NP-MRD: Showing NP-Card for (2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol (NP0201470)

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Record Information

Version

2.0

Created at

2022-09-04 20:31:26 UTC

Updated at

2022-09-04 20:31:26 UTC

NP-MRD ID

NP0201470

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol

Description

(+)-Alpha-Bisabolol, also known as bisabolol or levomenol, belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units (+)-alpha-Bisabolol is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, (+)-alpha-Bisabolol has been detected, but not quantified in, german camomiles. (2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol is found in Abies nephrolepis, Abies sibirica, Artemisia annua, Artemisia xanthochroa, Eremanthus incanus, Ferula hermonis, Helichrysum mimetes, Juniperus barbadensis, Lasiolaena morii, Libanotis buchtormensis, Seseli transcaucasicum, Lychnophora ericoides, Phlebia tremellosa, Microbiota decussata, Osyris quadripartita, Pellia epiphylla, Pinus pumila, Piper fimbriulatum and Valeriana officinalis. This could make (+)-alpha-bisabolol a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 42  0  0  0  0  0  0  0  0999 V2000
    5.3086    1.9044    0.1566 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2721    0.8123    0.2069 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3478   -0.2573    1.2245 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3084    0.8393   -0.6726 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.2091   -0.6772 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8852    0.3953   -0.4702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1117   -0.7023   -0.4863 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0089   -1.4379   -1.7984 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1777   -1.6437    0.5292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5292   -0.2765   -0.2838 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3528   -1.5604   -0.0935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7680   -1.1359   -0.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1099    0.0482    0.4136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5578    0.4592    0.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1502    1.0320    0.9710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7383    0.4858    1.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4016    2.2348   -0.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2816    1.5413    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9019    2.7467    0.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4225   -0.2349    1.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3602   -1.2363    0.6994 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2539   -0.1755    1.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2242    1.6110   -1.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3253   -0.8358   -1.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4112   -0.9053    0.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9267    0.9692    0.4734 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6893    1.0621   -1.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9876   -1.6026   -2.3000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5733   -0.8313   -2.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5306   -2.4012   -1.7216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1415   -1.1371    1.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9653    0.2636   -1.1218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1391   -2.3288   -0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1207   -1.8973    0.9593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5259   -1.7942   -0.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7570    1.1419    1.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7569    1.0001   -0.5223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1536   -0.4728    0.5183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1505    1.9134    0.2746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4409    1.4113    1.9682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6088   -0.1517    1.8795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0647    1.3558    1.1073 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 12  2  0
 12 11  1  0
 10  7  1  0
  7  8  1  0
  7  9  1  1
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
 11 10  1  0
 10 32  1  6
 16 41  1  0
 16 42  1  0
 15 39  1  0
 15 40  1  0
 14 36  1  0
 14 37  1  0
 14 38  1  0
 12 35  1  0
 11 33  1  0
 11 34  1  0
  8 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
  6 26  1  0
  6 27  1  0
  5 24  1  0
  5 25  1  0
  4 23  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
M  END


  Mrv1652307301922582D          

 17 17  0  0  0  0            999 V2000
 9999.629310000.4122    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.3439 9999.9999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.057110000.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.7723 9999.9999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.485510000.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.1987 9999.9999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.485510001.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.040910001.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.216010001.1254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7712 9998.7632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.6293 9999.5877    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9998.200610000.4131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.486110000.0006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.4861 9999.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2006 9998.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9151 9999.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.915110000.0006    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  8  1  1  0  0  0
  1  9  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  1 17  1  0  0  0  0
 17 11  1  6  0  0  0
 14 10  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201470

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]1(CCC(C)=CC1)[C@](C)(O)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O/c1-12(2)6-5-11-15(4,16)14-9-7-13(3)8-10-14/h6-7,14,16H,5,8-11H2,1-4H3/t14-,15+/m0/s1

> <INCHI_KEY>
RGZSQWQPBWRIAQ-LSDHHAIUSA-N

> <FORMULA>
C15H26O

> <MOLECULAR_WEIGHT>
222.3663

> <EXACT_MASS>
222.198365454

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
27.863086870988745

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-6-methyl-2-[(1R)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol

> <JCHEM_LOGP>
3.911965512666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4708710633739094

