NP-MRD: Showing NP-Card for (3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one (NP0246833)

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Record Information

Version

2.0

Created at

2022-09-07 08:25:26 UTC

Updated at

2022-09-07 08:25:27 UTC

NP-MRD ID

NP0246833

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one

Description

(3AR,7aS)-1-methyl-3a-{[(1R,5R,11R,12S,14R,17S,20R,21R)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]Docos-15-en-15-yl]methyl}-2,3,3a,6,7,7a-hexahydro-1H-indol-6-one belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. (3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one is found in Aconitum coreanum. Based on a literature review very few articles have been published on (3aR,7aS)-1-methyl-3a-{[(1R,5R,11R,12S,14R,17S,20R,21R)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]Docos-15-en-15-yl]methyl}-2,3,3a,6,7,7a-hexahydro-1H-indol-6-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072210252D          

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M  END

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M  END


  Mrv1652309072210252D          

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    1.7075   -0.3792    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4450   -0.8938    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2535   -1.7627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4652   -2.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2500   -2.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0922   -1.4823    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7939   -1.0439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7062   -0.0299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6266   -0.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2980   -1.3305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2185   -2.1517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0489   -0.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1284   -0.1677    0.0000 C   0  0  2  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  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 20  1  1  0  0  0
  7 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
 18 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
 27 28  1  0  0  0  0
 24 28  1  1  0  0  0
 28 29  1  0  0  0  0
 13 29  1  0  0  0  0
  5 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35  2  1  6  0  0  0
  5 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246833

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CC[C@]2(CC3=C[C@]45CC[C@H]6[C@]78CCC[C@@]6(C)CN6CCO[C@]76[C@H]4C[C@H]3C[C@H]58)C=CC(=O)C[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C31H42N2O2/c1-27-6-3-7-30-23(27)5-9-29-18-21(17-28-8-4-22(34)16-26(28)32(2)11-10-28)20(14-24(29)30)15-25(29)31(30)33(19-27)12-13-35-31/h4,8,18,20,23-26H,3,5-7,9-17,19H2,1-2H3/t20-,23-,24-,25+,26+,27+,28+,29+,30+,31-/m1/s1

> <INCHI_KEY>
MNQMVPGTCARFMJ-RXRFSQMPSA-N

> <FORMULA>
C31H42N2O2

> <MOLECULAR_WEIGHT>
474.689

> <EXACT_MASS>
474.3246286

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
54.567228134377004

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3aR,7aS)-1-methyl-3a-{[(1R,5R,11R,12S,14R,17S,20R,21R)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0^{1,11}.0^{5,20}.0^{7,11}.0^{12,17}.0^{17,21}]docos-15-en-15-yl]methyl}-2,3,3a,6,7,7a-hexahydro-1H-indol-6-one

> <JCHEM_LOGP>
4.2232903660000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.108257880750678

> <JCHEM_PKA_STRONGEST_BASIC>
9.184965276457893

> <JCHEM_POLAR_SURFACE_AREA>
32.78

> <JCHEM_REFRACTIVITY>
139.16559999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,7aS)-1-methyl-3a-{[(1R,5R,11R,12S,14R,17S,20R,21R)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0^{1,11}.0^{5,20}.0^{7,11}.0^{12,17}.0^{17,21}]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.680   0.138   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -5.212   0.602   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -4.724   2.063   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.184   2.050   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.720   0.582   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.567   1.603   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.106   1.115   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.297   1.808   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.761   1.097   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.654   2.431   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.222   2.363   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.128   1.038   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.307  -0.400   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.299  -1.578   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.907  -0.443   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.549   1.044   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.040   0.611   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.469  -0.255   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.945   0.327   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.179   0.052   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.608  -0.299   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.711  -1.420   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.187  -0.708   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.564  -1.668   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.207  -3.290   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.602  -4.832   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.067  -4.322   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       5.772  -2.767   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       7.082  -1.949   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.318  -0.056   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.170  -1.589   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.423  -2.484   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.275  -4.016   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -3.825  -1.846   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.973  -0.313   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   35                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   30   35                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   21                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   19   23                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15   29                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12   19   24                                             
CONECT   19   18    9   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20    7   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    9   24                                                  
CONECT   24   23   18   25   28                                             
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   24   29                                                  
CONECT   29   28   13                                                       
CONECT   30    5   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34    2    5                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₂N₂O₂

Average Mass

474.6890 Da

Monoisotopic Mass

474.32463 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CN1CC[C@]2(CC3=C[C@]45CC[C@H]6[C@]78CCC[C@@]6(C)CN6CCO[C@]76[C@H]4C[C@H]3C[C@H]58)C=CC(=O)C[C@H]12

InChI Identifier

InChI=1S/C31H42N2O2/c1-27-6-3-7-30-23(27)5-9-29-18-21(17-28-8-4-22(34)16-26(28)32(2)11-10-28)20(14-24(29)30)15-25(29)31(30)33(19-27)12-13-35-31/h4,8,18,20,23-26H,3,5-7,9-17,19H2,1-2H3/t20-,23-,24-,25+,26+,27+,28+,29+,30+,31-/m1/s1

InChI Key

MNQMVPGTCARFMJ-RXRFSQMPSA-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
Aconitum coreanum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Indole or derivatives
Alkaloid or derivatives
Cyclohexenone
Piperidine
N-alkylpyrrolidine
Oxazolidine
Pyrrolidine
Hemiaminal
Ketone
Tertiary amine
Tertiary aliphatic amine
Cyclic ketone
Oxacycle
Organoheterocyclic compound
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Amine
Organic oxygen compound
Carbonyl group
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

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

163022223

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one (NP0246833)

MOL for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

3D MOL for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

3D SDF for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

3D-SDF for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

PDB for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

3D PDB for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

SMILES for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

INCHI for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

Structure for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)

3D Structure for NP0246833 ((3ar,7as)-1-methyl-3a-{[(1r,5r,11r,12s,14r,17s,20r,21r)-5-methyl-10-oxa-7-azaheptacyclo[12.6.2.0¹,¹¹.0⁵,²⁰.0⁷,¹¹.0¹²,¹⁷.0¹⁷,²¹]docos-15-en-15-yl]methyl}-2,3,7,7a-tetrahydroindol-6-one)