NP-MRD: Showing NP-Card for (3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one (NP0238658)

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Record Information

Version

2.0

Created at

2022-09-06 22:05:05 UTC

Updated at

2022-09-06 22:05:05 UTC

NP-MRD ID

NP0238658

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one

Description

Dihydroreynosin belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. (3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one is found in Achillea biebersteinii, Achillea collina, Achillea millefolium, Artemisia herba-alba, Artemisia inculta, Inula helenium, Leucanthemopsis pectinata and Magnolia kachirachirai. (3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one was first documented in 2005 (PMID: 15997149). Based on a literature review a small amount of articles have been published on Dihydroreynosin (PMID: 22803366) (PMID: 33576270).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -1.1957    2.6590   -0.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5322    1.5208    0.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9746    1.1925    0.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2525   -0.2520   -0.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2381   -1.1423    0.6625 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5215   -2.4752    0.5295 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8566   -0.8222    0.1315 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9662   -0.7944   -1.3828 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0927   -1.8829    0.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5473   -1.4879    0.2916 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7693   -0.1883    0.9480 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8864    0.8596    0.2533 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4192    2.0397    0.8164 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7956    1.8657    0.8572 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6104    2.8185    0.9152 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1202    0.4125    0.8214 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9073    0.0066   -0.3607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5095    0.5582    0.6585 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1831    2.9861   -0.5501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9891    3.3431   -0.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3382    1.3621    1.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5674    1.8245   -0.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2440   -0.3227   -1.1071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2740   -0.5002    0.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2818   -0.8698    1.7560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828   -2.8042    1.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6737   -1.5837   -1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0098   -0.9797   -1.8873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3167    0.2166   -1.6633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0192   -2.0215    1.6745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1243   -2.8032    0.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1772   -2.2971    0.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6432   -1.4951   -0.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4699   -0.2375    1.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0160    0.8031   -0.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6939    0.1759    1.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3648   -0.4659   -1.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3787    0.9365   -0.7954 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7723   -0.6459   -0.0561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5517    0.4906    1.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 11  1  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  1  6
  7  5  1  0
  5  6  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 18  1  0
 18 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 12 11  1  0
 18  7  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
 16 36  1  1
 11 34  1  1
 10 32  1  0
 10 33  1  0
  9 30  1  0
  9 31  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  5 25  1  1
  6 26  1  0
  4 23  1  0
  4 24  1  0
  3 21  1  0
  3 22  1  0
  1 19  1  0
  1 20  1  0
 18 40  1  1
 12 35  1  6
M  END


  Mrv1652309072200052D          

 18 20  0  0  1  0            999 V2000
    2.2089   -2.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9943   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6043   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -0.0980    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6490    0.6290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -0.1238    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4736    0.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2982    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1228    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5127   -0.1753    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0781   -0.8765    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6108   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758   -1.6293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3140   -0.3719    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9440    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.8508    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 12 18  1  0  0  0  0
 18  2  1  1  0  0  0
  7 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0238658

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H]2CC[C@@]3(C)[C@H](O)CCC(=C)[C@@H]3[C@H]2OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O3/c1-8-4-5-11(16)15(3)7-6-10-9(2)14(17)18-13(10)12(8)15/h9-13,16H,1,4-7H2,2-3H3/t9-,10+,11-,12-,13+,15+/m1/s1

> <INCHI_KEY>
JWBPWNWPEVPCMJ-XBDPKTDKSA-N

> <FORMULA>
C15H22O3

> <MOLECULAR_WEIGHT>
250.338

> <EXACT_MASS>
250.156894568

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
27.873172947608523

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,3aS,5aR,6R,9aS,9bS)-6-hydroxy-3,5a-dimethyl-9-methylidene-dodecahydronaphtho[1,2-b]furan-2-one

> <JCHEM_LOGP>
2.0634632806666664

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.677998626299186

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9396434008567347

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
67.83250000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3R,3aS,5aR,6R,9aS,9bS)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3H-naphtho[1,2-b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       4.123  -4.254   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.395  -2.897   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.856  -2.849   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.128  -1.492   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.939  -0.183   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.211   1.174   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.479  -0.231   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.751   1.126   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.290   1.078   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.829   1.030   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.557  -0.327   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.746  -1.636   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.740  -2.812   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.166  -2.230   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.475  -3.041   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.053  -0.694   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.229   0.300   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.207  -1.588   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9   18                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   11   17                                                  
CONECT   17   16                                                            
CONECT   18   12    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Value	Source
1-Hydroxy-4(15),11(13)-eudesmadien-12,6-olide	MeSH
11-Epi-dihydroreynosin	MeSH

Chemical Formula

C₁₅H₂₂O₃

Average Mass

250.3380 Da

Monoisotopic Mass

250.15689 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H]2CC[C@@]3(C)[C@H](O)CCC(=C)[C@@H]3[C@H]2OC1=O

InChI Identifier

InChI=1S/C15H22O3/c1-8-4-5-11(16)15(3)7-6-10-9(2)14(17)18-13(10)12(8)15/h9-13,16H,1,4-7H2,2-3H3/t9-,10+,11-,12-,13+,15+/m1/s1

InChI Key

JWBPWNWPEVPCMJ-XBDPKTDKSA-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
Achillea biebersteinii	LOTUS Database	35616633
Achillea collina	LOTUS Database	35616633
Achillea millefolium	LOTUS Database	35616633
Artemisia herba-alba	LOTUS Database	35616633
Artemisia inculta	LOTUS Database	35616633
Inula helenium	LOTUS Database	35616633
Leucanthemopsis pectinata	LOTUS Database	35616633
Magnolia kachirachirai	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Sesquiterpenoid
Naphthofuran
Gamma butyrolactone
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00013041

Chemspider ID

67177134

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13895720

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang T, Ma L, Wu F, Chen R: [Chemical constituents from a portion of ethanolicextract of Saussurea lappa roots]. Zhongguo Zhong Yao Za Zhi. 2012 May;37(9):1232-6. [PubMed:22803366 ]
Duong TH, Nguyen VK, Sichaem J, Tran TN, Do TH, Pham NK, Nguyen TA, Nguyen TH, Mai DT, Nguyen NH, Huynh BL: Reticulatin, a novel C43-spiroterpenoid from the lichen Parmotrema reticulatum growing in Vietnam. Nat Prod Res. 2022 Jul;36(14):3705-3712. doi: 10.1080/14786419.2021.1885032. Epub 2021 Feb 12. [PubMed:33576270 ]
Yin HQ, Fu HW, Hua HM, Qi XL, Li W, Sha Y, Pei YH: Two new sesquiterpene lactones with the sulfonic acid group from Saussurea lappa. Chem Pharm Bull (Tokyo). 2005 Jul;53(7):841-2. doi: 10.1248/cpb.53.841. [PubMed:15997149 ]
LOTUS database [Link]

Showing NP-Card for (3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one (NP0238658)

MOL for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

3D MOL for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

3D SDF for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

3D-SDF for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

PDB for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

3D PDB for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

SMILES for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

INCHI for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

Structure for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)

3D Structure for NP0238658 ((3r,3as,5ar,6r,9as,9bs)-6-hydroxy-3,5a-dimethyl-9-methylidene-octahydro-3h-naphtho[1,2-b]furan-2-one)