NP-MRD: Showing NP-Card for (1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate (NP0185178)

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Record Information

Version

2.0

Created at

2022-09-04 00:30:47 UTC

Updated at

2022-09-04 00:30:47 UTC

NP-MRD ID

NP0185178

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042202302D          

 44 49  0  0  1  0            999 V2000
   11.9548   -3.3704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8849   -2.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5619   -2.0768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   11.0682   -1.3758    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.7451   -0.9043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309042202302D          

 44 49  0  0  1  0            999 V2000
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    6.3648   -2.8940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5923   -2.4933    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8901   -1.9178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1949   -1.0080    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5647   -0.4461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7153    0.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0863    0.9045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4896    0.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0997    0.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0462   -0.7766    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8580   -0.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3380    0.2510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9162    0.8504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7249    1.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7041    0.5759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4236    0.1338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0945    0.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8647    0.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9749   -0.4990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5510   -0.6972    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8993   -1.2031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0115   -2.0204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7755   -2.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3598   -2.5263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6248   -1.4983    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3232   -1.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0644   -1.9639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2436   -1.8801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7266   -1.2112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 19 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
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  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
  7 34  1  0  0  0  0
 31 35  1  0  0  0  0
  7 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
 25 40  1  0  0  0  0
 15 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 17 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 44  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0185178

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](OC(C)=O)[C@]12OCC\C(=C\C(=O)OC[C@]34CCC(C)=C[C@H]3O[C@@H]3C[C@@H](OC(=O)\C=C/C=C\1)[C@@]4(C)[C@]31CO1)[C@@H]2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H40O11/c1-19-9-12-31-17-38-28(37)15-23-10-13-39-32(20(2)41-21(3)34,29(23)42-22(4)35)11-7-6-8-27(36)44-24-16-26(43-25(31)14-19)33(18-40-33)30(24,31)5/h6-8,11,14-15,20,24-26,29H,9-10,12-13,16-18H2,1-5H3/b8-6-,11-7-,23-15-/t20-,24+,25+,26+,29-,30+,31+,32+,33-/m0/s1

> <INCHI_KEY>
PCFSOFHNZOHJSF-MILBEILXSA-N

> <FORMULA>
C33H40O11

> <MOLECULAR_WEIGHT>
612.672

> <EXACT_MASS>
612.257062108

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
61.43943281175213

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S)-1-[(1'E,2S,6'R,11'R,13'R,15'S,16'R,19'Z,21'E,23'R,27'S)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1^{13,16}.0^{6,11}.0^{6,15}]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate

> <JCHEM_LOGP>
2.6789469523333307

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.59515491695933

> <JCHEM_PKA_STRONGEST_BASIC>
-3.749227335680065

> <JCHEM_POLAR_SURFACE_AREA>
136.19000000000003

> <JCHEM_REFRACTIVITY>
156.08970000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S)-1-[(1'E,2S,6'R,11'R,13'R,15'S,16'R,19'Z,21'E,23'R,27'S)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1^{13,16}.0^{6,11}.0^{6,15}]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      22.316  -6.291   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      22.185  -4.757   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      23.449  -3.877   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      20.791  -4.103   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      20.661  -2.568   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.924  -1.688   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.266  -1.914   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.291  -3.499   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.910  -5.014   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.939  -6.236   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.541  -6.942   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.990  -6.814   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      14.238  -8.158   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      14.061  -5.549   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      13.087  -4.300   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.881  -5.402   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.439  -4.654   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.128  -3.580   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.697  -1.882   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.521  -0.833   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.802   0.692   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.628   1.688   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.247   1.213   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.386   0.159   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.286  -1.450   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.802  -0.825   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      13.698   0.468   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      14.777   1.587   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      14.420   3.085   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      16.248   1.075   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.591   0.250   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      18.843   1.187   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      20.281   0.609   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      20.486  -0.931   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      17.828  -1.301   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      16.612  -2.246   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      16.821  -3.771   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      18.248  -4.353   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      15.605  -4.716   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      12.366  -2.797   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      13.670  -1.977   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      11.320  -3.666   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       9.788  -3.509   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      10.690  -2.261   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   34   35                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   40                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   42                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   19   26   40                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   35                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33    7                                                       
CONECT   35   31    7   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   25   15   41   42                                             
CONECT   41   40                                                            
CONECT   42   40   17   43   44                                             
CONECT   43   42   44                                                       
CONECT   44   43   42                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₀O₁₁

Average Mass

612.6720 Da

Monoisotopic Mass

612.25706 Da

IUPAC Name

(1S)-1-[(1'E,2S,6'R,11'R,13'R,15'S,16'R,19'Z,21'E,23'R,27'S)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1^{13,16}.0^{6,11}.0^{6,15}]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H](OC(C)=O)[C@]12OCC\C(=C\C(=O)OC[C@]34CCC(C)=C[C@H]3O[C@@H]3C[C@@H](OC(=O)\C=C/C=C\1)[C@@]4(C)[C@]31CO1)[C@@H]2OC(C)=O

InChI Identifier

InChI=1S/C33H40O11/c1-19-9-12-31-17-38-28(37)15-23-10-13-39-32(20(2)41-21(3)34,29(23)42-22(4)35)11-7-6-8-27(36)44-24-16-26(43-25(31)14-19)33(18-40-33)30(24,31)5/h6-8,11,14-15,20,24-26,29H,9-10,12-13,16-18H2,1-5H3/b8-6-,11-7-,23-15-/t20-,24+,25+,26+,29-,30+,31+,32+,33-/m0/s1

InChI Key

PCFSOFHNZOHJSF-MILBEILXSA-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
Trichoderma cornu-damae	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	2.68	ChemAxon
pKa (Strongest Acidic)	12.6	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	136.19 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	156.09 m³·mol⁻¹	ChemAxon
Polarizability	61.44 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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate (NP0185178)

MOL for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

3D MOL for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

3D SDF for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

3D-SDF for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

PDB for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

3D PDB for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

SMILES for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

INCHI for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

Structure for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)

3D Structure for NP0185178 ((1s)-1-[(1'e,2s,6'r,11'r,13'r,15's,16'r,19'z,21'e,23'r,27's)-27'-(acetyloxy)-9',15'-dimethyl-3',18'-dioxo-4',12',17',24'-tetraoxaspiro[oxirane-2,14'-pentacyclo[21.3.1.1¹³,¹⁶.0⁶,¹¹.0⁶,¹⁵]octacosane]-1',9',19',21'-tetraen-23'-yl]ethyl acetate)