NP-MRD: Showing NP-Card for (1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate (NP0264091)

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Record Information

Version

2.0

Created at

2022-09-08 07:30:11 UTC

Updated at

2022-09-08 07:30:11 UTC

NP-MRD ID

NP0264091

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate

Description

Tasihalide B belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Based on a literature review very few articles have been published on Tasihalide B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082209302D          

 39 42  0  0  1  0            999 V2000
   -3.3769    1.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0022    0.6880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4514   -0.0040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1784    0.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8036   -0.0900    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2528   -0.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8781   -1.5170    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3273   -2.2090    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.0542   -1.5600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5034   -2.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6051   -0.8680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9798   -0.1330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5306    0.5590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2674   -1.1392    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6680   -0.2190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.4446   -4.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8269   -3.3796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2032   -4.4140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  7  8  1  6  0  0  0
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  9 10  1  6  0  0  0
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  5 12  1  0  0  0  0
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  9 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309082209302D          

 39 42  0  0  1  0            999 V2000
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    0.8759   -2.0660    0.0000 I   0  0  0  0  0  0  0  0  0  0  0  0
    0.5935   -1.6460    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1443   -2.3380    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5191   -3.0730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2725   -3.8378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4446   -4.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8269   -3.3796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6795   -2.2950    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1287   -2.9870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7540   -3.7220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0699   -3.7650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2032   -4.4140    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 11  9  1  1  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  1  0  0  0
 14 11  1  6  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 22  1  1  0  0  0
 14 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
  9 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0264091

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H](C[C@@H](Br)[C@]2(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]3[C@H]([C@H]12)[C@@H]1[C@@H](C[C@@]3(C)OC1(C)CI)OC(C)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H40BrIO9/c1-12-17(35-13(2)31)9-19(29)28(8)21(12)20-22-18(36-14(3)32)10-26(6,39-27(22,7)11-30)23(20)24(37-15(4)33)25(28)38-16(5)34/h12,17-25H,9-11H2,1-8H3/t12-,17-,18-,19-,20-,21+,22+,23-,24-,25+,26-,27?,28+/m1/s1

> <INCHI_KEY>
VTSUCPDRKZEUFW-QHGWMHHNSA-N

> <FORMULA>
C28H40BrIO9

> <MOLECULAR_WEIGHT>
727.427

> <EXACT_MASS>
726.09004

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
63.64563288888844

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3R,4S,5R,7R,8S,9R,10R,11R,12R,15R)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadecan-5-yl acetate

> <JCHEM_LOGP>
2.789991346

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.214557695825516

> <JCHEM_POLAR_SURFACE_AREA>
114.43

> <JCHEM_REFRACTIVITY>
150.79270000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3R,4S,5R,7R,8S,9R,10R,11R,12R,15R)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadecan-5-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.304   2.656   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.604   1.284   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -6.443  -0.007   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -4.066   1.204   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -3.367  -0.168   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.205  -1.460   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.506  -2.832   0.000  0.00  0.00           C+0
HETATM    8 Br   UNK     0      -4.344  -4.123   0.000  0.00  0.00          Br+0
HETATM    9  C   UNK     0      -1.968  -2.912   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.806  -4.204   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.129  -1.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.829  -0.248   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.990   1.043   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.499  -2.127   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.247  -0.409   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.785  -0.489   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.623   0.803   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.161   0.722   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.000   2.014   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.861  -0.650   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.484  -1.861   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.646  -3.153   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.345  -4.525   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.408  -2.122   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.942  -1.207   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.452  -1.597   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.024  -2.443   0.000  0.00  0.00           C+0
HETATM   28  I   UNK     0       1.635  -3.857   0.000  0.00  0.00           I+0
HETATM   29  C   UNK     0       1.108  -3.073   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.269  -4.364   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.969  -5.736   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.509  -7.164   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.830  -8.400   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -1.543  -6.309   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -1.268  -4.284   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -2.107  -5.576   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -1.407  -6.948   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.130  -7.028   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -2.246  -8.239   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   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   35                                             
CONECT   10    9                                                            
CONECT   11    9   12   14                                                  
CONECT   12   11    5   13                                                  
CONECT   13   12                                                            
CONECT   14   11   15   29                                                  
CONECT   15   14   16   25                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23   24   29                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   15   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
CONECT   29   22   14   30                                                  
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   30    9   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₄₀BrIO₉

Average Mass

727.4270 Da

Monoisotopic Mass

726.09004 Da

IUPAC Name

(1R,2S,3R,4S,5R,7R,8S,9R,10R,11R,12R,15R)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadecan-5-yl acetate

Traditional Name

(1R,2S,3R,4S,5R,7R,8S,9R,10R,11R,12R,15R)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadecan-5-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H](C[C@@H](Br)[C@]2(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]3[C@H]([C@H]12)[C@@H]1[C@@H](C[C@@]3(C)OC1(C)CI)OC(C)=O)OC(C)=O

InChI Identifier

InChI=1S/C28H40BrIO9/c1-12-17(35-13(2)31)9-19(29)28(8)21(12)20-22-18(36-14(3)32)10-26(6,39-27(22,7)11-30)23(20)24(37-15(4)33)25(28)38-16(5)34/h12,17-25H,9-11H2,1-8H3/t12-,17-,18-,19-,20-,21+,22+,23-,24-,25+,26-,27?,28+/m1/s1

InChI Key

VTSUCPDRKZEUFW-QHGWMHHNSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Tetracarboxylic acid or derivatives
Naphthalene
Oxane
Pyran
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organohalogen compound
Hydrocarbon derivative
Organic oxide
Alkyl halide
Alkyl bromide
Organic oxygen compound
Carbonyl group
Organobromide
Organoiodide
Organooxygen compound
Alkyl iodide
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	2.79	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	114.43 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	150.79 m³·mol⁻¹	ChemAxon
Polarizability	63.65 Å³	ChemAxon
Number of Rings	4	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

10190112

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21578692

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate (NP0264091)

MOL for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

3D MOL for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

3D SDF for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

3D-SDF for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

PDB for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

3D PDB for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

SMILES for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

INCHI for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

Structure for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)

3D Structure for NP0264091 ((1r,2s,3r,4s,5r,7r,8s,9r,10r,11r,12r,15r)-9,10,15-tris(acetyloxy)-7-bromo-14-(iodomethyl)-4,8,12,14-tetramethyl-13-oxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadecan-5-yl acetate)