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
72.1875

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-6-methyl-2-[(1R)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 30-JUL-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-JUL-19         0                                  
HETATM    1  C   UNK     0    8665.9758667.436   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8667.3098666.666   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8668.6408667.436   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8669.9758666.666   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8671.3068667.436   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8672.6388666.666   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8671.3068668.975   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8666.7438668.767   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0    8665.2038668.767   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0    8660.6408664.358   0.000  0.00  0.00           C+0
HETATM   11  H   UNK     0    8665.9758665.897   0.000  0.00  0.00           H+0
HETATM   12  C   UNK     0    8663.3088667.438   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8661.9748666.668   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8661.9748665.128   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8663.3088664.358   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8664.6428665.128   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8664.6428666.668   0.000  0.00  0.00           C+0
CONECT    1    2    8    9   17                                             
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    1                                                            
CONECT    9    1                                                            
CONECT   10   14                                                            
CONECT   11   17                                                            
CONECT   12   13   17                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   10                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   12   16    1   11                                             
MASTER        0    0    0    0    0    0    0    0   17    0   34    0
END

View in JSmol

Synonyms

Value	Source
(+)-a-Bisabolol	Generator
(+)-Α-bisabolol	Generator
Bisabolol, (+)-isomer	HMDB
Bisabolol	HMDB
(+)-(1'r,2R)-alpha-Bisabolol	HMDB
(+)-(1'r,2R)-Α-bisabolol	HMDB
(+)-(1’R,2R)-α-bisabolol	HMDB
(+)-6R,7R-alpha-Bisabolol	HMDB
(+)-6R,7R-Α-bisabolol	HMDB
(AlphaR,1R)-alpha,4-dimethyl-alpha-(4-methyl-3-penten-1-yl)-3-cyclohexene-1-methanol	HMDB
(ΑR,1R)-α,4-dimethyl-α-(4-methyl-3-penten-1-yl)-3-cyclohexene-1-methanol	HMDB
alpha-(+)-Bisabolol	HMDB
D-alpha-Bisabolol	HMDB
D-Α-bisabolol	HMDB
Α-(+)-bisabolol	HMDB
(+)-alpha-Bisabolol	HMDB

Chemical Formula

C₁₅H₂₆O

Average Mass

222.3663 Da

Monoisotopic Mass

222.19837 Da

IUPAC Name

(2R)-6-methyl-2-[(1R)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol

Traditional Name

(2R)-6-methyl-2-[(1R)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol

CAS Registry Number

Not Available

SMILES

[H][C@]1(CCC(C)=CC1)[C@](C)(O)CCC=C(C)C

InChI Identifier

InChI=1S/C15H26O/c1-12(2)6-5-11-15(4,16)14-9-7-13(3)8-10-14/h6-7,14,16H,5,8-11H2,1-4H3/t14-,15+/m0/s1

InChI Key

RGZSQWQPBWRIAQ-LSDHHAIUSA-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
Abies nephrolepis	LOTUS Database	35616633
Abies sibirica	LOTUS Database	35616633
Artemisia annua	LOTUS Database	35616633
Artemisia xanthochroa	LOTUS Database	35616633
Eremanthus incanus	LOTUS Database	35616633
Ferula hermonis	LOTUS Database	35616633
Helichrysum mimetes	LOTUS Database	35616633
Juniperus barbadensis var. lucayana	LOTUS Database	35616633
Lasiolaena morii	LOTUS Database	35616633
Libanotis buchtormensis	LOTUS Database	35616633
Libanotis transcaucasica	LOTUS Database	35616633
Lychnophora ericoides	LOTUS Database	35616633
Merulius tremellosus	LOTUS Database	35616633
Microbiota decussata	LOTUS Database	35616633
Osyris quadripartita	LOTUS Database	35616633
Pellia epiphylla	LOTUS Database	35616633
Pinus pumila	LOTUS Database	35616633
Piper fimbriulatum	LOTUS Database	35616633
Valeriana officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Bisabolane sesquiterpenoid
Sesquiterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	3.91	ChemAxon
pKa (Strongest Basic)	-0.47	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	4	ChemAxon
Refractivity	72.19 m³·mol⁻¹	ChemAxon
Polarizability	27.86 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0036198

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB015054

KNApSAcK ID

C00003103

Chemspider ID

1266723

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

1549992

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol (NP0201470)

MOL for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

3D MOL for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

3D SDF for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

3D-SDF for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

PDB for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

3D PDB for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

SMILES for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

INCHI for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

Structure for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)

3D Structure for NP0201470 ((2r)-6-methyl-2-[(1r)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol)