.254   6.154   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.144   5.086   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.665   5.513   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.555   4.446   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.076   4.873   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.706   6.368   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.226   6.795   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.815   7.435   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.445   8.930   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      12.295   7.008   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      18.583   3.805   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      19.693   4.873   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      19.323   6.368   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      21.172   4.446   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      22.282   5.513   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      23.762   5.086   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      24.871   6.154   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      26.351   5.727   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      26.721   4.232   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      28.200   3.805   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      25.611   3.164   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      24.132   3.591   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      18.953   2.310   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      20.433   1.883   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      17.843   1.242   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      18.213  -0.253   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      17.104  -1.321   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      17.473  -2.815   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      16.364  -3.883   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      14.884  -3.456   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      13.775  -4.524   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      14.514  -1.961   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      13.035  -1.534   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      15.624  -0.893   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   22                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14                                                       
CONECT   22    9   23   34                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   27                                                       
CONECT   34   22   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   45                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   38                                                       
MASTER        0    0    0    0    0    0    0    0   45    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₃₇N₃O₈

Average Mass

615.6830 Da

Monoisotopic Mass

615.25807 Da

IUPAC Name

(2E)-N-[(1E)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-N-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide

Traditional Name

(2E)-N-[(1E)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-N-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide

CAS Registry Number

Not Available

SMILES

NCCCNCCCC(N(C(=O)\C=C\C1=CC=C(O)C=C1)C(=O)\C=C\C1=CC=C(O)C(O)=C1)C(=O)\C=C\C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C34H37N3O8/c35-18-2-20-36-19-1-3-27(28(39)13-6-24-7-14-29(40)31(42)21-24)37(33(44)16-9-23-4-11-26(38)12-5-23)34(45)17-10-25-8-15-30(41)32(43)22-25/h4-17,21-22,27,36,38,40-43H,1-3,18-20,35H2/b13-6+,16-9+,17-10+

InChI Key

NKPFJFCCGJLPQU-FXYGUIBDSA-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
Fragaria x ananassa	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	2.93	ChemAxon
pKa (Strongest Acidic)	7.83	ChemAxon
pKa (Strongest Basic)	9.64	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	193.65 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	174.51 m³·mol⁻¹	ChemAxon
Polarizability	66.26 Å³	ChemAxon
Number of Rings	3	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide (NP0310572)

MOL for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

3D MOL for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

3D SDF for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

3D-SDF for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

PDB for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

3D PDB for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

SMILES for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

INCHI for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

Structure for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)

3D Structure for NP0310572 ((2e)-n-[(1e)-7-[(3-aminopropyl)amino]-1-(3,4-dihydroxyphenyl)-3-oxohept-1-en-4-yl]-3-(3,4-dihydroxyphenyl)-n-[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]prop-2-enamide)