NP-MRD: Showing NP-Card for 2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid (NP0168733)

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Record Information

Version

2.0

Created at

2022-09-03 04:35:22 UTC

Updated at

2022-09-03 04:35:22 UTC

NP-MRD ID

NP0168733

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid

Description

2-[9A-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)-2H,7H,9H,9aH-furo[3,2-g]isoquinolin-7-yl]propanoic acid belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. Based on a literature review very few articles have been published on 2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)-2H,7H,9H,9aH-furo[3,2-g]isoquinolin-7-yl]propanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032206352D          

 33 35  0  0  0  0            999 V2000
   -3.9080    4.2670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7149    4.4386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2670    3.8255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0120    3.0409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2051    2.8693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9501    2.0847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1432    1.9132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8882    1.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1345    0.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201    1.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201    2.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7056    0.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0089    1.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7233    0.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4378    1.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1523    0.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8668    1.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5812    0.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2208   -0.0275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6077   -0.5795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0277   -0.1990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4402    0.5155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9252   -0.1520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2472    0.6870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7992    0.0739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5022    1.4716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.3710    2.5993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.4329    3.5554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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    6.6369    1.8526   -0.9025 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1810    1.2267    0.3098 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1225    0.1004    0.2016 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6825   -1.1501   -0.4706 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2438    0.3392    1.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4344    0.7433    1.6921 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2545    0.3183    2.4514 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0995   -0.1640    1.9330 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3840   -1.4384    2.6045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0641    0.7774    1.8916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0590    1.8285    2.5063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1836    0.3432    1.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4134    0.7181    1.3287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5579    0.2896    0.5631 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8711    0.7857    0.9711 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -6.4379    1.7571   -0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4451   -0.4016   -0.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5692   -1.6289   -1.1018 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9674   -1.0615   -1.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3791    0.3930   -2.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9442    0.1152   -0.1003 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1223    1.7221   -0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3535    1.6256   -2.6417 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0985    0.0779   -2.1110 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0076    2.7371   -0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6415    2.0921    0.9227 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1236    0.4179   -0.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3873   -0.1973    1.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
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 33 64  1  0
M  END


  Mrv1652309032206352D          

 33 35  0  0  0  0            999 V2000
   -3.9080    4.2670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7149    4.4386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2670    3.8255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0168733

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(=O)C1=C2C=C3C=C(C=CC)N(C=C3C(=O)C2(C)OC1=O)C(C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H31NO6/c1-5-7-8-9-10-12-21(28)22-20-14-17-13-18(11-6-2)27(16(3)24(30)31)15-19(17)23(29)26(20,4)33-25(22)32/h6,11,13-16H,5,7-10,12H2,1-4H3,(H,30,31)

> <INCHI_KEY>
QIFKDKYLKWDIPS-UHFFFAOYSA-N

> <FORMULA>
C26H31NO6

> <MOLECULAR_WEIGHT>
453.535

> <EXACT_MASS>
453.215137722

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
51.091435914573935

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)-2H,7H,9H,9aH-furo[3,2-g]isoquinolin-7-yl]propanoic acid

> <ALOGPS_LOGP>
4.23

> <JCHEM_LOGP>
4.648757758333332

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.380863829280784

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.955577479337103

> <JCHEM_PKA_STRONGEST_BASIC>
-4.561478938792035

> <JCHEM_POLAR_SURFACE_AREA>
100.98

> <JCHEM_REFRACTIVITY>
128.03339999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.59e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.295   7.965   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.801   8.285   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.832   7.141   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.356   5.676   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.849   5.356   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.374   3.891   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.867   3.571   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.391   2.107   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.984   1.480   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.651   2.250   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.651   3.790   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.317   1.480   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.017   2.250   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.350   1.480   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.684   2.250   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.018   1.480   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.351   2.250   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.685   1.480   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.145  -0.051   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.001  -1.082   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -5.652  -0.371   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -6.422   0.962   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -7.327  -0.284   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -7.928   1.282   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -8.959   0.138   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -8.404   2.747   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -9.910   3.067   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0     -10.386   4.532   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0     -11.893   4.852   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -12.923   3.708   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -12.368   6.317   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0     -11.338   7.461   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0     -13.875   6.637   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   28                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19    9   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    8   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    6   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27    4   29                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
2-[9a-Methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)-2H,7H,9H,9ah-furo[3,2-g]isoquinolin-7-yl]propanoate	Generator

Chemical Formula

C₂₆H₃₁NO₆

Average Mass

453.5350 Da

Monoisotopic Mass

453.21514 Da

IUPAC Name

2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)-2H,7H,9H,9aH-furo[3,2-g]isoquinolin-7-yl]propanoic acid

Traditional Name

2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCC(=O)C1=C2C=C3C=C(C=CC)N(C=C3C(=O)C2(C)OC1=O)C(C)C(O)=O

InChI Identifier

InChI=1S/C26H31NO6/c1-5-7-8-9-10-12-21(28)22-20-14-17-13-18(11-6-2)27(16(3)24(30)31)15-19(17)23(29)26(20,4)33-25(22)32/h6,11,13-16H,5,7-10,12H2,1-4H3,(H,30,31)

InChI Key

QIFKDKYLKWDIPS-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Alpha-amino acid or derivatives
Aryl alkyl ketone
Aryl ketone
Alpha-acyloxy ketone
2-furanone
Dicarboxylic acid or derivatives
Pyridine
Heteroaromatic compound
Dihydrofuran
Vinylogous amide
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Ketone
Lactone
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Organic oxygen compound
Organopnictogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	4.23	ALOGPS
logP	4.65	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	3.96	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	100.98 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	128.03 m³·mol⁻¹	ChemAxon
Polarizability	51.09 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

85200480

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid (NP0168733)

MOL for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

3D MOL for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

3D SDF for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

3D-SDF for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

PDB for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

3D PDB for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

SMILES for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

INCHI for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

Structure for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)

3D Structure for NP0168733 (2-[9a-methyl-3-octanoyl-2,9-dioxo-6-(prop-1-en-1-yl)furo[3,2-g]isoquinolin-7-yl]propanoic acid)