NP-MRD: Showing NP-Card for abietyl alcohol (NP0291297)

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Record Information

Version

1.0

Created at

2022-09-09 22:20:10 UTC

Updated at

2022-09-09 22:20:11 UTC

NP-MRD ID

NP0291297

Secondary Accession Numbers

None

Natural Product Identification

Common Name

abietyl alcohol

Description

Abietinol, also known as abietyl alcohol, belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Abietinol is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Abietinol has been detected, but not quantified in, several different foods, such as malabar plums, red rices, nopals, conchs, and spirulina. abietyl alcohol is found in Abies firma, Abies pinsapo, Cedrus atlantica, Juniperus excelsa, Juniperus sabina, Juniperus thurifera, Picea glehnii and Solidago rugosa. It was first documented in 2000 (PMID: 11413487). This could make abietinol a potential biomarker for the consumption of these foods (PMID: 16902246) (PMID: 17374880) (PMID: 20044567).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    5.1004    0.5664   -0.9845 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6657   -0.0926    0.3304 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9550   -1.5677    0.1738 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2394    0.1542    0.5816 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3916   -0.8611    0.6449 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9947   -0.5771    0.8938 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2160   -1.5251    1.3896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2193   -1.1042    1.6037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6882   -0.6301    0.2303 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8306    0.4569   -0.2963 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1985    0.0726   -1.6440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6069    1.7423   -0.5887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    1.3402   -1.5457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6865    0.4972   -0.8172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1464   -0.3533    0.2723 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6109    0.2031    1.6213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8581   -1.7140    0.1608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2298   -1.5651    0.1905 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3473    0.7367    0.6244 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3930    1.6022   -0.0355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    1.5127    0.7778 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    0.0152   -1.7849 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2025    0.4002   -1.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8759    1.6371   -1.0012 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3050    0.3033    1.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0179   -1.7528   -0.0864 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6507   -2.0942    1.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3604   -1.9641   -0.6721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7146   -1.9061    0.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5668   -2.5131    1.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7561   -1.9949    1.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1765   -0.2957    2.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5291   -1.5338   -0.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7483   -0.4707   -1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8850   -0.6590   -2.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0138    0.9396   -2.2764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0462    2.1697    0.3135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9455    2.4395   -1.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3089    0.7786   -2.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2015    2.2464   -1.9244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2472   -0.0996   -1.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4838    1.1857   -0.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8654    0.8197    2.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5006    0.8736    1.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9663   -0.5795    2.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5489   -2.1147   -0.8291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5193   -2.4140    0.9293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5413   -1.4400   -0.7383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0259    1.2401    1.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5923    1.3365   -1.0830 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0263    2.6547    0.0090 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3574    1.5855    1.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3858    2.3126    0.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  6
 10 19  1  0
 19 20  1  0
 20 21  1  0
 21  4  1  0
 19  6  1  0
 10  9  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  5 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  6
 16 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 14 41  1  0
 14 42  1  0
 13 39  1  0
 13 40  1  0
 12 37  1  0
 12 38  1  0
 11 34  1  0
 11 35  1  0
 11 36  1  0
 19 49  1  1
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
M  END


  Mrv0541 05061308022D          

 21 23  0  0  0  0            999 V2000
    6.6809   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8742    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9557    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2684    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3237    0.8788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  5  1  0  0  0  0
 11  5  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 15  6  1  0  0  0  0
 15 12  2  0  0  0  0
 15 14  1  0  0  0  0
 16  7  2  0  0  0  0
 16 12  1  0  0  0  0
 17  8  1  0  0  0  0
 17 16  1  0  0  0  0
 18  9  1  0  0  0  0
 19  3  1  0  0  0  0
 19 10  1  0  0  0  0
 19 13  1  0  0  0  0
 19 18  1  0  0  0  0
 20  4  1  0  0  0  0
 20 11  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 13  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0291297

