NP-MRD: Showing NP-Card for 4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione (NP0224569)

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Record Information

Version

2.0

Created at

2022-09-06 03:02:03 UTC

Updated at

2022-09-06 03:02:03 UTC

NP-MRD ID

NP0224569

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione

Description

Frenolicin B, also known as am 3867I or UCF76 C, belongs to the class of organic compounds known as benzoisochromanequinones. These are benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton. Frenolicin B is an extremely weak basic (essentially neutral) compound (based on its pKa). 4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione is found in Streptomyces roseofulvus. Antibiotic feed additive especies for poultry and pigs.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 05061307352D          

 24 27  0  0  0  0            999 V2000
    2.4950   -2.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455   -1.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5828    2.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8017   -0.9142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7770    2.3093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8323    1.3459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7454    1.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2208    1.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2761    0.7366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5521   -0.1279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4968    0.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8373    1.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4703    0.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1083    0.4814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8588    1.2678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4150    1.8770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9141    0.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0530    1.4448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5257   -0.0498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2280    2.5523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655    2.6634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1637   -0.4820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7463    0.0492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6454    2.1621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
  6  3  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  2  0  0  0  0
 10  4  1  0  0  0  0
 11  7  1  0  0  0  0
 12  7  1  0  0  0  0
 13  8  2  0  0  0  0
 13  9  1  0  0  0  0
 14 10  1  0  0  0  0
 15 14  2  0  0  0  0
 16  8  1  0  0  0  0
 16 15  1  0  0  0  0
 17 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 11  1  0  0  0  0
 18 15  1  0  0  0  0
 19  9  1  0  0  0  0
 20 12  2  0  0  0  0
 21 16  2  0  0  0  0
 22 17  2  0  0  0  0
 23 10  1  0  0  0  0
 23 11  1  0  0  0  0
 24 12  1  0  0  0  0
 24 18  1  0  0  0  0
M  END


  Mrv0541 05061307352D          

 24 27  0  0  0  0            999 V2000
    2.4950   -2.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455   -1.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5828    2.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8017   -0.9142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7770    2.3093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8323    1.3459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7454    1.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2208    1.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2761    0.7366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5521   -0.1279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4968    0.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8373    1.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4703    0.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1083    0.4814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8588    1.2678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4150    1.8770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9141    0.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0530    1.4448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5257   -0.0498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2280    2.5523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655    2.6634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1637   -0.4820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7463    0.0492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6454    2.1621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
  6  3  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  2  0  0  0  0
 10  4  1  0  0  0  0
 11  7  1  0  0  0  0
 12  7  1  0  0  0  0
 13  8  2  0  0  0  0
 13  9  1  0  0  0  0
 14 10  1  0  0  0  0
 15 14  2  0  0  0  0
 16  8  1  0  0  0  0
 16 15  1  0  0  0  0
 17 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 11  1  0  0  0  0
 18 15  1  0  0  0  0
 19  9  1  0  0  0  0
 20 12  2  0  0  0  0
 21 16  2  0  0  0  0
 22 17  2  0  0  0  0
 23 10  1  0  0  0  0
 23 11  1  0  0  0  0
 24 12  1  0  0  0  0
 24 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0224569

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1OC2CC(=O)OC2C2=C1C(=O)C1=C(C=CC=C1O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H16O6/c1-2-4-10-14-15(18-11(23-10)7-12(20)24-18)16(21)8-5-3-6-9(19)13(8)17(14)22/h3,5-6,10-11,18-19H,2,4,7H2,1H3

> <INCHI_KEY>
AVCPRTNVVRPELB-UHFFFAOYSA-N

> <FORMULA>
C18H16O6

> <MOLECULAR_WEIGHT>
328.316

> <EXACT_MASS>
328.094688244

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
33.17257602842693

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3(8),4,6-tetraene-2,9,13-trione

> <ALOGPS_LOGP>
2.69

> <JCHEM_LOGP>
2.4245802486666665

> <ALOGPS_LOGS>
-2.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.412286959207568

> <JCHEM_PKA_STRONGEST_BASIC>
-4.222703861569621

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
83.38589999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.41e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3(8),4,6-tetraene-2,9,13-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       4.657  -4.312   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.192  -2.844   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.421   3.980   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.230  -1.707   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.917   4.311   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.887   2.512   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.391   2.196   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.879   3.173   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.849   1.375   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.764  -0.239   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.794   1.560   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.563   3.726   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.345   1.705   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.802   0.899   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.336   2.367   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.375   3.504   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.306   0.568   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.832   2.697   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.315  -0.093   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.426   4.764   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.909   4.972   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       7.772  -0.900   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       3.260   0.092   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.071   4.036   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    4                                                       
CONECT    3    5    6                                                       
CONECT    4    2   10                                                       
CONECT    5    3    8                                                       
CONECT    6    3    9                                                       
CONECT    7   11   12                                                       
CONECT    8    5   13   16                                                  
CONECT    9    6   13   19                                                  
CONECT   10    4   14   23                                                  
CONECT   11    7   18   23                                                  
CONECT   12    7   20   24                                                  
CONECT   13    8    9   17                                                  
CONECT   14   10   15   17                                                  
CONECT   15   14   16   18                                                  
CONECT   16    8   15   21                                                  
CONECT   17   13   14   22                                                  
CONECT   18   11   15   24                                                  
CONECT   19    9                                                            
CONECT   20   12                                                            
CONECT   21   16                                                            
CONECT   22   17                                                            
CONECT   23   10   11                                                       
CONECT   24   12   18                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Value	Source
AM 3867I	HMDB
Antibiotic am 3867I	HMDB
Antibiotic ucf76 C	HMDB
UCF76 C	HMDB

Chemical Formula

C₁₈H₁₆O₆

Average Mass

328.3160 Da

Monoisotopic Mass

328.09469 Da

IUPAC Name

4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3(8),4,6-tetraene-2,9,13-trione

Traditional Name

4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3(8),4,6-tetraene-2,9,13-trione

CAS Registry Number

Not Available

SMILES

CCCC1OC2CC(=O)OC2C2=C1C(=O)C1=C(C=CC=C1O)C2=O

InChI Identifier

InChI=1S/C18H16O6/c1-2-4-10-14-15(18-11(23-10)7-12(20)24-18)16(21)8-5-3-6-9(19)13(8)17(14)22/h3,5-6,10-11,18-19H,2,4,7H2,1H3

InChI Key

AVCPRTNVVRPELB-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
Streptomyces roseofulvus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoisochromanequinones. These are benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isochromanequinones

Sub Class

Benzoisochromanequinones

Direct Parent

Benzoisochromanequinones

Alternative Parents

Substituents

Benzoisochromanequinone
Naphthopyranone
Naphthopyran
Naphthoquinone
Naphthalene
Furopyran
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Gamma butyrolactone
Benzenoid
Pyran
Tetrahydrofuran
Furan
Vinylogous acid
Carboxylic acid ester
Ketone
Lactone
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
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	2.69	ALOGPS
logP	2.42	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	9.41	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	83.39 m³·mol⁻¹	ChemAxon
Polarizability	33.17 Å³	ChemAxon
Number of Rings	4	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

HMDB0034109

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB012376

KNApSAcK ID

C00018203

Chemspider ID

28587202

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13337184

PDB ID

Not Available

ChEBI ID

48201

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione (NP0224569)

MOL for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D MOL for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D SDF for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D-SDF for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

PDB for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D PDB for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

SMILES for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

INCHI for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

Structure for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)

3D Structure for NP0224569 (4-hydroxy-17-propyl-12,16-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-1(10),3,5,7-tetraene-2,9,13-trione)