NP-MRD: Showing NP-Card for (1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate (NP0218870)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 19:40:37 UTC

Updated at

2022-09-05 19:40:37 UTC

NP-MRD ID

NP0218870

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate

Description

(1S,6R,20S)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]Henicosa-8(16),9,14-trien-9-yl acetate belongs to the class of organic compounds known as piperidinones. Piperidinones are compounds containing a piperidine ring which bears a ketone. (1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate is found in Daphniphyllum macropodum. Based on a literature review very few articles have been published on (1S,6R,20S)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]Henicosa-8(16),9,14-trien-9-yl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052221402D          

 29 33  0  0  1  0            999 V2000
    1.6115   -0.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9325   -1.3490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3770   -0.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5800    0.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3430    0.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2977    1.1410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1490    0.1414    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9009   -0.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9828   -1.0191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7347   -1.3586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3128   -1.5005    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6080   -2.3394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8019   -2.1636    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0836   -2.5694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6815   -2.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9173   -1.4703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4462   -0.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7520   -0.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1177    0.5008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1717    1.3241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9116    1.6889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5976    1.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656    2.5122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5684    0.0916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0792   -0.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7734   -1.3225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5609   -1.1609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4790   -0.3400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6590   -0.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13  2  1  1  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  2  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  4 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
 21 23  2  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
 16 26  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END


  Mrv1652309052221402D          

 29 33  0  0  1  0            999 V2000
    1.6115   -0.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9325   -1.3490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3770   -0.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5800    0.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3430    0.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2977    1.1410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1490    0.1414    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9009   -0.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9828   -1.0191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7347   -1.3586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3128   -1.5005    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6080   -2.3394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8019   -2.1636    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0836   -2.5694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6815   -2.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9173   -1.4703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4462   -0.7930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7520   -0.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1177    0.5008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1717    1.3241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9116    1.6889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5976    1.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656    2.5122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5684    0.0916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0792   -0.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7734   -1.3225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5609   -1.1609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4790   -0.3400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6590   -0.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13  2  1  1  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  2  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  4 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
 21 23  2  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
 16 26  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0218870

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CN2C[C@H]3CCC4=C5C(CCO4)=C(OC(C)=O)C(=C5C3=C)C(=O)[C@@H]1CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H25NO5/c1-11-9-24-10-14-4-5-17-20-15(6-7-28-17)23(29-13(3)25)21(19(20)12(14)2)22(27)16(11)8-18(24)26/h11,14,16H,2,4-10H2,1,3H3/t11-,14-,16-/m1/s1

> <INCHI_KEY>
DIZCGIXPZFGBNL-DJSGYFEHSA-N

> <FORMULA>
C23H25NO5

> <MOLECULAR_WEIGHT>
395.455

> <EXACT_MASS>
395.173272909

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
41.721499913088216

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,6R,20S)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2^{3,6}.0^{8,16}.0^{10,15}]henicosa-8(16),9,14-trien-9-yl acetate

> <JCHEM_LOGP>
-0.15971574999999977

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.43862641612631

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5694466015972227

> <JCHEM_POLAR_SURFACE_AREA>
72.91

> <JCHEM_REFRACTIVITY>
109.1501

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,6R,20S)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2^{3,6}.0^{8,16}.0^{10,15}]henicosa-8(16),9,14-trien-9-yl acetate

> <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       3.008  -1.643   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.741  -2.518   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.704  -1.379   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.083   0.113   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.507   0.592   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.422   2.130   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.012   0.264   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.415  -0.370   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.568  -1.902   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.971  -2.536   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       4.317  -2.801   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       3.002  -4.367   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.497  -4.039   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.156  -4.796   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.272  -4.220   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.712  -2.745   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.833  -1.480   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.404  -0.050   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.220   0.935   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.320   2.472   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.702   3.153   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.982   2.297   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.802   4.689   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.928   0.171   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.881  -1.038   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.310  -2.469   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.914  -2.167   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.761  -0.635   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.230  -0.466   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4   17                                                  
CONECT    4    3    5   19                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   28                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12    2   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16    3   18                                                  
CONECT   18   17   19   24                                                  
CONECT   19   18    4   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   18   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   16                                                       
CONECT   27   11   28                                                       
CONECT   28   27    7   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
(1S,6R,20S)-20-Methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2,.0,.0,]henicosa-8(16),9,14-trien-9-yl acetic acid	Generator

Chemical Formula

C₂₃H₂₅NO₅

Average Mass

395.4550 Da

Monoisotopic Mass

395.17327 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1CN2C[C@H]3CCC4=C5C(CCO4)=C(OC(C)=O)C(=C5C3=C)C(=O)[C@@H]1CC2=O

InChI Identifier

InChI=1S/C23H25NO5/c1-11-9-24-10-14-4-5-17-20-15(6-7-28-17)23(29-13(3)25)21(19(20)12(14)2)22(27)16(11)8-18(24)26/h11,14,16H,2,4-10H2,1,3H3/t11-,14-,16-/m1/s1

InChI Key

DIZCGIXPZFGBNL-DJSGYFEHSA-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
Daphniphyllum macropodum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as piperidinones. Piperidinones are compounds containing a piperidine ring which bears a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Piperidines

Sub Class

Piperidinones

Direct Parent

Piperidinones

Alternative Parents

Substituents

Delta-lactam
Piperidinone
Enol ester
Tertiary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Ketone
Lactam
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Azacycle
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen 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
logP	-0.16	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

163035518

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate (NP0218870)

MOL for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

3D MOL for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

3D SDF for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

3D-SDF for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

PDB for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

3D PDB for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

SMILES for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

INCHI for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

Structure for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)

3D Structure for NP0218870 ((1s,6r,20s)-20-methyl-17-methylidene-4,7-dioxo-13-oxa-3-azapentacyclo[12.3.2.2³,⁶.0⁸,¹⁶.0¹⁰,¹⁵]henicosa-8(16),9,14-trien-9-yl acetate)