NP-MRD: Showing NP-Card for 5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one (NP0264921)

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Record Information

Version

2.0

Created at

2022-09-08 08:43:04 UTC

Updated at

2022-09-08 08:43:04 UTC

NP-MRD ID

NP0264921

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one

Description

5,6,7,22,23-Pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]Tetracos-15-en-17-one belongs to the class of organic compounds known as disaccharides. Disaccharides are compounds containing two carbohydrate moieties linked to each to each other through a glycosidic bond, no set of three or more glycosidically linked carbohydrate units. Based on a literature review very few articles have been published on 5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]Tetracos-15-en-17-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082210432D          

 32 34  0  0  0  0            999 V2000
    2.4794    2.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1565    1.7166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942    2.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6359    2.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4960    2.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2770    2.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6921    3.0237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9163    1.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3529    1.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5157    0.2474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3894   -0.5863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6382   -0.9522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5466   -1.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7832   -2.1962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9398   -2.3919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0915   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2491   -2.1762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7097   -1.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0222   -0.7561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8415    0.0893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8283    0.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0180    1.0841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8544   -0.6589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1839    0.0975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3387   -1.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1523   -1.1825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2493   -2.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1885   -3.0798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.6752   -2.3802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0680   -1.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8181   -0.7361    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
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
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  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 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
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 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
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  2 21  1  0  0  0  0
 21 22  2  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
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 31 32  1  0  0  0  0
M  END

     RDKit          3D

 66 68  0  0  0  0  0  0  0  0999 V2000
    5.4017   -0.6780   -0.8411 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9005    2.5594    0.5627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6710    2.5559   -0.0586 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5939    3.1492    1.7006 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9933    1.8298    1.5137 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2601    1.8224    0.6957 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0981    0.9566   -0.4100 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840    0.3352   -1.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3007    0.5458   -2.3793 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5042    3.2257    0.1907 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9749    4.0700    1.1718 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579    3.7997   -0.4572 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4651    5.1455   -0.6418 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2318   -3.4457    0.5993 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6361   -5.5443   -1.1417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1938   -4.7051   -1.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2467   -2.5112   -2.1611 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309082210432D          

 32 34  0  0  0  0            999 V2000
    2.4794    2.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1565    1.7166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942    2.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6359    2.6193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.2770    2.3107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8544   -0.6589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0264921

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCOC2OC(COC3OCC(OC(=O)C(C)=CCC1)C(O)C3O)C(O)C(O)C2O

> <INCHI_IDENTIFIER>
InChI=1S/C21H34O11/c1-10-4-3-5-11(2)19(27)31-12-8-29-20(17(25)15(12)23)30-9-13-14(22)16(24)18(26)21(32-13)28-7-6-10/h5,10,12-18,20-26H,3-4,6-9H2,1-2H3

> <INCHI_KEY>
QUOSEESBIZGJKC-UHFFFAOYSA-N

> <FORMULA>
C21H34O11

> <MOLECULAR_WEIGHT>
462.492

> <EXACT_MASS>
462.210111915

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.077457196685295

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1^{4,8}]tetracos-15-en-17-one

> <JCHEM_LOGP>
-0.06978397500000029

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.490911832598751

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.941886379807153

> <JCHEM_PKA_STRONGEST_BASIC>
-3.648667943910181

> <JCHEM_POLAR_SURFACE_AREA>
164.37

> <JCHEM_REFRACTIVITY>
107.57520000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1^{4,8}]tetracos-15-en-17-one

> <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       4.628   4.084   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.892   3.204   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.083   4.312   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.654   4.889   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.259   4.865   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.717   4.313   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.492   5.644   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.910   3.323   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.725   1.997   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      14.029   0.462   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      13.794  -1.094   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.391  -1.777   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      12.220  -3.347   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.795  -4.100   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.221  -4.465   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.637  -3.954   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.065  -4.062   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.058  -2.890   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.641  -1.411   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.304   0.167   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.279   1.734   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.767   2.024   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.195  -1.230   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.810   0.182   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.099  -2.462   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.618  -2.207   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      13.532  -4.213   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.418  -5.749   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      14.931  -3.562   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      16.194  -4.443   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      15.060  -2.015   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      16.460  -1.374   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   31                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20    2   22                                                  
CONECT   22   21                                                            
CONECT   23   19   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
CONECT   27   13   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   11   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₄O₁₁

Average Mass

462.4920 Da

Monoisotopic Mass

462.21011 Da

IUPAC Name

5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1^{4,8}]tetracos-15-en-17-one

Traditional Name

5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1^{4,8}]tetracos-15-en-17-one

CAS Registry Number

Not Available

SMILES

CC1CCOC2OC(COC3OCC(OC(=O)C(C)=CCC1)C(O)C3O)C(O)C(O)C2O

InChI Identifier

InChI=1S/C21H34O11/c1-10-4-3-5-11(2)19(27)31-12-8-29-20(17(25)15(12)23)30-9-13-14(22)16(24)18(26)21(32-13)28-7-6-10/h5,10,12-18,20-26H,3-4,6-9H2,1-2H3

InChI Key

QUOSEESBIZGJKC-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as disaccharides. Disaccharides are compounds containing two carbohydrate moieties linked to each to each other through a glycosidic bond, no set of three or more glycosidically linked carbohydrate units.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Disaccharides

Alternative Parents

Substituents

Disaccharide
Oxane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Carboxylic acid ester
Acetal
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Alcohol
Hydrocarbon derivative
Organic oxide
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
logP	-0.07	ChemAxon
pKa (Strongest Acidic)	11.94	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	164.37 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	107.58 m³·mol⁻¹	ChemAxon
Polarizability	47.08 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

163048462

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one (NP0264921)

MOL for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

3D MOL for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

3D SDF for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

3D-SDF for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

PDB for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

3D PDB for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

SMILES for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

INCHI for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

Structure for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)

3D Structure for NP0264921 (5,6,7,22,23-pentahydroxy-12,16-dimethyl-2,9,18,21,24-pentaoxatricyclo[17.2.2.1⁴,⁸]tetracos-15-en-17-one)