NP-MRD: Showing NP-Card for (1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol (NP0308277)

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Record Information

Version

2.0

Created at

2022-09-11 01:57:26 UTC

Updated at

2022-09-11 01:57:26 UTC

NP-MRD ID

NP0308277

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

Description

1H-Cycloprop[e]azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, [1ar-(1aalpha,4aalpha,7beta,7abeta,7balpha)]- belongs to the class of organic compounds known as 5,10-cycloaromadendrane sesquiterpenoids. These are aromadendrane sesquiterpenoids that arise from the C5-C10 cyclization of the aromadendrane skeleton. (1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol is found in Ageratina ligustrina, Aglaia forbesii, Aglaia foveolata, Anthemis aciphylla, Artabotrys hexapetalus, Artemisia annua, Artemisia monosperma, Artemisia vulgaris, Baccharis dracunculifolia, Baccharis incarum, Caesalpinia pulcherrima, Callicarpa japonica, Centaurea armena, Cistus incanus, Croton arboreus, Cyperus rotundus, Frullania lobulata, Hedyosmum orientale, Indocypraea montana, Kunzea ambigua, Lepidozia vitrea, Myrtus communis, Piper fimbriulatum, Prangos pabularia, Prangos tschimganica, Rhytisma fulvum, Santolina canescens and Valeriana officinalis. Based on a literature review very few articles have been published on 1H-Cycloprop[e]azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, [1ar-(1aalpha,4aalpha,7beta,7abeta,7balpha)]-.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
    0.2856    2.9844   -0.4094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1040    2.0661    0.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1178    2.1794    1.3041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0944    1.0799    1.2012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7414   -0.3038    1.1556 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5460   -0.9176    0.7195 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7837   -0.3491    0.7440 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1312    1.0594    0.6480 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1217    1.1481   -0.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8594   -0.1778   -0.3264 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6722   -1.1095   -0.2624 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0947   -2.4436    0.2776 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1166   -1.2089   -1.4933 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6111   -0.8874   -0.2705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7129   -0.0378   -1.4647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5629   -2.1042   -0.4321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4714    3.7626   -0.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1719    2.9573   -1.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6178    3.1361    1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7709    2.3486    2.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689    1.2982    0.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8092    1.2992    2.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3633   -0.9218    1.8987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4135   -2.0209    1.0284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2909   -0.6754    1.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7752    1.4528    1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5954    1.0489   -1.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8123    1.9948   -0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3455   -0.1418    0.6794 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5519   -0.3940   -1.1351 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6370   -2.6295    1.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8706   -3.2667   -0.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1979   -2.4708    0.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7996   -1.0555   -2.1860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6760    0.5468   -1.5548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9117    0.6312   -1.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7677   -0.7183   -2.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5907   -1.7549   -0.2082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2181   -2.8909    0.2635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4517   -2.5137   -1.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  1  0
 14  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  6
 11  7  1  0
  7  6  1  0
  6 14  1  0
  6  5  1  0
  7  8  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
  5 23  1  1
  4 21  1  0
  4 22  1  0
  3 19  1  0
  3 20  1  0
  1 17  1  0
  1 18  1  0
  8 26  1  1
  9 27  1  0
  9 28  1  0
 10 29  1  0
 10 30  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
  7 25  1  1
  6 24  1  1
M  END


  Mrv1652309112203572D          

 16 18  0  0  1  0            999 V2000
    2.0737    1.8074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6618    1.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4382    1.5078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1404    1.0746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2395    0.2556    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6609   -0.3326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8404   -0.2469    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3957    0.4480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5974    0.2398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5487   -0.5837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3169   -0.8846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1064   -1.6823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8901   -1.4779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4596   -0.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095   -1.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2732   -0.6761    0.0000 C   0  0  0  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
  5  4  1  1  0  0  0
  6  5  1  1  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  1  0  0  0
  6 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0308277

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@@H]2CCC(=C)[C@@H]3CC[C@](C)(O)[C@@H]3[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-9-5-6-11-13(14(11,2)3)12-10(9)7-8-15(12,4)16/h10-13,16H,1,5-8H2,2-4H3/t10-,11+,12-,13+,15-/m0/s1

> <INCHI_KEY>
FRMCCTDTYSRUBE-ARUSPNSKSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.356

> <EXACT_MASS>
220.182715393

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
26.397064036257365

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-decahydro-1H-cyclopropa[e]azulen-7-ol

> <JCHEM_LOGP>
2.8308566080000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.93392097088224

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6407029673361072

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
66.3775

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       3.871   3.374   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.969   2.294   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.418   2.815   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.729   2.006   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.914   0.477   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.834  -0.621   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.302  -0.461   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.472   0.836   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.982   0.448   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.891  -1.090   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.325  -1.651   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.932  -3.140   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.395  -2.759   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.325  -1.007   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.604  -2.521   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.843  -1.262   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    7   14                                                  
CONECT    7    6    8   11                                                  
CONECT    8    7    2    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    7   12   13                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    6    5   15   16                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O

Average Mass

220.3560 Da

Monoisotopic Mass

220.18272 Da

IUPAC Name

(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-decahydro-1H-cyclopropa[e]azulen-7-ol

Traditional Name

(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol

CAS Registry Number

Not Available

SMILES

CC1(C)[C@@H]2CCC(=C)[C@@H]3CC[C@](C)(O)[C@@H]3[C@H]12

InChI Identifier

InChI=1S/C15H24O/c1-9-5-6-11-13(14(11,2)3)12-10(9)7-8-15(12,4)16/h10-13,16H,1,5-8H2,2-4H3/t10-,11+,12-,13+,15-/m0/s1

InChI Key

FRMCCTDTYSRUBE-ARUSPNSKSA-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
Ageratina ligustrina	LOTUS Database	35616633
Aglaia forbesii	LOTUS Database	35616633
Aglaia foveolata	LOTUS Database	35616633
Anthemis aciphylla	LOTUS Database	35616633
Artabotrys hexapetalus	LOTUS Database	35616633
Artemisia annua	LOTUS Database	35616633
Artemisia monosperma	LOTUS Database	35616633
Artemisia vulgaris	LOTUS Database	35616633
Baccharis dracunculifolia	LOTUS Database	35616633
Baccharis incarum	LOTUS Database	35616633
Caesalpinia pulcherrima	LOTUS Database	35616633
Callicarpa japonica	LOTUS Database	35616633
Centaurea armena	LOTUS Database	35616633
Cistus incanus	LOTUS Database	35616633
Croton arboreus	LOTUS Database	35616633
Cyperus rotundus	LOTUS Database	35616633
Frullania lobulata	LOTUS Database	35616633
Hedyosmum orientale	LOTUS Database	35616633
Indocypraea montana	LOTUS Database	35616633
Kunzea ambigua	LOTUS Database	35616633
Lepidozia vitrea	LOTUS Database	35616633
Myrtus communis	LOTUS Database	35616633
Piper fimbriulatum	LOTUS Database	35616633
Prangos pabularia	LOTUS Database	35616633
Prangos tschimganica	LOTUS Database	35616633
Rhytisma fulvum	LOTUS Database	35616633
Santolina canescens	LOTUS Database	35616633
Valeriana officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 5,10-cycloaromadendrane sesquiterpenoids. These are aromadendrane sesquiterpenoids that arise from the C5-C10 cyclization of the aromadendrane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

5,10-cycloaromadendrane sesquiterpenoids

Alternative Parents

Substituents

5,10-cycloaromadendrane sesquiterpenoid
Guaiane sesquiterpenoid
Tertiary alcohol
Cyclic alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	2.83	ChemAxon
pKa (Strongest Acidic)	19.93	ChemAxon
pKa (Strongest Basic)	-0.64	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	66.38 m³·mol⁻¹	ChemAxon
Polarizability	26.4 Å³	ChemAxon
Number of Rings	3	ChemAxon
Rule of Five	Yes	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

65791273

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13854258

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol (NP0308277)

MOL for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

3D MOL for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

3D SDF for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

3D-SDF for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

PDB for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

3D PDB for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

SMILES for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

INCHI for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

Structure for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)

3D Structure for NP0308277 ((1ar,4ar,7s,7as,7br)-1,1,7-trimethyl-4-methylidene-octahydrocyclopropa[e]azulen-7-ol)