NP-MRD: Showing NP-Card for 2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol (NP0280158)

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Record Information

Version

2.0

Created at

2022-09-09 05:47:47 UTC

Updated at

2022-09-09 05:47:47 UTC

NP-MRD ID

NP0280158

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol

Description

Norecasantalol belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Norecasantalol is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, norecasantalol has been detected, but not quantified in, cereals and cereal products. 2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol is found in Santalum album. This could make norecasantalol a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 32  0  0  0  0  0  0  0  0999 V2000
    0.0705    1.7353    0.5802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1944    0.2949    0.1098 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4518   -0.2810    0.6439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6523    0.4493    0.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7415    0.3822   -1.2780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0722    0.1503   -1.3362 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4957    0.7377   -1.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1019   -0.0243   -0.2334 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5031   -1.3705   -0.3520 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4280   -1.3170   -1.4432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0361   -0.4317    0.6610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1452   -0.7567    2.0826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9700    1.9845    0.8875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3148    2.4393   -0.2469 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7146    1.9124    1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4169   -0.1320    1.7633 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5430   -1.3741    0.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6053    1.5416    0.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5761    0.0332    0.5907 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3435   -0.3773   -1.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5890    0.5332   -2.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4810    1.8241   -1.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9253    0.4411   -2.3681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1484    0.1306    0.0302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0201   -2.2967   -0.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8582   -1.5843   -2.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3847   -1.9829   -1.1279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5369   -0.0625    2.7092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6811   -1.7723    2.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1952   -0.8265    2.4065 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  1
 11  8  1  0
  8  7  1  0
  7  6  1  0
  6 10  1  0
 10  9  1  0
  6  2  1  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  0
  9 11  1  0
  2 11  1  0
  9  8  1  0
 12 28  1  0
 12 29  1  0
 12 30  1  0
  8 24  1  1
  7 22  1  0
  7 23  1  0
  6 21  1  6
 10 26  1  0
 10 27  1  0
  9 25  1  1
  1 13  1  0
  1 14  1  0
  1 15  1  0
  3 16  1  0
  3 17  1  0
  4 18  1  0
  4 19  1  0
  5 20  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -1.190   1.542   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.807   3.129   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.542   1.542   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.308   0.221   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.278  -0.661   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.014  -2.071   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.248  -3.129   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.248  -0.220   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.248   1.366   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.572   2.248   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.221   1.101   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.749  -0.572   0.000  0.00  0.00           C+0
CONECT    1    2    4    9   10                                             
CONECT    2    1                                                            
CONECT    3    4                                                            
CONECT    4    1    3    5   12                                             
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    9   12                                                       
CONECT    9    1    8   10                                                  
CONECT   10    1    9   11                                                  
CONECT   11   10   12                                                       
CONECT   12    4    8   11                                                  
MASTER        0    0    0    0    0    0    0    0   12    0   28    0
END

View in JSmol

Synonyms

Value	Source
10,11,12,13-Tetranor-a-santalan-9-ol	HMDB
Nortricycloekasantalol	HMDB

Chemical Formula

C₁₁H₁₈O

Average Mass

166.2600 Da

Monoisotopic Mass

166.13577 Da

IUPAC Name

2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethan-1-ol

Traditional Name

2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol

CAS Registry Number

Not Available

SMILES

CC12C3CC(CC13)C2(C)CCO

InChI Identifier

InChI=1S/C11H18O/c1-10(3-4-12)7-5-8-9(6-7)11(8,10)2/h7-9,12H,3-6H2,1-2H3

InChI Key

KIIXOVVGHFZKMM-UHFFFAOYSA-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
Santalum album	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Bornane monoterpenoid
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
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	2.39	ALOGPS
logP	1.45	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	17.5	ChemAxon
pKa (Strongest Basic)	-1.7	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	2	ChemAxon
Refractivity	48.42 m³·mol⁻¹	ChemAxon
Polarizability	19.87 Å³	ChemAxon
Number of Rings	3	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

HMDB0036815

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB015762

KNApSAcK ID

C00021846

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752057

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol (NP0280158)

MOL for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

3D MOL for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

3D SDF for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

3D-SDF for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

PDB for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

3D PDB for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

SMILES for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

INCHI for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

Structure for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)

3D Structure for NP0280158 (2-{2,3-dimethyltricyclo[2.2.1.0²,⁶]heptan-3-yl}ethanol)