NP-MRD: Showing NP-Card for 7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione (NP0225643)

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Record Information

Version

2.0

Created at

2022-09-06 04:25:44 UTC

Updated at

2022-09-06 04:25:44 UTC

NP-MRD ID

NP0225643

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione

Description

7-(2-Hydroxyethyl)-monascorubramine 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. 7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione was first documented in 2022 (PMID: 35608668). Based on a literature review very few articles have been published on 7-(2-hydroxyethyl)-monascorubramine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062206252D          

 31 33  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
    2.8668    2.0305    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
   -5.3091    1.6431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5641    2.4278    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3710    2.5993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6260    3.3839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0739    3.9970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 30 31  1  0  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
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    6.5668   -0.3580    0.8836 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2124   -0.2421   -0.4286 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8380   -1.8570   -0.7351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520   -2.3067   -1.1277 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2300   -1.8462    0.1138 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3116   -1.9138    1.6475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5884   -2.0197   -0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9197   -3.0238   -1.1045 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4956   -0.8780   -0.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7905   -1.0498   -0.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.7343   -1.4504    1.2139 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2940   -0.6311   -0.2547 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.5397   -1.5981   -2.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0270   -1.9123   -1.2351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5714   -2.9125    1.9875 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309062206252D          

 31 33  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
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M  END
> <DATABASE_ID>
NP0225643

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(=O)C1=C2C=C3C=C(\C=C/C)N(CCO)C=C3C(=O)C2(C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H31NO5/c1-4-6-7-8-9-11-21(28)22-20-15-17-14-18(10-5-2)26(12-13-27)16-19(17)23(29)25(20,3)31-24(22)30/h5,10,14-16,27H,4,6-9,11-13H2,1-3H3/b10-5-

> <INCHI_KEY>
NNVANSMEQBWXHJ-YHYXMXQVSA-N

> <FORMULA>
C25H31NO5

> <MOLECULAR_WEIGHT>
425.525

> <EXACT_MASS>
425.220223102

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
48.86341205473574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1Z)-prop-1-en-1-yl]-2H,7H,9H,9aH-furo[3,2-g]isoquinoline-2,9-dione

> <JCHEM_LOGP>
3.9119081956666664

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.380928934377835

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.565788325556337

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5512951045378394

> <JCHEM_POLAR_SURFACE_AREA>
83.91000000000001

> <JCHEM_REFRACTIVITY>
123.74719999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1Z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-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       5.351   3.790   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     -12.368   6.317   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -11.338   7.461   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                                                       
CONECT   30   29   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₁NO₅

Average Mass

425.5250 Da

Monoisotopic Mass

425.22022 Da

IUPAC Name

7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1Z)-prop-1-en-1-yl]-2H,7H,9H,9aH-furo[3,2-g]isoquinoline-2,9-dione

Traditional Name

7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1Z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione

CAS Registry Number

Not Available

SMILES

CCCCCCCC(=O)C1=C2C=C3C=C(\C=C/C)N(CCO)C=C3C(=O)C2(C)OC1=O

InChI Identifier

InChI=1S/C25H31NO5/c1-4-6-7-8-9-11-21(28)22-20-15-17-14-18(10-5-2)26(12-13-27)16-19(17)23(29)25(20,3)31-24(22)30/h5,10,14-16,27H,4,6-9,11-13H2,1-3H3/b10-5-

InChI Key

NNVANSMEQBWXHJ-YHYXMXQVSA-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
Aryl ketone
Aryl alkyl ketone
Alpha-acyloxy ketone
2-furanone
Pyridine
Dihydrofuran
Enoate ester
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Vinylogous amide
Carboxylic acid ester
Ketone
Lactone
Organoheterocyclic compound
Azacycle
Oxacycle
Carboxylic acid derivative
Alkanolamine
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organonitrogen compound
Organopnictogen compound
Alcohol
Organooxygen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Primary alcohol
Organic oxide
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	3.91	ChemAxon
pKa (Strongest Acidic)	15.57	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.91 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	123.75 m³·mol⁻¹	ChemAxon
Polarizability	48.86 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

78434708

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584399

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Troiano D, Orsat V, Dumont MJ: Solid-state co-culture fermentation of simulated food waste with filamentous fungi for production of bio-pigments. Appl Microbiol Biotechnol. 2022 Jun;106(11):4029-4039. doi: 10.1007/s00253-022-11984-1. Epub 2022 May 24. [PubMed:35608668 ]
LOTUS database [Link]

Showing NP-Card for 7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione (NP0225643)

MOL for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

3D MOL for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

3D SDF for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

3D-SDF for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

PDB for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

3D PDB for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

SMILES for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

INCHI for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

Structure for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)

3D Structure for NP0225643 (7-(2-hydroxyethyl)-9a-methyl-3-octanoyl-6-[(1z)-prop-1-en-1-yl]furo[3,2-g]isoquinoline-2,9-dione)