NP-MRD: Showing NP-Card for 2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol (NP0195544)

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Record Information

Version

2.0

Created at

2022-09-04 13:25:44 UTC

Updated at

2022-09-04 13:25:44 UTC

NP-MRD ID

NP0195544

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol

Description

Acorenol belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). 2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol is found in Juniperus chinensis and Tetraclinis articulata. 2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol was first documented in 2011 (PMID: 21990128). Based on a literature review a significant number of articles have been published on Acorenol (PMID: 30688448) (PMID: 28539061) (PMID: 34014675) (PMID: 27566837) (PMID: 24084795) (PMID: 22662164).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
    4.2619   -0.5294    0.3871 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8317   -0.5781    0.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3014   -0.1013   -1.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8433   -0.2290   -1.2513 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1202    0.2861   -0.0429 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7954   -0.1173    1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8531   -1.2134    1.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2827    1.8255   -0.1383 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1996    2.4835    1.1348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7002    2.1737   -1.2308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6863    1.0090   -1.3223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3442    0.2276   -0.0692 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1119   -0.9919   -0.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8851   -1.8877    1.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1326   -1.8876   -1.2224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4765   -0.5942    0.1302 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3356   -0.3066    1.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8101    0.2457   -0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7180   -1.5356    0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9220    0.3623   -1.7921 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5584    0.4333   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530   -1.2942   -1.4776 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0848   -0.4250    2.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3888    0.7157    1.6831 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4437   -2.0851    0.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3329   -1.4037    1.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3183    2.0884   -0.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4958    3.3361    1.3508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2030    2.9780    0.9951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3164    1.7964    1.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1928    2.3618   -2.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2963    3.0723   -0.9847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4701    0.4931   -2.2551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7358    1.3571   -1.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7016    0.9083    0.7680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1064   -1.3919    2.1544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6740   -2.6964    1.1055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263   -2.4229    1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0503   -2.5408   -1.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3076   -2.6253   -1.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2784   -1.3694   -2.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5558    0.0731    0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 13 16  1  0
 12  5  1  0
  5  6  1  1
  6  7  1  0
  7  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  5  8  1  0
  4  5  1  0
  9 28  1  0
  9 29  1  0
  9 30  1  0
  8 27  1  6
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  1
 14 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
M  END


  Mrv1652306132221112D          

 16 17  0  0  1  0            999 V2000
    1.0396   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2945    2.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8242    1.6096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2549    2.1195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
  9 12  1  0  0  0  0
  5 13  1  1  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195544

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@H](C(C)(C)O)[C@]11CCC(C)=CC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O/c1-11-7-9-15(10-8-11)12(2)5-6-13(15)14(3,4)16/h7,12-13,16H,5-6,8-10H2,1-4H3/t12-,13+,15-/m1/s1

> <INCHI_KEY>
XDVDHFJMCJWDPI-VNHYZAJKSA-N

> <FORMULA>
C15H26O

> <MOLECULAR_WEIGHT>
222.372

> <EXACT_MASS>
222.198365457

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
27.195433381343534

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1R,4R,5S)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol

> <JCHEM_LOGP>
3.4737942476666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.865347936103344

> <JCHEM_PKA_STRONGEST_BASIC>
-0.670696812748398

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
69.43399999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,4R,5S)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 13-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-JUN-22         0                                  
HETATM    1  C   UNK     0       1.941  -1.941   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.140   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.680   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.450   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.680  -0.564   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.140  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.990   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.941   3.481   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.416   4.945   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.405   3.005   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.476   3.956   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    2    7   11                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6                                                       
CONECT   12    9                                                            
CONECT   13    5   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₆O

Average Mass

222.3720 Da

Monoisotopic Mass

222.19837 Da

IUPAC Name

2-[(1R,4R,5S)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol

Traditional Name

2-[(1R,4R,5S)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@H](C(C)(C)O)[C@]11CCC(C)=CC1

