NP-MRD: Showing NP-Card for 3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid (NP0220918)

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Record Information

Version

2.0

Created at

2022-09-05 22:21:46 UTC

Updated at

2022-09-05 22:21:46 UTC

NP-MRD ID

NP0220918

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid

Description

3-{[5,6-Dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoic acid belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. 3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid is found in Aspergillus fumisynnematus. 3-{[5,6-Dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -1.0611    3.6837   -0.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6593    2.3057   -1.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2605    1.3305   -0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6800   -0.0465   -0.2459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6384   -0.5236   -1.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2296    0.3149   -2.0342 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0282   -1.8618   -1.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9838   -2.3859   -1.9497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4169   -2.6954   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4621   -2.2217    0.7107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0775   -0.9064    0.6882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0418   -0.6535    1.7199 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5283    0.3045    2.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147   -0.2389    1.1490 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -0.9895    0.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2800   -2.0502   -0.2548 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1150   -0.6272   -0.4756 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8206    0.4444   -0.1672 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0885    0.7439   -0.8324 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7726    1.7542   -0.5550 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5401   -0.1326   -1.8065 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1367   -1.9818    2.3522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505   -2.2016    3.3008 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8543    1.7255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1854    3.8202   -1.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8067    4.4526   -1.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7334    3.7495    0.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3937    2.2448   -1.7749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4792    1.6232    0.4922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9178   -0.0071   -2.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4479   -1.8611   -2.6236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7251   -3.7261   -0.1498 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0963    1.2242    2.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5880   -0.1871    3.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5569    0.6157    2.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6758    0.6311    1.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5416   -1.2733   -1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4248    1.0957    0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1056   -0.9130   -1.4946 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
  5  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 21  1  0
 19 20  2  0
 12 22  1  0
 22 23  2  0
 22 24  1  0
 11  4  1  0
 24 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  6 30  1  0
  8 31  1  0
  9 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 17 37  1  0
 18 38  1  0
 21 39  1  0
M  END


  Mrv1533004161522462D          

 24 25  0  0  0  0            999 V2000
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1154    1.8336    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305    2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9660    3.2547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8100    2.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3251    3.0823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4954    2.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8310    2.2423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9803    3.6635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  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
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 17  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 14 24  1  0  0  0  0
  4 24  1  0  0  0  0
 10 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0220918

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=CC1=C(O)C(O)=CC2=C1C(C)(NC(=O)C=CC(O)=O)C(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C16H15NO7/c1-3-4-8-13-10(7-9(18)14(8)22)24-15(23)16(13,2)17-11(19)5-6-12(20)21/h3-7,18,22H,1-2H3,(H,17,19)(H,20,21)

> <INCHI_KEY>
QWMZGLCXYLPQAZ-UHFFFAOYSA-N

> <FORMULA>
C16H15NO7

> <MOLECULAR_WEIGHT>
333.296

> <EXACT_MASS>
333.084851827

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.98326021604223

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

> <ALOGPS_LOGP>
2.17

> <JCHEM_LOGP>
1.5698108279999996

> <ALOGPS_LOGS>
-3.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.857699822583397

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.650543292947396

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0091756452979799

> <JCHEM_POLAR_SURFACE_AREA>
133.15999999999997

> <JCHEM_REFRACTIVITY>
84.29199999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       7.454   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.454   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.788   2.310   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.788  -0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.322  -0.476   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.877   0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.989   2.786   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       3.949   3.423   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.044   4.669   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.670   6.075   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.512   4.508   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.607   5.754   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.925   5.593   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.551   4.186   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -1.830   6.838   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   24                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   24                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   24                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   14    4   10                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoate	Generator

Chemical Formula

C₁₆H₁₅NO₇

Average Mass

333.2960 Da

Monoisotopic Mass

333.08485 Da

IUPAC Name

3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

Traditional Name

3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]carbamoyl}prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

CC=CC1=C(O)C(O)=CC2=C1C(C)(NC(=O)C=CC(O)=O)C(=O)O2

InChI Identifier

InChI=1S/C16H15NO7/c1-3-4-8-13-10(7-9(18)14(8)22)24-15(23)16(13,2)17-11(19)5-6-12(20)21/h3-7,18,22H,1-2H3,(H,17,19)(H,20,21)

InChI Key

QWMZGLCXYLPQAZ-UHFFFAOYSA-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
Aspergillus fumisynnematus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen 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-alpha amino acids and derivatives

Alternative Parents

Substituents

N-acyl-alpha amino acid or derivatives
Benzofuran
Coumaran
Styrene
1-hydroxy-2-unsubstituted benzenoid
Phenol
Dicarboxylic acid or derivatives
Benzenoid
Carboxylic acid ester
Lactone
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
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	2.17	ALOGPS
logP	1.57	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	2.65	ChemAxon
pKa (Strongest Basic)	-1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.16 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	84.29 m³·mol⁻¹	ChemAxon
Polarizability	31.98 Å³	ChemAxon
Number of Rings	2	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

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

73312051

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid (NP0220918)

MOL for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D MOL for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D SDF for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D-SDF for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

PDB for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D PDB for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

SMILES for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

INCHI for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

Structure for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)

3D Structure for NP0220918 (3-{[5,6-dihydroxy-3-methyl-2-oxo-4-(prop-1-en-1-yl)-1-benzofuran-3-yl]-c-hydroxycarbonimidoyl}prop-2-enoic acid)