NP-MRD: Showing NP-Card for 21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate (NP0214052)

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Record Information

Version

2.0

Created at

2022-09-05 13:14:26 UTC

Updated at

2022-09-05 13:14:27 UTC

NP-MRD ID

NP0214052

Secondary Accession Numbers

None

Natural Product Identification

Common Name

21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate

Description

GLAUCERINE belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom. 21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate is found in Delphinium barbeyi and Delphinium occidentale. Based on a literature review very few articles have been published on GLAUCERINE.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215142D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309052215142D          

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   -0.7304   -2.3031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6151   -0.8788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4471   -1.6547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4655   -2.5216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2204   -2.8584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7350   -2.2254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3863   -1.4403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2454   -1.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8655   -0.9696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7405   -1.1291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1594   -1.8905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5662   -0.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7221    0.5275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9900   -0.0456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6167    0.8713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4704   -0.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1102    0.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5628    0.9021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2769    1.4078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2006    2.2293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0265    1.0632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6997    1.5399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1027    0.2417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8674   -1.4201    0.0000 C   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
  5  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
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
  5 13  1  0  0  0  0
 13 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
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 23 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 19 40  1  0  0  0  0
  3 40  1  0  0  0  0
 12 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214052

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC2(C)CCC(OC)C34C2C(OC(C)=O)C2(OCOC22CC(OC)C5CC3(O)C2C5OC(=O)C(C)C)C14

> <INCHI_IDENTIFIER>
InChI=1S/C30H45NO9/c1-8-31-13-26(5)10-9-19(36-7)29-22(26)23(39-16(4)32)30(25(29)31)28(37-14-38-30)12-18(35-6)17-11-27(29,34)21(28)20(17)40-24(33)15(2)3/h15,17-23,25,34H,8-14H2,1-7H3

> <INCHI_KEY>
CTIUZFAMJMQFHC-UHFFFAOYSA-N

> <FORMULA>
C30H45NO9

> <MOLECULAR_WEIGHT>
563.688

> <EXACT_MASS>
563.309432033

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
60.03366679878229

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1^{2,5}.0^{1,13}.0^{3,8}.0^{8,12}.0^{16,20}]docosan-4-yl 2-methylpropanoate

> <JCHEM_LOGP>
1.011889364666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.840066319389294

> <JCHEM_PKA_STRONGEST_BASIC>
9.372795610009181

> <JCHEM_POLAR_SURFACE_AREA>
112.99000000000001

> <JCHEM_REFRACTIVITY>
140.0525

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1^{2,5}.0^{1,13}.0^{3,8}.0^{8,12}.0^{16,20}]docosan-4-yl 2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.761  -4.853   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.765  -4.344   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       1.931  -2.805   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       0.862  -1.478   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.509  -0.003   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.046   0.711   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.983   1.547   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.495   1.974   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.460   0.763   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.740   1.957   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.074   3.741   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.067  -0.840   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.817  -0.670   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.679  -2.337   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.117  -3.162   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.488  -3.032   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.363  -4.299   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.148  -1.640   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.568  -3.089   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.602  -4.707   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.011  -5.336   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.972  -4.154   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.321  -2.689   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.925  -2.889   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.082  -1.810   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      10.716  -2.108   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      11.497  -3.529   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.524  -0.268   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.948   0.985   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.581  -0.085   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.885   1.626   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.478  -1.094   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.672   0.303   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.517   1.684   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.850   2.628   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       9.708   4.161   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      11.249   1.985   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.506   2.875   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.392   0.451   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.486  -2.651   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   40                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   13                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   30   40                                             
CONECT   13   12    5   14                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20   23   40                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   19   24   32                                             
CONECT   24   23   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   12   31   32                                             
CONECT   31   30                                                            
CONECT   32   30   23   33                                                  
CONECT   33   32   28   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   19    3   12                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₅NO₉

Average Mass

563.6880 Da

Monoisotopic Mass

563.30943 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCN1CC2(C)CCC(OC)C34C2C(OC(C)=O)C2(OCOC22CC(OC)C5CC3(O)C2C5OC(=O)C(C)C)C14

InChI Identifier

InChI=1S/C30H45NO9/c1-8-31-13-26(5)10-9-19(36-7)29-22(26)23(39-16(4)32)30(25(29)31)28(37-14-38-30)12-18(35-6)17-11-27(29,34)21(28)20(17)40-24(33)15(2)3/h15,17-23,25,34H,8-14H2,1-7H3

InChI Key

CTIUZFAMJMQFHC-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
Delphinium barbeyi	LOTUS Database	35616633
Delphinium occidentale	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Aconitane-type diterpenoid alkaloids

Alternative Parents

Substituents

Aconitane-type diterpenoid alkaloid
Quinolidine
Alkaloid or derivatives
Azepane
Dicarboxylic acid or derivatives
Piperidine
Meta-dioxolane
Tertiary alcohol
Cyclic alcohol
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Acetal
Dialkyl ether
Ether
Oxacycle
Carboxylic acid derivative
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Amine
Alcohol
Organic oxygen 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

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

138310

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

157146

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate (NP0214052)

MOL for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

3D MOL for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

3D SDF for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

3D-SDF for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

PDB for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

3D PDB for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

SMILES for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

INCHI for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

Structure for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)

3D Structure for NP0214052 (21-(acetyloxy)-14-ethyl-2-hydroxy-6,19-dimethoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.1²,⁵.0¹,¹³.0³,⁸.0⁸,¹².0¹⁶,²⁰]docosan-4-yl 2-methylpropanoate)