InChI Identifier

InChI=1S/C15H26O/c1-11-7-9-15(10-8-11)12(2)5-6-13(15)14(3,4)16/h7,12-13,16H,5-6,8-10H2,1-4H3/t12-,13+,15-/m1/s1

InChI Key

XDVDHFJMCJWDPI-VNHYZAJKSA-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
Juniperus chinensis	LOTUS Database	35616633
Tetraclinis articulata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Tertiary alcohols

Alternative Parents

Hydrocarbon derivatives

Substituents

Tertiary alcohol
Hydrocarbon derivative
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	3.47	ChemAxon
pKa (Strongest Acidic)	19.87	ChemAxon
pKa (Strongest Basic)	-0.67	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	1	ChemAxon
Refractivity	69.43 m³·mol⁻¹	ChemAxon
Polarizability	27.2 Å³	ChemAxon
Number of Rings	2	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00021586

Chemspider ID

58828716

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101306697

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Jiang CX, Li J, Zhang JM, Jin XJ, Yu B, Fang JG, Wu QX: Isolation, Identification, and Activity Evaluation of Chemical Constituents from Soil Fungus Fusarium avenaceum SF-1502 and Endophytic Fungus Fusarium proliferatum AF-04. J Agric Food Chem. 2019 Feb 20;67(7):1839-1846. doi: 10.1021/acs.jafc.8b05576. Epub 2019 Feb 8. [PubMed:30688448 ]
Gu D, Fang C, Yang J, Li M, Liu H, Yang Y: Chemical composition and alpha-amylase inhibitory activity of the essential oil from Sabina chinensis cv. Kaizuca leaves. Nat Prod Res. 2018 Mar;32(6):711-713. doi: 10.1080/14786419.2017.1332612. Epub 2017 May 25. [PubMed:28539061 ]
Zhu J, Liu L, Wu M, Xia G, Lin P, Zi J: Characterization of a Sesquiterpene Synthase Catalyzing Formation of Cedrol and Two Diastereoisomers of Tricho-Acorenol from Euphorbia fischeriana. J Nat Prod. 2021 Jun 25;84(6):1780-1786. doi: 10.1021/acs.jnatprod.1c00126. Epub 2021 May 20. [PubMed:34014675 ]
Djouahri A, Saka B, Boudarene L, Baaliouamer A: Essential Oil Variability and Biological Activities of Tetraclinis articulata (Vahl) Mast. Wood According to the Extraction Time. Chem Biodivers. 2016 Dec;13(12):1691-1706. doi: 10.1002/cbdv.201600124. Epub 2016 Nov 23. [PubMed:27566837 ]
Citron CA, Dickschat JS: The stereochemical course of tricho-acorenol biosynthesis. Org Biomol Chem. 2013 Nov 21;11(43):7447-50. doi: 10.1039/c3ob41755g. [PubMed:24084795 ]
Wiemann P, Albermann S, Niehaus EM, Studt L, von Bargen KW, Brock NL, Humpf HU, Dickschat JS, Tudzynski B: The Sfp-type 4'-phosphopantetheinyl transferase Ppt1 of Fusarium fujikuroi controls development, secondary metabolism and pathogenicity. PLoS One. 2012;7(5):e37519. doi: 10.1371/journal.pone.0037519. Epub 2012 May 25. [PubMed:22662164 ]
Brock NL, Tudzynski B, Dickschat JS: Biosynthesis of sesqui- and diterpenes by the gibberellin producer Fusarium fujikuroi. Chembiochem. 2011 Nov 25;12(17):2667-76. doi: 10.1002/cbic.201100516. Epub 2011 Oct 11. [PubMed:21990128 ]
LOTUS database [Link]

Showing NP-Card for 2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol (NP0195544)

MOL for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

3D MOL for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

3D SDF for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

3D-SDF for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

PDB for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

3D PDB for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

SMILES for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

INCHI for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

Structure for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)

3D Structure for NP0195544 (2-[(1r,4r,5s)-4,8-dimethylspiro[4.5]dec-7-en-1-yl]propan-2-ol)