NP-MRD: Showing NP-Card for (1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one (NP0290864)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-09 21:44:24 UTC

Updated at

2022-09-09 21:44:24 UTC

NP-MRD ID

NP0290864

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one

Description

Debenzoyldunnianin belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. (1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one is found in Illicium floridanum. It was first documented in 1998 (PMID: 9548851). Based on a literature review very few articles have been published on Debenzoyldunnianin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
    3.3585    1.2577   -0.6078 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3818    0.5818    0.2796 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6148   -0.9092    0.4117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2224   -1.5679    0.4390 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0598   -2.1316   -0.8463 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1722   -1.2714   -1.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3749   -1.6635   -3.0988 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0497    0.1684   -1.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9540    0.6026   -0.2881 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2528    1.8831   -0.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2013    1.7881   -0.3007 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4622    2.1391   -1.6490 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8654    0.4802   -0.0603 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3967   -0.1429   -1.3594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0627    0.7728    0.6440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0685   -0.5120    0.7478 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5579   -0.3622    2.2040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5384   -1.9315    0.3981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8843   -2.0445    0.7013 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3770   -0.3758    0.7063 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8400    0.0928    1.9702 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9502    2.1606   -1.0868 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2066    1.6251    0.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8619    0.5724   -1.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3386    1.0976    1.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2446   -1.3259   -0.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1193   -1.0635    1.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1882   -2.3515    1.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9822    0.6330   -2.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2427    0.5877   -2.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6985    2.6915   -0.6590 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120    2.1606    1.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6794    2.6398    0.2753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4539    3.1300   -1.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3143   -0.7287   -1.1820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6690    0.6903   -2.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6791   -0.7636   -1.8787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7589    0.1154    0.4725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1130    0.5529    2.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6326   -0.2780    2.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2244   -1.2180    2.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9840   -2.5885    1.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2514   -2.2682   -0.5875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9729   -2.1999    1.6748 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8676   -0.7251    2.5407 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  9  8  1  6
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  1
 13 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 16 20  1  0
 20 21  1  1
  9  2  1  0
 20  9  1  0
 20  4  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  1
  3 26  1  0
  3 27  1  0
  4 28  1  1
  8 29  1  0
  8 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  1
 12 34  1  0
 14 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 21 45  1  0
M  END


  Mrv1652309092223442D          

 21 23  0  0  1  0            999 V2000
    0.2077    1.5127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4287    0.6515    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0292   -0.0347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2218   -0.8206    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0820   -1.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7923   -0.7699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7335   -1.0607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8179    0.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2507    0.7214    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0623    0.8693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5962    0.2403    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4524    0.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3184   -0.5365    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2441   -0.4948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3428   -1.5239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5068   -0.6844    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5918   -1.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7378   -1.6967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3891   -2.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729   -0.0554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0082    0.4503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  1  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  6  0  0  0
 13 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  1  0  0  0
 18 19  1  0  0  0  0
 16 20  1  0  0  0  0
  4 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0290864

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H]2OC(=O)C[C@]11C[C@@H](O)[C@](C)(O)[C@@](C)(CO)[C@@]21O

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O6/c1-8-4-10-15(20)12(2,7-16)13(3,19)9(17)5-14(8,15)6-11(18)21-10/h8-10,16-17,19-20H,4-7H2,1-3H3/t8-,9-,10+,12-,13+,14-,15+/m1/s1

> <INCHI_KEY>
UWEXQYMEOHSCLX-MNGXYHNASA-N

> <FORMULA>
C15H24O6

> <MOLECULAR_WEIGHT>
300.351

> <EXACT_MASS>
300.157288493

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
30.11012275675553

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3R,4R,5R,6R,7S,11R)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0^{1,6}]dodecan-9-one

> <JCHEM_LOGP>
-1.1989816720000006

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.572824251572854

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.825246755505855

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8279038916068364

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
72.34909999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,4R,5R,6R,7S,11R)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0^{1,6}]dodecan-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       0.388   2.824   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.800   1.216   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.055  -0.065   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.414  -1.532   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.020  -2.220   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.346  -1.437   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.103  -1.980   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.393   0.228   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.335   1.347   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.850   1.623   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.846   0.449   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.445   1.030   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.328  -1.002   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.056  -0.924   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.373  -2.845   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.813  -1.278   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.105  -2.275   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.244  -3.167   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.593  -4.709   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.816  -0.103   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.015   0.841   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8    2   10   20                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13   17   18   20                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18                                                            
CONECT   20   16    4    9   21                                             
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O₆

Average Mass

300.3510 Da

Monoisotopic Mass

300.15729 Da

IUPAC Name

(1R,3R,4R,5R,6R,7S,11R)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0^{1,6}]dodecan-9-one

Traditional Name

(1R,3R,4R,5R,6R,7S,11R)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0^{1,6}]dodecan-9-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H]2OC(=O)C[C@]11C[C@@H](O)[C@](C)(O)[C@@](C)(CO)[C@@]21O

InChI Identifier

InChI=1S/C15H24O6/c1-8-4-10-15(20)12(2,7-16)13(3,19)9(17)5-14(8,15)6-11(18)21-10/h8-10,16-17,19-20H,4-7H2,1-3H3/t8-,9-,10+,12-,13+,14-,15+/m1/s1

InChI Key

UWEXQYMEOHSCLX-MNGXYHNASA-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
Illicium floridanum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Not Available

Direct Parent

Lactones

Alternative Parents

Substituents

Caprolactone
Delta valerolactone
Delta_valerolactone
Oxepane
Oxane
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Polyol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Primary alcohol
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	-1.2	ChemAxon
pKa (Strongest Acidic)	12.83	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	72.35 m³·mol⁻¹	ChemAxon
Polarizability	30.11 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00050352

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

10709342

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Schmidt TJ, Schmidt HM, Muller E, Peters W, Fronczek FR, Truesdale A, Fischer NH: New Sesquiterpene Lactones from Illicium floridanum J Nat Prod. 1998 Feb 27;61(2):230-6. doi: 10.1021/np970434g. [PubMed:9548851 ]
LOTUS database [Link]

Showing NP-Card for (1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one (NP0290864)

MOL for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

3D MOL for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

3D SDF for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

3D-SDF for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

PDB for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

3D PDB for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

SMILES for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

INCHI for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

Structure for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)

3D Structure for NP0290864 ((1r,3r,4r,5r,6r,7s,11r)-3,4,6-trihydroxy-5-(hydroxymethyl)-4,5,11-trimethyl-8-oxatricyclo[5.3.2.0¹,⁶]dodecan-9-one)