NP-MRD: Showing NP-Card for 3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol (NP0163210)

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Record Information

Version

2.0

Created at

2022-09-02 21:46:40 UTC

Updated at

2022-09-02 21:46:41 UTC

NP-MRD ID

NP0163210

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol

Description

Piperitylmagnolol belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond. 3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol is found in Magnolia officinalis. Based on a literature review very few articles have been published on Piperitylmagnolol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022223462D          

 30 32  0  0  1  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
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  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
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 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 12 16  2  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
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 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 17 28  2  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  0  0  0  0
  9 30  2  0  0  0  0
  4 30  1  0  0  0  0
M  END

     RDKit          3D

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   -3.5007   -0.2166   -2.2816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8054   -0.0757   -3.7176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5520    0.1176   -1.2845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3838   -1.0055   -0.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0831   -0.7339    0.4543 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8646   -1.7608    1.5920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8086   -3.1477    1.0869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8074   -1.6168    2.7346 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4967   -0.1918   -0.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9248   -1.5256    0.0523 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1197    1.8272   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5257   -1.9146   -0.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5344    0.7468   -3.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3599   -1.0237   -3.9897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9218   -0.0661   -4.3689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4891    1.1017   -0.8365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5865   -0.0218   -1.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2304   -0.9298    0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4064   -1.9430   -0.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0829    0.2499    0.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1161   -3.9161    1.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
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 18 24  1  0
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  2 33  1  0
  1 31  1  0
  1 32  1  0
  5 36  1  0
  6 37  1  0
  8 38  1  0
M  END


  Mrv1652309022223462D          

 30 32  0  0  1  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
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  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
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M  END
> <DATABASE_ID>
NP0163210

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1CCC(C)=C[C@H]1C1=C(O)C(=CC(CC=C)=C1)C1=CC(CC=C)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H34O2/c1-6-8-20-11-13-27(29)24(15-20)26-17-21(9-7-2)16-25(28(26)30)23-14-19(5)10-12-22(23)18(3)4/h6-7,11,13-18,22-23,29-30H,1-2,8-10,12H2,3-5H3/t22-,23+/m0/s1

> <INCHI_KEY>
QIWQHZQTBNPZSG-XZOQPEGZSA-N

> <FORMULA>
C28H34O2

> <MOLECULAR_WEIGHT>
402.578

> <EXACT_MASS>
402.255880335

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
48.11397189877085

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(1S,6S)-3-methyl-6-(propan-2-yl)cyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol

> <ALOGPS_LOGP>
7.21

> <JCHEM_LOGP>
8.225517716333332

> <ALOGPS_LOGS>
-5.90

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.44692479349917

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.559647887466701

> <JCHEM_PKA_STRONGEST_BASIC>
-6.082884858848584

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
129.01899999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.06e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(1S,6S)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   30                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   30                                                  
CONECT   10    9   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   12   17                                                       
CONECT   17   16   18   28                                                  
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   18   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   17   10   29                                                  
CONECT   29   28                                                            
CONECT   30    9    4                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₄O₂

Average Mass

402.5780 Da

Monoisotopic Mass

402.25588 Da

IUPAC Name

3-[(1S,6S)-3-methyl-6-(propan-2-yl)cyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol

Traditional Name

3-[(1S,6S)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1CCC(C)=C[C@H]1C1=C(O)C(=CC(CC=C)=C1)C1=CC(CC=C)=CC=C1O

InChI Identifier

InChI=1S/C28H34O2/c1-6-8-20-11-13-27(29)24(15-20)26-17-21(9-7-2)16-25(28(26)30)23-14-19(5)10-12-22(23)18(3)4/h6-7,11,13-18,22-23,29-30H,1-2,8-10,12H2,3-5H3/t22-,23+/m0/s1

InChI Key

QIWQHZQTBNPZSG-XZOQPEGZSA-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
Magnolia officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Biphenyls and derivatives

Direct Parent

Biphenyls and derivatives

Alternative Parents

Substituents

Biphenyl
P-menthane monoterpenoid
Monoterpenoid
Monocyclic monoterpenoid
Aromatic monoterpenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	7.21	ALOGPS
logP	8.23	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	8.56	ChemAxon
pKa (Strongest Basic)	-6.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	129.02 m³·mol⁻¹	ChemAxon
Polarizability	48.11 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

9906886

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11732171

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol (NP0163210)

MOL for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

3D MOL for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

3D SDF for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

3D-SDF for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

PDB for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

3D PDB for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

SMILES for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

INCHI for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

Structure for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)

3D Structure for NP0163210 (3-[(1s,6s)-6-isopropyl-3-methylcyclohex-2-en-1-yl]-5,5'-bis(prop-2-en-1-yl)-[1,1'-biphenyl]-2,2'-diol)