NP-MRD: Showing NP-Card for 18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate (NP0241741)

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Record Information

Version

2.0

Created at

2022-09-07 01:53:48 UTC

Updated at

2022-09-07 01:53:48 UTC

NP-MRD ID

NP0241741

Secondary Accession Numbers

None

Natural Product Identification

Common Name

18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate

Description

18-Benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]Icosa-3,19-dien-2-yl acetate belongs to the class of organic compounds known as isoindoles and derivatives. These are polycyclic compounds containing an isoindole moiety, which is structurally characterized by a cyclohexadiene fused to a pyrrole ring. 18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate is found in Xylaria hypoxylon. 18-Benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]Icosa-3,19-dien-2-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191522362D          

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M  END

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M  END


  Mrv1533004191522362D          

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    0.8387   -3.4087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1516   -2.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4014   -0.7450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6180   -1.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0023   -0.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6610   -1.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8410   -0.1889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1699    0.3530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5870    0.8248    0.0000 O   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
  4  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
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  7 26  1  0  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 32 27  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0241741

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3=CC=CC=C3)NC(=O)C22C(C3OC3CC(C)C(=O)C(C)(O)C=CC2OC(C)=O)C2OC12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H37NO7/c1-15-13-20-24(37-20)23-26-29(5,38-26)16(2)22-19(14-18-9-7-6-8-10-18)31-27(34)30(22,23)21(36-17(3)32)11-12-28(4,35)25(15)33/h6-12,15-16,19-24,26,35H,13-14H2,1-5H3,(H,31,34)

> <INCHI_KEY>
KHJAUVJHBOZECO-UHFFFAOYSA-N

> <FORMULA>
C30H37NO7

> <MOLECULAR_WEIGHT>
523.626

> <EXACT_MASS>
523.257002535

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
55.547246466971046

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
18-benzyl-5-hydroxy-5,7,15,16-tetramethyl-6,20-dioxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icos-3-en-2-yl acetate

> <ALOGPS_LOGP>
2.76

> <JCHEM_LOGP>
2.5688497299999975

> <ALOGPS_LOGS>
-4.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.175694469143334

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.858567308659001

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3110916842672692

> <JCHEM_POLAR_SURFACE_AREA>
117.76000000000002

> <JCHEM_REFRACTIVITY>
138.0688

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.50e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
18-benzyl-5-hydroxy-5,7,15,16-tetramethyl-6,20-dioxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icos-3-en-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       0.903   2.561   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.893   1.257   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.656   2.594   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.164   2.281   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.574   1.662   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.333   0.750   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.541  -0.425   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.003   0.058   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.465   0.541   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.152  -0.967   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.765  -1.164   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.839  -2.474   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.040  -3.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.377  -2.957   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.758  -4.367   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.620  -5.728   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.771  -7.035   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.469  -8.407   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.630  -9.698   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.092  -9.617   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.393  -8.245   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.233  -6.953   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       4.225  -4.214   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       4.287  -2.905   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.577  -2.527   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.228  -1.933   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.765  -2.416   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.993  -4.059   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.599  -4.823   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.565  -6.363   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.283  -4.024   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.616  -1.391   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.154  -1.874   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.004  -0.849   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.234  -1.904   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -1.570  -0.353   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.317   0.659   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -1.096   1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4    6                                                       
CONECT    6    5    4    7                                                  
CONECT    7    6    8   26                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8   10                                                       
CONECT   10    9    8   11   12                                             
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   26                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   15   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    7   14   27                                             
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34    2   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Value	Source
18-Benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0,.0,.0,]icosa-3,19-dien-2-yl acetic acid	Generator
18-Benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetic acid	Generator

Chemical Formula

C₃₀H₃₇NO₇

Average Mass

523.6260 Da

Monoisotopic Mass

523.25700 Da

IUPAC Name

18-benzyl-5-hydroxy-5,7,15,16-tetramethyl-6,20-dioxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icos-3-en-2-yl acetate

Traditional Name

18-benzyl-5-hydroxy-5,7,15,16-tetramethyl-6,20-dioxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icos-3-en-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3=CC=CC=C3)NC(=O)C22C(C3OC3CC(C)C(=O)C(C)(O)C=CC2OC(C)=O)C2OC12C

InChI Identifier

InChI=1S/C30H37NO7/c1-15-13-20-24(37-20)23-26-29(5,38-26)16(2)22-19(14-18-9-7-6-8-10-18)31-27(34)30(22,23)21(36-17(3)32)11-12-28(4,35)25(15)33/h6-12,15-16,19-24,26,35H,13-14H2,1-5H3,(H,31,34)

InChI Key

KHJAUVJHBOZECO-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
Xylaria hypoxylon	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindoles and derivatives. These are polycyclic compounds containing an isoindole moiety, which is structurally characterized by a cyclohexadiene fused to a pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Not Available

Direct Parent

Isoindoles and derivatives

Alternative Parents

Substituents

Isoindole or derivatives
Oxepane
Acyloin
Monocyclic benzene moiety
Benzenoid
Pyrroline
Tertiary alcohol
Cyclic carboximidic acid
Carboxylic acid ester
Ketone
Cyclic ketone
Oxacycle
Azacycle
Carboxylic acid derivative
Organic 1,3-dipolar compound
Dialkyl ether
Oxirane
Ether
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Organic oxygen compound
Organopnictogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic oxide
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
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	2.76	ALOGPS
logP	2.57	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	12.86	ChemAxon
pKa (Strongest Basic)	-0.31	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.76 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	138.07 m³·mol⁻¹	ChemAxon
Polarizability	55.55 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

78420308

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate (NP0241741)

MOL for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

3D MOL for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

3D SDF for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

3D-SDF for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

PDB for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

3D PDB for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

SMILES for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

INCHI for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

Structure for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)

3D Structure for NP0241741 (18-benzyl-5,20-dihydroxy-5,7,15,16-tetramethyl-6-oxo-10,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0⁹,¹¹.0¹³,¹⁵]icosa-3,19-dien-2-yl acetate)