NP-MRD: Showing NP-Card for Epifriedelanol (NP0137500)

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Record Information

Version

2.0

Created at

2022-05-30 16:54:17 UTC

Updated at

2022-05-30 16:54:17 UTC

NP-MRD ID

NP0137500

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Epifriedelanol

Description

4,4A,6b,8a,11,11,12b,14a-octamethyl-docosahydropicen-3-ol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Epifriedelanol is found in Acritopappus heterolepis, Ageratum houstonianum, Aglaomorpha quercifolia, Ardisia japonica, Artemisia annua, Aster ageratoides, Aster baccharoides, Aster koraiensis, Aster scaber, Baccharis neaei, Bistorta officinalis, Bridelia ferruginea, Calophyllum calaba, Calophyllum inophyllum, Cannabis sativa, Castanopsis eyrei, Celastrus hindsii, Chrysoma pauciflosculosa, Chuquiraga ulicina, Clusia nemorosa, Clusia rosea, Cratoxylum arborescens, Cuphea appendiculata, Desmodium incanum, Dimocarpus longan, Dittrichia viscosa, Drypetes gossweileri, Drypetes inaequalis, Putranjiva roxburghii, Duhaldea cappa, Elephantopus mollis, Elephantopus scaber, Elliottia paniculata, Erigeron canadensis, Eschenbachia blinii, Eugenia uniflora, Euphorbia antiquorum, Euphorbia sapinii, Euphorbia tithymaloides, Goniothalamus thwaitesii, Gynura japonica, Haplopappus foliosus, Heliotropium ellipticum, Hippophae rhamnoides, Hololepis pedunculata, Holoptelea integrifolia, Hypericum ascyron, Lasiolaena morii, Leucosyke quadrinervia, Macaranga tanarius, Mallotus macrostachyus, Mallotus metcalfianus, Mallotus pallidus, Mangifera indica, Monteverdia rigida, Maytenus salicifolia, Monteverdia ilicifolia, Monteverdia truncata, Olearia paniculata, Oreocnide frutescens, Pachysandra terminalis, Paralychnophora bicolor, Pentaclethra eetveldeana, Peritassa campestris, Phyllanthus reticulatus, Plenckia populnea, Pleurostylia opposita, Pyrus pyrifolia, Quercus glauca, Quercus salicina, Relhania acerosa, Rhododendron caucasicum, Rhododendron degronianum, Rhododendron formosanum, Santolina oblongifolia, Scaevola taccada, Sideritis soluta, Sphagneticola trilobata, Stevia lucida, Syzygium grande, Taiwanofungus camphoratus, Tanacetum densum, Triumfetta rhomboidea, Ulmus davidiana, Ulmus pumila, Viguiera decurrens and Xylosma longifolia. 4,4A,6b,8a,11,11,12b,14a-octamethyl-docosahydropicen-3-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161508422D          

 31 35  0  0  0  0            999 V2000
    6.4895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
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  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
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 15 16  1  0  0  0  0
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 19 20  1  0  0  0  0
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 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
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 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
 17 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 83 87  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004161508422D          

 31 35  0  0  0  0            999 V2000
    6.4895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  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
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
 17 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137500

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(O)CCC2C1(C)CCC1C2(C)CCC2(C)C3CC(C)(C)CCC3(C)CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H52O/c1-20-21(31)9-10-22-27(20,5)12-11-23-28(22,6)16-18-30(8)24-19-25(2,3)13-14-26(24,4)15-17-29(23,30)7/h20-24,31H,9-19H2,1-8H3

> <INCHI_KEY>
XCDQFROEGGNAER-UHFFFAOYSA-N

> <FORMULA>
C30H52O

> <MOLECULAR_WEIGHT>
428.745

> <EXACT_MASS>
428.401816294

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
54.51870979318285

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,4a,6b,8a,11,11,12b,14a-octamethyl-docosahydropicen-3-ol

> <ALOGPS_LOGP>
6.38

> <JCHEM_LOGP>
7.7307665856666645

> <ALOGPS_LOGS>
-7.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.215333803187104

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9550129944859601

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
131.1343

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.11e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,4a,6b,8a,11,11,12b,14a-octamethyl-hexadecahydropicen-3-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      12.114   3.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      13.654   0.770   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.574   3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.034   3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.264  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.334   3.437   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    2    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   30                                                  
CONECT   13   12    7   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   30                                             
CONECT   18   17                                                            
CONECT   19   17   20   26                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   19   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   12   17   31                                             
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Value	Source
3beta-Friedelinol	MeSH
Friedelinol	MeSH
Epifriedelanol	MeSH
Friedelinol, (3beta)-isomer	MeSH
Epi-friedelinol	MeSH

Chemical Formula

C₃₀H₅₂O

Average Mass

428.7450 Da

Monoisotopic Mass

428.40182 Da

IUPAC Name

4,4a,6b,8a,11,11,12b,14a-octamethyl-docosahydropicen-3-ol

Traditional Name

4,4a,6b,8a,11,11,12b,14a-octamethyl-hexadecahydropicen-3-ol

CAS Registry Number

Not Available

SMILES

CC1C(O)CCC2C1(C)CCC1C2(C)CCC2(C)C3CC(C)(C)CCC3(C)CCC12C

InChI Identifier

InChI=1S/C30H52O/c1-20-21(31)9-10-22-27(20,5)12-11-23-28(22,6)16-18-30(8)24-19-25(2,3)13-14-26(24,4)15-17-29(23,30)7/h20-24,31H,9-19H2,1-8H3

