NP-MRD: Showing NP-Card for 5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol (NP0191315)

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Record Information

Version

2.0

Created at

2022-09-04 08:13:44 UTC

Updated at

2022-09-04 08:13:44 UTC

NP-MRD ID

NP0191315

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol

Description

5-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3S,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol is found in Piper peltatum. Based on a literature review very few articles have been published on 5-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3S,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042210132D          

 46 47  0  0  1  0            999 V2000
    1.9520   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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 16 46  1  0  0  0  0
M  END

     RDKit          3D

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 12 13  2  3
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 13 15  1  0
  3  2  1  1
  2  1  2  3
 24 25  1  0
 20 22  1  0
 39 95  1  0
 39 96  1  0
 39 97  1  0
 40 98  1  0
 40 99  1  0
 40100  1  0
 37 94  1  0
 36 92  1  0
 36 93  1  0
 35 90  1  0
 35 91  1  0
 34 87  1  0
 34 88  1  0
 34 89  1  0
 32 86  1  0
 31 84  1  0
 31 85  1  0
 30 82  1  0
 30 83  1  0
 27 76  1  0
 27 77  1  0
 27 78  1  0
 28 79  1  0
 29 80  1  0
 29 81  1  0
 41101  1  0
 43102  1  0
 45103  1  0
 24 75  1  0
 46104  1  0
 17 72  1  0
 19 73  1  0
 21 74  1  0
  4 50  1  0
  4 51  1  0
  4 52  1  0
  5 53  1  0
  5 54  1  0
  6 55  1  0
  6 56  1  0
  7 57  1  0
  9 58  1  0
  9 59  1  0
  9 60  1  0
 10 61  1  0
 10 62  1  0
 11 63  1  0
 11 64  1  0
 12 65  1  0
 14 66  1  0
 14 67  1  0
 14 68  1  0
 15 69  1  0
 15 70  1  0
 15 71  1  0
  2 49  1  0
  1 47  1  0
  1 48  1  0
M  END


  Mrv1652309042210132D          

 46 47  0  0  1  0            999 V2000
    1.9520   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    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
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   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
    2.8579    3.3000    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    4.5375    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
    4.2868    4.1250    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
    2.1434   -2.8875    0.0000 O   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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -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 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2539   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.0125    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
   -3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -9.4875    0.0000 C   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
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   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
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  6  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  2  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  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  3 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  6  0  0  0
 28 29  2  0  0  0  0
 26 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 25 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
 23 44  1  0  0  0  0
 44 45  1  0  0  0  0
 22 46  2  0  0  0  0
 16 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0191315

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\CC[C@](C)(C=C)C1=CC(O)=C(O)C(=C1)C1=CC(=CC(O)=C1O)[C@@](C)(CC\C=C(/C)CCC=C(C)C)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C42H58O4/c1-11-41(9,23-15-21-31(7)19-13-17-29(3)4)33-25-35(39(45)37(43)27-33)36-26-34(28-38(44)40(36)46)42(10,12-2)24-16-22-32(8)20-14-18-30(5)6/h11-12,17-18,21-22,25-28,43-46H,1-2,13-16,19-20,23-24H2,3-10H3/b31-21+,32-22+/t41-,42+

> <INCHI_KEY>
FBBLBOYXADGJGC-MWFZOWTOSA-N

> <FORMULA>
C42H58O4

> <MOLECULAR_WEIGHT>
626.922

> <EXACT_MASS>
626.433510348

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
76.11374337647335

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3S,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol

> <JCHEM_LOGP>
12.41634089

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.346450248545052

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.618357739575982

> <JCHEM_PKA_STRONGEST_BASIC>
-6.317065925328074

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
200.95020000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
5-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3S,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       3.644  -2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.874  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.206  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.207  -9.240   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.127  -9.240   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.357 -10.574   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.001 -13.090   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -6.668 -13.090   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -5.335 -15.400   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -6.668 -17.710   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -8.002 -18.480   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -8.002 -20.020   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -9.336 -17.710   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   16                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    3   17   46                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   46                                                  
CONECT   23   22   24   44                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   41                                                  
CONECT   26   25   27   28   30                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28                                                            
CONECT   30   26   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   25   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   23   45                                                  
CONECT   45   44                                                            
CONECT   46   22   16                                                       
MASTER        0    0    0    0    0    0    0    0   46    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₅₈O₄

Average Mass

626.9220 Da

Monoisotopic Mass

626.43351 Da

IUPAC Name

5-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3S,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol

Traditional Name

5-[(3R,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3S,6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\CC[C@](C)(C=C)C1=CC(O)=C(O)C(=C1)C1=CC(=CC(O)=C1O)[C@@](C)(CC\C=C(/C)CCC=C(C)C)C=C

InChI Identifier

InChI=1S/C42H58O4/c1-11-41(9,23-15-21-31(7)19-13-17-29(3)4)33-25-35(39(45)37(43)27-33)36-26-34(28-38(44)40(36)46)42(10,12-2)24-16-22-32(8)20-14-18-30(5)6/h11-12,17-18,21-22,25-28,43-46H,1-2,13-16,19-20,23-24H2,3-10H3/b31-21+,32-22+/t41-,42+

InChI Key

FBBLBOYXADGJGC-MWFZOWTOSA-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
Piper peltatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Farsesane sesquiterpenoid
Sesquiterpenoid
Biphenol
Biphenyl
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
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	12.42	ChemAxon
pKa (Strongest Acidic)	8.62	ChemAxon
pKa (Strongest Basic)	-6.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	200.95 m³·mol⁻¹	ChemAxon
Polarizability	76.11 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	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

163193782

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol (NP0191315)

MOL for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

3D MOL for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

3D SDF for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

3D-SDF for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

PDB for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

3D PDB for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

SMILES for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

INCHI for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

Structure for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)

3D Structure for NP0191315 (5-[(3r,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-5'-[(3s,6e)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl]-[1,1'-biphenyl]-2,2',3,3'-tetrol)