NP-MRD: Showing NP-Card for 12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate (NP0152484)

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Record Information

Version

2.0

Created at

2022-09-02 08:58:24 UTC

Updated at

2022-09-02 08:58:24 UTC

NP-MRD ID

NP0152484

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate

Description

12,14-Bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]Hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate is found in Phlegmariurus varius. 12,14-Bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]Hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251508282D          

 39 43  0  0  0  0            999 V2000
    6.5184    5.4721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0952    2.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2716    2.6542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0570    1.8158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5 36  2  0  0  0  0
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 37 38  2  0  0  0  0
  3 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004251508282D          

 39 43  0  0  0  0            999 V2000
    6.5184    5.4721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8330   -0.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9122   -0.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6629    0.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3345   -0.3106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2553   -1.1318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046   -1.4739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4254   -2.2950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6747   -2.6371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0031   -2.1579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0822   -1.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8214    4.2175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0893    4.9977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8990    5.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1669    5.9361    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 17 35  1  0  0  0  0
 26 35  1  0  0  0  0
  5 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
  3 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0152484

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CCC(=O)OC2C(OC(C)=O)C3C(OC(C)=O)C(C)CC45C2CCCN4CCCC35)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C30H41NO8/c1-17-16-30-21-7-5-13-31(30)14-6-8-22(30)28(29(38-19(3)33)26(21)27(17)37-18(2)32)39-25(35)12-10-20-9-11-23(34)24(15-20)36-4/h9,11,15,17,21-22,26-29,34H,5-8,10,12-14,16H2,1-4H3

> <INCHI_KEY>
PBYMARWOXNZTME-UHFFFAOYSA-N

> <FORMULA>
C30H41NO8

> <MOLECULAR_WEIGHT>
543.657

> <EXACT_MASS>
543.283217284

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
59.318989613194454

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate

> <ALOGPS_LOGP>
3.50

> <JCHEM_LOGP>
2.961277771359903

> <ALOGPS_LOGS>
-4.17

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.95830342499984

> <JCHEM_PKA_STRONGEST_BASIC>
8.398675834651282

> <JCHEM_POLAR_SURFACE_AREA>
111.6

> <JCHEM_REFRACTIVITY>
141.71189999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      12.168  10.215   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.668   8.758   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.156   8.463   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.656   7.006   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.145   6.711   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.644   5.255   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.107   4.954   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.706   3.389   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.190   2.977   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       4.571   2.276   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.182   0.571   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.058  -0.404   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.438   0.551   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.629   1.952   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.911   1.951   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.398   3.285   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.633  -1.601   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.475  -0.784   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.075  -1.374   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.103  -2.529   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.619  -3.991   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.611  -2.217   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.710   0.161   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.534   1.830   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.029  -0.734   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.288  -1.857   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.436  -0.324   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.837   0.315   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.091  -0.580   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.943  -2.113   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       6.542  -2.751   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       6.394  -4.284   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.993  -4.923   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.739  -4.028   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.887  -2.495   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.133   7.873   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.633   9.329   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.145   9.624   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.645  11.081   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   38                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   36                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   27                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12   18   35                                                  
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   31   35                                             
CONECT   27   26   11   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   17   26                                                  
CONECT   36    5   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37    3   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
12,14-Bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0,.0,]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoic acid	Generator
12,14-Bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoic acid	Generator

Chemical Formula

C₃₀H₄₁NO₈

Average Mass

543.6570 Da

Monoisotopic Mass

543.28322 Da

IUPAC Name

12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate

Traditional Name

12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate

CAS Registry Number

Not Available

SMILES

COC1=CC(CCC(=O)OC2C(OC(C)=O)C3C(OC(C)=O)C(C)CC45C2CCCN4CCCC35)=CC=C1O

InChI Identifier

InChI=1S/C30H41NO8/c1-17-16-30-21-7-5-13-31(30)14-6-8-22(30)28(29(38-19(3)33)26(21)27(17)37-18(2)32)39-25(35)12-10-20-9-11-23(34)24(15-20)36-4/h9,11,15,17,21-22,26-29,34H,5-8,10,12-14,16H2,1-4H3

InChI Key

PBYMARWOXNZTME-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
Phlegmariurus varius	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Azaspirodecane
Methoxyphenol
Quinolizidine
Quinolidine
Tricarboxylic acid or derivatives
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acid ester
Benzenoid
Fatty acyl
Piperidine
Monocyclic benzene moiety
Tertiary aliphatic amine
Tertiary amine
Amino acid or derivatives
Carboxylic acid ester
Organoheterocyclic compound
Azacycle
Carboxylic acid derivative
Ether
Hydrocarbon derivative
Amine
Organonitrogen compound
Carbonyl group
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
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	3.5	ALOGPS
logP	2.96	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	9.96	ChemAxon
pKa (Strongest Basic)	8.4	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	111.6 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	141.71 m³·mol⁻¹	ChemAxon
Polarizability	59.32 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate (NP0152484)

MOL for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

3D MOL for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

3D SDF for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

3D-SDF for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

PDB for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

3D PDB for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

SMILES for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

INCHI for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

Structure for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)

3D Structure for NP0152484 (12,14-bis(acetyloxy)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadecan-11-yl 3-(4-hydroxy-3-methoxyphenyl)propanoate)