NP-MRD: Showing NP-Card for terpineol; terpineols (NP0294965)

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Record Information

Version

2.0

Created at

2022-09-10 03:43:58 UTC

Updated at

2022-09-10 03:43:58 UTC

NP-MRD ID

NP0294965

Secondary Accession Numbers

None

Natural Product Identification

Common Name

terpineol; terpineols

Description

1196157-69-3 Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. terpineol; terpineols is found in Aristolochia asclepiadifolia, Artemisia tridentata, Carica papaya, Chaerophyllum bulbosum, Chrysanthemum indicum, Cymbopogon citratus, Melaleuca alternifolia, Narcissus tazetta, Ocimum campechianum and Osmitopsis asteriscoides. Based on a literature review very few articles have been published on 1196157-69-3.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 58 58  0  0  0  0  0  0  0  0999 V2000
   -2.6922   -1.1781    0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3136   -0.0620    0.1513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2408    1.0952    0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9978    0.0219   -0.4859 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1364    1.1412    0.0257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0384    0.6521    0.8380 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9462   -0.2638    0.0900 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1822    0.4295   -0.4332 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3139   -1.3007    0.9747 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1586   -0.9259   -1.0222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2102   -1.2556   -0.4069 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2008    0.8748   -0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0582   -0.0059    0.1141 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3739    0.0788    1.2719 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2256   -0.8693    1.4317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6812   -0.8859    0.2528 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7351    0.1769    0.4098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6739    0.1742   -0.7903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1806    1.5611    0.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358   -0.0885    1.5867 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0647   -0.7988   -1.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5367   -1.0536   -0.8256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6527   -1.2606    1.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0364   -2.0287    0.7052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2538    0.8019    0.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8970    1.9159    0.8321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3457    1.4627   -0.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1789    0.2082   -1.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2715    1.7489   -0.8086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6979    1.8524    0.6732 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7172    0.2443    1.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6346    1.5690    1.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893    1.0515    0.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9400   -0.3049   -0.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9272    1.0652   -1.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0409   -1.0085    1.5778 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6469   -1.8118   -1.4232 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866   -0.2116   -1.8783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0532   -1.5490    0.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6870   -2.0986   -0.9128 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3185    1.1529   -1.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1583    0.4779    0.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0355    1.8455    0.3942 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6601    0.8009    2.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2808   -0.5751    2.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6135   -1.9032    1.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2399   -1.8676    0.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6856   -0.8088   -1.2902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3912    0.9803   -1.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6896    0.3813   -0.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4620    1.7225    1.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0392    2.2475    0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6709    1.8619   -0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5678   -1.0744    1.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0253    0.2170   -1.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2902   -1.5267   -1.7898 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7071   -2.0274   -0.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0962   -1.0683   -1.7665 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  1
  7 10  1  0
 10 11  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 21  1  0
 21 22  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 17 20  1  0
 11  4  1  0
 22 13  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  1 23  1  0
  1 24  1  0
  4 28  1  6
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  8 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  6
 21 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
M  END


  Mrv1652309102205432D          

 22 22  0  0  0  0            999 V2000
    0.7145   -1.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.3899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.5649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.1524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303    1.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303    1.7171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.1524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8966    2.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8966    1.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6111    0.9375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6111    0.1125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8966   -0.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8966   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8966   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0716   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7216   -1.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1821    0.1125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1821    0.9375    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 13 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0294965

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C1CCC(C)(O)CC1.CC1=CCC(CC1)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/2C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11;1-8(2)9-4-6-10(3,11)7-5-9/h4,9,11H,5-7H2,1-3H3;9,11H,1,4-7H2,2-3H3

> <INCHI_KEY>
MGABGZGUMNDCSN-UHFFFAOYSA-N

> <FORMULA>
C20H36O2

> <MOLECULAR_WEIGHT>
308.506

> <EXACT_MASS>
308.271530399

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
18.830790442429034

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol; 2-(4-methylcyclohex-3-en-1-yl)propan-2-ol

> <JCHEM_LOGP>
2.2322311779999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.002116372471004

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0482742986811822

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
47.3894

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
terpineol; β-terpineol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  -3.364   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -2.594   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -3.364   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -1.054   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -0.284   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334   1.256   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   2.026   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.990   3.205   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.990   3.205   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.334   1.256   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -0.284   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.274   4.060   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.274   2.520   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.607   1.750   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.607   0.210   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.274  -0.560   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.274  -2.100   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.274  -3.640   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.734  -2.100   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.814  -2.100   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.940   0.210   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.940   1.750   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10    4                                                       
CONECT   12   13                                                            
CONECT   13   12   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17                                                            
CONECT   21   16   22                                                       
CONECT   22   21   13                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₆O₂

Average Mass

308.5060 Da

Monoisotopic Mass

308.27153 Da

IUPAC Name

1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol; 2-(4-methylcyclohex-3-en-1-yl)propan-2-ol

Traditional Name

terpineol; β-terpineol

CAS Registry Number

Not Available

SMILES

CC(=C)C1CCC(C)(O)CC1.CC1=CCC(CC1)C(C)(C)O

InChI Identifier

InChI=1S/2C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11;1-8(2)9-4-6-10(3,11)7-5-9/h4,9,11H,5-7H2,1-3H3;9,11H,1,4-7H2,2-3H3

InChI Key

MGABGZGUMNDCSN-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
Aristolochia asclepiadifolia	LOTUS Database	35616633
Artemisia tridentata	LOTUS Database	35616633
Carica papaya	LOTUS Database	35616633
Chaerophyllum bulbosum	LOTUS Database	35616633
Chrysanthemum indicum	LOTUS Database	35616633
Cymbopogon citratus	LOTUS Database	35616633
Melaleuca alternifolia	LOTUS Database	35616633
Narcissus tazetta	LOTUS Database	35616633
Ocimum campechianum	LOTUS Database	35616633
Osmitopsis asteriscoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Menthane monoterpenoids

Alternative Parents

Substituents

P-menthane monoterpenoid
Monocyclic monoterpenoid
Cyclohexanol
Tertiary alcohol
Cyclic alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Not Available

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	2.23	ChemAxon
pKa (Strongest Acidic)	19	ChemAxon
pKa (Strongest Basic)	-1	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	47.39 m³·mol⁻¹	ChemAxon
Polarizability	18.83 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

Not Available

Chemspider ID

17339370

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16211350

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for terpineol; terpineols (NP0294965)

MOL for NP0294965 (terpineol; terpineols)

3D MOL for NP0294965 (terpineol; terpineols)

3D SDF for NP0294965 (terpineol; terpineols)

3D-SDF for NP0294965 (terpineol; terpineols)

PDB for NP0294965 (terpineol; terpineols)

3D PDB for NP0294965 (terpineol; terpineols)

SMILES for NP0294965 (terpineol; terpineols)

INCHI for NP0294965 (terpineol; terpineols)

Structure for NP0294965 (terpineol; terpineols)

3D Structure for NP0294965 (terpineol; terpineols)