InChI Key

XCDQFROEGGNAER-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
Acritopappus heterolepis	LOTUS Database	35616633
Ageratum houstonianum	LOTUS Database	35616633
Aglaomorpha quercifolia	LOTUS Database	35616633
Ardisia japonica	LOTUS Database	35616633
Artemisia annua	LOTUS Database	35616633
Aster ageratoides	LOTUS Database	35616633
Aster baccharoides	LOTUS Database	35616633
Aster koraiensis	LOTUS Database	35616633
Aster scaber	LOTUS Database	35616633
Baccharis neaei	LOTUS Database	35616633
Bistorta officinalis	LOTUS Database	35616633
Bridelia ferruginea	LOTUS Database	35616633
Calophyllum calaba	LOTUS Database	35616633
Calophyllum inophyllum	LOTUS Database	35616633
Cannabis sativa	LOTUS Database	35616633
Castanopsis eyrei	LOTUS Database	35616633
Celastrus hindsii	LOTUS Database	35616633
Chrysoma pauciflosculosa	LOTUS Database	35616633
Chuquiraga ulicina	LOTUS Database	35616633
Clusia nemorosa	LOTUS Database	35616633
Clusia rosea	LOTUS Database	35616633
Cratoxylum arborescens	LOTUS Database	35616633
Cuphea appendiculata	LOTUS Database	35616633
Desmodium incanum	LOTUS Database	35616633
Dimocarpus longan	LOTUS Database	35616633
Dittrichia viscosa	LOTUS Database	35616633
Drypetes gossweileri	LOTUS Database	35616633
Drypetes inaequalis	LOTUS Database	35616633
Drypetes roxburghii	LOTUS Database	35616633
Duhaldea cappa	LOTUS Database	35616633
Elephantopus mollis	LOTUS Database	35616633
Elephantopus scaber	LOTUS Database	35616633
Elliottia paniculata	LOTUS Database	35616633
Erigeron canadensis	LOTUS Database	35616633
Eschenbachia blinii	LOTUS Database	35616633
Eugenia uniflora	LOTUS Database	35616633
Euphorbia antiquorum	LOTUS Database	35616633
Euphorbia sapinii	LOTUS Database	35616633
Euphorbia tithymaloides	LOTUS Database	35616633
Goniothalamus thwaitesii	LOTUS Database	35616633
Gynura japonica	LOTUS Database	35616633
Haplopappus foliosus	LOTUS Database	35616633
Heliotropium ellipticum	LOTUS Database	35616633
Hippophae rhamnoides	LOTUS Database	35616633
Hololepis pedunculata	LOTUS Database	35616633
Holoptelea integrifolia	LOTUS Database	35616633
Hypericum ascyron	LOTUS Database	35616633
Lasiolaena morii	LOTUS Database	35616633
Leucosyke quadrinervia	LOTUS Database	35616633
Macaranga tanarius	LOTUS Database	35616633
Mallotus macrostachyus	LOTUS Database	35616633
Mallotus metcalfianus	LOTUS Database	35616633
Mallotus pallidus	LOTUS Database	35616633
Mangifera indica	LOTUS Database	35616633
Maytenus rigida	LOTUS Database	35616633
Maytenus salicifolia	LOTUS Database	35616633
Monteverdia ilicifolia	LOTUS Database	35616633
Monteverdia truncata	LOTUS Database	35616633
Olearia paniculata	LOTUS Database	35616633
Oreocnide frutescens	LOTUS Database	35616633
Pachysandra terminalis	LOTUS Database	35616633
Paralychnophora bicolor	LOTUS Database	35616633
Pentaclethra eetveldeana	LOTUS Database	35616633
Peritassa campestris	LOTUS Database	35616633
Phyllanthus reticulatus	LOTUS Database	35616633
Plenckia populnea	LOTUS Database	35616633
Pleurostylia opposita	LOTUS Database	35616633
Pyrus pyrifolia	LOTUS Database	35616633
Quercus glauca	LOTUS Database	35616633
Quercus salicina	LOTUS Database	35616633
Relhania acerosa	LOTUS Database	35616633
Rhododendron caucasicum	LOTUS Database	35616633
Rhododendron degronianum	LOTUS Database	35616633
Rhododendron formosanum	LOTUS Database	35616633
Santolina oblongifolia	LOTUS Database	35616633
Scaevola frutescens	LOTUS Database	35616633
Sideritis soluta	LOTUS Database	35616633
Sphagneticola trilobata	LOTUS Database	35616633
Stevia lucida	LOTUS Database	35616633
Syzygium grande	LOTUS Database	35616633
Taiwanofungus camphoratus	LOTUS Database	35616633
Tanacetum densum	LOTUS Database	35616633
Triumfetta rhomboidea	LOTUS Database	35616633
Ulmus davidiana	LOTUS Database	35616633
Ulmus pumila	LOTUS Database	35616633
Viguiera decurrens	LOTUS Database	35616633
Xylosma longifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
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	6.38	ALOGPS
logP	7.73	ChemAxon
logS	-7	ALOGPS
pKa (Strongest Acidic)	19.22	ChemAxon
pKa (Strongest Basic)	-0.96	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	0	ChemAxon
Refractivity	131.13 m³·mol⁻¹	ChemAxon
Polarizability	54.52 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

348029

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Epifriedelanol (NP0137500)

MOL for NP0137500 (Epifriedelanol)

3D MOL for NP0137500 (Epifriedelanol)

3D SDF for NP0137500 (Epifriedelanol)

3D-SDF for NP0137500 (Epifriedelanol)

PDB for NP0137500 (Epifriedelanol)

3D PDB for NP0137500 (Epifriedelanol)

SMILES for NP0137500 (Epifriedelanol)

INCHI for NP0137500 (Epifriedelanol)

Structure for NP0137500 (Epifriedelanol)

3D Structure for NP0137500 (Epifriedelanol)