NP-MRD: Showing NP-Card for (1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione (NP0323560)

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Record Information

Version

2.0

Created at

2022-09-12 03:03:47 UTC

Updated at

2022-09-12 03:03:48 UTC

NP-MRD ID

NP0323560

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione

Description

(1R,2S,3S,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]Hexadeca-8,15-diene-7,13-dione belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. (1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione is found in Fibraurea tinctoria. Based on a literature review very few articles have been published on (1R,2S,3S,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]Hexadeca-8,15-diene-7,13-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122205032D          

 37 42  0  0  1  0            999 V2000
    2.4501   -0.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8992    0.4555    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    4.4725   -1.0575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4166   -2.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6816   -2.3759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0981   -1.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1723    1.1045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  1  6  0  0  0
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 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 19 37  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309122205032D          

 37 42  0  0  1  0            999 V2000
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  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5  9  2  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 16  1  6  0  0  0
  2 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  1  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  6  0  0  0
 22 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 19 37  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0323560

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12C[C@@H](OC(=O)C1=CC[C@]1(C)[C@H]2[C@@H]2OC(=O)[C@@]1(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C=C2)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H30O11/c1-24-9-15(12-5-8-33-11-12)34-21(31)13(24)3-6-25(2)20(24)14-4-7-26(25,23(32)36-14)37-22-19(30)18(29)17(28)16(10-27)35-22/h3-5,7-8,11,14-20,22,27-30H,6,9-10H2,1-2H3/t14-,15-,16-,17-,18+,19-,20+,22-,24-,25-,26+/m1/s1

> <INCHI_KEY>
CLMFOKCFOQCBFM-MLNGZWRGSA-N

> <FORMULA>
C26H30O11

> <MOLECULAR_WEIGHT>
518.515

> <EXACT_MASS>
518.178811786

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
49.47601995030615

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3S,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadeca-8,15-diene-7,13-dione

> <JCHEM_LOGP>
0.46737070999999913

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.199382234641352

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.208737519997069

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8646278282254474

> <JCHEM_POLAR_SURFACE_AREA>
165.12

> <JCHEM_REFRACTIVITY>
123.51340000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadeca-8,15-diene-7,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       4.573  -0.441   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.412   0.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.111  -0.522   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.649  -0.602   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.349  -1.974   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.870  -2.215   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.111  -3.736   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.739  -4.435   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.650  -3.346   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.488   0.690   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.788   2.062   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.627   3.353   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.250   2.142   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.551   3.514   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.013   3.594   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.175   2.303   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.712   2.222   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.874   0.931   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.036  -0.361   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.341   0.437   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.874   1.352   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.637   2.383   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.937   3.755   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.776   5.047   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.314   4.966   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.152   6.258   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.690   6.178   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.389   4.806   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.453   7.630   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.291   8.922   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.915   7.710   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.215   9.082   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.076   6.418   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -0.462   6.499   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.798   1.091   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.740   1.171   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       1.498  -0.281   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   13   18                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    5                                                       
CONECT   10    4   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    2   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   22                                             
CONECT   17   16                                                            
CONECT   18   16    2   19                                                  
CONECT   19   18   20   37                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23   35                                             
CONECT   23   22   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   24   34                                                  
CONECT   34   33                                                            
CONECT   35   22   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   19                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₀O₁₁

Average Mass

518.5150 Da

Monoisotopic Mass

518.17881 Da

IUPAC Name

(1R,2S,3S,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadeca-8,15-diene-7,13-dione

Traditional Name

(1R,2S,3S,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0^{2,11}.0^{3,8}]hexadeca-8,15-diene-7,13-dione

CAS Registry Number

Not Available

SMILES

C[C@@]12C[C@@H](OC(=O)C1=CC[C@]1(C)[C@H]2[C@@H]2OC(=O)[C@@]1(O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C=C2)C1=COC=C1

InChI Identifier

InChI=1S/C26H30O11/c1-24-9-15(12-5-8-33-11-12)34-21(31)13(24)3-6-25(2)20(24)14-4-7-26(25,23(32)36-14)37-22-19(30)18(29)17(28)16(10-27)35-22/h3-5,7-8,11,14-20,22,27-30H,6,9-10H2,1-2H3/t14-,15-,16-,17-,18+,19-,20+,22-,24-,25-,26+/m1/s1

InChI Key

CLMFOKCFOQCBFM-MLNGZWRGSA-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
Fibraurea tinctoria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Naphthopyran
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Naphthalene
Delta valerolactone
Dihydropyranone
Delta_valerolactone
Pyran
Oxane
Dicarboxylic acid or derivatives
Monosaccharide
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Heteroaromatic compound
Furan
Secondary alcohol
Carboxylic acid ester
Lactone
Polyol
Carboxylic acid derivative
Organoheterocyclic compound
Acetal
Oxacycle
Primary alcohol
Carbonyl group
Organooxygen compound
Alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	0.47	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	165.12 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	123.51 m³·mol⁻¹	ChemAxon
Polarizability	49.48 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

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

162978109

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,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione (NP0323560)

MOL for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

3D MOL for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

3D SDF for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

3D-SDF for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

PDB for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

3D PDB for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

SMILES for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

INCHI for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

Structure for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)

3D Structure for NP0323560 ((1r,2s,3s,5r,11r,12r)-5-(furan-3-yl)-3,11-dimethyl-12-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6,14-dioxatetracyclo[10.2.2.0²,¹¹.0³,⁸]hexadeca-8,15-diene-7,13-dione)