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC2=CCC3C(C)(CO)CCCC3(C)C2CC1

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h7,12,14,17-18,21H,5-6,8-11,13H2,1-4H3

> <INCHI_KEY>
GQRUHVMVWNKUFW-UHFFFAOYSA-N

> <FORMULA>
C20H32O

> <MOLECULAR_WEIGHT>
288.4675

> <EXACT_MASS>
288.245315646

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
36.28114792669106

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthren-1-yl]methanol

> <ALOGPS_LOGP>
5.72

> <JCHEM_LOGP>
4.480101304666667

> <ALOGPS_LOGS>
-4.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.65208138301447

> <JCHEM_PKA_STRONGEST_BASIC>
-1.201379603069471

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
91.27169999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-1-yl)methanol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      12.471  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.471   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.499   3.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.311  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.231  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.391  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.081   3.437   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.851  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.541   3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.461   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.771  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.391   2.104   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.784   2.630   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.701   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.161   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.851   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.081   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.771   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.231   2.104   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.541   0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.604   1.640   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5   10   11                                                       
CONECT    6    8   15                                                       
CONECT    7    9   16                                                       
CONECT    8    6   17                                                       
CONECT    9    7   18                                                       
CONECT   10    5   19                                                       
CONECT   11    5   20                                                       
CONECT   12   15   16                                                       
CONECT   13   19   21                                                       
CONECT   14    1    2   15                                                  
CONECT   15    6   12   14                                                  
CONECT   16    7   12   17                                                  
CONECT   17    8   16   20                                                  
CONECT   18    9   19   20                                                  
CONECT   19    3   10   13   18                                             
CONECT   20    4   11   17   18                                             
CONECT   21   13                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Value	Source
Abieta-7,13-dien-18-ol	HMDB
Abieta-7,13-diene-18-ol	HMDB
Abietadienol	HMDB
Abietol	HMDB
Abietyl alcohol	HMDB

Chemical Formula

C₂₀H₃₂O

Average Mass

288.4675 Da

Monoisotopic Mass

288.24532 Da

IUPAC Name

[1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,6,10,10a-decahydrophenanthren-1-yl]methanol

Traditional Name

(7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-1-yl)methanol

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC2=CCC3C(C)(CO)CCCC3(C)C2CC1

InChI Identifier

InChI=1S/C20H32O/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h7,12,14,17-18,21H,5-6,8-11,13H2,1-4H3

InChI Key

GQRUHVMVWNKUFW-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
Abies firma	LOTUS Database	35616633
Abies pinsapo	LOTUS Database	35616633
Cedrus atlantica	LOTUS Database	35616633
Juniperus excelsa	LOTUS Database	35616633
Juniperus sabina	LOTUS Database	35616633
Juniperus thurifera	LOTUS Database	35616633
Picea glehnii	LOTUS Database	35616633
Solidago rugosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

a diterpenoid (CPD-8691 )
an alcohol (CPD-8691 )

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	5.72	ALOGPS
logP	4.48	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	18.65	ChemAxon
pKa (Strongest Basic)	-1.2	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	91.27 m³·mol⁻¹	ChemAxon
Polarizability	36.28 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

HMDB0034736

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102461

PDB ID

Not Available

ChEBI ID

29510

Good Scents ID

Not Available

References

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
LOTUS database [Link]

Showing NP-Card for abietyl alcohol (NP0291297)

MOL for NP0291297 (abietyl alcohol)

3D MOL for NP0291297 (abietyl alcohol)

3D SDF for NP0291297 (abietyl alcohol)

3D-SDF for NP0291297 (abietyl alcohol)

PDB for NP0291297 (abietyl alcohol)

3D PDB for NP0291297 (abietyl alcohol)

SMILES for NP0291297 (abietyl alcohol)

INCHI for NP0291297 (abietyl alcohol)

Structure for NP0291297 (abietyl alcohol)

3D Structure for NP0291297 (abietyl alcohol)