NP-MRD: Showing NP-Card for 1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone (NP0220869)

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Record Information

Version

1.0

Created at

2022-09-05 22:18:10 UTC

Updated at

2022-09-05 22:18:10 UTC

NP-MRD ID

NP0220869

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone

Description

Drummondone A belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms. 1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone is found in Sesbania drummondii. It was first documented in 2022 (PMID: 36051722). Based on a literature review a significant number of articles have been published on Drummondone A (PMID: 36050584) (PMID: 36044365) (PMID: 36043368) (PMID: 36038174).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
    3.4803    0.0802    0.2503 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392   -1.1163   -0.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1956   -2.1699   -0.3674 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1812   -1.0455   -0.1852 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5229   -0.6567    1.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8047   -0.0577    0.8616 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6633   -0.0527    1.9287 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5259   -0.6233   -0.3630 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1782   -1.9225   -0.1184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5823    0.4911   -0.4713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8002    1.6191   -0.4140 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6771    1.3792    0.3298 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4901    2.3189    1.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5168    1.3491   -0.6078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6825   -0.0276   -1.2162 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5468   -0.0342   -2.2801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7076   -0.5331   -1.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5220   -0.2674    0.4482 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0988    0.5962    1.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5659    0.7902   -0.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7779   -2.0456   -0.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4783   -1.4945    1.8333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1700    0.1177    1.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2031   -0.2797    2.7726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5446   -2.7805   -0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5387   -1.9721    0.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0950   -1.9883   -0.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1614    0.4254    0.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1805    0.3896   -1.3709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2829    2.1115    2.2199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5012    2.1421    1.9216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6297    3.3647    1.1410 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2974    2.0275   -1.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4133    1.7341   -0.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1863   -0.4327   -3.0916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5651   -1.5524   -2.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1460    0.1159   -2.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  1
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 15  4  1  0
 12  6  1  0
 17  8  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  6
  5 22  1  0
  5 23  1  0
  7 24  1  0
  9 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
 14 33  1  0
 14 34  1  0
 16 35  1  0
 17 36  1  0
 17 37  1  0
M  END


  Mrv1652309062200182D          

 17 19  0  0  1  0            999 V2000
    5.1303    1.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6642    0.4810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -0.2630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8416    0.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3073   -0.1141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5189    0.2430    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2121   -0.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7994    0.4948    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5612   -0.2950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9719    0.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3176    1.4618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1186    1.1333    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3899    0.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7173    1.7597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4129    1.2795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0180    1.8402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6738    0.8447    0.0000 C   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  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  8 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220869

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C1C[C@]2(O)[C@@]3(C)CO[C@]2(C)CC1(O)C3

> <INCHI_IDENTIFIER>
InChI=1S/C13H20O4/c1-8(14)9-4-13(16)10(2)5-12(9,15)6-11(13,3)17-7-10/h9,15-16H,4-7H2,1-3H3/t9?,10-,11-,12?,13+/m1/s1

> <INCHI_KEY>
LDUXISPHWOIQAZ-HDPSNQDDSA-N

> <FORMULA>
C13H20O4

> <MOLECULAR_WEIGHT>
240.299

> <EXACT_MASS>
240.136159124

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
25.059104725712928

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(3R,6R,7S)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0^{3,7}]decan-9-yl]ethan-1-one

> <JCHEM_LOGP>
-0.38762752666666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.292186278207371

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.207045012155952

> <JCHEM_PKA_STRONGEST_BASIC>
-3.130894634095827

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
60.9926

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-[(3R,6R,7S)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0^{3,7}]decan-9-yl]ethanone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       9.577   2.168   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.706   0.898   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.372  -0.491   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       7.171   1.016   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.174  -0.213   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.702   0.454   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.129  -0.976   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.359   0.924   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.914  -0.551   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.814   1.316   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.460   2.729   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.955   2.116   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.595   1.394   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.072   3.285   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.371   2.388   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.500   3.435   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.991   1.577   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8   12                                             
CONECT    7    6                                                            
CONECT    8    6    9   10   17                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    6   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    4   16   17                                             
CONECT   16   15                                                            
CONECT   17   15    8                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₂₀O₄

Average Mass

240.2990 Da

Monoisotopic Mass

240.13616 Da

IUPAC Name

1-[(3R,6R,7S)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0^{3,7}]decan-9-yl]ethan-1-one

Traditional Name

1-[(3R,6R,7S)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0^{3,7}]decan-9-yl]ethanone

CAS Registry Number

Not Available

SMILES

CC(=O)C1C[C@]2(O)[C@@]3(C)CO[C@]2(C)CC1(O)C3

InChI Identifier

InChI=1S/C13H20O4/c1-8(14)9-4-13(16)10(2)5-12(9,15)6-11(13,3)17-7-10/h9,15-16H,4-7H2,1-3H3/t9?,10-,11-,12?,13+/m1/s1

InChI Key

LDUXISPHWOIQAZ-HDPSNQDDSA-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
Sesbania drummondii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Oxepane
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Ketone
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	-0.39	ChemAxon
pKa (Strongest Acidic)	13.21	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	60.99 m³·mol⁻¹	ChemAxon
Polarizability	25.06 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

316009

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

355979

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wako M, Kono H, Koyama K, Fujimaki T, Furuya N, Haro H: The Anatomical Position of Graf's Standard Plane and Its Relationship With Pelvic Morphology: A Computed Tomography-Based Study. Cureus. 2022 Jul 28;14(7):e27424. doi: 10.7759/cureus.27424. eCollection 2022 Jul. [PubMed:36051722 ]
Jayroe M, Aguilar DR, Porter A, Cima M, Chai S, Hayman K: Transmission Analysis of COVID-19 Outbreaks Associated with Places of Worship, Arkansas, May 2020-December 2020. J Relig Health. 2022 Sep 1. pii: 10.1007/s10943-022-01653-y. doi: 10.1007/s10943-022-01653-y. [PubMed:36050584 ]
Belik AA, Khalyavin DD, Matsushita Y, Yamaura K: Triple A-Site Cation Ordering in the Ferrimagnetic Y2CuGaMn4O12 Perovskite. Inorg Chem. 2022 Sep 12;61(36):14428-14435. doi: 10.1021/acs.inorgchem.2c02343. Epub 2022 Aug 31. [PubMed:36044365 ]
Siwach P, Sikarwar P, Rajput SA, Antharjanam S, Chandiran AK: The effect of halogenated spacer cations on structural symmetry-breaking in 2D halide double perovskites. Chem Commun (Camb). 2022 Aug 31. doi: 10.1039/d2cc02747j. [PubMed:36043368 ]
Abukhadijah HJ, Turk-Adawi KI, Dewart N, Grace SL: Qualitative study measuring the usability of the International Cardiac Rehabilitation Registry. BMJ Open. 2022 Aug 29;12(8):e064255. doi: 10.1136/bmjopen-2022-064255. [PubMed:36038174 ]
LOTUS database [Link]

Showing NP-Card for 1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone (NP0220869)

MOL for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

3D MOL for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

3D SDF for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

3D-SDF for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

PDB for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

3D PDB for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

SMILES for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

INCHI for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

Structure for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)

3D Structure for NP0220869 (1-[(3r,6r,7s)-1,7-dihydroxy-3,6-dimethyl-4-oxatricyclo[4.3.1.0³,⁷]decan-9-yl]ethanone)